WO2010027516A2

WO2010027516A2 - Transgenically preventing establishment and spread of transgenic algae in natural ecosystems

Info

Publication number: WO2010027516A2
Application number: PCT/US2009/005067
Authority: WO
Inventors: Jonathan Gressel; Shai Ufaz; Ofra Chen; Doron Eisenstadt
Original assignee: Jonathan Gressel; Shai Ufaz; Ofra Chen; Doron Eisenstadt
Priority date: 2008-09-05
Filing date: 2009-09-08
Publication date: 2010-03-11
Also published as: EP2384366A2; EP2384366A4; WO2010027516A3

Abstract

genetic mechanism for mitigating the effects of introgression of a genetically engineered genetic trait of cultivated algae or cyanobacteria to its wild type or to an undesirable, interbreeding related species. As well as preventing the establishment of the transgenic algae or cynobacteria in natural ecosystems.

Description

TITLE: TRANSGENICALLY PREVENTING ESTABLISHMENT AND SPREAD OF TRANSGENIC ALGAE IN NATURAL ECOSYSTEMS

INVENTORS: Jonathan GRESSEL, Shai UFAZ, Ofra CHEN, Doron EISENSTADT

PRIORITY: This application claims priority of US provisional applications numbers 61/191,169 filed on 09/05/2008; 61/191,167 filed on 09/05/2008; 61/191,453 filed on 09/09/2008; 61/192,447 filed on 09/18/2008; 61/274,608 filed on 08/19/2009; and US nonprovisional application number 12/322,686 that was filed on February 5* 2009.

Assignee: TransAlgae (Israel) Ltd.

FIELD AND BACKGROUND OF THE INVENTION

The present invention relates to a genetic mechanism for preventing the establishment of transgenic algae and cyanobacteria in natural ecosystems should they be released from enclosed cultivation.

Algae and cyanobacteria have recently attracted much interest as biofactories for production of foods, bioactive compounds and biofuels. Since algae and cyanobacteria need sunlight, carbon-dioxide, and water for growth, they can be cultivated in open or enclosed water bodies. These systems are vulnerable to being contaminated by other algal species and cyanobacteria. Similarly, the cultivated algae may escape outside the cultivation. This may become a serious concern when the cultivated cells are transgenically modified.

The release of organisms containing introgressed genetically engineered genetic traits may have negative environmental impacts and be of regulatory concern, and thus it is imperative that algae and cyanobacteria containing transgenic traits not establish outside of their place of cultivation. Various methods have been described for prevention of transgene flow in crop plants. We have previously described a method to mitigate the establishment of transgenes from crops that might disperse to the wild, either through seed or through gene introgression into weedy or wild relatives of crops, described in U.S. Patent applications 09/889,737 and 10/774,388 of which this application is a continuation in part. Both of the previous applications are incorporated herein by reference.

While the major type of introgression from transgenic crops is sexual interspecific genetic gene flow, and in some cases sexual gene flow to related species, in the case of algae and cyanobacteria it is mainly that they themselves will establish and propagate asexually, as sexual exchanges are quite rare with most algal and cyanobacterial species. Still, cyanobacteria can be subject to horizontal gene flow through phages and possibly by conjugation. Horizontal gene flow is rare in eukaryotic organisms including algae, but conjugation-like processes have been confirmed, intra-specifically in the laboratory by protoplast fusion (Sivan and Arad, 1998). What can occur in the laboratory at high frequency intra-specifically, can happen at much lower frequencies in nature, posing a finite risk, possibly even between related species. Thus, we here extend the concept described for higher plants in the above mentioned patent application to algae and cyanobacteria; tandemly combine a gene that is needed in the transgenic algae or cyanobacteria and poses a risk in natural ecosystems, with another gene that is either useful or neutral to the cultivated algae or cyanobacteria, but would be deleterious to the organisms in natural ecosystems such that there is a net fitness disadvantage. Because of the tandem construct, they remain genetically linked through asexual or sexual propagation, or gene flow. In cases where there is no sexual or asexual recombination, the genes may be introduced separately.

Thus, a series of genes that have either a neutral or desirable effect on the algae and cyanobacteria in cultivation but will prevent competition and establishment in the environment are genetically engineered into the algae and cyanobacteria. These would override any selective advantage derived from other possible transgenes that might provide a modicum of advantage in natural ecosystems.

Rapid domestication of algae and cyanobacteria as crops for Industrial and agricultural uses by transgenesls

Higher plants have been domesticated as crops since prehistory, by farmers who selected against a large number of traits that were valuable for wild species, but undesirable in agronomic practice. These differences between wild species and crops were further accentuated by selective breeding, and even more so by genetic engineering, which allowed introducing traits that were non-existent in the gene pool of the species, genus, family, or kingdom of the crop. Algae and cyanobacteria have only recently been considered for wide scale cultivation with domestication limited to mainly selection of organisms, occasionally with selection of strains or mutants with desired traits. Unlike crops, millennia of efforts have not been invested in their domestication, and in many cases the traits needed do not exist within the species. Genetic engineering allows one to rapidly fill the void of needed traits for rapid domestication (e.g. Gressel, 2008a). Indeed, large scale cultivation of algae has been plagued by problems that are analogous to agricultural production of crops (Gressel 2008b; Sheehan et al., 2004). These problems include contamination by other algae and cyanobacteria (analogous to weeds in crops), fungi, bacteria, viruses (analogous to pathogens of crops), zooplankton (analogous to arthropod pests of crops), low productivity, and especially of desired traits (dealt with in crops by breeding for millennia). With crops, the analogous problems with cultivation, light penetration, light use efficiency, heating, mineral nutrition, harvesting have been dealt with by breeding coupled with development of novel cultivation procedures, and are being continued with the added tools of genetic engineering, which allows bringing in traits not available in the organism's genome.

Introgression of genetically engineered traits: Needed traits could be artificially forced horizontally into the algae and cyanobacteria by genetic engineering to enhance cost-effectiveness (higher yields, new products, resistances to contaminations, adaptability to cultivation with high levels of light and carbon dioxide not presently occurring in their natural ecosystems). Detractors of both the process of genetic engineering and its products have raised the possibilities that the engineered algae and cyanobacteria would become uncontrollable problems if there was an inadvertent leak or spill from such cultivation into natural ecosystems. The benefits that accrue from cultivating transgenic algae and cyanobacteria, with their much higher primary productivity than terrestrial crops, could have great benefits to humanity by providing equivalent products on far less land area than conventional agriculture, often using seawater instead of potable fresh water, with far less fertilizer, and without fertilizer or pesticide run-off, allowing removing of agricultural land from production and putting the land to more environmentally sound use.

Risk analysis and risk mitigation: Tomes have been written on how to assess the risks of introgression in crops - some with continuing generalizations and some discussing how and why this assessment must be undertaken on a case by case basis (Regal, 1994; Keeler et al, 1996; Kareiva et al, 1996; de Kathen, 1998; Williamson, 1993; Timmons et al, 1996; Kjellsson et al, 1998; Sindel, 1997; Gressel and Rotteveel, 2000, Galun and Breman, 1997; Krimsky and Wrubel, 1996). There have been no published assessments on risks from transgenic algae, but it is clear that some traits being engineered into algae or cyanobacteria could give them a selective advantage in competing with other algae and cyanobacteria in natural ecosystems. This would include genes encoding enzymes that enhance utilization of fixed carbon and its sequestration into stored products such as fructose- 1 ,6-bisphosphate aldolase (ALD) and triose phosphate isomerase (TPI) as well as phosphoribosylphosphate synthetase (Ma et al. 2007; Kang, et al., 2005). Transgenes encoding resistance to viruses or phages could easily be predicted to supply a competitive advantage to the recipient. Similarly, genes for herbicide resistance could provide a selective advantage in the few areas where herbicides are used (typically in freshwater, not marine habitats). It might be harder to predict the competitive advantages of other genes such as enhanced or modified lipid, amino acid, protein or carbohydrate contents, but precaution might prevent the utilization of such genes, unless there are mechanisms in place to prevent their establishment in natural ecosystems, should they escape cultivation.

Two general approaches deal with the problems of transgene flow from crops that could be considered for use in algae and cyanobacteria: containment of the transgenes within the transgenic crop, and transgenic mitigation of the effects of the primary transgenic trait should it escape and move to an undesired target. Many containment efforts have depended upon physical containment (see Physical Gene Flow Barriers, page 61; in: Environmental issue report, No. 28, European Environmental Agency Publication No. 28, 2002), but it is breaches in physical containment that require precaution. Of the biological means such as apomixis, cleistogamy, male sterility and plastid transformation proposed for crops (see Biological Gene Flow Barriers, pages 60 and 61 ; in: Environmental issue report, No. 28, European Environmental Agency Publication No. 28, 2002, and Daniell (2002) and the recoverable block of function concept introduced in US Pat No. 6,849,776 or introduction lethal traits under control of inducible promoters (US Pat No. 5,723,765), none would preclude establishment of transgenic algae or cyanobacteria, except for cases where there might be rare sexual transmission. Thus, establishment of transgenic algae and cyanobacteria themselves, not just their introgressed offspring must be mitigated. Unfortunately, discussions of the hazards and risk assessment rarely consider how biotechnologies can be used to mitigate the risk of crop gene establishment in natural ecosystems (see Gressel 2008a as an exception), and there has been no discussion how this might be done for transgenic algae and cyanobacteria. There is thus a recognized need for, and it would be highly advantageous to have, failsafe anti-establishment, establishment-mitigating mechanisms to reduce the possibility of establishment of algae and cyanobacteria released to natural ecosystems that will also preclude establishment of rare cases where the transgenes interspecifically introgress into other algae or cyanobacteria.

SUMMARY OF THE INVENTION

According to the present invention a method is provided to obtain transgenic algae or cyanobacteria bearing at least one genetically engineered, commercially desirable genetic trait that is at risk of establishing in natural ecosystems (Table 1) but is tandemly linked to, and co-expressing at least one transgene (mitigating gene) that is desirable in or neutral to the cultivated transgenic algae or cyanobacteria but rendering the transgenic algae or cyanobacteria incapable of establishing by itself or in introgressed offspring in natural ecosystems (Table 2), thereby obtaining a cultivated algae or cyanobacteria capable of mitigating the effects of release of said genetically engineered, commercially desirable genetic trait of the algae or cyanobacteria in natural ecosystems. The sequence encoding the desirable genetic trait and the sequence of the mitigating gene remain genetically linked in the transgenic algae or cyanobacteria according to this invention, because of the introduction of the sequences in tandem. If there is no recombination in the species, the genes need not be tandemly linked. According to the present invention the transgene that prevents the establishment of the algae or cyanobacteria may be, one or more of the following:

1. a transgene encoding a reduced content of RUBISCO (ribulose 1,5 bis phosphate carboxylase/oxygenase) (such as an antisense or RNAi construct of the small or the large subunit of RUBISCO) which allows normal algae or cyanobacteria growth only at artificially high carbon dioxide concentrations, but not in natural environments; '

2. a transgene encoding reduced photosystem 2 antennae size such as tla\, which allows growth only at high light intensities but allows greater packing of cells in commercial production facilities with less light energy wasted as heat; such organisms would not have enough chlorophyll to compete with indigenous organisms in natural ecosystems. In cases where there is no recombination in the species, the gene of choice can be introduced into a mutant strain having a reduced antennae.

3. an antisense or RNAi construct of any of the genes encoding cilia or flagella (or similar motility organ) formation or action such that the transgenic algae or cyanobacteria cannot optimally position themselves based on environmental stimuli. Such movement is required to compete in natural ecosystems, but is unnecessary and utilizes energy in commercial cultivation;

4. a transgenic mutant form of the phytoene desaturase ipds) gene conferring resistance to phytoene desaturase inhibiting herbicides, which synthesizes less beta- carotene. The herbicide resistance allows controlling unwanted species in commercial culture and the less carotene is of little consequence in dense commercial culture but provides photoprotection to organisms in the natural environments and organisms with less beta carotene are less competitive in the natural ecosystems. Similarly, other herbicide resistances can be used;

5. a transgene in the anti-sense or RNAi form encoding one or more of the polymers of the cell walls such that the algae or cyanobacteria has a thinner cell wall. This thinner cell wall is of little consequence in commercial production, and the cell walls are the least commercially valued part of the cell, but organisms with thinner cell walls cannot compete in the variable vicissitudes of environmental conditions in natural ecosystems;

6. a transgene encoding a storage polymer such as inulin, levan or, graminan that the cell cannot later degrade for use as energy when needed, especially if coupled with a transgene in the RNAi or antisense form such as starch phosphorylase, precluding storage as starch. This is desirable in commercial production when the new polymer has a greater value than starch, but renders an organism that cannot mobilize reserves less fit in a natural environment, where it cannot compete with organisms that can mobilize reserves in times of need; or 7. any other transgene that is neutral or beneficial to the algae or cyanobacteria when cultivated commercially, but renders the algae or cyanobacteria unfit to compete in natural ecosystems, overcoming any benefit that may derive from the transgene tandem Iy bound to it.

Thus a method is provided to obtain a cultivated algae or cyanobacteria having multiple transgenes in tandem, (or in some cases separately introduced), derived from different sources with at least one of the transgenes capable of mitigating the fitness effects preventing stable establishment of at least one genetically engineered, commercially desirable genetic trait of the algae or cyanobacteria in natural ecosystems. According to yet another aspect of the present invention there is provided a method of obtaining a cultivated algae or cyanobacteria capable of mitigating the effects of self propagation or of asexual or sexual introgression of at least one genetically engineered, commercially desirable genetic trait to an undesirable species related to the cultivated algae or cyanobacteria, the method comprising transforming a population of the cultivated algae or cyanobacteria to express at least one genetically engineered commercially desirable genetic trait in the algae or cyanobacteria under genetic control of at least one genetic control element which is inexpressible by said undesirable interbreeding species related to the cultivated algae or cyanobacteria, thereby obtaining a cultivated algae or cyanobacteria capable of mitigating the effects of self propagation or of introgression of said genetically engineered, commercially desirable genetic trait of the cultivated algae or cyanobacteria to said undesirable species related thereto. According to a further aspect of the present invention there is provided a genetic construct for genetically modifying a cultivated algae or cyanobacteria to express a genetically engineered, commercially desirable genetic trait while mitigating the effects of establishment of self propagation or sexual or asexual gene introgression of said genetically engineered, commercially desirable genetic trait of the algae or cyanobacteria to an undesirable species related to the cultivated algae or cyanobacteria, the genetic construct comprising a first polynucleotide encoding said genetic trait and at least one additional polynucleotide comprising at least one control element which is expressible by the cultivated algae or cyanobacteria, said control element being inexpressible by said undesirable interbreeding species.

