WO2002010209A1

WO2002010209A1 - Nucleotide sequences which code for the meth gene

Info

Publication number: WO2002010209A1
Application number: PCT/EP2001/008220
Authority: WO
Inventors: Brigitte Bathe; Bettina Möckel; Walter Pfefferle; Klaus Huthmacher; Christian RÜCKERT; Jörn Kalinowski; Alfred Pühler; Michael Binder; Dieter Greissinger; Georg Thierbach
Original assignee: Degussa Ag
Priority date: 2000-08-02
Filing date: 2001-07-17
Publication date: 2002-02-07
Also published as: WO2002010209A8; AU2001285844A1; EP1307475A1

Abstract

The invention relates to an isolated polynucleotide comprising a polynucleotide sequence chosen from the group consisting of a) polynucleotide which is identical to the extent of at least 70 % to a polynucleotide which codes for a polypeptide which comprises the amino acid sequence of SEQ ID No. 2, b) polynucleotide which codes for a polypeptide which comprises an amino acid sequence which is identical to the extent of at least 70 % to the amino acid sequence of SEQ ID No. 2, c) polynucleotide which is complementary to the polynucleotides of a) or b), and d) polynucleotide comprising at least 15 successive nucleotides of the polynucleotide sequence of a), b) or c), and processes for the fermentative preparation of L-amino acids using coryneform bacteria in which at least the metH gene coding for 5 -methyltetrahydrofolate homocysteine methyltransferase (EC 2.1.1.13) is present in enhanced form, and the use of the polynucleotide sequences as hybridization probes.

Description

Nucleotide sequences which code for the metH gene

Field of the Invention

The invention provides nucleotide sequences from coryneform bacteria which code for the metH gene and a process for the fermentative preparation of amino acids, in particular L- methionine, using bacteria in which the metH gene is enhanced.

Prior Art

L-Amino acids, in particular L-methionine, are used in human medicine and in the pharmaceuticals industry, in the foodstuffs industry and very particularly in animal nutrition.

It is known that amino acids are prepared by fermentation from strains of coryneform bacteria, in particular Corynebacteriu gluta icum. Because of their great importance, work is constantly being undertaken to improve the preparation processes. Improvements to the process can relate to fermentation measures, such as, for example, stirring and supply of oxygen, or the composition of the nutrient media, such as, for example, the sugar concentration during the fermentation, or the working up to the product form by, for example, ion exchange chro atography, or the intrinsic output properties of the microorganism itself.

Methods of mutagenesis, selection and mutant selection are used to improve the output properties of these microorganisms. Strains which are resistant to antimetabolites, such as e.g. the methionine analogue α- methyl-methionine, ethionine, norleucine, N- acetylnorleucine, S-trifluoromethylhomocysteine, 2-amino-5- heprenoitic acid, seleno-methionine, methionine- sulfoxi ine, methoxine, 1-aminocyclopentane-carboxylic acid, or are auxotrophic for metabolites of regulatory importance and produce amino acids, such as e.g. L- methionine, are obtained in this manner.

Methods of the recombinant DNA technique have also been employed for some years for improving the strain of Corynebacterium strains which produce L-amino acid, by amplifying individual amino acid biosynthesis genes and investigating the effect on the amino acid production.

Object of the Invention

The inventors had the object of providing new measures for improved fermentative preparation of amino acids, in particular L-methionine.

Summary of the Invention

When L-methionine or methionine are mentioned in the following, the salts, such as e.g. methionine hydrochloride or methionine sulfate are also meant, by this.

The invention provides an isolated polynucleotide from coryneform bacteria, comprising a polynucleotide sequence which codes for the metH gene, chosen from the group consisting of

a) polynucleotide which is identical to the extent of at least 70% to a polynucleotide which codes for a polypeptide which comprises the amino acid sequence of SEQ ID No. 2,

b) polynucleotide which codes for a polypeptide which comprises an amino acid sequence which is identical to the extent of at least 70% to the amino acid sequence of SEQ ID No. 2,

c) polynucleotide which is complementary to the polynucleotides of a) or b) , and d) polynucleotide comprising at least 15 successive nucleotides of the polynucleotide sequence of a) , b) or c), the polypeptide preferably having the activity of ho ocysteine methyltransferase II.

The invention also provides the above-mentioned polynucleotide, this preferably being a DNA which is capable of replication, comprising:

(i) the nucleotide sequence shown in SEQ ID No. 1, or

(ii) at least one sequence which corresponds to sequence (i) within the* range of the degeneration of the genetic code, or

(iii) at least -one sequence which hybridizes with the sequence complementary to sequence (i) or (ii) , and optionally

(iv) sense mutations of neutral function in (i) .

The invention also provides

a polynucleotide comprising the nucleotide sequence as shown in SEQ ID No. 1;

a polynucleotide which codes for a polypeptide which comprises the amino acid sequence as shown in SEQ ID No. 2,

a vector containing the polynucleotide according to the invention, in particular a shuttle vector or plasmid vector, and and coryneform bacteria serving as the host cell, which contain the vector or in which the metH gene is enhanced. The invention also provides polynucleotides which substantially comprise a polynucleotide sequence, which are obtainable by screening by means of hybridization of a corresponding gene library, which comprises the complete gene with the polynucleotide sequence corresponding to SEQ ID No. 1, with a probe which comprises the sequence of the polynucleotide mentioned, according to SEQ ID No. 1 or a fragment thereof, and isolation of the DNA sequence mentioned.

Detailed Description of the Invention

Polynucleotides which comprise the sequences according to the invention are suitable as hybridization probes for RNA, cDNA and DNA, in order to isolate, in the full length, nucleic acids or polynucleotides or genes which code for homocysteine methyltransferase II or to isolate those nucleic acids or polynucleotides or genes which have a high similarity of sequence with that of the homocysteine methyltransferase II gene.

Polynucleotides which comprise the sequences according to the invention are furthermore suitable as primers with the aid of which DNA of genes which code for homocysteine methyltransferase II can be prepared by the polymerase chain reaction (PCR) .

Such oligonucleotides which serve as probes or primers comprise at least 30, preferably at least 20, very particularly preferably at least 15 successive nucleotides. Oligonucleotides which have a length of at least 40 or 50 nucleotides are also suitable. Oligonucleotides with a length of at least 100, 150, 200, 250 or 300 nucleotides are optionally also suitable.

"Isolated" means separated out of its natural environment. "Polynucleotide" in general relates to polyribonucleotides and polydeoxyribonucleotides, it being possible for these to be non-modified RNA or DNA or modified RNA or DNA.

"Polypeptides" are understood as meaning peptides or proteins which comprise two or more amino acids bonded via peptide bonds.

The polypeptides according to the invention include a polypeptide according to SEQ ID No. 2, in particular those with the biological activity of homocysteine methyltransferase II, and also those which are at least

70%, preferably at least 80%_. and in particular which are at , least 90% to 95% identical to the polypeptide according to .SEQ ID No. 2 and have the activity mentioned.

The invention moreover provides a process for the fermentative preparation of amino acids, in particular L- methionine, using coryneform bacteria which in particular already produce amino acids, and in which the nucleotide sequences which code for the metH gene are enhanced, in particular over-expressed. The term "enhancement" in this connection describes the increase in the intracellular activity of one or more enzymes (proteins) in a microorganism which are coded by the corresponding DNA, for example by increasing the number of copies of the gene or genes, using a potent promoter or using a gene or allele which codes for a corresponding enzyme (protein) having a high activity, and optionally combining these measures.

