Nucleotide sequences which code for the acp gene
AssigneeDegussa AG
InventorsBettina Mockel, Anke Weissenborn, Walter Pfefferle, Hermann Sahm, Lothar Eggeling, Madhavan Nampoothiri
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AssigneeDegussa AG
InventorsBettina Mockel, Anke Weissenborn, Walter Pfefferle, Hermann Sahm, Lothar Eggeling, Madhavan Nampoothiri
Estimating the term…
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), a process for the fermentative preparation of L-amino acids with enhancement of the acp gene and the use of the polynucleotide as a primer or hybridization probe.
Isolated polynucleotide from coryneform bacteria, comprising a polynucleotide sequence chosen from the group consisting of
Process for the fermentative preparation of L-amino acids, in particular L-lysine, characterized in that the following steps are carried out:
Process according to one or more of the preceding claims, characterized in that microorganisms of the genus Corynebacterium glutamicum are employed.
Dependencies are inferred from the claim text.