According to yet another aspect of the present invention there is provided a method of obtaining cultivated asexual, non-conjugating algae or cyanobacteria capable of mitigating the effects of self propagation of at least one genetically engineered, commercially desirable genetic trait in natural ecosystems, the method comprising transforming a population of the cultivated algae or cyanobacteria to express at least one genetically engineered, commercially desirable genetic trait into algae or cyanobacteria bearing a natural or induced mutation that acts as a mitigating genetic trait, wherein said mitigating genetic trait is selected such that a self propagated said mitigating genetic trait is less fit than native algae or cyanobacteria not expressing said mitigating genetic trait.

According to yet another aspect of the present invention there is provided a method of obtaining a cultivated algae or cyanobacteria capable of mitigating the effects of self propagation or of introgression of at least one genetically engineered, commercially desirable genetic trait to an undesirable, uncultivated interbreeding species related to the cultivated algae or cyanobacteria, the method comprising transforming a population of the cultivated algae or cyanobacteria to co-express at least one genetically engineered, commercially desirable genetic trait, and at least one genetically linked, mitigating genetic trait, wherein said mitigating genetic trait is selected such that a self propagated or undesirable, species introgressing genes from the transgenic alga or cyanobacterium related to the cultivated algae or cyanobacteria expressing said mitigating genetic trait is less fit than an undesirable uncultivated interbreeding/introgressing species related to the cultivated algae or cyanobacteria not expressing said mitigating genetic trait, thereby obtaining a cultivated algae or cyanobacteria capable of mitigating the effects of introgression of the at least one genetically engineered, commercially desirable genetic trait of the cultivated algae or cyanobacteria to the undesirable, uncultivated interbreeding species related thereto. According to further features in preferred embodiments of the invention described below, at least one commercially desirable genetic trait is selected from the group consisting of herbicide resistance, disease or zooplankton resistance, environmental stress resistance, the ability to fluoresce near ultraviolet light to photosynthetically usable light, high productivity, modified polysaccharide, protein or lipid qualities and quantities, enhanced yield, expression of heterologous products and other genetically modified algae and cyanobacteria products.

According to yet further features in preferred embodiments of the invention described below, the at least one mitigating genetic trait is selected from the group consisting of decreased RUBISCO, decreased storage or cell wall polysaccharides, decreased chlorophyll and/or carotene, decreased or eliminated motility organs, and increased non self metabolizable storage materials.

According to still further features in preferred embodiments of the invention described below, the at least one mitigating genetic trait is a reduced expression of endogenous genetic trait of said cultivated algae or cyanobacteria. According to further features in preferred embodiments of the invention described below, the cultivated algae or cyanobacteria is one of the following Synechococcus PCC7002, Phaeodactylum tricornutum, Nannochloropsis sp CS 246, Nannochloropsis oculata, Nannochloropsis salina, Pavlova lutheri CS 182, Synechococcus PCC7942, Synechosystis PCC6803, Chlamydomonas reinhardtii, Chlorella vulgaris, Chlorella ssp., Isochrysis sp. CS- 177 Tetraselmis chuii CS-26 Tetraselmis suecica CS- 187, and the commercially desirable genetic trait is single double or triple herbicide resistance, virus resistance, the ability to fluoresce near ultraviolet light as blue or red light, protein content modified to high lysine and methionine and enhanced non self metabolizable storage polysaccharides and the mitigating genetic trait is selected from the group consisting of reduced RUBISCO, lack of motility organs, reduced photosystem II antenna size, reduced carotene synthesis as part of resistance to phytoene desaturase inhibiting herbicides, and reduced storage starch formation. According to another aspect of the present invention there is provided a genetic construct for mitigating the effects of establishment by self propagation or introgression of a genetically engineered commercially desirable genetic trait of a cultivated algae or cyanobacteria to an undesirable species related to the cultivated algae or cyanobacteria, the genetic construct comprising a first polynucleotide encoding the at least one commercially desirable genetic trait and a second polynucleotide encoding at least one mitigating genetic trait, wherein said at least one mitigating genetic trait is selected such that an undesirable, species related to the cultivated algae or cyanobacteria expressing said at least one mitigating genetic trait is less fit than the undesirable species related to the cultivated algae or cyanobacteria not expressing said at least one mitigating genetic trait and wherein expression of said commercially desirable and said at least one mitigating genetic trait is genetically linked, and a genetically modified cultivated algae or cyanobacteria comprising the genetic construct. According to further features in preferred embodiments of the invention described below, said first and said second polynucleotides are covalently linked.

According to still further features in preferred embodiments of the invention described below, the first and said second polynucleotides are functionally linked.

According to yet further features in preferred embodiments of the invention described below, the first and second polynucleotides are co-transformed.

According to still further features in preferred embodiments of the invention described below, the first and second polynucleotides are integrated into the same chromosomal locus.

According to still further features in preferred embodiments of the invention described below, the first and second polynucleotides are integrated separately into an organism that has no known ability to exchange DNA among cells.

According to further features in preferred embodiments of the invention described below, the at least one commercially desirable genetic trait is selected from the group consisting of herbicide resistance, disease or zooplankton resistance, environmental stress resistance, the ability to fluorescence near ultraviolet light to photosynthetically usable light, high productivity, modified polysaccharide, protein or lipid qualities and quantities, enhanced yield, and expression of heterologous products and other genetically modified algae and cyanobacteria products.

The present invention successfully addresses the shortcomings of the presently known configurations by conceiving and providing a mechanism for mitigating the establishment of the transgenic algae or cyanobacteria and its progeny from establishing by self-propagation or the effects of introgression of a genetically engineered genetic trait of a alga or cyanobacteria to competing organisms. In the case of asexual organisms, where conjugation is unknown, it is sufficient that the mitigating gene be an irreversible mutation to a mitigating form.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention is herein described, by way of example only, with reference to the accompanying drawings. With specific reference now to the drawings in detail, it is stressed that the particulars shown are by way of example and for purposes of illustrative discussion of the preferred embodiments of the present invention only, and are presented in the cause of providing what is believed to be the most useful and readily understood description of the principles and conceptual aspects of the invention

Figure 1. Schematic diagram used to induce glyphosate resistant epsps in tandem with tlal RNAi in C. reinhardtii. The coding region of epsps is cloned under the control of the RbcS promoter. The RNAi cassette of tlal is cloned in tandem to the epsps, upstream to the RbcS terminator.

Figure 2. Schematic diagram used to induce HPPD in background mutant algae with reduced antenna size. The coding region of HPPD is cloned under the control of the RbcS promoter.

Figure 3. Schematic diagram used to induce the virus CAPSID and RbcS RNAi cassette in C. reinhardtii. The coding region of the CAPSID is cloned under the control of the RbcS promoter. The RbcS RNAi cassette is cloned in tandem to the CAPSID, upstream to the RbcS terminator.

Figure 4. Schematic diagram used to induce the virus CAPSID and RbcS antisense in the green alga C. reinhardtii. The coding region of the CAPSID is cloned under the control of the RbcS promoter and upstream to the RbcS terminator. The RbcS is cloned in an antisense orientation in tandem to the CAPSID, downstream to the RbcS promoter and upstream to the RbcS terminator.

Figure 5. Schematic diagram used to induce the virus CAPSID and RbcS antisense in cyanobacteria Synechococcus PCC7002. The coding region of the CAPSID is cloned under the control of the RbcS promoter and upstream to the RbcS terminator. The RbcS is cloned in an antisense orientation in tandem to the CAPSID, downstream to the RbcS promoter and upstream to the RbcS terminator.

Figure 6. Schematic diagram used to induce pds together with the high lysine BHL8 protein or high methionine 2S albumin protein in C. reinhardtii. The coding region of PDS is cloned under the control of the hsp70A and the RbcS promoters and upstream to the RbcS terminator. The BHL8 or 2S are cloned in tandem to PDS, downstream to the RbcS promoter and upstream to the RbcS terminator.

Figure 7. Schematic diagram used to induce pds together with the high lysine BHL8 protein or high methionine 2S albumin protein in cyanobacteria Synechococcus PCC7002. The coding region of pds is cloned under the control of RbcS promoter and upstream to the RbcS terminator. The BHL8 of 2S are cloned in tandem to pds, downstream to the RbcS promoter and upstream to the RbcS terminator.

Figure 8. Schematic diagram used to induce the MERA and MERE genes together with RNAi of stal (A) and the l-S5Tand 1 -FFT genes (B) in C. reinhardtii. The coding region of MERA is cloned under the control of the RbcS promoter and upstream to the RbcS terminator in tandem to merB, which is cloned under the control of the RbcS promoter and upstream to the RbcS terminator. This is in tandem to RNAi cassette of sta\ or staβ, which are cloned under the control of the RbcS promoter and upstream to the RbcS terminator. This together with the 1-SST and 1-FFT genes cloned each under the control of the RbcS promoter and upstream to the RbcS terminator.

Figure 9. Schematic diagram used to induce the BFP in the C. reinhardtii mutant odal2-l. The coding region of BFP is cloned under the control of the RbcS promoter and upstream to the RbcS terminator.

Figure 10. Schematic diagram used to induce the BFP and PiH antisense in cyanobacteria Synechococcus PCC7002. The coding region of BFP is cloned under the control of the RbcS promoter and upstream to the RbcS terminator. The PiIT is cloned in an antisense orientation in tandem to BFP, downstream to the RbcS promoter and upstream to the RbcS terminator.

Figure 11. Schematic diagram used to induce the PPO in the C. reinhardtii mutant oda 12-1.

DETAILED DESCRIPTION OF THE INVENTION

The present invention is of genetic mechanisms that can be used for preventing the establishment of transgenic algae or cyanobacteria in natural ecosystems and mitigating the effects of introgression of a genetically engineered genetic trait of a cultivated algae or cyanobacteria to an undesirable, related species of the algae or cyanobacteria. Specifically, the present invention can be used to preclude the establishment of self-propagated transgenic algae or cyanobacteria and mitigating the effects of introgression of genetically engineered traits related algae or cyanobacteria.

Before explaining at least one embodiment of the invention in detail, it is to be understood that the invention is not limited in its application to the details of construction and the arrangement of the components set forth in the following description or illustrated in the drawings. The invention is capable of other embodiments or of being practiced or carried out in various ways. Also, it is to be understood that the phraseology and terminology employed herein is for the purpose of description and should not be regarded as limiting.

Generally, the nomenclature used herein and the laboratory procedures in recombinant DNA technology described below are those well known and commonly employed in the art. Standard techniques are used for cloning, DNA and RNA isolation, amplification and purification. Generally enzymatic reactions involving

DNA ligase, DNA polymerase, restriction endonucleases and the like are performed according to the manufacturers' specifications. Generally, the nomenclature used herein and the laboratory procedures utilized in the present invention include molecular, biochemical, microbiological and recombinant DNA techniques. Such techniques are thoroughly explained in the literature. See, for example, Sambrook et al., (1989); Ausubel, R. M., ed. (1994); Ausubel et al (1989); Perbal, (1988); Watson et al., (1998); methodologies as set forth in U.S. Pat. Nos. 4,666,828; 4,683,202;

4,801,531; 5,192,659 and 5,272,057; Cellis, J. E., ed. (1994); Coligan J. E., ed. (1994); Stites et al. (eds), (1994); Mishell and Shiigi (eds), (1980); available immunoassays are extensively described in the patent and scientific literature, see, for example, U.S.

Pat. Nos. 3,791,932; 3,839,153; 3,850,752; 3,850,578; 3,853,987; 3,867,517;

3,879,262; 3,901,654; 3,935,074; 3,984,533; 3,996,345; 4,034,074; 4,098,876;

4,879,219; 5,011,771 and 5,281,521 ; Gait, M. J., ed. (1984); Hames, B. D., and Higgins S. J., eds. (1985); Hames, B. D., and Higgins S. J., eds. (1984); " Freshney,

R. L, ed. (1986); " (1986); Perbal, B., (1984) and "Methods in Enzymology" Vol. 1-

317, Academic Press; " (1990); Marshak et al., (1996).

Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, suitable methods and materials are described below.

As used herein the term genetically linked refers to a genetic distance smaller than 50 centiMorgan, preferably smaller than 40 centiMorgan, more preferably smaller than 30 centiMorgan, more preferably smaller than 20 centiMorgan, more preferably smaller than 10 centiMorgan, more preferably smaller than 5 centiMorgan, more preferably smaller than 1 centiMorgan, most preferably in the range of 0 to 1 centiMorgan, wherein 0 centiMorgan refers to juxtaposed sequences.

One of the greatest advantages of herbicide-resistant algae and cyanobacteria is that they allow control of closely-related algae and cyanobacteria that have the same herbicide selectivity spectrum as the cultivated algae and cyanobacteria and could not be previously controlled. Similarly, an advantage of disease resistant algae and cyanobacteria is that they will not be decimated by pathogens. Highly productive algae and cyanobacteria are also advantageous, as are algae and cyanobacteria with modified product such as different types of starch and oils. These, and other genetic traits have been or could be transgenically introduced into algae or cyanobacteria of various types (see Table 1, herein below).

Table 1: Commercially desirable traits that can be engineered into algae and cyanobacteria that may be undesirable if algae or cyanobacteria released into natural ecosystems

The advantages of transgenics are well appreciated, if there is no danger of establishment of the transgenic algae or cyanobacteria in natural ecosystems or introgression into a related alga or cyanobacterium. Because the advantages of transgenics are so great, as in the above cases, new modified transgenic algae and cyanobacteria are being developed.