By enhancement measures, in particular over-expression, the activity or concentration of the corresponding protein is in general increased by at least 10%, 25%, 50%, 75%, 100%, 150%, 200%, 300%, 400% or 500%, up to a maximum of 1000% or 2000%, based on the starting microorganism. The microorganisms which the present invention provides can prepare L-amino acids, in particular L-methionine, from glucose, sucrose, lactose, fructose, maltose, molasses, starch, cellulose or from glycerol and ethanol. They can be representatives of coryneform bacteria, in particular of the genus Corynebacterium. Of the genus Corynebacterium, there may be mentioned in particular the species Corynebacterium glutamicum, which is known among experts for its ability to produce L-amino acids. Suitable strains of the genus Corynebacterium, in particular of the species Corynebacterium glutamicum (C. glutamicum) , are in particular the known wild-type strains

Corynebacterium glutamicum ATCC13032 - Corynebacterium aσetoglutamicum ATCC15806 Corynebacterium acetoacidophiϊum ATCC13870

Corynebacterium thermoaminogenes FERM BP-1539 Corynebacterium elassecola ATCC17965 Brevibacterium flavum ATCC14067 Brevibacterium lactofer entum ATCC13869 and Brevibacterium divaricatum ATCC14020

or L-amino acid-producing mutants or strains prepared therefrom, such as, for example, the L-methionine-producing strain

Corynebacterium glutamicum ATCC21608. The new metH gene from C. glutamicum which codes for the enzyme homocysteine methyltransferase II (EC 2.1.1.13) has been isolated.

To isolate the metH gene or also other genes of C. glutamicum, a gene library of this microorganism is first set up in Escherichia coli (E. coli) . The setting up of gene libraries is described in generally known textbooks and handbooks. The textbook by Winnacker: Gene und Klone, Eine Einfϋhrung in die Gentechnologie (Verlag Chemie, Weinheim, Germany, 1990) , or the handbook by Sambrook et al.: Molecular Cloning, A Laboratory Manual (Cold Spring Harbor Laboratory Press, 1989) may be mentioned as an example. A well-known gene library is that of the E. coli K-12 strain W3110 set up in λ vectors by Kohara et al . (Cell 50, 495 -508 (1987)). Bathe et al . (Molecular and General Genetics, 252:255-265, 1996) describe a gene library of C. glutamicum ATCC13032, which was set up with the aid of the cos id vector SuperCos I (Wahl et al . , 1987, Proceedings of the National Academy of Sciences USA,

84:2160-2164) in the E. coli K-12 strain NM554 (Raleigh et al., 1988, Nucleic Acids Research 16:1563-1575).

Bδrmann et al. (Molecular Microbiology 6(3), 317-326) (1992) ) in turn describe a gene library of C. glutamicum ATCC13032 using the cosmid pHC79 (Hohn and Collins, Gene 11, 291-298 (1980)). To prepare a gene library of C. ^■ glutamicum in E. coli it is also possible to use plasmids such as pBR322 (Bolivar, Life Sciences, 25, 807-818 (1979)) or pUC9 (Vieira et al . , 1982, Gene,^" 19:259-268). Suitable hosts are, in particular, those E. coli strains which are restriction- and recombination-defective. An example of these is the strain DH5αmcr, which has been described by Grant et al. (Proceedings of the National Academy of Sciences USA, 87 (1990) 4645-4649) . The long DNA fragments cloned with the aid of cosmids can in turn be subcloned in the usual vectors suitable for sequencing and then sequenced, as is described e.g. by Sanger et al. (Proceedings of the National Academy of Sciences of the United States of America, 74:5463-5467, 1977). The resulting DNA sequences can then be investigated with known algorithms or sequence analysis programs, such as e.g. that of Staden (Nucleic Acids Research 14, 217- 232(1986)), that of Marck (Nucleic Acids Research 16, 1829- 1836 (1988)) or the GCG program of Butler (Methods of Biochemical Analysis 39, 74-97 (1998)). The new DNA sequence of C. glutamicum which codes for the metH gene and which, as SEQ ID No. 1, is a constituent of the present invention has been found. The amino acid sequence of the corresponding protein has furthermore been derived from the present DNA sequence by the methods described above. The resulting amino acid sequence of the metH gene product is shown in SEQ ID No. 2.

Coding DNA sequences which result from SEQ ID No. 1 by the degeneracy of the genetic code are also a constituent of the invention. In the same way, DNA sequences which hybridize with SEQ ID No. 1 or parts of SEQ ID No. 1 are a constituent of the invention. Conservative amino acid exchanges, such as e.g. exchange of glycine for alanine or of aspartic acid for glutamic acid in proteins, are furthermore known among experts as "sense mutations" which do not lead to a fundamental change in the activity of the protein, i.e. are of neutral function. It is furthermore known that changes on the N and/or C terminus of a protein cannot substantially impair or can even stabilize the function thereof. Information in this context can be found by the expert, inter alia, in Ben-Bassat et al. (Journal of Bacteriology 169:751-757 (1987)), in 0' Regan et al. (Gene 77:237-251 (1989)), in Sahin-Toth et al. (Protein Sciences 3:240-247 (1994)), in Hochuli et al. (Bio/Technology 6:1321-1325 (1988)) and in known textbooks of genetics and molecular biology. Amino acid sequences which result in a corresponding manner from SEQ ID No. 2 are also a constituent of the invention.

In the same way, DNA sequences which hybridize with SEQ ID No. 1 or parts of SEQ ID No. 1 are a constituent of the invention. Finally, DNA sequences which are prepared by the polymerase chain reaction (PCR) using primers which result from SEQ ID No. 1 are a constituent of the invention. Such oligonucleotides typically have a length of at least 15 nucleotides. Instructions for identifying DNA sequences by means of hybridization can be found by the expert, inter alia, in the handbook "The DIG System Users Guide for Filter Hybridization" from Boehringer Mannheim GmbH (Mannheim, Germany, 1993) and in Liebl et al. (International Journal of Systematic Bacteriology (1991) 41: 255-260) . Instructions for amplification of DNA sequences with the aid of the polymerase chain reaction (PCR) can be found by the expert, inter alia, in the handbook by Gait: Oligonucleotide Synthesis: A Practical Approach (IRL Press, Oxford, UK, 1984) and in Newton and Graham: PCR (Spektrum Akademischer Verlag, Heidelberg, Germany, 1994) .

It has been found that coryneform bacteria produce amino acids, in particular L-methionine, in an improved manner after over-expression of the metH gene.

To achieve an over-expression, the number of copies of the corresponding genes can be increased, or the promoter and regulation region or the ribosome binding site upstream of the structural gene can be mutated. Expression cassettes which are incorporated upstream of the structural gene act in the same way. By inducible promoters, it is additionally possible to increase the expression in the course of fermentative L-methionine production. The expression is likewise improved by measures to prolong the life of the m- RNA. Furthermore, the enzyme activity is also increased by preventing the degradation of the enzyme protein. The genes or gene constructs can either be present in plasmids with a varying number of copies, or can be integrated and amplified in the chromosome. Alternatively, an over- expression of the genes in question can furthermore be achieved by changing the composition of the media -and the culture procedure.

Instructions in this context can be found by the expert, inter alia, in Martin et al. (Bio/Technology 5, 137-146 (1987)), in Guerrero et al. (Gene 138, 35-41 (1994)), Tsuchiya and Morinaga (Bio/Technology 6, 428-430 (1988)), in Eik anns et al. (Gene 102, 93-98 (1991)), in European Patent Specification 0 472 869, in US Patent 4,601,893, in Schwarzer and Pϋhler (Bio/Technology 9, 84-87 (1991), in Reinscheid et al. (Applied and Environmental Microbiology 60, 126-132 (1994)), in LaBarre et al . (Journal of Bacteriology 175, 1001-1007 (1993)), in Patent Application WO 96/15246, in Malumbres et al. (Gene 134, 15 - 24 (1993)), in Japanese Laid-Open Specification JP-A-10-229891, in Jensen and Hammer (Biotechnology and Bioengineering 58, 191-195 (1998)), in Makrides (Microbiological Reviews 60:512-538 (1996)) and in known textbooks of genetics and molecular biology.

By way of example, for enhancement the metH gene according to the invention was over-expressed with the aid of episomal plasmids. Suitable plasmids are those which are replicated in coryneform bacteria. Numerous known plasmid vectors, such as e.g. pZl (Menkel et al . , Applied and Environmental Microbiology (1989) 64: 549-554), pEKExl (Eikmanns et al., Gene 102:93-98 (1991)) or pHS2-l (Sonnen et al., Gene 107:69-74 (1991)) are based on the cryptic plasmids pHM1519, pBLl or pGAl. Other plasmid vectors, such as e.g. those based on pCG4 (US-A 4,489,160), or pNG2 (Serwold-Davis et al., FEMS Microbiology Letters 66, 119- 124 (1990)), or pAGl (US-A 5,158,891), can be used in the same manner.

