IP Library › Granted Patent US 11,905,539
Granted Patent B2
US 11,905,539 · App. 17/156,998 · Granted Feb 20, 2024

Isopropylmalate synthase variant and a method of producing L-leucine using the same

Inventors: Ji Hye Lee (Gyeonggi-do, KR); Byeong Cheol Song (Gyeonggi-do, KR); Ae Ji Jeon (Seoul, KR); Jong Hyun Kim (Gyeonggi-do, KR); Hye Won Kim (Gyeonggi-do, KR)
Assignee: CJ Cheiljedang Corporation
C12P13/06C12N9/1025C12N15/52C12N15/74C12N15/77C12Y203/03013
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Quick Facts
Patent No.
US 11,905,539
App. No.
17/156,998
Granted
Feb 20, 2024
Kind
B2
Abstract

A novel modified polypeptide having an isopropylmalate synthase activity, a polynucleotide encoding the same, a microorganism including the polypeptide, and a method of producing L-leucine by culturing the microorganism.

Claims (19)

1. A modified microorganism belonging to the genus of Corynebacterium for producing L-leucine, comprising a modified polypeptide having an isopropylmalate synthase activity,

wherein glycine at position 561 from a N-terminus of a polypeptide consisting of the amino acid sequence of SEQ ID NO: 1 is substituted with aspartic acid in the modified polypeptide, and

wherein the modified microorganism has a resistance to norleucine or L-leucine, and

wherein a native promoter of a polynucleotide encoding the modified polypeptide in the microorganism is substituted with a promoter which enhances an expression of the polynucleotide compared to the native promoter.

2. The modified microorganism of claim 1 , wherein the promoter which enhances an expression of the polynucleotide compared to the native promoter is a PCJ7 promoter.

3. The modified microorganism of claim 1 , wherein the modified microorganism belonging to the genus of Corynebacterium is derived from a Corynebacterium glutamicum.

4. A method of producing L-leucine, comprising:

(a) culturing a modified microorganism belonging to the genus of Corynebacterium for producing L-leucine, in a medium to produce L-leucine, wherein the microorganism comprises a polynucleotide encoding a modified polypeptide having an isopropylmalate synthase activity, wherein glycine at position 561 from a N-terminus of a polypeptide consisting of the amino acid sequence of SEQ ID NO: 1 is substituted with aspartic acid in the modified polypeptide, wherein the modified microorganism has a resistance to norleucine or L-leucine, and wherein a native promoter of a polynucleotide encoding the modified polypeptide in the microorganism is substituted with a promoter which enhances an expression of the polynucleotide compared to the native promoter; and

(b) recovering L-leucine from the cultured microorganism or the cultured medium.

5. The method of claim 4 , wherein the promoter which enhances an expression of the polynucleotide compared to the native promoter is a PCJ7 promoter.

6. The method of claim 4 , wherein the modified microorganism belonging to the genus of Corynebacterium is derived from a Corynebacterium glutamicum.

7. The modified microorganism of claim 1 , wherein said modified microorganism is transformed with a vector comprising:

i) the polynucleotide encoding the modified polypeptide having an isopropylmalate synthase activity; and

ii) the promoter that is operatively connected to the polynucleotide, wherein the promoter is a non-native promoter of the polynucleotide and the expression of the polynucleotide is driven by the promoter, not the native promoter; and wherein the promoter enhances the expression of the polynucleotide, compared to the native promoter, thereby enhancing the productivity of L-leucine.

8. The modified microorganism of claim 7 , wherein the promoter that enhances productivity of L-leucine operatively linked to the polynucleotide is a PCJ7 promoter.

9. The method of claim 4 , wherein the microorganism is transformed with a vector comprising:

i) the polynucleotide encoding the modified polypeptide having an isopropylmalate synthase activity; and

ii) the promoter that is operatively connected to the polynucleotide, wherein the promoter is a non-native promoter of the polynucleotide and the expression of the polynucleotide is driven by the promoter, not the native promoter; and wherein the promoter enhances the expression of the polynucleotide, compared to the native promoter, thereby enhancing the productivity of L-leucine.

10. The method of claim 9 , wherein the promoter that enhances productivity of L-leucine linked to the polynucleotide is a PCJ7 promoter.

Priority Claims (1)
KR 10-2016-0181343 · Dec 28, 2016 · national
Continuity (2)
Continuation 16473941
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