Hence, while conceiving the present invention, the concept of mitigating the risks of establishment in natural ecosystems or introgression of a genetically engineered trait from the cultivated algae or cyanobacteria, it was conceived that the primary gene of choice having the desired trait should be in tandem constructs with "anti-establishment", mitigating genes (Table 2) conferring a disadvantage on the algae or cyanobacteria when in natural ecosystems or into introgessed progeny, while being benign or advantageous to the cultivated algae or cyanobacteria. This coupling can either be physical, where the two genes are covalently linked prior to transformation or by the same physical juxtaposition commonly achieved by co- transformation. Both will heretofore be termed "tandem", as the result in tightly linked genes. These would render individuals released to natural ecosystems unfit to act as competitors with its own wild type as well as other algae and cyanobacteria species.

In a special case, if the cultivated algae or cyanobacteria are asexual and non- conjugating, it is only necessary to mitigating the effects of self propagation. In that case the genetically engineered, commercially desirable genetic trait can be transformed into a population of the cultivated algae or cyanobacteria that express an irreversible (e.g. deletion) mutation conferring a mitigating trait. Such mutations exist in culture collections or can be obtained by mutagenesis, preferably by ultraviolet or gamma irradiation that causes deletions that cannot be reversed. Chemical mutagenesis, which typically causes point mutations in a single nucleotide can be reversed. Such mutations have been reported, e.g. in chloroplast antenna (Melis et al. 1998, Lee et al., 2002), with reduced RUBISCO (Khrebtukova and Spreitzer. 1996), lacking organs of motility (Okamoto and Ohmori 2002; Tanner et.al 2008). If the genetically engineered, commercially desirable genetic trait(s) is/are transformed into algae or cyanobacteria bearing such a natural or induced mutation that acts as a mitigating genetic trait, then they will be less fit than native algae or cyanobacteria and not be able to establish themselves in natural ecosystems.

As further detailed and exemplified herein below, genes that decrease RUBISCO or starch, remove cilia or other movement organelles among others would all be useful for that purpose, as they would often be benign or advantageous to the cultivated algae or cyanobacteria while detrimental establishment in the wild.

Table 2: Example of commercially desirable traits that can be engineered into algae and cyanobacteria that would render algae or cyanobacteria unfit and non-competitive if released into natural ecos stems.

A transgene encoding reduced content of RUBISCO (ribulose 1,5 bis phosphate carboxylase/oxygenase) (such as an antisense or RNAi construct of the small or the large subunit of RUBISCO) allows normal algae or cyanobacteria growth only at artificially high carbon dioxide concentrations.

A transgene or a mutation encoding reduced chlorophyll a oxygenase or reduced photosystem II antennae size, allows growth only at high light intensities but allows greater cell packing in commercial production facilities with less light energy wasted as heat; such organisms would not have enough chlorophyll to compete with indigenous organisms in natural ecosystems.

An antisense or RNAi construct of any of the genes encoding cilia or flagella (or similar motility organ) formation or action prevents the transgenic alga or cyanobacterium to position itself optimally based on environmental stimuli. Such movement is required to compete in natural ecosystems, but is unnecessary and wastes energy in commercial cultivation. A transgenic mutant form of the phytoene desaturase (pds) gene conferring resistance to phytoene desaturase inhibiting herbicides synthesizes less beta-carotene. The herbicide resistance allows controlling unwanted species in commercial culture and the less carotene is of little consequence in dense commercial culture but provides photoprotection to organisms in the natural environments and organisms with less beta carotene are less competitive in the natural ecosystems.

A transgene in the anti-sense or RNAi form encoding one of the genes encoding one or more of the polymers of the cell walls causes the alga or cyanobacterium to form a thinner cell wall. This thinner cell wall is of little consequence in commercial production, and the cell walls are the least commercially valued part of the cell, but organisms with thinner cell walls cannot compete in the variable vicissitudes of environmental conditions in natural ecosystems.

A transgene encoding a storage polymer such as inulin, levan, or graminan that is not degradable for use as energy when needed, especially if coupled with RNAi or antisense form of for example starch phosphorylase encoding gene whereby energy storage as starch becomes prevented. This is desirable in commercial production when the new polymer has a greater value than starch, but renders an organism that cannot mobilize reserves, less fit in a natural environment where it cannot compete with organisms that can mobilize reserves in times of need. A transgene in the anti-sense or RNAi form targeting the reduction of the nitrate reductase gene that catalyzes the last steps in the reduction of nitrate to NH₃. Unless ammonia is supplied exogenously this transgene will not be able to survive in a natural environment, where bacteria rapidly metabolize ammonia to nitrate.

A transgene in the anti-sense or RNAi form targeting the reduction of carbonic anhydrase or either encoding over expression of the gene, which also allows normal algae or cyanobacteria growth only at artificially high carbon dioxide concentrations, but not in natural environments.

Any other transgene that is neutral or beneficial to the algae or cyanobacteria when cultivated commercially, but renders the algae or cyanobacteria unfit to compete in natural ecosystems, overcoming any benefit that may derive form the transgene tandemly bound to it may be used as well. The present invention also provides a genetic construct for mitigating the effects of establishment or introgression of a genetically engineered commercially desirable genetic trait of a cultivated alga or cyanobacterium. The genetic construct comprises a first polynucleotide encoding at least one commercially desirable genetic trait and a second polynucleotide encoding at least one mitigating genetic trait.

Expression of the commercially desirable and the mitigating genetic trait is genetically linked. The polynucleotide encoding the first, primary genetic trait is preferably flanked on both sides by polynucleotides encoding the second, mitigating genetic trait, to thereby reduce the risk of losing the second, mitigating genetic trait due to mutation, etc.

However, it will be appreciated that in many cases while using conventional transformation techniques genetic traits carried on two different vectors integrate to the same locus.

Thus, according to a further aspect of the present invention there is provided a cultivated algae or cyanobacteria genetically modified to include the above described genetic constructs and to express the traits encoded thereby.

In one embodiment, the second, mitigating genetic trait is selected from the group consisting of reduced RUBISCO, reduced photosynthetic antennae, or reduced starch content or removal of cilia or other propelling organelles Numerous specific examples of such genetic traits are listed herein and are further discussed in the

Examples section that follows.

One such mitigating trait is reduced RUBISCO content. Genetically reduced

RUBISCO would be neutral or advantageous to the algae or cyanobacteria growing in saturating carbon dioxide, but deleterious to the algae or cyanobacteria in the wild, by themselves or in introgressed progeny, where carbon dioxide is limiting and there would not be enough enzyme to fix carbon dioxide.

Another such mitigating trait is decreased starch content. Such algae or cyanobacteria would be desirable as they would funnel more photosynthate to more valuable products, but without starch, such algae and cyanobacteria would not have the desired storage components to compete and exist in natural ecosystems

Yet another such mitigating trait is the reducing of the photosystem II antennae size by reducing the chlorophyll content (anti-sense or RNAi of the tlal or similar transgene, or a mutation encoding a reduced antenna) or by reducing the carotenoid content (using the mutant pds gene conferring herbicide resistance to fluridone and related herbicides). This is advantageous in high light intensity photobioreactors and shallow ponds, as it allows more biomass production and less photoinhibition, but in light-limiting natural ecosystems is highly deleterious.

Still another such mitigating trait is using mutants that are obtained transgenically that are less mobile.

Thus, these anti-establishment in natural ecosystem, introgression-mitigating traits are combined, according to the present invention, with the desirable genetically engineered traits, which genetically engineered traits include, but are not limited to, traits imposing resistance to herbicides, disease, zooplankton pests, and pathogens, resistance to environmental stress such as, but not limited to, heat, salinity, etc., and traits affecting yield, modified product and by-product quality, bioremediation, as well as expression of heterologous products and genetically modified products such as starches and oils, etc. Such traits for which genes has been isolated are well known in the art, for example, genes modifying fatty content [delta(12)-fatty acid dehydrogenase (fad2), fatty acid desaturase, and thioesterase (TE)], PAT), herbicide tolerance genes that collaterally control many bacteria and fungal pathogens (5-enolpyruvylshikimate- 3-phosphate synthase (EPSPS), acetolactate synthase, glyphosate oxidoreductase, nitrilase, phosphinothricin N-acetyltransferase), genes conferring favorable mutations (acetolactate synthase (ALS) and acetyl-CoA-carboxylase), and numerous viral resistance genes (helicase replicase and various specific viral coat protein genes). Additional suitable genes are listed in Table land summarized in many recent texts.

Once a gene responsible for a mitigating trait has been selected, it must be engineered for algal or cyanobacterial expression along with the desirable trait that confers an advantage thereto. To introduce such genes into algae or cyanobacteria, a suitable chimeric gene and transformation vector must be constructed. A typical chimeric gene for transformation will include a promoter region, a heterologous structural DNA coding sequences and a 3' non-translated polyadenylation site for algae. A heterologous structural DNA coding sequence means a structural coding sequence that is not native to the algae or cyanobacteria being transformed. Heterologous with respect to the promoter means that the coding sequence does not exist in nature in the same gene with the promoter to that it is now attached. Chimeric means a novel non-naturally occurring gene that is comprised of parts of different genes. In preparing the transformation vector, the various DNA fragments may be manipulated as necessary to create the desired vector. This includes using linkers or adaptors as necessary to form suitable restriction sites or to eliminate unwanted restriction sites or other like manipulations that are known to those of ordinary skill in the art.

Promoters that are known or found to cause transcription of a selected gene or genes in plant and bacterial cells can be used to implement the present invention in algae or cyanobacteria, respectively. Such promoters may be obtained from plants, plant pathogenic bacteria or plant viruses and include, but are not necessarily limited to, strong constitutive promoter such as a 35S promoter (Odell et al (1985) ), a 35S'3 promoter (Hull and Howell (1987) ) and the 19S promoter of cauliflower mosaic virus (CaMV35S and CaMV19S), the full-length transcript promoter from the figwort mosaic virus (FMV35S) and promoters isolated from plant genes such as EPSP synthase, ssRUBISCO genes. Selective expression in green tissue can be achieved by using, for example, the promoter of the gene encoding the small subunit of Rubisco ( EP 0 242 246). All of these promoters have been used to create various types of DNA constructs that have been expressed in plants. See, for example WO 84/02913 ). The particular promoter selected should be capable of causing sufficient expression to result in the production of an effective amount of the respective proteins to confer the traits.

A particularly useful promoter for use in some embodiments of the present invention is the full-length transcript promoter from the figwort mosaic virus (FMV35S). The FMV35S promoter is particularly useful because of its ability to cause uniform and high levels of expression in plant tissues. The DNA sequence of a FMV.35S promoter is presented in U.S.5,512,466 and is identified as SEQ ID NO:17 therein. The promoters used for expressing the genes according to the present invention may be further modified if desired to alter their expression characteristics. For example, the CaMV35S promoter may be ligated to the portion of the ssRUBISCO gene which represses the expression of ssRUBISCO in the absence of light, to create a promoter which is active in leaves but not in roots. The resulting chimeric promoter may be used as described herein. As used herein, the phrase "CaMV35S" or "FMV35S" promoter includes variations of these promoters, e.g., promoters derived by means of ligation with operator regions, random or controlled mutagenesis, addition or duplication of enhancer sequences, etc. The 3' non-translated region contains a polyadenylation signal that functions in algae (but not cyanobacteria) to cause the addition of polyadenylated nucleotides to the 3' end of an RNA sequence. Examples of suitable 3' regions are the 3' transcribed, non-translated regions containing the polyadenylation signal of plant genes like the 7s soybean storage protein genes and the pea E9 small subunit of the RuBP carboxylase gene (ssRUBISCO).

The RNAs produced by a DNA construct of the present invention also preferably contains a 5' non-translated leader sequence. This sequence can be derived from the promoters selected to express the genes, and can be specifically modified so as to increase translation of the mRNAs. The 5' non-translated regions can also be obtained from viral RNA's, from suitable eukaryotic genes, or from a synthetic gene sequence. The present invention is not limited to constructs wherein the non- translated region is derived from the 5' non-translated sequence that accompanies the promoter sequence. Rather, the non-translated leader sequences can be part of the 5' end of the non-translated region of the native coding sequence for the heterologous coding sequence, or part of the promoter sequence, or can be derived from an unrelated promoter or coding sequence as discussed above.

In a preferred embodiment according to the present invention, the vector that is used to introduce the encoded proteins into the host cells of the algae or cyanobacteria will comprise an appropriate selectable marker. In a more preferred embodiment according to the present invention the vector is an expression vector comprising both a selectable marker and an origin of replication. In another most preferred embodiment according to the present invention the vector will be a shuttle vector, which can propagate both in E. coli (wherein the construct comprises an appropriate selectable marker and origin of replication) and be compatible for propagation or integration in the genome of the plant organism of choice. In yet another embodiment, the construct comprising the promoter of choice, and the gene of interest is placed in a viral vector which is used to infect the cells. This virus may be integrated in the genome of the organism of choice or may remain non-integrated.

According to some embodiments of the present invention secretion of the protein or proteins out of the cell is preferred. In this embodiment the construct will comprise a signal sequence to effect secretion as is known in the art. For some applications, a signal sequence that is recognized in the active growth phase will be most preferred. As will be recognized by the skilled artisan, the appropriate signal sequence should be placed immediately downstream of the translational start site (ATG), and in frame with the coding sequence of the gene to be expressed. Introduction of the construct into the cells is accomplished by any conventional method for transfection, infection or the like as is known in the art including electroporation and biolistic transformations. In constructs comprising a selectable marker the cells may be selected for those bearing functional copies of the construct. If the plasmid comprising the gene of interest is episomal, the appropriate selective conditions will be used during growth. Stable transfectants and stable cell lines may be derived from the transfected cells in appropriate cases, in order to conveniently maintain the genotype of interest. Cell growth is accomplished in accordance with the cell type, using any standard growth conditions as may be suitable to support the growth of the specific cell line. A DNA construct of the present invention can be inserted into the genome of algae or cyanobacteria by any suitable method. Such methods may involve, for example, the use of liposomes, electroporation, chemicals that increase free DNA uptake such as polyethylene glycol (PEG), vacuum filtration, particle gun technology (biolistic bombardment with tungsten or gold particles; see, for example, U.S. 4,945,050; McCabe et al. (1988) ). Also see, Weissinger et al. (1988) Datta et al. (1990) Klein et al. (1988) ; Klein et al. (1988) ; Klein et al. (1988) ; Fromm et al. (1990) ; and Tomes et al. (1995); Hooydaas-Van Slogteren & Hooykaas (1984) ; Bytebier et al. (1987) ) and other mechanical DNA transfer techniques, and transformation using viruses Such techniques include, but are not limited to, injection methods or microprojectile methods, as described in detail herein below. Application of these systems to different species depends upon the ability to regenerate that particular algal or cyanobacterial species from protoplasts. An additional advantage of using a dual (tandem) system including a gene that may have an advantage in natural ecosystems with a mitigating gene is that the pair can be chosen in such a manner that one of the pair can have traits that will allow it to be used as a selectable marker, obviating the need for a separate selectable marker. Confirmation of the transgenic nature of the algal or cyanobacterial cells may be performed by PCR analysis, antibiotic or herbicide resistance, enzymatic analysis and/or Southern blots to verify transformation. Progeny of the initial algal or cyanobacterial strains may be obtained by continuous sub-culturing may be obtained and analyzed to verify whether the transgenes are heritable. Heritability of the transgene is further confirmation of the stable transformation of the transgene in the algae or cyanobacteria. The transgenic algae or cyanobacteria are then grown and harvested using conventional procedures.

