Method for production of L-glutamine
View Patent ↗A polypeptide comprising an amino acid sequence in which one or more amino acids are deleted, substituted or added in the amino acid sequence of a glutamine synthetase 2 derived from a microorganism belonging to a coryneform bacterium, wherein the coryneform bacterium producing the polypeptide has L-glutamine productivity, a DNA encoding the polypeptide, a recombinant DNA comprising the DNA, a microorganism comprising the DNA or the recombinant DNA, and a process for producing L-glutamine using the microorganism are provided.
1. A isolated DNA encoding a modified polypeptide having glutamine synthetase 2 activity, wherein the polypeptide comprises the amino acid sequence of SEQ ID NO: 1, wherein the modification is the substitution of glutamic acid at position 64 from the N-terminal of SEQ ID NO: 1 (corresponding to codon or nucleotides 190-192 of SEQ ID NO: 2) with an amino acid other than glutamic acid and further comprising deletion, substitution or addition of 1-20 amino acids in the sequence of SEQ ID NO: 1, wherein said DNA when expressed in Coryneform bacterium as a host cell results in increased L-glutamine production as compared unmodified wild type Coryneform bacterium.
2. The isolated DNA of claim 1 , wherein the codon encoding the glutamic amino acid encodes lysine.
3. The isolated DNA of claim 1 or 2 , wherein the coryneform bacterium belongs to the genus Corynebacterium, Brevibacterium or Mycobacterium.
4. An isolated DNA encoding a modified polypeptide having glutamine synthetase 2 activity which is at least 95% identical to the nucleotide sequence of SEQ ID NO:2, and comprises a nucleotide sequence in which a region corresponding to the nucleotide sequence at positions 190 to 192 from the 5′-terminal in the nucleotide sequence of SEQ ID NO:2 is a codon encoding a basic amino acid, wherein a production amount of L-glutamine in a transformant obtained by introducing the DNA into a wild type coryneform bacterium is larger than that of the wild type coryneform bacterium.
5. The isolated DNA of claim 4 , wherein the codon encoding the basic amino acid encodes lysine.
6. An isolated microorganism transformed with the isolated recombinant DNA of claim 1 or 4 .
7. An isolated microorganism which comprises, on its chromosomal DNA, the isolated DNA of claim 1 or 4 .
8. The isolated microorganism of claim 6 , which has an ability of producing a polypeptide comprising an amino acid sequence in which from one to twenty amino acids are deleted, substituted or added in the amino acid sequence of LtsA obtained from a microorganism belonging to a coryneform bacterium, and has lysozyme sensitivity, wherein the polypeptide comprises an amino acid sequence in which an amino acid at a position corresponding to the amino acid at position 80 from the N-terminal in the amino acid sequence of SEQ ID NO:10 is aspartic acid.
9. The isolated microorganism according to of claim 7 , wherein the amino acid sequence of LtsA is SEQ ID NO:10.
10. The isolated microorganism of claim 6 , wherein the microorganism belongs to the genus Corynebacterium, Brevibacterium or Mycobacterium.
11. The isolated microorganism of claim 10 , wherein the microorganism is Corynebacterium glutamicum.
12. A process for producing L-glutamine, which comprises culturing the microorganism of claim 6 in a medium to form and accumulate L-glutamine in a culture, and recovering L-glutamine from the culture.