Plasmid vectors which are furthermore suitable are also those with the aid of which the process of gene amplification by integration into the chromosome can be used, as has been described, for example, by Reinscheid et al. (Applied and Environmental Microbiology 60, 126-132 (1994) ) for duplication or amplification of the hom-thrB operon. In this method, the complete gene is cloned in a plasmid vector which can replicate in a host (typically E. coli) , but not in C. glutamicum. Possible vectors are, for example, pSUP301 (Simon et al., Bio/Technology 1, 784-791 (1983)), pKlδmob or pK19mob (Schafer et al., Gene 145, 69- 73 (1994)), pGEM-T (Promega corporation, Madison, WI, USA), pCR2.1-TOPO (Shuman (1994) . Journal of Biological Chemistry 269:32678-84; US-A 5, 487, 993) , pCR®Blunt (Invitrogen, Groningen, Holland; Bernard et al., Journal of Molecular Biology, 234: 534-541 (1993)), pEMl (Schrumpf et al, 1991, Journal of Bacteriology 173:4510-4516) or pBGS8 (Spratt et al.,1986, Gene 41: 337-342). The plasmid vector which contains the gene to be amplified is then transferred into the desired strain of C. glutamicum by conjugation or transformation. The -method of conjugation is described, for example, by Schafer et al. (Applied and Environmental Microbiology 60, 756-759 (1994)). Methods for transformation are described, for example, by Thierbach et al. (Applied Microbiology and Biotechnology 29, 356-362 (1988)), Dunican and Shivnan (Bio/Technology 7, 1067-1070 (1989)) and Tauch et al.' (FEMS Microbiological Letters 123, 343-347 (1994)). After homologous recombination by means of a "cross over" event, the resulting strain contains at least two copies^' of the gene in question.

In addition, it may be advantageous for the production of amino acids, in particular L-methionine, to enhance one or more enzymes of the particular biosynthesis pathway, of glycolysis, of anaplerosis, of the citric acid cycle or of amino acid export, in addition to the metH gene.

Thus for the preparation of amino acids, in particular L- methionine, one or more genes chosen from the group consisting of

• the gap gene which codes for glyceraldehyde 3-phosphate dehydrogenase (Eikmanns (1992), Journal of Bacteriology 174:6076-6086),

• the tpi gene which codes for triose phosphate isomerase (Eikmanns (1992), Journal of Bacteriology 174:6076-6086), • the pgk gene which codes for 3-phosphoglycerate kinase (Eikmanns (1992), Journal of Bacteriology 174:6076-6086),

• the pyc gene which codes for pyruvate carboxylase (Eikmanns (1992), Journal of Bacteriology 174:6076-6086),

• the lysC gene which codes for a feed-back resistant aspartate kinase (ACCESSION NUMBER P26512; EP-B-0387527; EP-A-0699759) ,

• the metA gene which codes for homoserine 0- acetyltransferase (ACCESSION Number AF052652) ,

• the metB gene which codes for cystathionine gamma- synthase (ACCESSION Number AF126953) ,

• the aecD gene which codes for cystathionine gamma-lyase (ACCESSION Number M89931)

• the glyA gene which codes for serine hydroxymethyltransferase (JP-A-08107788) ,

• the metY gene which codes for O-acetylhomoserine- sulfhydrylase (DSM 13556)

can be enhanced, in particular over-expressed.

It may furthermore be advantageous for the production of amino acids, in particular L-methionine, in addition to the enhancement of the metH gene, for one or more genes chosen from the group consisting of

• the thrB gene which codes for homoserine kinase (ACCESSION Number P08210) ,

• the ilvA gene which codes for threonine dehydratase (ACCESSION Number Q04513) ,

• the thrC gene which codes for threonine synthase (ACCESSION Number P23669) , • the ddh gene which codes for meso-diaminopimelate D-dehydrogenase (ACCESSION Number Y00151) ,

• the pck gene which codes for phosphoenol pyruvate carboxykinase (DE 199 50 409.1; DSM 13047),

• the pgi gene which codes for glucose 6-phosphate isomerase (US 09/396,478; DSM 12969),

• the poxB gene which codes for pyruvate oxidase

(DE: 1995 1975.7; DSM 13114)

. to be attenuated, in particular for the expression thereof . to be reduced.

The term "attenuation" in this connection describes the reduction or elimination of the intracellular activity of one or more enzymes (proteins) in a microorganism which are coded by the corresponding. DNA, for example by using a weak promoter or using a gene or allele which codes for a

- corresponding enzyme with a low activity or inactivates the corresponding gene or enzyme (protein) , and optionally combining these measures.

By attenuation measures, the activity or concentration of the corresponding protein is in general reduced to 0 to 50%, 0 to 25%, 0 to 10% or 0 to 5% of the activity or concentration of the wild-type protein.

In addition to over-expression of the metH gene it may furthermore be advantageous, for the production of amino acids, in particular L-methionine, to eliminate undesirable side reactions, (Nakayama: "Breeding of Amino Acid Producing Micro-organisms", in: Overproduction of Microbial Products, Krumphanzl, Sikyta, Vanek (eds.), Academic Press, London, UK, 1982) .

The microorganisms prepared according to the invention can be cultured continuously or discontinuously in the batch process (batch culture) or in the fed batch (feed process) or repeated fed batch process (repetitive feed process) for the purpose of production of amino acids, in particular L-methionine. A summary of known culture methods is described in the textbook by Chmiel (Bioprozesstechnik 1. Einfuhrung in die Bioverfahrenstechnik (Gustav Fischer Verlag, Stuttgart, 1991)) or in the textbook by Storhas (Bioreaktoren und periphere Einrichtungen (Vieweg Verlag, Braunschweig/Wiesbaden, 1994) ) . The culture medium to be used must meet the requirements of the particular strains in a suitable manner. Descriptions of culture media for various microorganisms are contained in the handbook "Manual of Methods for General Bacteriology" of the American Society for Bacteriology (Washington D.C., USA, 1981).

Sugars and carbohydrates, such as e.g. glucose, sucrose, lactose, fructose, maltose, molasses, starch and cellulose, oils and fats, such as e.g. soya-oil, sunflower oil, groundnut oil and coconut fat, fatty acids, such as e.g. palmitic acid, stearic acid and linoleic acid, alcohols, such as e.g. glycerol and ethanol, and organic acids, such as e.g. acetic acid, can be used as the source of carbon. These substances can be used individually or as a mixture.

Organic nitrogen-containing compounds, such as peptones, yeast extract, meat extract, malt extract, corn steep liquor, soya bean flour and urea, or inorganic compounds, such as ammonium sulfate, ammonium chloride, ammonium phosphate, ammonium carbonate and ammonium nitrate, can be used as the source of nitrogen. The sources of nitrogen can be used individually or as a mixture.

Organic and inorganic sulfur-containing compounds, such as, for example, sulfides, sulfites, sulfates and thiosulfates, can be used as a source of sulfur, in particular for the preparation of methionine. Phosphoric acid, potassium dihydrogen phosphate or dipotassium hydrogen phosphate or the corresponding sodium- containing salts can be used as the source of phosphorus. The culture medium must furthermore comprise salts of metals, such as e. g. magnesium sulfate or iron sulfate, which are necessary for growth. Finally, essential growth substances, such as amino acids and vitamins, can be employed in addition to the above-mentioned substances. Suitable precursors can moreover be added to the culture medium. The starting substances mentioned can be added to the culture in the form of a single batch, or can be fed in during the culture in a suitable manner.

