Modified microorganisms for chemical production

Patent metadata

Field	Value
Publication number	US-10125178-B2
Application number	US-201615176866-A
Country	US
Kind code	B2
Filing date	Jun 8, 2016
Priority date	Jun 12, 2015
Publication date	Nov 13, 2018
Grant date	Nov 13, 2018

Abstract

The present invention relates to increasing xylose utilization in industrial microbe by inducing mutations in the regulator genes, crp and xylR. Thus the invention is directed to isolated nucleic acid sequences that encode mutations in the crp gene and the xylR gene and recombinant bacterium that express mutated CRP and XylR. In some embodiments, the mutation results in a point mutation at residue 142 of the CRP protein and/or at point mutation at residues 121, 182 and/or 363 of the XylR protein (based on the protein sequences in E. coli). The invention also includes methods of using the recombinant bacterium.

First claim

What is claimed:

1. A method for increasing xylose utilization in microbes of the Enterobacteriaceae family, the method comprising mutating the microbial genomes of the microbes to produce a mutated microbe of the Enterobacteriaceae family having a mutated XylR protein,
wherein the mutated XylR protein comprises a point mutation substituting the proline at position 363, wherein the amino acid positioning corresponds to the amino acid sequence positioning set forth in SEQ ID NO:13.

2. The method of claim 1 , wherein the mutated microbe of the Enterobacteriaceae family further comprises a mutated CRP protein comprising a point mutation substituting the glycine at position 142, wherein the amino acid positioning corresponds to the amino acid sequence positioning set forth in SEQ ID NO:2.

3. The method of claim 2 , wherein the mutated XylR protein further comprises a point mutation substituting the arginine at position 121.

4. The method of claim 3 , wherein the arginine at position 121 is substituted with a cysteine, a serine, a glycine, a valine, a proline, or a conservative substitution thereof.

5. The method of claim 2 , wherein the glycine at position 142 is substituted with an aspartate, a proline, a histidine, or a conservative substitution thereof.

6. The method of claim 2 , wherein the mutated CRP protein comprises the amino acid sequence the sequence set forth in SEQ ID NO:11.

7. The method of claim 2 , wherein the mutated CRP protein comprises the amino acid sequence the sequence set forth in SEQ ID NO:11 and the mutated XylR protein comprises the amino acid sequence the sequence set forth in SEQ ID NO:27.

8. The method of claim 2 , wherein the mutated CRP protein comprises the amino acid sequence the sequence set forth in SEQ ID NO:11 and the mutated XylR protein comprises the amino acid sequence the sequence set forth in SEQ ID NO:28.

9. The method of claim 1 , wherein the mutated microbe of the Enterobacteriaceae family is a member of a genus selected from the group consisting of Escherichia, Erwinia, Providencia , and Serratia.

10. The method of claim 1 , wherein the mutated XylR protein further comprises a point mutation substituting the proline at position 182.

11. The method of claim 1 , wherein the proline at position at 363 is substituted with a serine, a lysine, an arginine, or a conservative substitution thereof.

12. The method of claim 1 , wherein the mutated XylR protein comprises the amino acid sequence the sequence set forth in SEQ ID NO:27.

13. The method of claim 1 , wherein the mutated XylR protein comprises the amino acid sequence the sequence set forth in SEQ ID NO:28.

14. The method of claim 1 , wherein the mutated XylR protein further comprises a point mutation substituting the arginine at position 121.

15. The method of claim 14 , wherein the arginine at position 121 is substituted with a cysteine, a serine, a glycine, a valine, a proline, or a conservative substitution thereof.

16. A method for improved chemical production from woody biomass comprising culturing a recombinant bacterium having increased xylose utilization with woody biomass, wherein the recombinant bacterium having increased xylose utilization expresses a mutated XylR protein;
wherein the mutated XylR protein has the amino acid sequence selected from the group consisting of SEQ ID NO:27 and SEQ ID NO:28, wherein:
Xaa at position 363 in SEQ ID NO:27 is selected from the group consisting of: S, K, R, and conservative substitutions thereof,
Xaa at position 121 in SEQ ID NO:28 is selected from the group consisting of: C, S, G, V, P, and conservative substitutions thereof, and
Xaa at position 363 in SEQ ID NO:28 is selected from the group consisting of: S, K, R, and conservative substitutions thereof.

17. The method of claim 16 , wherein the recombinant bacterium having increased xylose utilization further expresses a mutated CRP protein having the amino acid sequence set forth in SEQ ID NO:11, wherein Xaa at position 142 is selected from the group consisting of: D, P, H, and conservative substitutions thereof.

18. The method of claim 16 , wherein the mutated XylR protein has the amino acid sequence set forth in SEQ ID NO:27.

19. The method of claim 16 , wherein the mutated XylR protein has the amino acid sequence set forth in SEQ ID NO:28.

20. The method of claim 19 , wherein the recombinant bacterium having increased xylose utilization further expresses a mutated CRP protein having the amino acid sequence set forth in SEQ ID NO:11, wherein Xaa at position 142 is selected from the group consisting of: D, P, H, and conservative substitutions thereof.

Assignees

• Univ Arizona State

Inventors

• Wang Xuan
• Cartwright Reed
• Sievert Christian
• Loeffler Taylor
• Nieves Lizbeth
• Panyon Larry
• Morris Chandler

Classifications

• C12P7/56

  Lactic acid · CPC title

• C12N9/0006

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

• C12Y101/01307

  D-Xylose reductase (1.1.1.307) · CPC title

• C07K14/245 Primary

  Escherichia (G) · CPC title