Additional objects, advantages, and novel features of the present invention will become apparent to one ordinarily skilled in the art upon examination of the following examples, which are not intended to be limiting. Additionally, each of the various embodiments and aspects of the present invention as delineated herein above and as claimed in the claims section below finds experimental support in the following examples.

EXAMPLES

Reference is now made to the following examples, which together with the above descriptions, illustrate the invention in a non-limiting fashion. The concept of using genetic engineering to mitigate any positive effects transgenes may confer when released from controlled culture conditions into the natural environment, preventing the establishment of the transgenic algae or cyanobacteria and the products they may have from introgression to other species, is based on the following premise: If a transgene construct has in totality a small fitness disadvantage, it will remain localized as a very small proportion of the population. Therefore, gene establishment and flow should be mitigated by lowering the fitness of recipients below the fitness of the wild type so that they will not spread. This concept of "transgenic mitigation" (TM) was proposed for higher plants WO 04/46362, from which the present invention claims priority) and in a subsequent publication (Gressel, 1999: , see Figs. 9 and 10) in which mitigator genes are added to the desired primary transgene, which would reduce the fitness advantage to hybrids and their rare progeny, and thus considerably reduce risk. It is now extended to transgenic algae and cyanobacteria.

The TM approach is based on the facts that: 1) tandem constructs act as tightly linked genes, and their segregation from each other is exceedingly rare, far below the natural mutation rate; and 2) The TM traits chosen are selected to be nearly neutral or favorable to the cultivated crops, but deleterious to non-crop progeny (weeds, etc) due to a negative selection pressure; and 3) Individuals bearing even mildly harmful TM traits will be kept at exceedingly low frequencies in weed populations because weeds typically have a very high seed output and strongly compete amongst themselves, eliminating even marginally unfit individuals (Gressel, 1999). That this approach has been effective in higher plants has been illustrated in the following scientific publications: Al-Ahmad, et al., (2004; 2005; 2006, Al-Ahmad and Gressel, 2006).

Basically, in the cases of algae and cyanobacteria, these findings can be extended by tandemly combining almost any commercially useful trait that might spread in natural environments (Table 1) with a commercially neutral or advantageous trait that would render organisms unfit to compete in natural ecosystems (Table 2) as demonstrated in these few non-exclusive examples.

Example 1

Prevention of establishment and introgression ofglyphosate herbicide resistance by coupling with mutation in the tlal gene conferring a smaller photosynthetic antenna

One of the traits suitable for Transgenic Mitigation in constructs with a primary, desirable trait is down regulation of a form of the tlal gene (e.g. AF534571) that reduces the number of chlorophyll molecules in the antennae of photosystem II.

Such strains can live only in the high light intensity of bioreactors and shallow ponds, where they allow greater packing, but cannot compete with the superior light capture of organisms with full size antennae. Such organisms with full size antennae are kept out of the culture ponds by having traits such as glyphosate herbicide resistance. Rare algae or cyanobacteria introgressing the TM construct could also no longer compete with native organisms in natural ecosystems. In order to determine whether co- transformation of a desirable transgene with a mitigator gene would prevent proliferation of transgenic strains having the tandem construct can compete in the case of breach of containment, a tandem construct was made containing an EPSP synthase gene (enolphosphate shikimate phosphate synthase) gene (SEQ ID NO: 1) for glyphosate herbicide resistance as the primary desirable gene, and a RNAi cassette of the tlal gene (SEQ ID NO: 2) as a mitigator, and used to transform Synechococcus PCC7002, Phaeodactylum tricornutum, Nannochloropsis sp CS 246, Nannochloropsis oculata, Nannochloropsis salina, Pavlova lutheri CS 182, Synechococcus PCC7942, Synechosystis PCC6803, Chlamydomonas reinhardtii, Chlorella vulgaris, Chlorella ssp., Isochrysis sp. CS- 177 Tetraselmis chuii CS-26 Tetraselmis suecica CS- 187.

Experimental Procedures Assembling the tandem construct

A DNA fragment corresponding to nucleotides 1 to 293 of the C. reinhardtii tlal gene (AF534571) is de novo synthesized in sense and antisense orientation with a 50-bp DNA spacer separating the sense and antisense fragments (SEQ ID NO:2). This fragment is cloned under the control of the C. reinhardtii rbcS2B promoter and downstream to the de novo synthesized EPSPS gene (SEQ ID NO:1) in the plasmid pSP124s (Lumbreras et al. 1998) to generate plasmid pEPSPS-tlal (Fig. 1).

Another option: The de novo synthesized EPSPS gene for algae under the control of rbcS2 promoter and 3 'rbcS2 terminator, downstream to the ble selectable marker in the plasmid pSP124s (Lumbreras, Stevens et al. 1998) is transformed into the C. reinhardtii tlal mutant (Polle et al., 2003). The transformed algae will express the EPSPS gene on the background of the tlal deficient mutant.

Transformation of Algae

Algae cells in 0.4 ml of growth medium containing 5% PEG6000 were transformed with the pEPSPS-tlal plasmid (l±5mg) by the glass bead vortexing method (Kindle, 1990). The transformation mixture was then transferred to 10 ml of non-selective growth medium for recovery. The cells were kept for at least 18 h at 25⁰C in the light. Cells were collected by centrifugation and plated at a density of 10⁸ cells per 80 mm plate. Transformants were selected on fresh TAP agar plates containing 10 mM glyphosate, for 7-10 days at 30⁰C. Conditions are modified for each organism according to its needs, based on modifications of standard protocols.

Gene integration analyses of algal or cyanobacterial transformants Genomic DNA was isolated using either Stratagene's (La Jolla, Calif.) DNA purification kit or a combination of QIAGEN's (Valencia, Calif.) DNeasy plant mini kit and phenol chloroform extraction (Davies et al. 1992). Total RNA was isolated using either QIAGENS's Plant RNeasy Kit or the Trizol Reagent (Invitrogen, Carlsbad, Calif.). The DNA was analyzed by PCR for the presence of intact tandemly linked epsps and tla\ genomic insert. Four different DNA segments within the genomic TM T-DNA insert were amplified over the positions indicated in Figure 1 with the following primers: EPSPS forward primer 1 (SEQ ID NO:3): TCCCCGGCGACAAGAGCAT Tlal reverse primer 1 (SEQ ID NO:4): AAGAGCGCGGTTTGGTCAGC EPSPS forward primer 2 (SEQ ID NO:5): CACCGCATCGCCATGAGCTT Tlal Reverse primer 2 (SEQ ID NO:6): GCTGACCAAACCGCGCTCTT PCR reactions were carried out in 50 μL aliquots containing about 200 ng genomic DNA, 5 μL of 10 X DyNAzyme™ II buffer (Finnzymes Oy, ESPOO, Finland), 1.5 U of DyNAzyme™ II DNA polymerase (Finnzymes Oy, ESPOO, Finland), 5 μL of 2.5 mM of each dNTP(s) (Roche Diagnostics, GmbH), and 35 pmol of each primer, in sterile distilled water. The mixture was denatured for 3 min at 94° C and amplified for 35 cycles (94° C for 30 s, 51⁰C (DNA segments A and C) or 57° C (segments B and D) for 30 s, 72° C for 1 min) with a final cycle of 7 min at 72° C. The PCR products (15μL) were loaded directly onto 1% (w/v) agarose gels to verify single bands. The remaining PCR products were purified using the QIAquick PCR Purification Kit^® (Qiagen, Hilden, Germany) according to the manufacturer's instructions, and sequenced to confirm the integration of the TM T-DNA.

In vivo epsps assay. Putative transformed algal or cyanobacterial cells were cultured in a solution of 10 mM glyphosate in standard algae or cyanobacteria culture media. At this concentration, all non-transgenic cells are killed. In vivo tlal assay Putatively transformed algae or cyanobacteria cells were diluted and plated out and cultured on agar plates in standard algae or cyanobacteria culture media such that single cells develop into colonies. These colonies were light yellow green in color vs. wild type colonies that are dark green in color. Inheritance of the TM construct transgenes

Productivity of algae or cyanobacteria transformants at high light intensities: The transformants are analyzed for high productivity in full sunlight and lack of photoinhibition as previously demonstrated by US 20080120749 and by Poll et al., 2003. Competition of TM transgenics with the wild type algae and cyanobacteria

The transgenic TM algae or cyanobacteria were used to compete with natural species in simulated conditions. 1000 transgenic cells per ml were pipetted into unfiltered sea water in aquaria and cultivated in 100 μEin per cm² per sec light fluence, to simulate light conditions in the sea at a nominal depth. Aliquots were removed initially at daily, and later at weekly intervals, and the dwindling proportion of yellow green colonies are counted. Aliquots at the same dilutions were plated in parallel on the same media, but containing 10 mM glyphosate.

Within a few months, neither light yellow green colonies tlal colonies nor glyphosate resistant colonies could be found in the aquaria. All glyphosate resistant colonies were light green in color, demonstrating that the tandem traits do not segregate.

Example 2

Prevention of establishment and introgression of HPPD inhibiting herbicide resistance by coupling with a selected mutation a gene conferring a smaller photosynthetic antennae

One of the traits suitable for Mitigation in constructs with a primary, desirable trait is down regulation of a form of the tlal gene, as described in Example 1. Such modification of antenna size can be achieved by mutagenesis of the organism prior to introducing the commercial gene of choice. Such mutant strains can live only in the high light intensity of bioreactors and shallow ponds, where they allow greater packing, but cannot compete with the superior light capture of organisms with full size antennae. Such organisms with full size antennae are kept out of the culture ponds by having traits such as herbicide resistance, in this example resistance to inhibitors of the enzyme HPPD (4-hydroxyphenyl-pyruvate-dioxygenase). Rare escapes of algae or cyanobacteria bearing the HPPD gene in this background could no longer compete with native organisms in natural ecosystems. In order to determine whether transformation of a desirable transgene into an organism with a mutant mitigator gene would prevent proliferation of transgenic strains having the commercially desirable transgenic trait can compete in the case of breach of containment, a construct of Fig. 2 was made containing a HPPD ( AF000228) gene (SEQ ID NO:9) conferring resistance to the herbicide isoxaflutole (and related HPPD inhibiting herbicides), as the primary desirable gene, and used to transform Synechococcus PCC7002, Phaeodactylum tricornutum, Nannochloropsis sp CS 246, Nannochloropsis oculata, Nannochloropsis salina, Pavlova lutheri CS 182, Synechococcus PCC7942, Synechosystis PCC6803, Chlamydomonas reinhardtii, Chlorella vulgaris, Chlorella ssp, Isochrysis sp. CS- 177 Tetraselmis chuii CS-26 Tetraselmis suecica CS-187, bearing a mutation conferring small antennae size.

Experimental Procedures

Attaining reduced antennae mutants by UV mutagenesis with metronidazole selection. Metronidazole (2-methyl-5-nitroimidazole-l -ethanol) was shown to be effective for the selective enrichment of mutants of Chlamydomonas reinhardtii that possess impaired photosynthetic electron transport. More than 99.9% of wild-type cells were killed when incubated in the presence of 6-10 mM metronidazole for 24 hr under illumination of 7500 lux. Survival of wild-type cells in darkness and of mutants that are blocked at different steps in photosynthetic electron transport was nearly 100% when incubated in the presence of the drug under identical conditions (Schmidt et al. 1977).

We applied similar principles on Nannochloropsis sp. (strains CS 246 and CS 179). Cells were grown in Artificial Sea Water (ASW) (Guillard, 1962) enriched with f/2. 25ml of each cell culture in liquid media was placed in Petri dish and was exposed to UV irradiation (UV-C Lamp 30W) for 6.5 min. resulting in cell death of approximately 90%. The remaining cells were allowed a recovery time of 15 hrs. under dark conditions, then centrifuged (4000 rpm, 5 min.), re-suspended in 2 ml. 50- lOOμl were plated on 1% Bacto Agar ASW plates containing 1OmM metronidazole + 172 mineral supplement+ 1OmM HCO₃ ^" . Light intensity was maintained at -2000 lux with light duration of 14 hrs followed by 10 hrs. dark. The temperature was kept at 25°C.

To assess physiological properties of reduced antennae sized algae compared with their relevant wild type strains we performed a set of procedures that enabled us to evaluate each strain.

Initially, each modified strain is checked for the trait modified, (reduced antennae size). A screening process is established where colonies of mutant algae are allowed to grow on metronidazole containing agar plates to verify that the desired trait, i.e. reduced antennae size has been established and is maintained. Next, pale green growing colonies where picked and transferred to liquid medium for further physiological evaluation. This includes: Growth rate, Photosynthetic activity, Respiration activity, and Chlorophyll content

An overall report is generated for each strain that is used to estimate the feasibility of using the strain. Those with a near normal photosynthetic rate at high light intensities without photoinhibition , and a near normal growth rate are then used as a mitigation platform for further development. That they are unable to compete with wild type algae under open sea conditions is ascertained as in example 1.

Assembling the HPPD construct

The de novo synthesized HPPD gene for algae is cloned under the control of rbcS2 promoter and 3 'rbcS2 terminator, downstream to the ble selectable marker in the plasmid pSP124s (Lumbreras et al. 1998) and transformed into the algae bearing a mutation conferring small antennae size.

