Process for the production of L-lysine
AssigneeEvonik Degussa GmbH
InventorsWilfried Claes, Brigitte Bathe
Life of this patent
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Abstract
The invention relates to mutants of coryneform bacteria in which genes have been enhanced by the use of a mutated promoter region, and to processes for the production of amino acids using bacteria according to the invention.
Claims26
An isolated mutant coryneform bacterium comprising a DNA fragment with promoter activity operably linked to a polynucleotide coding for a protein with dihydrodipicolinate reductase activity, wherein said DNA fragment comprises the sequence of SEQ ID NO:12 but with one or more substitutions selected from the group consisting of:
- a) substitution of the nucleobase thymine at position 36 of SEQ ID NO:12 by guanine;
- b) substitution of the nucleobase cytosine at position 37 of SEQ ID NO:12 by guanine;
- c) substitution of the nucleobase guanine at position 40 of SEQ ID NO:12 by thymine;
- d) substitution of the nucleobase cytosine at position 42 of SEQ ID NO:12 by adenine;
- and wherein:
- i) relative to a bacterial parent strain which does not carry said DNA fragment operably linked to a polynucleotide coding for a protein with dihydrodipicolinate reductase activity, said mutant coryneform bacterium produces more L-lysine when fermented in nutrient medium and under conditions suitable for lysine production;
- and
- ii) relative to a DNA fragment of SEQ ID NO:12 without any of said substitutions, said DNA fragment with the sequence of SEQ ID NO:12 with one or more of said substitutions has increased transcriptional activity.
An isolated mutant of a coryneform bacterium which comprises a DNA fragment with promoter activity, wherein said DNA fragment has the sequence of SEQ ID NO:12 but with all of the following substitutions:
- a) substitution of the nucleobase thymine at position 36 of SEQ ID NO:12 by guanine;
- b) substitution of the nucleobase cytosine at position 37 of SEQ ID NO:12 by guanine;
- c) substitution of the nucleobase guanine at position 40 of SEQ ID NO:12 by thymine;
- d) substitution of the nucleobase cytosine at position 42 of SEQ ID NO:12 by adenine;
- and wherein, relative to a DNA fragment comprising the sequence of SEQ ID NO:12 without any of said substitutions, said DNA fragment with said substitutions has increased transcriptional activity.
Dependencies are inferred from the claim text.