IP Library Granted Patent US 9,493,795
Granted Patent B2
US 9,493,795 · App. 14/718,663 · Granted Nov 15, 2016

Metabolically enhanced cyanobacterial cell for the production of ethanol

Inventors: Ulf Dühring (Fredersdorf, DE); Heike Enke (Berlin, DE); Karl Ziegler (Zeuthen, DE); Torsten Schwecke (Berlin, DE)
Assignee: Algenol Biotech LLC
C12P7/065C12N9/0006C12N9/88C12Y101/01001C12Y401/01001Y02E50/17Y02P20/52
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Quick Facts
Patent No.
US 9,493,795
App. No.
14/718,663
Granted
Nov 15, 2016
Kind
B2
Abstract

A metabolically enhanced cyanobacterial cell for the production of ethanol is provided. The metabolically enhanced cyanobacterial cell for the production of ethanol comprises at least one recombinant gene encoding a pyruvate decarboxylase enzyme (Pdc) converting pyruvate to acetaldehyde, and at least one recombinant gene encoding a first Zn 2+ dependent alcohol dehydrogenase enzyme (Adh) converting acetaldehyde to ethanol. The invention also provides a method for producing the metabolically enhanced cyanobacterium , a method for producing ethanol with the metabolically enhanced cyanobacterium , and a method for screening of alcohol dehydrogenase enzyme expressing cyanobacterial strains for the presence of NADPH-dependent native alcohol dehydrogenase enzymes.

Claims (30)

1. A cyanobacterial cell for the production of ethanol, comprising:

at least one recombinant gene encoding a pyruvate decarboxylase enzyme (Pdc) converting pyruvate to acetaldehyde, and

at least one recombinant gene encoding a first Zn 2+ dependent alcohol dehydrogenase enzyme (Adh) converting acetaldehyde to ethanol, wherein the alcohol dehydrogenase enzyme has an amino acid sequence that is at least 95% identical to an Adh amino acid sequence selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, and SEQ ID NO: 8;

wherein the transcription of both the recombinant gene encoding the pyruvate decarboxylase enzyme and the recombinant gene encoding the alcohol dehydrogenase enzyme is controlled by a single promoter.

2. The cyanobacterial cell of claim 1 , wherein said single promoter is an inducible promoter.

3. The cyanobacterial cell of claim 1 , wherein the recombinant gene encoding the pyruvate decarboxylase enzyme is arranged upstream of the recombinant gene encoding the alcohol dehydrogenase enzyme.

4. The cyanobacterial cell of claim 1 , wherein the recombinant gene encoding the alcohol dehydrogenase enzyme is arranged upstream of the recombinant gene encoding the pyruvate decarboxylase enzyme.

5. The cyanobacterial cell of claim 4 , wherein the transcription of the alcohol dehydrogenase gene occurs before transcription of the pyruvate decarboxylase gene.

6. The cyanobacterial cell of claim 1 , wherein the pyruvate decarboxylase enzyme activity is higher than the alcohol dehydrogenase enzyme activity.

7. The cyanobacterial cell of claim 1 , wherein ethanol is produced in an amount that is at least 0.017% (v/v) per day over a period of at least 30 days.

8. The cyanobacterial cell of claim 2 , wherein the inducible promoter is an endogenous promoter.

9. The cyanobacterial cell of claim 2 , wherein the inducible promoter is a metal-inducible promoter.

10. The cyanobacterial cell of claim 9 , wherein the metal inducible promoter is selected from the group consisting of PziaA (SEQ ID NO: 38), PaztA (SEQ ID NO: 40), PsmtA (SEQ ID NO: 39), PcorT (SEQ ID NO: 41), PnrsB (SEQ ID NO: 42), Porf0316 (SEQ ID NO: 67), and PpetJ (SEQ ID NO: 43).

11. The cyanobacterial cell of claim 2 , wherein the inducible promoter is a nitrate-inducible promoter.

12. The cyanobacterial cell of claim 11 , wherein the nitrate-inducible promoter is selected from the group consisting of PnirA, PnrtA, and PnarB.

13. A method for producing ethanol in a cyanobacterial cell, comprising:

a) providing a cyanobacterial cell of claim 1 ;

b) growing said cyanobacterial cell in a culture medium suitable for producing ethanol; and

c) obtaining ethanol from the culture medium.

14. The method of claim 13 , wherein the single promoter is an inducible promoter.

15. The method of claim 13 , wherein the recombinant gene encoding the pyruvate decarboxylase enzyme is arranged upstream of the recombinant gene encoding the alcohol dehydrogenase enzyme.

16. The method of claim 15 , wherein the recombinant gene encoding the alcohol dehydrogenase is arranged upstream of the recombinant gene encoding the pyruvate decarboxylase enzyme.

17. The method of claim 16 , wherein the transcription of the alcohol dehydrogenase gene occurs before transcription of the pyruvate decarboxylase gene.

18. The method of claim 13 , wherein the pyruvate decarboxylase enzyme activity is higher than the alcohol dehydrogenase enzyme activity.

19. The method of claim 13 , wherein ethanol is produced in an amount that is at least 0.017% (v/v) per day over a period of at least 30 days.

20. The method of claim 14 , wherein the inducible promoter is an endogenous promoter.

21. The method of 14 , wherein the inducible promoter is a metal-inducible promoter.

22. The method of claim 21 , wherein the metal inducible promoter is selected from the group consisting of PziaA (SEQ ID NO: 38), PaztA (SEQ ID NO: 40), PsmtA (SEQ ID NO: 39), PcorT (SEQ ID NO: 41), PnrsB (SEQ ID NO: 42), Porf0316 (SEQ ID NO: 67), and PpetJ (SEQ ID NO: 43).

23. The method of claim 14 , wherein the inducible promoter is a nitrate-inducible promoter.

24. The method of claim 23 , wherein the nitrate-inducible promoter is selected from the group consisting of PnirA, PnrtA, and PnarB.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 3, 2018
From: DUHRING, ULF; ENKE, HEIKE; ZIEGLER, KARL; SCHWECKE, TORSTEN
To: ALGENOL BIOFUELS INC.
Reel/Frame 044526/0643 →
Continuity (3)
Continuation 14305781 · Jun 16, 2014
Provisional Application 61835086 · Jun 14, 2013
Related Publication 20150259708A1 · Sep 17, 2015