Process for preparing L-amino acids
View Patent ↗A process for preparing L-amino acids employing coryneform bacteria in which the AmtR regulator has been attenuated is provided. Recombinant bacteria, polynucleotides and vectors corresponding to or having the attenuated AmtR regulator are disclosed.
1. A recombinant polynucleotide that encodes a polypeptide that is at least 95% identical to SEQ ID NO: 2, but that is not SEQ ID NO: 2; and comprises one or more amino acid exchanges at positions 3, 24, 31, 32, or 36 of SEQ ID NO: 2, and wherein the polypeptide is active as an AmtR transcription regulator.
2. The recombinant polynucleotide of claim 1 that encodes a polypeptide that is at least 98% identical to SEQ ID NO: 2.
3. The recombinant polynucleotide of claim 1 that encodes a polypeptide is at least 99% identical to SEQ ID NO: 2.
4. The recombinant polynucleotide of claim 1 that encodes the polypeptide of SEQ ID NO: 2 except that it compries two or three amino acid exchanges at positions 3, 24, 31, 32, or 36 of SEQ ID NO: 2.
5. The recombinant polynucleotide of claim 1 that encodes the polypeptide of SEQ ID NO: 2 except that it comprises one amino acid exchange at position 3, 24, 31, 32, or 36 of SEQ ID NO: 2.
6. A vector that comprises the isolated polynucleotide sequence of claim 1 .
7. An isolated host cell comprising the vector of claim 6 .
8. The host cell of claim 7 that is a Corynebacterium.
9. The host cell of claim 7 that is a Corynebacterium glutamicum.
10. The host cell of claim 7 that releases more L-amino acid into the culture medium than a host cell comprising a vector encoding the polypeptide of SEQ ID NO: 2.
11. The host cell of claim 7 that accumulates in its interior more L-amino acid than a host cell comprising a vector encoding the polypeptide of SEQ ID NO: 2.
12. An isolated host cell comprising the polynucleotide of claim 1 .
13. A method for producing an L-amino acid comprising culturing the host cell of claim 7 in a suitable medium and recovering the L-amino acid.
14. A method for producing an L-amino acid comprising culturing the host cell of claim 12 in a suitable medium and recovering the L-amino acid.