Basic compounds, such as sodium hydroxide, potassium hydroxide, ammonia or aqueous ammonia, or acid compounds, such as phosphoric acid or sulfuric acid, can be employed in a suitable manner to control the pH of the culture. Antifoams, such as e.g. fatty acid polyglycol esters, can be employed to control the development of foam. Suitable substances having a selective action, such as e.g. antibiotics, can be added to the medium to maintain the stability of plasmids. To maintain aerobic conditions, oxygen or oxygen-containing gas mixtures, such as e.g. air, are introduced into the culture. The temperature of the culture is usually 20°C to 45°C, and preferably 25°C to 40°C. Culturing is continued until a maximum of the desired product has formed. This target is usually reached within 10 hours to 160 hours.

The fermentation broths obtained in this way, in particular containing L-methionine, usually have a dry weight of 7.5 to 25 wt.% and contain L-methionine. It is furthermore also advantageous if the fermentation is conducted in a sugar- limited procedure at least at the end, but in particular over at least 30% of the duration of the fermentation. That is to say, the concentration of utilizable sugar in the fermentation medium is reduced to > 0 to 3 g/1 during this period.

The fermentation broth prepared in this manner, in particular containing L-methionine, is then further processed. Depending on requirements, all or some of the biomass can be removed from the fermentation broth by separation methods, such as e.g. centrifugation, filtration, decanting or a combination thereof, or it can be left completely in this. This broth is then thickened or concentrated by known methods, such as e.g. with the aid of a rotary evaporator, thin film evaporator, falling film evaporator, by reverse osmosis, or by nanofiltration. This concentrated - fermentation broth can then be worked up by ".^' methods' of freeze drying, spray drying, spray granulation or by other processes to give a preferably free-flowing, finely divided powder.

This free-flowing, finely divided powder can then in turn by converted by suitable compacting or granulating processes into a coarse-grained, readily free-flowing, storable and largely dust-free product. In the granulation or compacting it is advantageous to employ conventional organic or inorganic auxiliary substances or carriers, such as starch, gelatin, cellulose derivatives or similar substances, such as are conventionally used as binders, gelling agents or thickeners in foodstuffs or feedstuffs processing, or further substances, such as, for example, silicas, silicates or stearates.

"Free-flowing" is understood as meaning powders which flow unimpeded out of the vessel with the opening of 5 mm (millimeters) of a series of glass outflow vessels with outflow openings of various sizes (Klein, Seifen, Ole, Fette, Wachse 94, 12 (1968)).

As described here, "finely divided" means a powder with a predominant content (> 50 %) with a particle size of 20 to 200 μm diameter. "Coarse-grained" means products with a predominant content (> 50 %) with a particle size of 200 to 2000 μm diameter. In this context, "dust-free" means that the product contains only small contents (< 5 %) with particle sizes of less than 20 μm diameter. The particle size determination can be carried out with methods of laser diffraction spectrometry. The corresponding methods are described in the textbook on "Teilchengrδβenmessung in der Laborpraxis" by R. H. Muller and R. Schuhmann, Wissenschaftliche Verlagsgesellschaft Stuttgart (1996) or in the textbook "Introduction to Particle Technology" by M. Rhodes, Verlag Wiley & Sons (1998).

"Storable" in the context of this invention means a product which can be stored for up to 120 days, preferably up to 52 weeks, particularly preferably 60 months, without a^' substantial loss (< 5%) of methionine occurring.

Alternatively, however, the product can be absorbed on to an organic or inorganic carrier substance which is known and conventional in feedstuffs processing, such as, for example, silicas, silicates, grits, brans, meals, starches, sugars or others, and/or mixed and stabilized with conventional thickeners or binders. Use examples and processes in this context are described in the literature (Die Mϋhle + Mischfuttertechnik 132 (1995) 49, page 817). Finally, the product can be brought into a state in which it is stable to digestion by animal stomachs, in particular the stomach of ruminants, by coating processes ("coating") using film-forming agents, such as, for example, metal carbonates, silicas, silicates, alginates, stearates, starches, gums and cellulose ethers, as described in DE-C-4100920.

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QJ ι-3 3 \ CO l-¹ o *« QJ CO LQ μ- <! μ- μ- hi μ- O CO H H • : rt O o H ft) 3 Φ Hi l-" l-J⁴ Ω o- O G C ts H -* CU μ- rt CO ^■ O 3 TJ C Φ C Φ O Hi Ω 0 α Ω ft) Hi

!-^■ Φ Φ Φ hi tr Φ rt CO H- 3 Φ rt ft) rt TJ rt . μ- hi tr Hi S Hi c Φ rt Φ CQ CO

^ CO TJ CO H- Ω h μ- 0⁾ 3 μ- rt μ- CO O CO φ TJ Φ TJ rt rt CO ff Φ CO rt φ H- Φ rt rt O o Ω O Ω u 3 μ- 3 O 3 ^■-a Ω α ri^¬ hi rt hi tr " CO α ft)

O 3 3 3' ft⁾ h 3 ff ft) hi 3 μ- 3 ιQ Ό ιQ r ^{^} C ft) ft) rt O ft) rt φ Φ φ rt

1-1 o P. Φ 3 Ω ft) 3 3^" Φ ft) Ω 3 σ 0 tr 0 CO Z QJ μ- tr a. hi CQ H- Ω rt Q⁾ H- Φ Ω ω O ft) O CO hi Φ Ω h-* N) I-^* φ μ- . ff 3 3 φ μ- ft) iQ O 3 hi Φ ff h-¹ CO α i μ- < DO Ol Hi 3 Hi φ ⁽Q 0. Φ ^■ : I-¹ o • ; ^o a 3 Φ α rt

CQ ft) H ιQ CU CO Φ ft⁾ α μ- I-¹ • φ CO o dp o rt < H TS TJ μ-

3 H- Ω O 3 to r+ > . . <! tr* μ- 0. 3 o\o o\o Φ Φ Φ p^j ftJ H <!

3 H- O Φ TJ hti i Ό ft) Ό μ- H 1 3 μ- μ- o -. O J -- 3 3 hi hi φ φ

H- Ω 3 3 H- hi Φ O h-¹ 3 _^-_^ ft⁾ rt 3- H Ω tr 3 3 Hi rt rt rt Φ rt

X o H- 3 o CO hi Hi Φ tr μ- Ω 3 0⁾ Φ ; h-¹ Ω tr T rt TJ μ- ff μ- o ft) rt O hi hi Ω Ω x H- C _^ μ- 3 rt 3 *- ω c: ft) H μ- hi ft O hi O O Φ TJ Ω 3 Ω

£ C Φ I-^* c n Φ 3 Ω ft) O μ- μ- rt n o Φ ff Φ Hi 3 CO hi μ- Ω hi σ μ*¹ •O, 3 C Ω Φ X ft) ft) ff ts 3 rt 3 μ- 3 φ ff α 3 Hi Φ I-¹ Hi Φ φ h-* 3 o

Φ CO H- C H- rt C hi Ω O 3" 3 Φ Φ μ- Φ • ft) Φ o Φ C CQ ft) &) hi co rt (O H- x H- . μ- Φ Ω . . Ω Φ ω Ω •_^ tr¹ rt CO hi tr o hi T3 rt tr Φ hi 3 ft) 0 hi rt 3 H- TJ Ω r+ ft) ft O 3 h-> μ-* 1 3 μ- o co ft) μ- o\o ft) tr cu 3 rt μ- r+ 3 H- Φ c ιQ h H μ- H O tr μ- ■C t-< ft) μ- o H tr 0 . tr rt φ <! rt O 3

O Ω 3 H Φ ft> Ω hi Ω ft⁾ Ω _^-, α 1 3 Ω 3 iQ μ- h-" 3 μ- O Φ H TJ iQ

Φ φ φ "* rt Ω O h-¹ rt Φ <5 μ- hi ft) O ^ . ft⁾ •- σ μ- ιQ hi rt 01 Hi 3 1 ff H- Ό ft) ft) ^{^} ft) 3 o rt ^■ 3 to H μ- 3 3 ft) O rt tr 0 rt D 3 φ r+ α Ω o 3^* 3 Ω μ- <! hH O 0 O μ- CO f= CΛ 3 C o 0 O 3 TJ O

