Mutants having capability to produce 1, 4-butanediol and method for preparing 1, 4-butanediol using the same

Patent metadata

Field	Value
Publication number	US-9920325-B2
Application number	US-201514802681-A
Country	US
Kind code	B2
Filing date	Jul 17, 2015
Priority date	Sep 7, 2007
Publication date	Mar 20, 2018
Grant date	Mar 20, 2018

Abstract

A mutant capable of producing 1,4-butanediol and a method of preparing 1,4-butanediol using the same are provided. The mutant microorganism is prepared by introducing and amplifying genes encoding enzymes converting succinate into 4-hydroxybutyrate and 4-hydroxybutyrate into 1,4-butanediol in a microorganism capable of producing succinate. The method includes culturing the mutant in a medium containing carbohydrate and obtaining 1,4-butanediol from the culture. Thus, 1,4-butanediol, which is essential in chemical industry, can be prepared in a biological process.

First claim

The invention claimed is:

1. An isolated mutant microorganism exhibiting high production of 1,4-butanediol, which is prepared by introducing or amplifying genes encoding enzymes converting succinate into 4-hydroxybutyrate, and 4-hydroxybutyrate into 1,4-butanediol, in a Lumen bacteria capable of producing succinate,
wherein the Lumen bacteria have inactive genes encoding lactate dehydrogenase (ldhA) and pyruvate-formate lyase (pfl), and produce succinate in high concentration without substantial production of other organic acids in an anaerobic condition, and
wherein the gene encoding the enzyme converting succinate into 4-hydroxybutyrate is selected from the group consisting of genes encoding succinyl-CoA transferase (Cat1), succinate semialdehyde dehydrogenase (SucD), 4-hydroxybutyrate dehydrogenase (4hbD) and 4-hydroxybutyrate dehydrogenase (GHB).

2. The isolated mutant microorganism according to claim 1 , wherein the Lumen bacteria have inactive genes encoding lactate dehydrogenase (ldhA), pyruvate-formate lyase (pfl), phosphotransacetylase (pta) and acetate kinase (ackA), and produce succinate in high concentration without substantial production of other organic acids in an anaerobic condition.

3. The isolated mutant microorganism according to claim 1 , wherein the Lumen bacteria have inactive genes encoding lactate dehydrogenase (ldhA), pyruvate-formate lyase (pfl) and phosphopyruvate carboxylase (ppc), and produce succinate in high concentration without substantial production of other organic acids in an anaerobic condition.

4. The isolated mutant microorganism according to claim 1 , wherein the Lumen bacteria are selected from the group consisting of Mannheimia species, Actinobacillus species and Anaerobiospirillum species.

5. The isolated mutant microorganism according to claim 4 , wherein the Lumen bacteria are Mannheimia species.

6. The isolated mutant microorganism according to claim 5 , wherein the Lumen bacteria are selected from the group consisting of Mannheimia succiniciproducens MBEL55E (KCTC 0769BP), and Mannheimia species LPK (KCTC 10558BP), LPK4 and LPK7 (KCTC 10626BP).

7. The isolated mutant microorganism according to claim 1 , wherein the gene encoding the enzyme converting succinate into 4-hydroxybutyrate is isolated from Clostridium kluyveri.

8. The isolated mutant microorganism according to claim 1 , wherein the gene encoding Cat1 has a nucleotide sequence of SEQ ID NO: 1, the gene encoding SucD has a nucleotide sequence of SEQ ID NO: 2, the gene encoding 4hbD has a nucleotide sequence of SEQ ID NO: 3, and the gene encoding GHB has a nucleotide sequence of SEQ ID NO: 4.

9. The isolated mutant microorganism according to claim 1 , wherein the mutant comprises a gene encoding Cat1; a gene encoding SucD; and a gene encoding 4hbD or a gene encoding GHB.

10. The isolated mutant microorganism according to claim 1 , wherein the gene encoding the enzyme converting 4-hydroxybutyrate into 1,4-butanediol is isolated from Clostridium acetobutylicum.