Transformation of Algae

Algae cells in 0.4 ml of growth medium containing 5% PEG6000 were transformed with the pHPPD plasmid (l±5mg) by the glass bead vortexing method (Kindle, 1990). The transformation mixture was then transferred to 10 ml of nonselective growth medium for recovery. The cells were kept for at least 18 h at 25°C in the light. Cells were collected by centrifugation and plated at a density of 10⁸ cells per 80 mm plate. Transformants were selected on fresh TAP agar plates containing 10 mM isoxaflutole, for 7-10 days at 30⁰C. Conditions are modified for each organism according to its needs, based on modifications of standard protocols.

Gene integration analyses of algal or cyanobacterial transformants

Genomic DNA was isolated using either Stratagene's (La Jolla, Calif.) DNA purification kit or a combination of QIAGEN's (Valencia, Calif.) DNeasy plant mini kit and phenol chloroform extraction (Davies et al. 1992). Total RNA was isolated using either QIAGENS's Plant RNeasy Kit or the Trizol Reagent (Invitrogen,

Carlsbad, Calif.).

The DNA was analyzed by PCR for the presence of intact HPPD insert as indicated in Figure 2 with the following primers:

HPPD forward primer 1 (SEQ ID NO:7): ATGG GCCACCAAAA CGCCGC HPPD reverse primer 2 (SEQ ID NO:8): CCCACTAACTGTTTGGCTTC

PCR reactions were carried out in 50 μL aliquots containing about 200 ng genomic DNA, 5 μL of 10 X DyNAzyme™ II buffer (Finnzymes Oy, ESPOO, Finland), 1.5 U of DyNAzyme™ II DNA polymerase (Finnzymes Oy, ESPOO, Finland), 5 μL of 2.5 mM of each dNTP(s) (Roche Diagnostics, GmbH), and 35 pmol of each primer, in sterile distilled water. The mixture was denatured for 3 min at 94⁰C and amplified for 35 cycles (94° C for 30 s, 51⁰C (DNA segments A and C) or 57° C (segments B and D) for 30 s, 72⁰C for 1 min) with a final cycle of 7 min at 72⁰C. The PCR products (15μL) were loaded directly onto 1% (w/v) agarose gels to verify single bands. The remaining PCR products were purified using the QIAquick PCR Purification Kit^® (Qiagen, Hilden, Germany) according to the manufacturer's instructions, and sequenced to confirm the integration of the TM T-DNA.

In vivo HPPD assay. Putative transformed algal or cyanobacterial cells were cultured in a solution of 10 mM isoxaflutole in standard algae or cyanobacteria culture media. At this concentration, all non-transgenic cells are killed.

Productivity of algae or cyanobacteria transformants at high light intensities: The transformants are analyzed for high productivity in full sunlight and lack of photoinhibition as previously demonstrated by US20080120749 and by Poll et al., 2003.

Competition of TM transgenics with the wild type algae and cyanobacteria

The transgenic TM algae or cyanobacteria were used to compete with natural species in simulated conditions. 1000 transgenic cells per ml were pipetted into unfiltered sea water in aquaria and cultivated in 100 μEin per cm per sec light fluence, to simulate light conditions in the sea at a nominal depth. Aliquots were removed initially at daily, and later at weekly intervals, and the dwindling proportion of yellow green colonies are counted. Aliquots at the same dilutions were plated in parallel on the same media, but containing 10 mM isoxaflutole.

Within a few months, neither light yellow green colonies mutant colonies nor isoxaflutole resistant colonies could be found in the aquaria. All isoxaflutole resistant colonies were light green in color, demonstrating that the traits do not segregate.

Example 3Prevention of establishment and introgression of virus resistance by coupling with the transgenes conferring a lowered RUBISCO content

One of the traits suitable for Transgenic Mitigation in constructs with a primary, desirable trait is using an antisense or RNAi form of one or both of the subunits of the RUBISCO gene (such as GenBank Accessions XM_001702356, NC_005353) that cause the reduction of the number of RUBISCO molecules in the algae or cyanobacteria. Such strains can live only in the carbon dioxide levels artificially created by using carbon dioxide enrichment - such as from flue gasses from industrial sources to facilitate high levels of carbon fixation in bioreactors and shallow ponds. In this situation, lower levels of the low affinity RUBISCO are needed as the carbon dioxide levels in the ponds are at least 100 fold greater than ambient levels. Algae and cyanobacteria with less RUBISCO cannot compete in natural ecosystems with the superior carbon dioxide capture of native organisms with full RUBISCO content at the low ambient levels of carbon dioxide. Such organisms with full RUBISCO complement are kept out of the culture ponds by having traits such as herbicide resistance (Example 1). Rare algae or cyanobacteria introgressing the TM construct can also no longer compete with native organisms in natural ecosystems. In order to determine whether co-transformation of a desirable transgene with a mitigator gene would prevent proliferation of transgenic strains having the tandem construct can compete in the case of breach of containment, a tandem construct is made containing a desirable gene encoding a gene conferring virus resistance ( M85052) as the primary desirable gene, and the rubisco mutant gene as a mitigator ( XM OO 1702356). Genes conferring resistance to viruses or phages specifically pathogenic to Synechococcus PCC7002, Phaeodactylum tricornutum, Nannochloropsis sp CS 246, Nannochloropsis oculata, Nannochloropsis salina, Pavlova lutheri CS 182, Synechococcus PCC7942, Synechosystis PC

Assembling the tandem construct

Generation of Chlamydomonas reinhardtii expressing the virus CAPSID and the RNAi of rbcS2B under the control of the rbcS2 promoter

The chlorella virus capsid sequence is chemically synthesized using the published sequence ( M85052 ) with modifications according to the codon usage of the green algae Chlamydomonas reinhardtii (SEQ ID NO: 12). The gene is cloned under the control of the RbcS2 promoter in the plasmid pSP124S (Sizova et al. 2001).

For generation of RNAi of rbcS2B, a 248 bp fragment corresponding to the coding sequence of rbcS is amplified with primers : TCTAGA CTGCAG CGCCGTCATTGCCAAGTCCT (SEQ ID NO: 10) adding Xbal and Pstl and GGATCC AAGCTT AATGTAGTCGACCTGGGCGG (SEQ ID NO: 1 1) adding BamHI and HindIII restriction in their 5' flanking region. The PCR product is cloned in forward and reverse orientations into the Pstl/BamHI and Hindlll/Xbal sites of the pSTBlue-1 vector (Novagen, Madison, WI, USA), flanking a 200-bp DNA spacer previously inserted into the EcoRV site. The rbcS RNAi cassette is then excised from pSTBlue-1 by Xbal digestion and is cloned downstream to the virus capsid in the corresponding site of pSP124S (Lumbreras, Stevens et al. 1998) (Fig. 3).

Generation of Chlamydomonas reinhardtii expressing the virus CAPSID and the antisense rbcS2B gene under the control of the rbcS2 promoter The chlorella virus CAPSID sequence is chemically synthesized using the published sequence (M85052 ) with modifications according to the codon usage of the green algae Chlamydomonas reinhardtii (SEQ ID NO: 12). The gene is cloned into pGEM-T vector (Promega) and then transferred under the control of the RbcS2 promoter in the plasmid pSP124S (Sizova et al. 2001).

For generation of antisense of rbcS2B gene, the 567 bp fragment of the C. reinhardtii rbcS2B gene (SEQ ID NO:57) is PCR amplified with the forward primer: TCTAGA ATGGCCGCCGTCATTGCCAAG (SEQ ID NO: 13) and the reverse primer:

TCTAGA ACGAGCGCCTCCATTTACACG (SEQ ID NO: 14), containing the Xbal site in their 5' region, and is cloned into pGEM-T (Promega). The Xbal fragment is then cloned downstream to the virus capsid in the corresponding site of pSP124S (Lumbreras, Stevens et al. 1998) (Fig. 4).

Transformation of Algae

Algae cells in 0.4 ml of growth medium containing 5% PEG6000 are transformed with the pCAPSID- (anti)RUBISCO plasmid (l±5mg) by the glass bead vortexing method (Kindle, 1990). The transformation mixture is then transferred to 10 ml of non-selective growth medium for recovery. The cells are kept for at least 18 h at 25° C in the light. Cells were collected by centrifiigation and plated at a density of 10⁸ cells per 80 mm plate. Selection is made according to (Van Etten et al., 1983). Briefly, transformants are grown to a density of 2 x 10⁷ to 3 x 10⁷ algae per milliliter, concentrated by centrifiigation, and resuspended in MBBIM (Van Etten et al., 1983) at 38 x 10⁷ algae per milliliter. Two hundred microliters of algae (7.6 x 10⁷ algae) plus 100 μl of appropriate dilutions of the virus are added to 2.5 ml of 0.7 percent agar in MBBM (48⁰C to 50⁰C) and immediately overlaid on petri plates containing 15 ml of MBBM plus 1.5 percent agar. The plates are then incubated at 25°C in continuous light. Plaques are visible after 2-4 days. Conditions are modified for each organism according to its needs, based on modifications of standard protocols.

Generation of cyanobacteria Synechococcus PCC7002 expressing the virus capsid and the antisense of rbcS gene under the control of the rbcS2 promoter

The Synechococcus virus (Syn9) capsid gene is chemically synthesized using the published sequence ( 4239190 ) (SEQ ID NO: 15) and is directly cloned downstream to the RbcS promoter in the pCB4 plasmid. The coding sequence of Synechococcus PCC7002 rbcS2B (SEQ ID NO:66) is amplified using the forward primer: (SEQ ID NO: 16) and the reverse primer: GTAACGGGTTTGGTTGGGC (SEQ ID NO: 17) harboring BamHI restriction sites in their 5' ends, followed by cloning into pGEM-T plasmid (Promega). The 333 bp fragment is then excised from the pGEM-T plasmid and cloned into the BamHI site in the shuttle vector pCB4 in an antisense orientation downstream to the virus capsid gene (Fig. 5).

Transformation of Cyanobacteria For transformation of Synechococcus PCC7002, cells are cultured in 100 ml of BG-1 1 liquid medium at 28°C under white fluorescent light and subcultured at the mid-exponential phase of growth. To 1.0 ml of cell suspension containing 2x10⁸ cells, which are cultured at the mid-exponential phase of growth, 0.5 or 1.0 μg of donor DNA (in 10 mM Tris/1 mM EDTA, pH 8.0) is added, and the mixture is incubated in the dark at 26°C overnight. After incubation for a further 6h in the light, the transformants are selected on BG-I l agar plates using the plaque selection assay which is preformed as described in (Wilson et al. 1993). Serial dilutions of the cyanophage filtrates are added to separate 0.5-ml volumes of a 4Ox concentration (ca. 8 x 10⁹ cells ml^"1) of exponentially growing Synechococcus PCC7002 that are incubated at 25° C for 1 h with occasional agitation to encourage cyanophage adsorption. Each phage-cell suspension is then added to 2.5 ml of 0.4% molten ASW agar (42° C); these suspensions are mixed gently and then poured evenly onto a solid 1% ASW agar plate (diameter, 85mm) before being left to set at room temperature for 1 h. Incubation of the plates is carried out at 25⁰ C under constant illumination (15 to 25 microeinsteins m^~2 s^"1), and the plates are monitored daily for the formation of plaques. Conditions are modified for each organism according to its needs, based on modifications of standard protocols.

Gene integration analyses of algal or cyanobacterial transformants Genomic DNA was isolated using either Stratagene's (La Jolla, Calif.) DNA purification kit or a combination of QIAGEN's (Valencia, Calif.) DNeasy plant mini kit and phenol chloroform extraction (Davies et al. 1992). Total RNA was isolated using either QIAGENS's Plant RNeasy Kit or the Trizol Reagent (Invitrogen, Carlsbad, Calif.).

The DNA was analyzed by PCR for the presence of intact tandemly linked

PBCV-I virus CAPSID -gene encoding resistance to Chlamydomonas virus, and low rubisco genomic insert. Four different DNA segments within the genomic TM T-

DNA insert were amplified over the positions indicated in Figure 4 with the following primers for algae: For CAPSID and RNAi of RUBISCO:

CAPSID Forward primer: ATGGCCGGCGGCCTGAGCCA (SEQ ID NO: 18)

Rubisco reverse of RNAi Reverse primer: AATGTAGTCGACCTGGGCGG (SEQ ID NO: 19)

For capsid and antisense of rubisco:

CAPSID Forward primer: ATGGCCGGCGGCCTGAGCCA (SEQ ID NO:20) rubisco Reverse primer: GTGTAAATGGAGGCGCTCGT (SEQ ID NO:21)

And the following primers for cyanobacteria CAPSID Forward primer: ATGTCTTTCCAAAACCTCCA (SEQ ID NO:22) rubisco Reverse primer: AGCCCAACCAAACCCGTTAC (SEQ ID NO:23)

In vivo virus assay. Putatively transformed and serially diluted algae or cyanobacteria cells are cultured in Petri dishes on standard algae or cyanobacteria culture media in an incubator with high carbon dioxide until colonies derived from single cells are apparent. The dishes are then inoculated with a solution containing virus, such that all non-transformed cells are killed.

In vivo rubisco assay Healthy colonies from the algae or cyanobacteria cells are picked and plated in marked replicates on agar plates in standard algae or cyanobacteria culture media. Two replicates of each colony are cultured in ambient carbon dioxide and two in >10% carbon dioxide. The colonies that grow the largest on the high carbon dioxide but hardly develop on ambient carbon dioxide are candidates for verification by western immunoblotting with commercial anti- RUBISCO antibody to demonstrate that indeed the amount of RUBISCO per cell is quite reduced

Competition of TM transgenics with the wild type algae and cyanobacteria The transgenic TM algae or cyanobacteria are used to compete with natural species in simulated conditions. 1000 transgenic cells per ml are pipetted into unfiltered sea water in aquaria and cultivated in 100 μEin per cm² per sec light fluence, to simulate light conditions in the sea at a nominal depth at ambient carbon dioxide levels. Aliquots are removed initially at daily, and later at weekly intervals, and the dwindling proportion of virus resistant colonies are counted.

Results Within a few months, no virus-resistant colonies can be found in the aquaria.