Φ 3 hi CO φ ^•< hj • μ- 3 Φ μ- μ- 0⁾ μ- μ- hi Ω Φ TJ _"* T o\° 3 rt O μ- O

Φ 3 •> tr¹ rt Φ 0- φ H 3 α 3 rt 3 ft⁾ iQ rt TJ ft) ft⁾ O Ω hi rt hi 3 1 t H- - •^• _^ O — — ' μ- 0) Φ Ω ft) ff tr ft) rt TJ 3 rt co tr h-¹ rt tr

Φ rt ft) 3 H- U CU μ- rt (-^■ 3 3 ** H- 3 Φ ^•• H O hi O O T CO Φ C CO μ- Φ ω £ CO Φ O TJ h-* 3 h-¹ O — ' φ μ- O- μ- 1 ft) Φ rt hi Φ rt C o

S-. O hi rt 3 H O ft> ft⁾ • 3 < — 3 tr* O O IT¹ TJ r+ n Hi ff ⁽.3 φ 0 3 μ- σ 3 μ- h-¹ 3 H- cu ff H- O O H Ω rt μ- μ- CO 1 3 1 hi Φ o\° Φ Φ C 1 Hi ft) O CO 3 rt Φ 3 H- 3 <l Φ h-¹ ft tf ^ Ω rt rh Ω co 3 o hi hj o\o Φ 3 CO 3 ri^¬ O <i

H- α iQ Ω O Φ φ • ^*•< μ- hi ff o 0⁾ < Ω p- tr Φ α QJ hi φ ft) Hi φ

3 O 3 _^ Ω Φ Φ rt 3 μ- ff H o Φ rt c o tr ft) ft) tr TJ μ- 3 3 ιQ Ω ftJ 3 H- CU rt ι-3 Φ •< μ- μ- fi- O (0 co 3 ff Ω Hi h-^* O ft) tr CD QJ 3 O rt rt ft) Ω 3 3 ff tr rt ft⁾ 3 3 ft) ω O Φ TJ μ- rt hh TJ 3 H hi Φ ff H-

O 3 to Φ Φ O. Φ Φ 3¹ Ω ^" Ω μ- μ- 3 φ 3 3 H o CΛ φ α •< QJ rt CO (0 O ι-f C 3 \ CO Φ μ- ft) 3 Ω W μ- 3 μ- O 3 c Ω rt ff 3 tr H- rt O Φ ^• α h Ω σs 3 3 Hi ^• μ- s: TJ rt c Φ CD

Φ rt H Ω hi tr H Hi Φ hi Φ 3 tr TJ α ft⁾ ft⁾ ft⁾ O ro hi O α Φ μ- rt O tr σ rt 3 D H X ιs> 0 3 Ω O Hi r+ o μ- h-* Φ 1 * Φ 3 μ- tr O H Ω Φ o H 1 3 Hi ff

concentrated fermentation broth, or also during the drying or granulation process. It is likewise possible to add an organic substance or a mixture of several organic substances to the fermentation broth and a further organic substance or a further mixture of several organic substances during a later process step, for example granulation. t The product described above is suitable as a feedstuffs additive, i.e. feed additive, for animal nutrition.

The L-methionine content of the . animal feedstuffs additive 'is conventionally 1 wt.%^* to 80 wt.%, preferably 2 wt.% to 80 wt.%, particularly preferably ,4 wt.% to 80 wt.%, and very particularly preferably 8 wt.% to 80 wt.%, based on the dry weight of the animal feedstuffs additive. Contents of 1 wt.% to 60 wt.%, 2 wt.% to 60 wt.%, 4 wt.% to 60 wt.%, 6 wt.% to 60 wt.%, .1 wt.%. to 40 wt.%, 2 wt.% to 40 wt.% or 4 wt.% to 40 wt.% are likewise possible. The water content of the feedstuffs additive is conventionally up to 5 wt.%, . preferably up to 4 wt.%, and particularly preferably less than 2 wt.%.

The invention accordingly also provides a process for the preparation of an L-methionine-containing animal feedstuffs additive from fermentation broths, which comprises the steps

a) culture and fermentation of an L-methionine-producing microorganism in a fermentation medium;

b) removal of water from the L-methionine-containing fermentation broth (concentration) ;

c) removal of an amount of 0 to 100 wt.% of the biomass formed during the fermentation; and d) drying of the fermentation broth obtained according to a) and/or b) to obtain the animal feedstuffs additive in the desired powder or granule form.

If desired, one or more of the following steps can furthermore be carried out in the process according to the invention:

e) addition of one or more organic substances, including L-methionine and/or D-methionine and/or the racemic mixture D, L-methionine, to the products obtained, according to a) , b) and/or c) ; f) addition of auxiliary substances chosen from the group consisting of silicas, silicates, stearates, grits and bran to the substances obtained according to a) to d) for stabilization and to increase the storability; or g) conversion of the substances obtained according to a) ■ to e) into a form stable to the animal stomach, in particular rumen, by coating with film-forming agents.

The analysis of L-methionine can be carried out by ion exchange chromatography with subsequent ninhydrin derivation, as described by Spackman et al. (Analytical Chemistry, 30, (1958), 1190).

The process according to the invention is used for the fermentative preparation of amino acids, in particular L- methionine.

The following microorganism was deposited as a pure culture on 14th June 2001 at the Deutsche Sammlung fur Mikroorganismen und Zellkulturen (DSMZ = German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany) in accordance with the Budapest Treaty: • Escherichia coli DH5αmcr/pCREmetH as DSM 14354. The present invention is explained in more detail in the following with the aid of embodiment examples.

Example 1

Preparation of a genomic cosmid gene library from Corynebacterium glutamicum ATCC 13032

Chromosomal DNA from Corynebacterium glutamicum ATCC 13032 was isolated as described by Tauch et al. (1995, Plasmid 33:168-179) and partly cleaved with the restriction enzyme Sau3AI (Amersham Pharmacia, Freiburg, Germany, Product Description Sau3AI, Code no. 27-0913-02). The DNA fragments were dephosphorylated with shrimp alkaline phosphatase (Roche Diagnostics GmbH, Mannheim, Germany, Product Description SAP, Code no. 1758250) .

The DNA of the cosmid vector SuperCosl (Wahl et al. (1987) Proceedings of the National Academy of Sciences USA

84:2160-2164), obtained from Stratagene (La Jolla, USA, Product Description SuperCosl Cosmid Vector Kit, Code no. 251301) was cleaved with the restriction enzyme Xbal (Amersham Pharmacia, Freiburg, Germany, Product Description Xbal, Code no. 27-0948-02) and likewise dephosphorylated with shrimp alkaline phosphatase. The cosmid DNA was then cleaved with the restriction enzyme BamHI (Amersham Pharmacia, Freiburg, Germany, Product Description BamHI, Code no. 27-0868-04) . The cosmid DNA treated in this manner was mixed with the treated ATCC13032 DNA and the batch was treated with T4 DNA ligase (Amersham Pharmacia, Freiburg, Germany, Product Description T4-DNA-Ligase, Code no.27- 0870-04) . The ligation mixture was then packed in phages with the aid of Gigapack II XL Packing Extract (Stratagene, La Jolla, USA, Product Description Gigapack II XL Packing Extract, Code no. 200217) .

For infection of the E. coli strain NM554 (Raleigh et al. 1988, Nucleic Acid Research 16:1563-1575) the cells were taken up in 10 mM MgS0₄ and mixed with an aliquot of the phage suspension. The infection and titering of the cosmid library were carried out as described by Sambrook et al. (1989, Molecular Cloning: A laboratory Manual, Cold Spring Harbor) , the cells being plated out on LB agar (Lennox, 1955, Virology, 1:190) with 100 mg/1 ampicillin. After incubation overnight at 37 °C, recombinant individual clones were selected.