11. The isolated mutant microorganism according to claim 1 , wherein the gene encoding the enzyme converting 4-hydrxoybutyrate into 1,4-butanediol is a gene encoding 4-hydroxybutyrate-CoA transferase and a gene encoding alcohol dehydrogenase reducing 4-hydroxybutyrate-CoA; or a gene encoding phosphotransbutyrylase, a gene encoding butyryl kinase and a gene encoding alcohol dehydrogenase reducing 4-hydroxybutyrate-CoA.

12. The isolated mutant microorganism according to claim 11 , wherein the gene encoding 4-hydroxybutyrate-CoA transferase has a nucleotide sequence of SEQ ID NO: 5.

13. The isolated mutant microorganism according to claim 11 , wherein the gene encoding phosphotransbutyrylase and the gene encoding butyryl kinase have nucleotide sequences of by SEQ ID NOs: 6 and 7, respectively.

14. The isolated mutant microorganism according to claim 11 , wherein the alcohol dehydrogenase is butyl-CoA dehydrogenase isolated from Clostridium acetobutylicum.

15. The isolated mutant microorganism according to claim 14 , wherein the gene encoding butyl-CoA dehydrogenase has a nucleotide sequence of SEQ ID NO: 8 or 9.

16. The isolated mutant microorganism according to claim 1 , wherein the mutant has an inactive gene associated with conversion of succinate semialdehyde into succinate.

17. The isolated mutant microorganism according to claim 16 , wherein the gene associated with conversion of succinate semialdehyde into succinate is a gene encoding succinic semialdehyde dehydrogenase (GabD).

18. The isolated mutant microorganism according to claim 17 , wherein the gene encoding GabD has a nucleotide sequence of SEQ ID NO: 10.

19. The isolated mutant microorganism according to claim 1 , wherein a gene encoding C4-dicarboxylate transport protein (DctA) associated with transport of succinate is further introduced or amplified in the mutant.

20. The isolated mutant microorganism according to claim 19 , wherein the gene encoding DctA has a nucleotide sequence of SEQ ID NO: 11.

21. An isolated mutant microorganism exhibiting high production of 1,4-butanediol, which is prepared by introducing or amplifying:
a gene encoding succinyl-CoA transferase (Cat1);
a gene encoding succinate semialdehyde dehydrogenase (SucD);
a gene encoding 4-hydroxybutyrate dehydrogenase (4hbD) or 4-hydroxybutyrate dehydrogenase (GHB);
a gene encoding 4-hydroxybutyrate-CoA transferase, or a gene encoding phosphotransbutyrylase (Ptb) and a gene encoding butyryl kinase (Buk); and
a gene encoding butyl-CoA dehydrogenase,
in a Lumen bacteria capable of producing succinate,
wherein the Lumen bacteria have inactive genes encoding lactate dehydrogenase (ldhA) and pyruvate-formate lyase (pfl), and produce succinate in high concentration without substantial production of other organic acids in an anaerobic condition.

22. The isolated mutant microorganism according to claim 21 , wherein a gene encoding GabD is inactivated in the mutant.

23. The isolated mutant microorganism according to claim 21 , wherein a gene encoding DctA associated with transport of succinate is introduced or amplified in the mutant.

24. A method of preparing 1,4-butanediol, comprising:
culturing the mutant microorganism according to claim 1 in a medium containing a carbon source; and
obtaining 1,4-butanediol from the medium.

Assignees

• Lg Chemical Ltd
• Korea Advanced Inst Sci & Tech

Inventors

• Park Si Jae
• Lee Sang Hyun
• Lee Sang Yup
• Lee Eun Jeong

Classifications

• C12N9/0006

  acting on CH-OH groups as donors (1.1) · CPC title

• C12N9/001

  acting on the CH-CH group of donors (1.3) · CPC title

• C12N15/77 Primary

  for Corynebacterium; for Brevibacterium · CPC title

• C12Y103/99002

  Butyryl-CoA dehydrogenase (1.3.99.2), i.e. short chain acyl-CoA dehydrogenase · CPC title

• C12Y102/01024

  Succinate-semialdehyde dehydrogenase (NAD+) (1.2.1.24) · CPC title