Example 4 Prevention of establishment of balanced protein containing transgenic lines of algae by engineering balanced protein into algae with fitness-lowering phytoene desaturase herbicide resistance

One of the traits suitable for Transgenic Mitigation in constructs with a primary, desirable trait is using a mutant form of the pds (phytoene desaturase) gene (e.g.AY639658) that confers resistance to the herbicide fluridone and related herbicides, but also reduces the carotene levels leaving algae more subject photoinhibition and to UV light^induced damage. Such strains can live only under high light intensity of bioreactors and shallow ponds, but in dense cultures, but cannot compete with the superior light capture of organisms with full size antennae with its complete complement of carotenoids. Such organisms with full size antennae are kept out of the culture ponds by having traits such as herbicide resistance, which is needed to prevent contamination in any event. Rare algae or cyanobacteria introgressing the TM construct could also no longer compete with native organisms in natural ecosystems. In order to determine whether co-transformation of a desirable transgene with a mitigator gene would prevent proliferation of transgenic strains having the tandem construct can compete in the case of breach of containment, a tandem construct was made. This tandem construct contained a modified high lysine or a modified high methionine or a fusion storage protein containing high levels of both as one of the primary desirable genes together with expression of feedback insensitive bacterial DHDPS (dihydrodipicolinate synthase) and with RNAi of LKR/SDH (lysine-ketoglutarate reductase/saccharopine dehydrogenase) as described previously (Zhu and Galili, 2004) to increase free lysine level or overexpression of cystathionine γ-synthase (CGS). CGS is the enzyme that controls the synthesis of the first intermediate metabolite in the methionine pathway to increase free methionine (Avraham et al., 2005). In addition the construct contained mutant pds gene (AY639658) for herbicide resistance as a mitigator gene as well as a desirable gene in its own right, and as a selectable marker to isolate transformants. The construct was used to transform Synechococcus PCC7002, Phaeodactylum tricornutum, Nannochloropsis sp CS 246, Nannochloropsis oculata, Nannochloropsis salina, Pavlova lutheri CS 182, Synechococcus PCC7942, Synechosystis PCC6803, Chlamydomonas reinhardtii, Chlorella vulgaris, Chlorella ssp., Isochrysis sp. CS-177 Tetraselmis chuii CS-26 Tetraselmis suecica CS- 187.

Experimental Procedures

Assembling the tandem construct

Generation of Chlamydomonas reinhardtii expressing PDS together with the high lysine BHL8 protein or high methionine 2S albumin protein For expression the de novo synthesized pds gene (SEQ ID NO:24) together with the high lysine BHL8 protein coding gene (SEQ ID NO:25) or high methionine 2S albumin coding gene (SEQ ED NO:26) in C. reinhardtii, the two genes are cloned under the control of the C. reinhardtii rbcS2 promoter and terminator and then combined into pSP124s replacing the ble selectable marker coding sequence (Fig. 6).

Generation of cyanobacteria Synechococcus PCC7002 expressing PDS together with the high lysine BHL8 protein or high methionine 2S albumin protein

For cyanobacteria, the de novo synthesized pds (SEQ ID NO:27) genes together with high lysine BHL8 protein coding gene (SEQ ID NO:28) or high methionine 2S albumin coding gene (SEQ ID NO:29) are cloned under the control of the constitutive promoter of the rbcLS operon (Deng and Coleman 1999) in the plasmid pCB4 by BamHI restriction sites, as well into various expression vectors, allowing various levels of expression driven by different promoters, including constitutive, inducible, and log phase temporal promoters (Fig. 7).

Transformation into algae was conducted as described in example 1. Transformation of Cyanobacteria

For transformation of Synechococcus PCC7002, cells are cultured in 100 ml of BG-1 1 liquid medium at 28°C under white fluorescent light and subcultured at the mid-exponential phase of growth. To 1.0 ml of cell suspension containing 2xlO⁸ cells, which are cultured at the mid-exponential phase of growth, 0.5 or 1.0 μg of donor

DNA (in 10 mM Tris/1 mM EDTA, pH 8.0) is added, and the mixture is incubated in the dark at 26° C overnight. After incubation for a further 6 h in the light, the transformants are directly selected on BG-11 agar plates containing 1.5% agar, 1 mM sodium thiosulfate and fluridone. The transformation frequency is calculated by counting the number of transformants.

Gene integration analyses of algae or cyanobacteria transformants

Genomic DNA is isolated using either Stratagene's (La Jolla, Calif.) DNA purification kit or a combination of QIAGEN's (Valencia, Calif.) DNeasy plant mini kit and phenol chloroform extraction (Davies et al. 1992). Total RNA was isolated using either QIAGENS's Plant RNeasy Kit or the Trizol Reagent (Invitrogen, Carlsbad, Calif.).

The DNA is analyzed by PCR for the presence of intact tandemly linked pds and BHL8 genomic insert. Four different DNA segments within the genomic TM T- DNA insert were amplified over the positions indicated in Figs. 6 and 7 with the following primers: forward primer: (SEQ ID NO:30): ATGACTGTTGCTAGGTCGGT (PDS) Reverse primer: (SEQ ID NO:31): GCACTTGGGGGTCTTGGCGA (BHL8)

PCR reactions is carried out in 50 μL aliquots containing about 200 ng genomic DNA, 5 μL of 10 X DyNAzyme™ II buffer (Finnzymes Oy, ESPOO, Finland), 1.5 U of DyNAzyme™ II DNA polymerase (Finnzymes Oy, ESPOO, Finland), 5 μL of 2.5 mM of each dNTP(s) (Roche Diagnostics, GmbH), and 35 pmol of each primer, in sterile distilled water. The mixture is denatured for 3 min at 94⁰C and amplified for 35 cycles (94⁰C for 30 s, 51° C (DNA segments A and C) or 57° C (segments B and D) for 30 s, 72⁰C for 1 min) with a final cycle of 7 min at 72⁰C. The PCR products (15μL) are loaded directly onto 1% (w/v) agarose gels to verify single bands. The remaining PCR products are purified using the QIAquick PCR Purification Kit^® (Qiagen, Hilden, Germany) according to the manufacturer's instructions, and sequenced to confirm the integration of the TM T-DNA.

In vivo pds assay. Putative algae or cyanobacteria cells are cultured in a solution of 100 μM fluridone in standard algae or cyanobacteria culture media and cultured in high light. At this concentration, all non-transgenic cells are bleached and eventually die.

In vivo meth/lys protein assay Picked colonies putative algae or cyanobacteria cells are separately cultured in wells of 96 well microplate dishes in standard algae or cyanobacteria culture media containing fluridone, until the cultures become dense. Dimethyl sulfoxide is added to each well and the cultures are allowed to bleach in the light. The bleached cultures are reacted with a fluorescent tagged antibody specific for the high lysine/methionine storage protein used in the transformation and the levels are measured with a microplate reader. Crude proteins are isolated from the cultures indicated to have acceptable growth rates and high levels antigenic proteins, digested and the proportion of lysine and methionine in crude protein is measured in a Moore- Stein type automated amino-acid analyzer.

Inheritance of the TM construct transgenes

Productivity of algae or cyanobacteria transformants at high light intensities: The transformants are analyzed for high productivity in full sunlight and freedom from undesirable algae and cyanobacteria in the presence of fluridone.

Competition of TM transgenics with the wild type algae and cyanobacteria The transgenic TM algae or cyanobacteria are used to compete with natural species in simulated conditions. 1000 transgenic cells per ml are pipetted into unfiltered sea water in aquaria and cultivated in 100 μEin per cm² per sec light fluence, to simulate light conditions in the sea at a nominal depth. Aliquots are removed initially at daily, and later at weekly intervals, and plated on dishes with and without fluridone. The dwindling proportion of fluridone resistant colonies are counted.

Results Within a few months, fluridone resistant colonies cannot be found in the aquaria. Example 5 Prevention of establishment of algal individuals transgenically resistant to PPO inhibiting herbicides by engineering PPO resistance into mutant algae lacking motility

One of the traits suitable for Transgenic Mitigation in constructs with a primary, desirable trait is to have cells incapable of phototactic/chemotactic or thermotactic motility such that they cannot swim in a direction that is optimal survival (such as odal-12 mutant for Chlamydomonas and the PUT accession NC_010475 for cyanobacteria). Such strains do not need motility to exist in continually mixed high cell density bioreactors and ponds, but cannot compete with native organisms in a natural ecosystem, where they must^' be able to swim towards optimal light and away from danger. Because they do not waste energy on motility, they have more energy available for making commercially needed components Potentially contaminating cells organisms are kept out of the culture ponds by having traits such as herbicide resistance. Rare non-motile algae or cyanobacteria introgressing the TM construct could also no longer compete with native organisms in natural ecosystems. In order to determine whether co-transformation of a desirable transgene with a mitigator gene prevents proliferation of transgenic strains having the tandem construct can compete in the case of breach of containment, a construct was made containing a PPO (protoporphyrinogen oxidase) gene ( DQ3861 14) (SEQ ID NO: 32) conferring pyrazoxyfen herbicide resistance (and other PPO related herbicides) as the primary desirable gene, in the background of the odal2-l mutant in algae or in tandem to the PiIT gene (SEQ ID NO:33) (NC_010475) from cyanobacteria conferring non swimming as a mitigator, and used to transform Synechococcus PCC7002, Phaeodactylum tricornutum, Nannochloropsis sp CS 246, Nannochloropsis oculata, Nannochloropsis salina, Pavlova lutheri CS 182, Synechococcus PCC7942, Synechosystis PCC6803, Chlamydomonas reinhardtii, Chlorella vulgaris, Chlorella ssp., Isochrysis sp. CS-177 Tetraselmis chuii CS-26 Tetraselmis suecica CS- 187. Transformants were selected on fresh TAP agar plates containing 10 mM pyrazoxyfen, for 7-10 days at 30⁰C. Conditions are modified for each organism according to its needs, based on modifications of standard protocols Experimental Procedures Assembling the tandem construct

Generation of Chlamydomonas containing a PPO herbicide resistant gene in the background of the odal2-l mutant

The odal2-l mutant lacks the entire LC2 + LClO genes. This strain exhibits a flagellar beat frequency that is consistently less than that observed for strains that fail to assemble the entire outer arm and docking complex (Tanner 2008). Therefore the PPO herbicide resistant construct is transformed in the background of the odal2-l mutant .

The PPO herbicide resistant sequence ( Patzoldt 2006) is synthesized using the published sequence ( DQ386114) (SEQ ID NO:32) with modifications according to the codon usage of the green algae C. reinhardtii. The gene is cloned into pGEM-T vector (Promega) and then transferred into pSP124S (Sizova et al. 2001) under the control of the RbcS2 promoter and 3 ' RbcS2 terminator. Fig. 1 1.

Another option is to produce either RNAi or antisense constructs directed against dynein heavy/light chains in tandem with the PPO herbicide resistant gene under the control of the RbcS2 promoter and 3 ' RbcS2 terminator in the pSP124S vector.

Transformation of algae

Algae cells in 0.4 ml of growth medium containing 5% PEG6000 are transformed with plasmid from examples 1 and 2 (l±5mg) by the glass bead vortexing method (Kindle 1990) or electroporation (Chow and Tung 1999). The transformation mixture is then transferred to 10 ml of non-selective growth medium for recovery. The cells are kept for at least 18 h at 25° C in the light. Cells are collected by centrifugation and plated at a density of 10⁸ cells per 80 mm plate.

For selection transformants were grown on fresh TAP agar plates containing 10 mM pyrazoxyfen, for 7-10 days at 30°C. Conditions are modified for each organism according to its needs, based on modifications of standard protocols Generation of cyanobacteria Synechococcus PCC7002 expressing a PPO herbicide resistant gene and the antisense of PUT gene under the control of the rbcS2 promoter

The PPO herbicide resistant gene (Patzoldt 2006) is chemically synthesized using the published sequence (DQ386114) (SEQ ID NO:32) with modifications according to the codon usage of Synechococcus PCC7002 (SEQ ID NO:35) and with the addition of BamHI restriction sites in its both ends. The gene is cloned into pGEM-T vector (Promega) and then transferred into the BamHI site of pCB4 plasm id

(Deng and Coleman, 1999) downstream to the Synechococcus rbcLS promoter and upstream to antisense of PUT gene (SEQ ID NO:33), followed by rbcLS terminator.

The coding sequence of Synechococcus PCC7002 PUT gene is amplified using the forward primer: ATGGATTACATGATCGAAGA (SEQ ID NO:36) and the reverse primer: GCGACGTTTTGCGGTTGGGC (SEQ ID NO:37) followed by cloning into pGEM-T plasmid (Promega). The fragment is then excised from the pGEM-T plasmid and cloned into the shuttle vector pCB4 in an antisense orientation downstream to the PPO herbicide resistant gene.

Transformation of cyanobacteria

For transformation of Synechococcus PCC7002, cells are cultured in 100 ml of ASN-III liquid medium at 28°C under white fluorescent light and subcultured at the mid-exponential phase of growth. To 1.0 ml of cell suspension containing 2x10⁸ cells, which are cultured at the mid-exponential phase of growth, 0.5 or 1.0 μg of donor DNA (in 10 mM Tris/1 mM EDTA, pH 8.0) is added, and the mixture is incubated in the dark at 26° C overnight. For selection transformants were grown on fresh TAP agar plates containing 10 mM pyrazoxyfen, for 7-10 days at 30⁰C.

Conditions are modified for each organism according to its needs, based on modifications of standard protocols. Surviving cells are then transferred for future culturing and further examination.

Gene integration analyses of algae or cyanobacteria transformants

Genomic DNA is isolated using either Stratagene's (La Jolla, Calif.) DNA purification kit or a combination of QIAGEN's (Valencia, Calif.) DNeasy plant mini kit and phenol chloroform extraction (Davies et al. 1992). Total RNA is isolated using either QIAGENS's Plant RNeasy Kit or the Trizol Reagent (Invitrogen, Carlsbad, Calif.).

The DNA is analyzed by PCR for the presence of intact PPO. primers for algae:

Forward primer: (SEQ ID NO:38) ATGGTAATTC AATCCATTAC

Reverse primer: (SEQ ID NO:39) CGGTCTTCTCATCCATCTTC And the following primers for cyanobacteria: Forward primer: CTGG ACTCTC ATATATACGT

(SEQ ID NO:40) from the PPO

Reverse primer: C AACCGC AAAACGTCGCTAA (SEQ ID NO 41) from PUT In vivo PPO assay. Putative transformed algal or cyanobacterial cells were cultured in a solution of 10 mM pyrazoxyfen in standard algae or cyanobacteria culture media. At this concentration, all non-transgenic cells are killed.