Example 2

Isolation and sequencing of the metH gene

The cosmid DNA of an individual colony was isolated with the Qiaprep Spin Miniprep Kit (Product No. 27106, Qiagen, Hilden, Germany) in accordance with the manufacturer's instructions and partly cleaved with the restriction enzyme Sau3AI (Amersham Pharmacia, Freiburg, Germany, Product Description Sau3AI, Product No. 27-0913-02). The DNA fragments were dephosphorylated with shrimp alkaline phosphatase (Roche Diagnostics GmbH, Mannheim, Germany, Product Description SAP, Product No. 1758250) . After separation by gel electrophoresis, the cosmid fragments in the size range of 1500 to 2000 bp were isolated with the QiaExII Gel Extraction Kit (Product No. 20021, Qiagen, Hilden, Germany) .

The DNA of the sequencing vector pZero-1, obtained from Invitrogen (Groningen, The Netherlands, Product Description Zero Background Cloning Kit, Product No. K2500-01) was cleaved with the restriction enzyme BamHI (Amersham Pharmacia, Freiburg, Germany, Product Description BamHI, Product No. 27-0868-04) . The ligation of the cosmid fragments in the sequencing vector pZero-1 was carried out as described by Sambrook et al. (1989, Molecular Cloning: A laboratory Manual, Cold Spring Harbor), the DNA mixture being incubated overnight with T4 ligase (Pharmacia Biotech, Freiburg, Germany) . This ligation mixture was then J K> μ^ h-¹ o Cπ o 01 o j Hi > 1-3 > € ι-3 J I-¹ rt ι-3 CD -2 rt ø tu ~~3 •X) α tα Ω ι-3 < CO Φ ff H 3 tr φ μ- ff N J-. ff tr Φ Φ ^•^1 ff co μ- ?0 *> hi μ- μ- PJ ff μ- -J hi N3 (--

Φ OJ ft) Φ CO rt Φ Φ ._* Φ Φ H lO M Φ Φ o tr .. O α H H Φ hi .. 0 LO Φ

3 h-> Φ tr H r 3 0 CO 0 CJi Ω Φ 0- hi O Ω .. Ω

3 φ << H tf) Ω O > CΛ H ft) Φ . Ω CQ α — . JS. Φ o φ μ- TJ μ-¹ n Φ LO rt φ CO Φ H el^¬ O I-¹ rt ft) 3 3 h-¹ h Φ co cu μ> σ-i Φ p 3 φ h-* o α-. Φ it--. hi rt o μ- CO Ω s' 3 1 Q⁾ s: ^ Ω ^• ; ι-3 rt 3 U3 ω α ><; QJ iQ π 0. ω 0

X Hi CΛ C tr Φ TJ IV) — Φ e tr Φ μ- Ω 1 μ- CO ^> 1 μ- 1 TJ

H c Φ Φ co • hi ?3 ft) Φ Φ 3 3 o CTi 3 Ω cπ o 3 > α-> 3 O ιQ ω 0 rt X rt hi μ- 3 Φ o 3 3 co -* it-. ιQ tr Φ 0 μ- 01 vQ ~~- hi

Φ o-i Hi μ- μ> z Φ μ- — - Λ H rt μ- Ω CO ι-3 σi O H rt α I-¹ ti--. CO QJ

3 σi 3 •fc. hi <1 J ø hi ff μ- Φ . — . Φ -3 μ- 3 .. μ- r+

Φ IV) rt in • • i ) 1 ft) <! H Φ O Φ 3 TJ •τ) hi ^' C — o 3 o ≤, J -¹ O 3 Φ tr t ft) rt Φ 0 3 3 -\ lQ h 3 Ω Hi 3 μ- h o Hi rt

Ω tr φ 3 μ¹ TJ CO μ- hi ιQ Ω W CO hi O μ- ^■S rt ^• rt φ o ft) O

O ft) ø hi CQ <! O hi Φ <τ) Q⁾ μ- hi ft) 3 Φ μ- rt Φ tr TJ ' — 3 rt _^ — .

CO 3 Ω 1 o μ- φ μ- ft) M H co Φ rt d ft) μ- rt ff H . J ff rt ι-3 φ Φ ø h-¹ > IQ ω CO o 3 α h-¹ .ft⁾ ft) --H- Ω rt Ω ff Φ 3 ω hi s: Φ ff QJ

CO 0 Φ LO hi rt 3 ft> CO Ω Ω O rt O μ- ι-3 μ- 0⁾ μ- TJ Φ ø

TJ H O h-¹ ft) Φ z J rt J hi H rt 3 hj 3 a 3 ff o rt rt (-^■ Z Ω hh ft) φ <ϊ — 3 φ <£> ft⁾ OJ TJ 0 ^ μ- a- Ω 0 QJ Q⁾ Φ H μ- tr QJ QJ M ff o μ- o μ- • H -J Ω I-** ff H O tr 0 O μ- rt rt o 0 rt rt hi H rt α. Ω Φ 1 0 μ- Φ ft) p ^> >< 0- μ- μ- μ- CD tr 3 Oi Φ μ- Φ O μ- Φ CJ O o ft) σ Φ 3 Ω ω Hi o o Φ o o α O Ω rt ft) rt α. ft) U3 rt μ- s; vQ *-. h-¹ μ- 3 3 ^■-a rt 0 3 O φ CO QJ μ- CO Φ OJ Q α Φ Φ o Φ J Ω ft) 0 Hi 3 o ft) μ-* QJ

TJ s. φ α 3 CO 1-3 μ- w Φ Φ hi CO φ ft> H 3 Φ VJD >Q C- μ- h-* hi tr CQ ^•X3 Φ φ 3" _^-_^ 3 μ- H 3 Φ o ω CO π- φ 3 OΛ rt ^. rt .

O μ- φ 0 _^ 3 Φ μ- φ o 3 Φ *. Φ φ μ- ^■ rt Ω o tr -- co rt Ω ^•£. φ hi lO O ft) o Ω h-¹ ^•£! QJ o Ω ff μ- o Φ O Ω rt h-¹

Φ ff 0 3 Φ I-¹ μ- 00 3 φ OJ Φ C H 3 ft) O 3 N 3 0⁾ H < ⁾ μ- Φ Ω I-¹ ιQ φ 3 en •c ω • h-¹ H O Φ Ω ω * α ιQ _^-_^ H Φ α QJ VD

3 ≤: 3 Φ <£> μ- α α Φ rt — H rt εi 3 tr Φ >T3 Φ O tr¹ φ μ- a) Ω 00 o μ- H Φ _-_^ μ- H Φ Ω •_^ ft) 3 o « hi Ω Ω 133 3 3

O CO Φ μ- σi 3 rt <1 3 Φ 3 - κ> φ O μ- μ- Ω

-_^ ^• Hi ft) 0 o μ-

Hi ω o μ- c ω μ- υ_> α J rt 3 ¹ Ω ω !__ 3 QJ D "3

Ω CO ft) Ω rt rt .. tr φ iQ 00 O 0 ω c; ff . vQ o ffi t? ft) tr ω 3 3 0) 0 μ^{j "} .. — . ff μ¹ o o hi .. hi Hi Ω Ω μ- QJ hh CJl S f-O μ-* 0 tr C ft⁾ ft) φ Φ si — - i= H O t h-¹ 3 QJ rt 3 H ω

!O h-¹ Z o Ω h-* Ω h-* μ- 3 Φ rt rt Φ rt μ- O μ- ω Q hi QJ ω h-¹ 3

Φ Φ s. μ- ^ o Ω μ- tr _^-. CO QJ rt Ti 3 Ω φ hi a 3 _— . Ω Ω S

3 Φ CQ 3 O J rt Φ HJ μ- μ- _; -J ιQ μ- hi μ- o rt tr> μ- H μ-

OJ μ- μ- rt Φ H φ hi 3 Cfl rt - — Φ φ . Φ φ Ω

3 rt μ- Ω o μ- Λ Ω 0 hi 3 0 Hi . rt 3 φ α Ω 3 3 . . hj μ- tr 3 3 y ø μ- Ω CO ft⁾ ft) hi O Ω rt U) H 3 Ω Q O

3 ^■ ø Φ Q. Φ rt a c: 3 0 i-3 φ 0 o 0 0 Φ h t o 0 CO Ω ft) 0 2 CO CQ PJ H Ω 3 Φ ^'3 - N ω QJ 0 o 3 X CQ OJ μ-

