Recombinant strain producing L-lysine and construction methods therefor and use thereof
AssigneeHeilongjiang Eppen Biotech Co., Ltd.
InventorsGang Meng, Aiying Wei, Huiping Jia, Fengyong Ma, Xiaoqun Zhou, Chunguang Zhao, Xiaowei Guo, Bin Tian, Xiaohang Gao
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Abstract
Provided are a method for introducing point mutations to the coding sequence of NCg12176 gene or improving the expression thereof in Corynebacterium glutamicum, and a method for performing point mutations on the promoter region sequence of dapB gene in Corynebacterium glutamicum. The fermentation yield of L-lysine produced by a strain with the mutations can be increased by means of the methods.
Claims4
A method for producing L-lysine, comprising culturing a first recombinant strain contains a polynucleotide encoding a polypeptide that comprise an amino acid sequence of SEQ ID NO:
- 3, wherein the lysine residue at position 176 is substituted with an asparagine residue;
- the polynucleotide sequence is formed by mutation of the base at position 528 of the polynucleotide sequence shown in SEQ ID NO:
- 1;
- and the mutation includes base mutation of adenine (A) to cytosine (C) at position 528 of the polynucleotide sequence shown in SEQ ID NO:
- 1;
- or a second recombinant strain contains the promoter nucleotide sequence comprises the nucleotide sequence obtained by mutating the bases at positions −49, −51 and −54 to −58 in the promoter region shown in SEQ ID NO:
- 29;
- or an expression cassette comprising the promoter nucleotide sequence comprises the nucleotide sequence obtained by mutating the bases at positions −49, −51 and −54 to −58 in the promoter region shown in SEQ ID NO:
- 29;
- or a second recombinant vector comprises the promoter nucleotide sequence comprises the nucleotide sequence obtained by mutating the bases at positions −49, −51 and −54 to −58 in the promoter region shown in SEQ ID NO:
- 29;
- wherein in the second recombinant strain or in the second recombinant vector or in the expression cassette, the nucleotide at position −49 of the promoter region shown in SEQ ID NO:
- 29 is mutated from cytosine (C) to adenine (A), the nucleotide at position −51 is mutated from guanine (G) to thymine (T), and the nucleotide sequence from positions −54 to −58 is mutated from CTGCA to GGTGT;
- and
- both the first recombinant strain and the second recombinant strain use Corynebacterium glutamicum YP97158 as the host strain, and recovering L-lysine from the culture.
Dependencies are inferred from the claim text.