In vivo motility assay Picked pyrazoxyfen resistant algae or cyanobacteria cells are placed on a microscope slide and observed. The slide is then unilaterally illuminated and movement towards or away from the light (depending on intensity) is observed in wild type but not mutant cells . Competition of TM transgenics with the wild type algae and cyanobacteria

The transgenic TM algae or cyanobacteria are used to compete with natural species in simulated conditions. 1000 transgenic cells per ml are pipetted into unfiltered sea water in aquaria and cultivated in 100 μEin per cm² per sec light fluence, to simulate light conditions in the sea at a nominal depth. Aliquots are removed initially at daily, and later at weekly intervals and plated out, and the dwindling proportion of colonies that fluoresce in blue light are counted.

Results Within a few months, blue fluorescing colonies cannot be found in the aquaria.

Example 6 Prevention of establishment of algal individuals transgenically resistant to mercury in flue gas by engineering them into mutant algae lacking the ability to store complex carbohydrates

One of the traits suitable for Transgenic Mitigation in constructs with a primary, desirable trait is using an antisense or RNAi form of starch synthesizing genes that confer non-storage of starch (such as stal, GenBank Accession: XM OO 1693395) coupled to genes encoding enzymes responsible for the synthesis of polysaccharides such a inulin (such as 1-SST and 1-FFT, AJ009757, AJ009756) or levan (such as SacB from Bacillus subtilis (NC 000964) or Bacillus amyloliquifaciens (NC_009725) or levan sucrase gene from Erwinia amylovora (AJ831832) or ftf gene from Streptococcus mutans, NC 004350) or graminan, a highly branched levan found in wheat, barley and other graminae that the algae or cyanobacteria are capable of storing but are incapable of mobilizing in times of need. Such strains can live only in bioreactors and ponds, where other traits are separately used to prevent the establishment of competing organisms. Rare algae or cyanobacteria introgressing the TM construct in natural ecosystems could also no longer compete with native organisms in the natural ecosystems. In order to determine whether co-transformation of a desirable transgene with a mitigator gene would prevent proliferation of transgenic strains having the tandem construct can compete in the case of breach of containment, the merA (SEQ TD NO:64; NC_002134) and merB genes (SEQ ID NO:65,U77087) conferring mercury resistance are used as the primary desirable genes, and a tandem construct is made containing the above starch reducing/inulin over-producing genes as a mitigator and used to transform Synechococcus PCC7002, Phaeodactylum tricornutum, Nannochloropsis sp CS 246, Nannochloropsis oculata, Nannochloropsis salina, Pavlova lutheri CS 182, Synechococcus PCC7942, Synechosystis PCC6803, Chlamydomonas reinhardtii, Chlorella vulgaris, Chlorella ssp., lsochrysis sp. CS-177 Tetraselmis chuii CS-26 Tetraselmis suecica CS-187. In this case the mercury resistant trait is used as a selectable marker.

Experimental Procedures

Assembly the tandem construct Generation of Chlamydomonas reinhardtii expressing RNAi ofstal (for reduced starch) together with the merΛ and nterB genes conferring mercury resistance and the ISST and 1-FFT genes encoding enzymes responsible for the synthesis of inulin For generation of a tandem construct including the RNAi of C. reinhardtii stal gene encodes for AGPase large subunit (which are later used together with the merA and merB genes conferring mercury resistance), The primer for stal is: GCTCTAGAGCATGC TGTTAATGGCGACGCCTGG (SEQ ID NO: 42), and primer: GC GGATCCAAGCTT GAACCACTCCTTGTCGGTGG (SEQ ID NO:43) containing the Xbal+Sphl and BamHI+Hindlll restriction in their 5' flanking region are used for amplification of exons number 2,3,4 and introns 2,3 (597-1649 gDNA) of C. reinhardtii stal gene (SEQ ID NO: 67) using gDNA (genomic DNA) as a template and exons 2,3,4 (40-504 CDS) of C. reinhardtii staicDNA using cDNA as template. The 1053 bp genomic fragment was cloned into pSTBlue-1 (Novagene) in Sphl/BamHI restriction sites and the 465 bp cDNA fragment is cloned into Hindlll/Xbal sites of the same pSTBlue-1 plasmid in antisense orientation downstream to the sense genomic sequence. The stal RNAi cassette is then excised from pSTBlue-1 by Xbal digestion and cloned into the corresponding site of pSP124s, in the ble 3'UTR. Then a de novo synthesized merA and merB is synthesized according to the appropriate codon usage of the desired algae, each cloned under the control of rbcS2 promoter and terminator, is introduced into the same plasmid replacing the ble selectable marker, upstream to the stal RNAi cassette (Fig. 8A).

For generation of a construct including genes encoding enzymes responsible for the synthesis of inulin (such as Helianthus tuberosus ISST (SEQ ID NO: 44) and 1-FFT (SEQ ID NO:45); AJ009757, AJ009756, respectively ) or levans,such as SacB from Bacillus subtilis (NC 000964) (SEQ ID NO:69)or Bacillus amyloliquifaciens (NC 009725) or levan sucrase gene from Erwinia amylovora (AJ831832) orftfgene from Streptococcus mutans, NC_004350) the coding sequence of each gene is de novo synthesized according to the appropriate codon usage of the desired algae and cloned under the control of rbcS2 promoter and terminator. The tandem construct is introduced into the pSP124s plasmid downstream to the ble 3'UTR (Fig. 8B). Co-transformation of the two plasmids into Chlamydomonas reinhardtii is analyzed using inverse PCR with specific primers (arrows indicates primers positions in Figs. 8A and B).

Generation of cyanobacteria Synechococcus PCC7002 expressing antisense ofstal (for reduced starch) together with the merA and merB genes conferring mercury resistance and the ISST and 1-FFT genes encoding enzymes responsible for the synthesis ofinulin

For cyanobacteria the glgC (glucose- 1 -phosphate adenyltransferase) (SEQ ID NO:68) is cloned in antisense orientation using primers:

PrimeπGTGTGTTGTTGGCAATCGAG (SEQ ID NO:46) and PrimerCTAGATTACCGTGCCGTCGG (SEQ ID NO:47) for amplification of glgC cDNA from Synecocysitis PCC 6803 and the PCR product is cloned into pGEM-T T/A vector (Promega). The fragment containing the complete AGPase coding sequence is cloned into the plasmid pCB4 in an antisense orientation downstream to the rbcLS promoter. Then the de novo synthesized merA and merB synthesized according to the cyanobacteria codon usage of the desired algae each cloned under the control of rbcLS promoter and terminator, is introduced into the same plasmid upstream to the glgC antisense sequence. For generation of a construct including genes encoding enzymes responsible for the synthesis of inulin (e.g. Helianthus tuberosus J-SST and 1-FFT, AJ009757, AJ009756) the coding sequence of each gene is de novo synthesized according to the appropriate codon usage of the desired cyanobacteria and cloned under the control of rbcLS promoter and terminator in pCB4 plasmid. Co-transformation of the two plasmids into Synechococcus PCC7002 is analyzed using inverse PCR with specific primers and genomic DNA as a template.

Gene integration analyses of algae or cyanobacteria transformants

The DNA is analyzed by inverse PCR as described by Ochman et al., 1998, for the presence of intact tandem linked merA, merB, and 1-FFT, ISST genomic inserts. Two different DNA segments within the genomic TM T-DNA insert are amplified over the positions indicated in Fig. 8 with the following primers: Forward primer 1 (SEQ ID NO:48): TCTCATCGCATTGCGCTGCA (merB) Reverse primer 1 (SEQ ID NO:49): CCAACTTTCCTGGAACCCGC (merA) forward primer 2 (SEQ ID NO: 50): CACGTTTAGTTCCCATGATC (FFT-I) Reverse primer 2 (SEQ ID NO: 51^ CAAGCGTGGAACACATCTAC (SST-I)

The PCR products are purified using the QIAquick PCR Purification Kit^® (Qiagen, Hilden, Germany) according to the manufacturer's instructions, and sequenced to confirm the integration of the TM T-DNA. In vivo merA/merB assay. Putative algae or cyanobacteria cells are plated on

5-10 μM PMA (phenyl mercury acetate, replacing methyl mercury) in standard algae or cyanobacteria culture media. At this concentration, all non-transgenic cells are killed.

In vivo starch assay Mercury resistant transgenic algae or cyanobacteria cells from numbered colonies of picked cells are cultured in 96-well dishes in standard algae or cyanobacteria culture media such that single cells develop into cultures. When cultures are dense, they are bleached with DMSO as in Example 3, and then stained for the absence of starch with iodine / potassium iodide solution.

Inulin determination The best cultures, most rapidly growing mercury resistant/low starch cultures able to attain the most dense growth are analyzed for inulin content according to Cairns (2003) and references therein.

Competition of TM transgenics with the wild type algae and cyanobacteria The transgenic TM algae or cyanobacteria are used to compete with natural species in simulated conditions. 1000 transgenic cells per ml are pipetted into unfiltered sea water in aquaria and cultivated in 100 μEin per cm² per sec light fluence, to simulate light conditions in the sea at a nominal depth. Aliquots are removed initially at daily, and later at weekly intervals, and the dwindling proportion of yellow green colonies are counted. Aliquots at the same dilutions were plated in parallel on the same media, but containing 10 μM PMA.

Results Within a few months, no methyl mercury resistant cells can be found in the aquaria.

Example 7

Prevention of establishment and introgression of enhanced photosynthesis and UV resistance by coupling with a gene preventing flagella/cilia formation resulting in cells lacking self motility One of the traits suitable for Transgenic Mitigation in constructs with a primary, desirable trait is to have cells incapable of phototactic/chemotactic or thermotactic motility such that they cannot swim in a direction that is optimal survival (such as odal-12 mutant for Chlamydomonas and the PUT NC Ol 0475 for cyanobacteria). Such strains do not need motility to exist in continually mixed high cell density bioreactors and ponds, but cannot compete with native organisms in a natural ecosystem, where they must be able to swim towards optimal light and away from danger. Because they do not waste energy on motility, they have more energy available for making commercially needed components Potentially contaminating cells organisms are kept out of the culture ponds by having traits such as herbicide resistance. Rare non-motile algae or cyanobacteria introgressing the TM construct could also no longer compete with native organisms in natural ecosystems. In order to determine whether co-transformation of a desirable transgene with a mitigator gene prevents proliferation of transgenic strains having the tandem construct can compete in the case of breach of containment, a tandem construct was made containing a BFP- blue fluorescing protein (SEQ ID NO:53) that converts cell damaging near ultraviolet light to blue light that can be used in photosynthesis, and the odal2-l mutant in algae / PiIT gene in cyanobacteria conferring non swimming as a mitigator (NC Ol 0475), and used to transform Synechococcus PCC7002, Phaeodactylum tricornutum, Nannochloropsis sp CS 246, Nannochloropsis oculata, Nannochloropsis salina, Pavlova lutheri CS 182, Synechococcus PCC7942, Synechosystis PCC6803, Chlamydomonas reinhardtii, Chlorella vulgaris, Chlorella ssp., Isochrysis sp. CS-177 Tetraselmis chuii CS-26 Tetraselmis suecica CS- 187. The resistance to UV damage and the ability to photosynthesize the blue fluorescence emanating from incident near UV light is used as a selectable marker for transformations.

Experimental Procedures Assembling the construct

Generation of Chlamydomonas containing an BFP-blue fluorescing protein gene in the background of odal 2-1 mutant The odal 2-1 mutant lacks the entire LC2 + LClO genes. This strain exhibits a flagellar beat frequency that is consistently less than that observed for strains that fail to assemble the entire outer arm and docking complex (Tanner 2008). Therefore the BFP-azurite construct is built in with the background of the odal 2-1 mutant. The BFP-azurite construct sequence (Mena et al. 2006) is chemically synthetized using the published sequence with modifications according to the codon usage of the green algae C. reinhardtii (SEQ ID NO:54).

The gene is cloned into pGEM-T vector (Promega) and then transferred into pSP124S (Sizova et al. 2001).under the control of the RbcS2 promoter and 3 ' RbcS2 terminator (Fig. 9). Another option is to produce either RNAi or antisense constructs directed against dynein heavy/light chains in tandem with the BFP-blue fluorescing protein gene under the control of the RbcS2 promoter and 3 ' RbcS2 terminator in the pSP124S vector.

Transformation of algae

Algae cells in 0.4 ml of growth medium containing 5% PEG6000 are transformed with plasmid from examples 1 and 2 (l±5mg) by the glass bead vortexing method (Kindle 1990) or electroporation (Chow and Tung 1999). The transformation mixture is then transferred to 10 ml of non-selective growth medium for recovery. The cells are kept for at least 18 h at 25° C in the light. Cells are collected by centrifugation and plated at a density of 10⁸ cells per 80 mm plate. Transformants are grown on fresh TAP agar plates for 7 days in 30° C. For selection, transformants are grown on fresh TAP agar plates for 7 days at 30° C. Colonies are transferred to micro-well plates at a dilution of 1-2 cells per microwell using medium, and cultured under UV light until it is apparent that there cells growing in most wells. BFP fluorescence is monitored at excitation of 383 nm and emission of 450 nm. DsRed and any other FP used are monitored with their specific excitation and emission spectra. Cells from microwells producing the highest fluorescent signal are collected and cultured as single cell colonies under UV light (duration and intensity are set at LD 99% of wild type cells). Surviving cells are then transferred for future culturing and further examination.

Generation of cyanobacteria Synechococcus PCC7002 expressing a BFP-blue fluorescing protein gene and the antisense of PUT gene under the control of the rbcS2 promoter

The BFP-azurite sequence (Mena et al. 2006) is chemically synthesized using the published sequence (SEQ ID NO:52) with modifications according to the codon usage of Synechococcus PCC7002 (SEQ ID NO:55) and with the addition of BamHI restriction sites in its both ends. The gene is cloned into pGEM-T vector (Promega) and then transferred into the BamHI site of pCB4 plasmid (Deng and Coleman, 1999) downstream to the Synechococcus rbcLS promoter and upstream to antisense of PUT gene (SEQ ID NO:53), followed by rbcLS terminator.