3 J M μ- CO c Ω CO rt ?d hi Φ μ- -> rt r-o Φ 3 o c Φ φ lO α CO Φ ?α Φ rt o o BJ

-« 3 ^■τ) g G . o O C rt (-^■

Ω rt 3 CO J co Φ H S rt 3 ft) M 3 y tr o μ> . **« μ- tc hi Ω CO μ- O μ- BJ 3 w Φ c/_ _^--. _^ ≤ ^D ui t-¹ hi α Φ 0 0 φ 0 o TJ H s J H • H¹ OJ ( l . Φ ω ιQ Φ TJ 3 H cu O 3 tr • TJ 3 l£> rt O ui > ⁽£⁾ rf

• Φ ft) s ft) rt hi μ- o CO J ,ft⁾ -J ff μ- UD rt

3 Q. o hi μ- rt Ω

. 3 ϋύ H μ- s; μ- 3 • -J Φ OJ •_* O Φ

Φ μ- Φ (Q ff tr ιQ -^1 Φ co μ- 3 ιQ H

3 α Φ •_^ -J. CQ (ϋ φ O μ-¹ o O. Φ 3

Hi rt

Example 3

Preparation of the strain C. glutamicum ATCCl3032/pCREmetH

3.1 Amplification of the metH gene

From the strain ATCC13032, chromosomal DNA was isolated by the method of Eikmanns et al. (Microbiology 140: 1817 -1828 (1994)). Starting from the nucleotide sequences of the methionine biosynthesis genes metH (SEQ ID No. 1) of C. glutamicum ATCC13032, the following oligonucleotides were chosen for the polymerase chain reaction (PCR) (see SEQ ID No. -3 and SEQ ID No. 4) :

metH-EVP5:

5 ' -GATCTAAGATCTAAAGGAGGACAACCATGTCTACTTCAGTTACTTCACCAGC-3 '

^■ metH-EVP3 :

5 ' -GATCTAGTCGACCCCTCTCAAAGGT.GTTAGAC-3 ' The primers shown were synthesized by MWG-Biotech AG

(Ebersberg, Germany) and the PCR reaction was carried out by the standard PCR method of Innis et al. (PCR Protocols. A Guide to Methods and Applications, 1990, Academic Press) with Pwo-Polymerase from Roche Diagnostics GmbH (Mannheim, Germany) . With the aid of the polymerase chain reaction, the primers allow amplification of a DNA fragment 3718 bp in size, which carries the metH gene.

Furthermore, the primer metH-EVP5 contains the sequence for the cleavage site of the restriction endonuclease Bglll and the primer metH-EVP3 the cleavage site of the restriction endonuclease Sail, which are marked by underlining in the nucleotide sequence shown above.

The metH fragment 3718 bp in size was cleaved with the restriction endonucleases Bglll and Sail. The batch was separated by gel electrophoresis and the metH fragment

(approx. 3700 bp) was then isolated from the agarose gel with the QiaExII Gel Extraction Kit (Product No. 20021, Qiagen, Hilden, Germany) .

3.2 Cloning of metH in the vector pZ8-l

The E. coli - C. glutamicum shuttle expression vector pZ8-l (EP 0 375 889) was used as the base vector for the expression.

DNA of the plasmid pZ8-l was cleaved completely with the restriction enzymes BamHI and Sail and then dephosphorylated with shrimp alkaline phosphatase (Roche Diagnostics GmbH, Mannheim, Germany, Product Description SAP, Product No. 1758250) .

The metH fragment approx. 3700 bp in size isolated from the agarose gel in example 3.1 and cleaved with the restriction endonucleases Bglll and Sail was mixed with the vector pZ8- 1 prepared in this way and the batch was treated with T4

DNA ligase (Amersham Pharmacia, Freiburg, Germany, Product Description T4-DNA-Ligase, Code no.27-0870-04) .

The ligation batch was transformed in the E. coli strain DH5αmcr (Hanahan, In: DNA cloning. A Practical Approach. Vol. I. IRL-Press, Oxford, Washington DC, USA). Selection of plasmid-carrying cells was made by plating out the transformation batch on LB agar (Lennox, 1955, Virology, 1:190) with 50 mg/1 kanamycin. After incubation overnight at 37°C, recombinant individual clones were selected. Plasmid DNA was isolated from a transformant with the Qiaprep Spin Miniprep Kit (Product No. 27106, Qiagen, Hilden, Germany) in accordance with the manufacturer's instructions and checked by restriction cleavage. The resulting plasmid was called pCREmetH. The strain E. coli DH5αmcr/pCREmetH was deposited as a pure culture on 14th June 2001 at the Deutsche Sammlung fur Mikroorganismen und Zellkulturen (DSMZ = German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany) in accordance with the Budapest Treaty as DSM 14354.

3.3 Preparation of the strain C. glutamicum ATCCl3032/pCREmetH

The vector pCREmetH obtained in example 3.2 was electroporated in the strain C. glutamicum ATCC13032 using the electroporation method described by Liebl et al. (FEMS Microbiology Letters, 53:299-303 (1989)). Selection of the plasmid-carrying cells took place on LBHIS agar comprising 18.5 g/1 brain-heart infusion broth, 0.5 M sorbitol, 5 g/1 " Bacto-tryptone, 2.5 g/1 Bacto-yeast extract, 5 g/1 NaCl and 18 g/1 Bacto-agar, which had bee.n supplemented with 25 mg/1 kanamycin. Incubation was carried out for 2 days at 33°C.

Plasmid DNA was isolated from a transformant by conventional methods (Pete-rs-Wendisch et al., 1998,

Microbiology 144, 915-927) and checked by restriction cleavage. The resulting strain was called ATCC13032pCREmetH.

Example 4 Preparation of methionine with the strain C. glutamicum ATCCl3032/pCREmetH

The C. glutamicum strain ATCC13032/pCREmetH obtained in example 3 was cultured in a nutrient medium suitable for the production of methionine and the methionine content in the culture supernatant was determined.

For this, the strain was first incubated on an agar plate with the corresponding antibiotic (brain-heart agar with kanamycin (25 mg/1) ) for 24 hours at 33°C. Starting from this agar plate culture, a preculture was seeded (10 ml medium in a 100 ml conical flask) . The medium MM was used as the medium for the preculture . Medium MM

CSL (corn steep liquor) 5 g/1

MOPS (morpholinopropanesulfonic acid) 20 g/1

Glucose (autoclaved separately) 50g/l

Salts:

(NH₄)₂S0₄ 25 g/1

KH₂P0₄ 0.1 g/1

MgS0₄ * 7 H₂0 1.0 g/1

CaCl₂ * 2. H₂0 10 mg/1

FeS0 .* 7 H₂0 - 10 mg/1

MnS0₄ * H₂0 5.0mg/l

Biotin (sterile-filtered) 0.01 mg/1

Vitamin B12 (sterile-filtered) 0.02 mg/1

Thiamine * HC1 (sterile-filtered) 0.2 mg/1

CaC0₃ 25 g/1

The CSL, MOPS and the salt solution were brought to pH 7 with aqueous ammonia and autoclaved. The sterile substrate and vitamin solutions were then added, as well as the CaC0₃ autoclaved in the dry state.

Kanamycin (25 mg/1) was added to this. The preculture was incubated for 16 hours at 33°C at 240 rpm on a shaking machine. A main culture was seeded from this preculture such that the initial OD (660 nm) of the main culture was 0.1. Medium MM was also used for the main culture. Culturing is carried out in a 10 ml volume in a 100 ml conical flask with baffles. Kanamycin (25 mg/1) was added. Culturing was carried out at 33°C and 80% atmospheric humidity.

After 72 hours, the OD was determined at a measurement wavelength of 660 nm with a Biomek 1000 (Beckmann Instruments GmbH, Munich) . The amount of methionine formed was determined with an amino acid analyzer from Eppendorf- BioTronik (Hamburg, Germany) by ion exchange chromatography and post-column derivation with ninhydrin detection.

