IP Library Granted Patent US 8,692,024
Granted Patent B2
US 8,692,024 · App. 13/368,506 · Granted Apr 8, 2014

Method of producing n-butyraldehyde

Inventors: Jay Kouba (Chicago, IL); Mounir Izallalen (Savoy, IL); Jill Bradshaw (Champaign, IL)
Assignee: Eastman Renewable Materials, LLC
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Quick Facts
Patent No.
US 8,692,024
App. No.
13/368,506
Granted
Apr 8, 2014
Kind
B2
Abstract

The invention provides method of producing n-butyraldehyde using recombinant solventogenic bacteria and recombinant microorganisms.

Claims (27)

1. A method of producing n-butyraldehyde comprising:

(a) providing a recombinant solventogenic bacterium with reduced or knocked-out expression of at least one enzyme involved in either:

i) n-butyraldehyde biodegradation, or

ii) synthesis of n-butyraldehyde reaction products, and

(b) culturing the recombinant solventogenic bacterium to produce n-butyraldehyde.

2. A method of claim 1 , wherein said recombinant solventogenic bacterium has reduced or knocked-out expression of butanol dehydrogenase.

3. The method of claim 2 , wherein a parent bacterium of the recombinant solventogenic bacterium is from Clostridium sp.

4. The method of claim 3 , wherein the recombinant solventogenic bacterium is derived from a bacterium selected from the group consisting of C. acetobutylicum, C. beijerinckii, C. saccharobutylicum , and C. saccharobutylacetonicum.

5. The method of claim 4 , wherein the recombinant solventogenic bacterium is derived from a C. beijerinckii bacterium which contains at least one butanol dehydrogenase gene;

comprising a nucleic acid sequence which is at least about 70% identical SEQ ID NO: 1, SEQ ID NO. 2, or SEQ ID NO. 3.

6. The method of claim 5 , wherein the butanol dehydrogenase gene comprises a nucleic acid sequence at least about 80% identical to SEQ ID NO:. 1, SEQ ID NO. 2, or SEQ ID NO. 3.

7. The method of claim 5 , wherein the butanol dehydrogenase gene comprises a nucleic acid sequence which is at least about 90% identical to SEQ ID NO said comparative sequence selected from the group consisting of SEQ ID NO. 1, SEQ ID NO. 2, or SEQ ID NO. 3.

8. The method of claim 5 , wherein the recombinant solventogenic bacterium is derived from a C. beijerinckii bacterium which contains the butanol dehydrogenase gene containing SEQ ID NO: 1.

9. The method of claim 5 , wherein the recombinant solventogenic bacterium is derived from a C. beijerinckii bacterium which contains the butanol dehydrogenase gene containing SEQ ID NO: 2.

10. The method of claim 5 , wherein the recombinant solventogenic bacterium is derived from a C. beijerinckii bacterium which contains the butanol dehydrogenase gene containing SEQ ID NO: 3.

11. The method of claim 5 wherein at least one of SEQ ID NO: 1, SEQ ID NO: 2 and SEQ ID NO: 3 is reduced or knocked out in the recombinant solventogenic bacterium.

12. The method of claim 5 wherein the SEQ ID NO: 2 is knocked out in the recombinant solventogenic bacterium.

13. The method of claim 4 , wherein the recombinant solventogenic bacterium is derived from a C. beijerinckii which is NCIMB 8052 or BA 101.

14. The method of claim 2 , wherein the bacterium is selected from recombinant Lactococcus lactis and recombinant Lactobacillus buchneri.

15. The method of claim 2 , wherein the recombinant solventogenic bacterium constitutively expresses butyraldehyde dehydrogenase.

16. The method of claim 2 , wherein the recombinant solventogenic bacterium comprises a nucleic acid sequence encoding butyraldehyde dehydrogenase operably linked to a constitutive promoter.

17. The method of claim 2 , wherein the recombinant solventogenic bacterium has reduced or knocked-out expression of alcohol dehydrogenase as compared to a parent bacterium.

18. The method claim 2 , wherein the recombinant solventogenic bacterium has reduced or knocked-out expression of lactate dehydrogenase as compared to a parent bacterium.

19. The method of claim 2 , wherein the recombinant solventogenic bacterium has reduced or knocked-out expression of a hydrogen-evolving hydrogenase as compared to a parent bacterium.

20. The method of claim 2 , wherein the recombinant solventogenic bacterium has reduced or knocked-out expression of formate dehydrogenase as compared to a parent bacterium.

21. The method of claim 2 , further comprising isolating n-butyraldehyde.

22. The method of claim 21 , wherein the n-butyraldehyde is isolated by a method selected from the group consisting of using a sweep gas, gas stripping with carbon dioxide, distillation, solvent extraction, solid adsorption, and membrane separation.

Assignments (2)
CORRECTION TO NAME OF ASSIGNEE PREVIOUSLY RECORDED ON REEL 027889 AND FRAME 0658 Recorded Sep 25, 2012
From: KOUBA, JOY; IZALLALEN, MOUNIR; BRADSHAW, JILL
To: EASTMAN RENEWABLE MATERIALS
Reel/Frame 029059/0025 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 16, 2012
From: KOUBA, JAY; IZALLALEN, MOUNIR; BRADSHAW, JILL
To: EASTMAN CHEMICAL COMPANY
Reel/Frame 027889/0658 →
Continuity (2)
Provisional Application 61442599 · Feb 14, 2011
Related Publication 20120209021A1 · Aug 16, 2012