The coding sequence of Synechococcus PCC7002 PUT gene is amplified using the forward primer: ATGGATTACATGATCGAAGA (SEQ ID NO:58) and the reverse primer: GCGACGTTTTGCGGTTGGGC (SEQ ID NO:59) followed by cloning into pGEM-T plasmid (Promega). The fragment is then excised from the pGEM-T plasmid and cloned into the shuttle vector pCB4 in an antisense orientation downstream to the BFP gene ( Fig. 11).

Transformation of cyanobacteria

For transformation of Synechococcus PCC7002, cells are cultured in 100 ml of ASN-III liquid medium at 28°C under white fluorescent light and subcultured at the mid-exponential phase of growth. To 1.0 ml of cell suspension containing 2x10⁸ cells, which are cultured at the mid-exponential phase of growth, 0.5 or 1.0 μg of donor DNA (in 10 mM Tris/1 mM EDTA, pH 8.0) is added, and the mixture is incubated in the dark at 26° C overnight. For selection, transformants are grown on fresh TAP Agar plates for 7 days at 30° C. Colonies are transferred to micro-well plates at a dilution of 1-2 cells per microwell using medium, and cultured with a 16/8 h light/dark period under white fluorescent light at 30° C until it is apparent that there cells growing in most wells. BFP fluorescence is monitored at excitation of 383 nm and emission of 450 nm. DsRed and any other FP used are monitored with their specific excitation and emission spectra. Cells from microwells producing the highest fluorescent signal are collected and cultured as single cell colonies under UV light (duration and intensity are set at LD 99% of wild type cells). Surviving cells are then transferred for future culturing and further examination.

Gene integration analyses of algae or cyanobacteria transformants

Genomic DNA is isolated using either Stratagene's (La Jolla, Calif.) DNA purification kit or a combination of QIAGEN's (Valencia, Calif.) DNeasy plant mini kit and phenol chloroform extraction (Davies et al. 1992). Total RNA is isolated using either QIAGENS's Plant RNeasy Kit or the Trizol Reagent (Invitrogen, Carlsbad,

Calif.).

The DNA is analyzed by PCR for the presence of intact tandemly linked BFP- blue fluorescing protein gene and PUT gene in an antisense orientation. Four different DNA segments within the genomic TM T-DNA insert are amplified over the positions indicated in Fig. 11 with the following primers for algae:

Forward primeπATGAGCAAGGGCGAGGAGCT (SEQ ID NO:60) Reverse primer: GTGGTGGTGGTGGTGGTGCT (SEQ ID NO:61) And the following primers for cyanobacteria:

Forward primer: AACACCACCACCACCACCAC (SEQ ID NO:62) from the BFP

Reverse primer: CAACCGCAAAACGTCGCTAA (SEQ ID NO 63) from PUT In vivo UV resistance assay. Putative algae or cyanobacteria cells are plated on Petri dishes and placed in a box where the sole irradiation is near UV light. Green colonies that develop are expected to contain the BFP gene. In vivo motility assay Picked UV resistant algae or cyanobacteria cells are placed on a microscope slide and observed. The slide is then unilaterally illuminated and movement towards or away from the light (depending on intensity) is observed in wild type but not mutant cells . Competition of TM transgenics with the wild type algae and cyanobacteria

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Claims

TransAlgae MitigationCLAIMS:What is claimed is:

1. A method to mitigate effects of release of at least one advantageous genetically engineered trait of an alga or a cyanobacterium into natural ecosystems, said method comprising a step of transforming an alga or a cyanobacterium to express said at least one advantageous genetically engineered trait, and at least one mitigating genetic trait, wherein: said at least one advantageous genetically engineered trait is encoded by at least one advantageous gene, and said at least one advantageous gene being operably linked with promoter sequences, and said at least one mitigating genetic trait is encoded by at least one mitigating gene, said at least one mitigating gene being optionally operably linked with promoter sequences; and said at least one advantageous gene and said at least one mitigating gene being introduced into the alga or cyanobacterium in tandem, whereby encoding sequences of the advantageous and mitigating genes remain genetically linked in the transgenic alga or cyanobacterium; and said at least one mitigating gene further being desirable in or neutral to the transgenic alga or cyanobacterium when cultivated but rendering the transgenic alga or cyanobacterium incapable of establishing itself or its introgressed offspring in natural ecosystems.

2. The method of claim 1, wherein the alga is selected from the group of algal strains consisting of : Nannochloropsis sp CS 246, Nannochloropsis oculata, Phaeodactylum tricornutum, Nannochloropsis salina, Pavlova lutheri CS 182, Chlamydomanas reinhardtii, Isochrysis sp. Tetraselmis sp., Nannochloris sp. and Chlorella sp. TransAlgae Mitigation

3. The method of claim 1, wherein the cyanobacterium is selected from the group of cyanobacterial strains consisting of:

Synechococcus PC 7942, Synechococcus PCC7002, and Synechocystis PCC6803,

4. The method of claim 1, wherein the mitigating trait is selected from the group consisting of: reduced content of ribulose 1,5 bis phosphate carboxylase/oxygenase (RUBISCO), reduced photosystem 2 antenna size, modified cilia or flagella formation or action, reduced carotene content in photosystems, reduced content of cell wall polymers, reduced ability to take up carbon dioxide, suppressed ability to convert nitrate to ammonia, and reduced biosynthesis of storage polymers.

5. The method of claim 4, wherein the mitigating trait is reduced content of

RUBISCO and the trait is conferred by an antisense oriented gene sequence encoding large or small subunit of RUBISCO or by RNAi casette of the gene.

6. The method of claim 4, wherein the mitigating trait is reduced photosystem 2 antenna size, and the trait is conferred by an antisense oriented tlal, or reduced chlorophyll a oxygenase or similar gene or by RNAi of the gene.

7. The method of claim 4, wherein the mitigating trait is modified cilia or flagella formation or action, and the trait is conferred by/»//T-gene in antisense orientation.

8. The method of claim 4, wherein the mitigating trait is reduced carotene content of photosystems and the trait is conferred by a mutant pds-gene.

9. The method of claim 4, wherein the mitigating trait is reduced content of cell wall polymers. TransAlgae Mitigation

10. The method of claim 4, wherein the mitigating trait is modified biosynthesis of storage polymers.

11. The method of claim 10, wherein starch storage is reduced and nondegradable polysaccharide storage is enhanced.

12. The method of claim 11, wherein the non degradable polysaccharide is selected from the group consisting of inulin, levan and graminan.

13. The method of claim 10, wherein starch storage is reduced by Αstal gene in antisense orientation or by an RNAi cassette of the gene.

14. The method of claim 12, wherein the non degradable polysaccharide is inulin and the trait is conferred by ISST or IFFT encoding sequences.

15. The method of claim 12, wherein the non degradable polysaccharide is levan and the trait is conferred by SacB or fif gene. The method of claim 4, wherein the mitigating trait is reduced ability to reduce nitrate to ammonia.

16. The method of claim 4, wherein the mitigating trait is reduced ability to reduce nitrate to ammonia.

17. The method of claim 16, wherein the reduced ability to reduce nitrate to ammonia is conferred by antisense or RNAi suppression of nitrate or nitrite reductase.

18. The method of claim 4, wherein the mitigating trait is suppressed activity of carbon concentrating mechanism.

19. The method of claim 18, wherein the suppressed carbon concentrating mechanism is achieved by low carbonic anhydrase activity or production. TransAlgae Mitigation

20. The method of claim 1, wherein the advantageous trait is selected from the group consisting of modified fatty acid composition, enhanced photosynthesis, increased methionine content, increased lysine content, herbicide resistance, mercury resistance, and virus resistance.

21. The method of claim 20, wherein the advantageous trait is modified fatty acid composition and the trait is conferred by a gene encoding delta(12)-fatty acid dehydrogenase.

22. The method of claim 20, wherein the advantageous trait is modified fatty acid composition and the trait is conferred by a gene encoding fatty acid desaturase.

23. The method of claim 20, wherein the advantageous trait is modified fatty acid composition and the trait is conferred by a gene encoding dithioesterase.

24. The method of claim 20, wherein the advantageous trait is enhanced photosynthesis and the trait is conferred by Tlal gene.

25. The method of claim 20, wherein the advantageous trait is enhanced photosynthesis and the trait is conferred by reducing expression of chlorophyll a oxygnase-gene.

26. The method of claim 20, wherein the advantageous trait is enhanced photosynthesis and the trait is conferred by overexpression of aldolase, triosephosphate isomerase or fructose 1,6 bisphosphatase genes.

27. The method of claim 20, wherein the advantageous trait is enhanced photosynthesis and the trait is conferred by a gene encoding Blue Fluorescent Protein (BFP). TransAlgae Mitigation

28. The method of claim 20, wherein the advantageous trait is increased methionine content and the trait is conferred by a gene encoding high methionine 2S albumin.

29. The method of claim 20, wherein the advantageous trait is increased lysine content, and the trait is conferred by a gene encoding high lysine BHL8 protein.

30. The method of claim 20, wherein the advantageous trait is herbicide resistance and the trait is conferred by a gene selected from a group consisting of genes encoding phosphinothricin N-acetyltransferase, glyphosate oxidoreductase, or herbicide resistant forms of 5- enolpyruvylshikimate-3-phosphate synthase (EPSPS), acetolactate synthase (ALS), 4-hydroxyphenyl-pyruvate dehydrogenase (HPPD) and protoporphyrinogen oxidase (PPO).

31. A genetic construct for mitigating effects of release of a genetically engineered genetic trait of an alga or cyanobacterium into natural ecosystems, said construct comprising a first polynucleotide sequence encoding a desirable genetic trait and a second polynucleotide sequence encoding a mitigating genetic trait, wherein the first and the second polynucleotide sequences are covalently linked.

32. The genetic construct of claim 31 , wherein the first polynucleotide sequence is operably linked to a promoter sequence.

33. The genetic construct of claim 32, wherein the first polynucleotide sequence is EPSPS coding sequence, the promoter sequence is RbcS promoter sequence, and the second polynucleotide sequence is a tlal encoding sequence in anti-sense orientation. TransAlgae Mitigation

34. The genetic construct of claim 32, wherein the first polynucleotide sequence is virus CAPSID coding sequence, the promoter sequence is RbcS promoter sequence, and the second polynucleotide comprises RbcS RNAi casette.

35. The genetic construct of claim 32, wherein the first polynucleotide sequence is virus CAPSID coding sequence, the promoter sequence is RbcS promoter sequence, and the second polynucleotide sequence is RbcS encoding sequence in antisense orientation operably linked to RbcS promoter sequence.

36. The genetic construct of claim 32, wherein the first polynucleotide sequence is mutant PDS coding sequence, the promoter sequence is

linked to 5 'end of rbcS2, and the second polynucleotide sequence is BHL8 coding sequence or 2S albumin protein coding sequence.

37. The genetic construct of claim 32, wherein the first polynucleotide sequence is mutant PDS coding sequence, the promoter sequence is RbcLS promoter sequence, and the second polynucleotide sequence is

BHL8 coding sequence or 2S albumin protein coding sequence.

38. The genetic construct of claim 32, wherein the first polynucleotide sequence is BFP encoding sequence, the promoter sequence is RbcS promoter sequence, and the second polynucleotide sequence is PiIT encoding sequence in antisense orientation operably linked RbcS promoter sequence.

39. A genetic construct for mitigating effects of release of a genetically engineered genetic trait of an alga or cyanobacterium in to natural ecosystems, said construct comprising a first cassette and a second cassette, said first cassette comprising a first and a second polynucleotide TransAlgae Mitigation

sequences operably linked to a first and a second promoter sequences and encoding a first and a second desirable genetic trait, said second cassette comprising a polynucleotide sequence encoding a mitigating trait, said polynucleotide sequence being operably linked to a promoter sequence; and said first and second cassettes being covalently linked.

40. The genetic construct of claim 39, wherein the first polynucleotide sequence is merA coding sequence, first promoter sequence is RbcS promoter sequence, the second polynucleotide sequence is merB coding sequence, second promoter sequences is RbcS promoter sequence and the polynucleotide sequence encoding mitigating trait is stal or staό RNAi cassette.

41. A method to mitigate effects of release of at least one advantageous genetically engineered trait of an alga or a cyanobacterium into natural ecosystems, said method comprising steps of:

a. selecting a mutated alga or a cyanobacterium to express said at least one mitigating trait, and b. transforming the mutated alga or cyanobacterium with said at least one advantageous trait, wherein said at least one advantageous genetically engineered trait is encoded by at least one advantageous gene, and said at least one advantageous gene being operably linked with promoter sequences, and said at least one mitigating trait being desirable in or neutral to the transformed alga or cyanobacterium when cultivated but rendering the alga or cyanobacterium incapable of establishing itself or its introgressed offspring in natural ecosystems.

42. The method of claim 41 , wherein the mitigating trait is decreased antenna size and the advantageous trait is herbicide resistance. TransAlgae Mitigation

43. The method of claim 42, wherein the mutated alga or cyanobacteria is transformed with an expression vector comprising HPPD resistance encoding gene sequence under control of rbcS2 promoter.

44. The method of claim 41, wherein the mitigating trait is impaired motility and the advantageous trait is herbicide resistance.

45. The method of claim 44, wherein the mutated alga is transformed with an expression vector comprising PPO herbicide resistance encoding gene sequence under control of rbcS2 promoter.

46. The method of claim 41, wherein the mutated alga is odal-12 or tla-1 mutant of Chlamydomonas reinhardtii.

47. The method of claim 41, wherein the mutated cyanobacteria is PiIT mutant.

48. A method to mitigate effects of release of at least one advantageous genetically engineered trait of an asexual, or non-conjugating alga or a cyanobacterium into natural ecosystems, said method comprising a step of transforming an alga or a cyanobacterium to express said at least one advantageous genetically engineered trait, and at least one mitigating genetic trait, wherein: said at least one advantageous genetically engineered trait is encoded by at least one advantageous gene, and said at least one advantageous gene being operably linked with promoter sequences, and said at least one mitigating genetic trait is encoded by at least one mitigating gene, said at least one mitigating gene being optionally operably linked with promoter sequences; and said at least one mitigating gene further being desirable in or neutral to the transgenic alga or cyanobacterium when cultivated but rendering the transgenic alga or cyanobacterium incapable to compete in natural ecosystems.