The result of the experiment is shown in table 1.

Table 1

Brief description of the figure:

Figure 1 : Plasmid pCREmetH

The abbreviations used in the figures have the following meaning:

Km: Resistance gene for kanamycin metH: metH gene of C. glutamicum Ptac: tac promoter Tl T2: Terminator T1T2 of the rrnB gene of E. coli rep: Plas id-coded replication origin for C. glutamicum (of pHM1519)

EcoRI ; Cleavage site of the restriction enzyme EcoRI

Sail: Cleavage site of the restriction enzyme Sail

Claims

W■hat: is claimed is:

1. An isolated polynucleotide from coryneform bacteria, comprising a polynucleotide sequence chosen from the group consisting of

c) polynucleotide which is complementary to the polynucleotides of a) or b) , and

d) polynucleotide comprising at least 15 successive nucleotides of the polynucleotide sequence of a) , b) or c) .

2. A polynucleotide as claimed in claim 1, wherein the polynucleotide is a preferably recombinant DNA which is capable of replication in coryneform bacteria.

3. A polynucleotide as claimed in claim 1, wherein the polynucleotide is an RNA.

4. A polynucleotide as claimed in claim 2, comprising the nucleic acid sequence as shown in SEQ ID No. 1.

5. A DNA as claimed in claim 2 which is capable of replication, comprising

(i) the nucleotide sequence shown in SEQ ID No. 1, or (ii) at least one sequence which corresponds to sequence (i) within the range of the degeneration of the genetic code, or

(iii) at least .one sequence which hybridizes with the sequence complementary to sequence (i) or (ii) , and optionally

(iv) sense mutations of neutral function in (i) .

6. A polynucleotide sequence as claimed in claim 2, which codes for a polypeptide which comprises the amino acid sequence, in SEQ ID No. 2.

7. A coryneform bacterium in which the metH gene is enhanced, in particular over-expressed.

8. A coryneform bacterium serving as the host cell, which contains a vector which carries a polynucleotide as claimed in claim 1.

9. Escherichia coli strain DH5αmcr/pCREmetH as DSM 14354 deposited at the Deutsche Sammlung fur Mikroorganismen und Zellkulturen [German Collection of Microorganisms and Cell Cultures] , Braunschweig, Deutschland.

10. A process for the fermentative preparation of L-amino acids, in particular L-methionine, which comprises carrying out the following steps:

a) fermentation of the coryneform bacteria which produce the desired L-amino acid and in which at least the metH gene or nucleotide sequences which code for it are enhanced, in particular over- expressed;

b) concentration of the L-amino acid in the medium or in the cells of the bacteria, and

c) isolation of the L-amino acid.

11. A process as claimed in claim 10, wherein bacteria in which further genes of the biosynthesis pathway of the desired L-amino acid are additionally enhanced are employed.

12. A process as claimed in claim 10, wherein bacteria in which the metabolic pathways which reduce the formation of the desired L-amino acid are at least partly eliminated are employed.

13. A process as claimed in claim 10, wherein a strain transformed with a plasmid vector is employed, and the plasmid vector carries the nucleotide sequence which codes for the metH gene.

14. A process as claimed in claim 10, wherein the expression of the polynucleotide (s) which code(s) for the metH gene is enhanced, in particular over- expressed.

15. A process as claimed in claim 10, wherein the catalytic properties of the polypeptide (enzyme protein) for which the polynucleotide metH codes are increased.

16. A process as claimed in claim 10, wherein for the preparation of L-amino acids, in particular L- methionine, coryneform microorganisms in which at the same time one or more of the genes chosen from the group consisting of

16.1 the lysC gene which codes for a feed back resistant aspartate kinase,

16.2 the gap gene which codes for glycerolaldehyde 3-phosphate dehydrogenase,

16.3 the pgk gene which codes for 3-phosphoglycerate kinase,

16.4 the pyc gene which codes for pyruvate carboxylase,

16.5 the tpi gene which codes for triose phosphate iso erase

16.6 the metA gene which codes for homoserine 0- acetyltransferase

16.7 the metB gene which codes for cystathionine gamma-synthase

16.8 the aecD gene which codes for cystathionine gamma-lyase

16.9 the glyA gene which codes for serine hydroxymethyltransferase

16.10 the etY gene which codes for 0- acetylhomoserine-sulfhydrylase is or are enhanced or over-expressed, are fermented.

17. A process as claimed in claim 10, wherein for the preparation of L-amino acids, in particular L- methionine, coryneform microorganisms in which at the same time one or more of the genes chosen from the group consisting of

17.1 the thrB gene which codes for homoserine kinase

17.2 the ilvA gene which codes for threonine dehydratase

17.3 the thrC gene which codes for threonine synthase

17.4 the ddh gene which codes for eso- diaminopimelate D-dehydrogenase

17.5 the pck gene which codes for phosphoenol pyruvate carboxykinase

17.6 the pgi gene which codes for glucose 6- phosphate isomerase 17.7 the poxB gene which codes for pyruvate oxidase

is or are attenuated are fermented.

18. A process as claimed in one or more of claims 10 to 17, wherein microorganisms of the species Corynebacterium glutamicum are employed.

19. A process as claimed in claim 18, wherein the

Corynebacterium glutamicum strain ATCC13032/pCREmetH is employed.

20. A process for the preparation of an L-methionine- containing animal feedstuffs additive from fermentation broths, which comprises the steps

a) culture and fermentation of an L-methionine- producing microorganism in a fermentation medium;

c) removal of an amount of 0 to 100 wt.% of the biomass formed during the fermentation; and

d) drying of the fermentation broth obtained according to b) and/or c) to obtain the animal feedstuffs additive in the desired powder or granule form.

21. A process as claimed in claim 20, wherein microorganisms in which further genes of the biosynthesis pathway of L-methionine are additionally enhanced are employed.

22. A process as claimed in claim 20, wherein microorganisms in which the metabolic pathways which reduce the formation of L-methionine are at least partly eliminated are employed.

23. A process as claimed in claim 20, wherein the expression of the polynucleotide (s) which code(s) for the metH gene is enhanced, in particular over- expressed.

24. A process as claimed in one or more of claims 20 to 23, wherein microorganisms of the species Corynebacterium glutamicum are employed.

25. A process as claimed in claim 24, wherein the Corynebacterium glutamicum strain ATCC13032/pCREmetH is employed.

26. A process as claimed in claim 20, wherein one or more of the following steps is or are additionally carried out:

e) addition of one or more organic substances, including L-methionine and/or D-methionine and/or the racemic mixture D, L-methionine, to the products obtained according to b) , c) and/or d) ;

f) addition of auxiliary substances chosen from the group consisting of silicas, silicates, stearates, grits and bran to the substances obtained according to b) to e) for stabilization and to increase the storability; or

g) conversion of the substances obtained according to b) to f) into a form stable to the animal stomach, in particular rumen, by coating with film-forming agents.

27. A process as claimed in claim 26, wherein a portion of the biomass is removed.

28. A process as claimed in claim 27, wherein up to 100% of the biomass is removed.

29. A process as claimed in claim 26, wherein the water content is up to 5 wt . % .

30. A process as claimed in claim 29, wherein the water content is less than 2 wt.%.

31. A process as claimed in claims 27, 28, 29, 30 or 31, wherein the film-forming agents are metal carbonates, silicas, silicates, alginates, stearates, starches, gums of cellulose ethers.

32. An animal feedstuffs additive prepared as claimed in claims 20 to 31.

33. An animal feedstuffs additive as claimed in claim 32, which comprises 1 wt.% to 80 wt.% L-methionine, D- methionine, D, L-methionine or a mixture thereof, based on the dry weight of the animal feedstuffs additive.

34. A process for discovering RNA, cDNA and DNA in order to isolate nucleic acids, or polynucleotides or genes which code for homocysteine methyltransferase II or have a high similarity with the sequence of the homocysteine methyltransferase II gene, which comprises employing the polynucleotide sequences as claimed in claim 1, 2, 3 or 4 as hybridization probes.