IP Library Granted Patent US 9,611,487
Granted Patent B2
US 9,611,487 · App. 14/137,524 · Granted Apr 4, 2017

Cell-free system for converting methane into fuel and chemical compounds

Inventors: William Jeremy Blake (Winchester, MA); James R. Swartz (Menlo Park, CA)
Assignee: GreenLight Biosciences, Inc.
C12P7/16C12P7/40C12P7/649Y02E50/10Y02E50/13
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,611,487
App. No.
14/137,524
Granted
Apr 4, 2017
Kind
B2
Abstract

The present disclosure relates, in some aspects, to cell-free methods and systems for large-scale conversion of methane to isobutanol, comprising combining, in a bioreactor at elevated pressure, methane, oxygen, and cell lysates containing methane monooxygenase, methanol dehydrogenase, and enzymes that catalyze the conversion of formaldehyde to isobutanol, to form a cell-free reaction mixture, and incubating under suitable conditions the cell-free reaction to convert methane to isobutanol.

Claims (64)

1. A cell-free method for large-scale conversion of methane to pyruvate, comprising:

combining, in a bioreactor, methane, oxygen, and a cell lysate mixture of at least two cell lysates, at least one of which is obtained from recombinant cells, wherein the cell lysate mixture contains the following enzymes: a methane monooxygenase, a methanol dehydrogenase, a hexulose-6-phosphate synthase, a 6-phospho-3-hexuloisomerase, a 6-phosphofructokinase, a fructose bisphosphate aldolase, a triose phosphate isomerase, a transketolase, a ribose-5-phosphate isomerase or a ribulose-5-phosphate 3-epimerase, a glyceraldehyde 3-phosphate dehydrogenase, a phosphoglycerate kinase, a phosphoglycerate mutase, an enolase, and a pyruvate kinase, wherein the recombinant cells overexpress at least one of the foregoing enzymes, to form a cell-free reaction mixture; and

incubating under suitable conditions the cell-free reaction mixture to convert methane to pyruvate, thereby producing pyruvate at a production rate of at least 1 g/L-h.

2. The cell-free method of claim 1 , wherein the cell lysate mixture further contains an acetolactate synthase, an acetohydroxy acid isomeroreductase, a dihydroxy acid dehydratase, an alpha-ketoisovalerate decarboxylase, and an isobutanol dehydrogenase, and wherein the method results in the conversion of pyruvate to isobutanol.

3. The cell-free method of claim 2 , wherein

(i) the methane monooxygenase has EC number 1.14.13.25 or 1.14.18.3,

(ii) the methanol dehydrogenase has EC number 1.1.1.244, 1.1.2.7, or 1.1.99.37,

(iii) the hexulose-6-phosphate synthase has EC number 4.1.2.43,

(iv) the 6-phospho-3-hexuloisomerase has EC number 5.3.1.27,

(v) the 6-phosphofructokinase has EC number 2.7.1.11,

(vi) the fructose bisphosphate aldolase has EC number 4.1.2.13,

(vii) the triose phosphate isomerase has EC number 5.3.1.1,

(viii) the transketolase has EC number 2.2.1.1,

(xi) the ribose-5-phosphate isomerase has EC number 5.3.1.6, or the ribulose-5-phosphate 3-epimerase has EC number 5.1.3.1,

(xii) the glyceraldehyde 3-phosphate dehydrogenase has EC number 1.2.1.12,

(xiii) the phosphoglycerate kinase has EC number 2.7.2.3,

(xiv) the phosphoglycerate mutase has EC number 5.4.2.11 or 5.4.2.12,

(xv) the enolase has EC number 4.2.1.11,

(xvi) the pyruvate kinase has EC number 2.7.1.40,

(xvii) the acetolactate synthase has EC number 2.2.1.6,

(xviii) the acetohydroxy acid isomeroreductase has EC number 1.1.1.86,

(xix) the dihydroxy acid dehydratase has EC number 4.2.1.9,

(xx) the alpha-ketoisovalerate decarboxylase has EC number 4.1.1.72, and

(xxi) the isobutanol dehydrogenase has EC number 1.1.1.1.

4. The cell-free method of claim 2 , wherein the pressure in the bioreactor is at least 1 bar.

5. The cell-free method of claim 4 , wherein the pressure in the bioreactor is at least 2 bar.

6. The cell-free method of claim 2 , wherein the isobutanol is produced at a production rate of at least 1 g/L-h.

7. The cell-free method of claim 6 , wherein the isobutanol is produced at a production rate of at least 10 g/L-h.

8. The cell-free method of claim 2 , wherein the bioreactor comprises a gas phase and an aqueous phase.

9. The cell-free method of claim 8 , wherein the bioreactor further comprises an organic solvent.

10. The cell-free method of claim 9 , wherein the organic solvent is selected from the group consisting of pentane, hexane, heptane, octane, nonane, and decane.

11. The cell-free method of claim 2 , wherein the methane monooxygenase is obtained from a methanotroph.

12. The cell-free method of claim 11 , wherein the methanotroph is a Methylococcus capsulatus Bath methanotroph.

13. The method of claim 2 , wherein the methanol dehydrogenase is a heterologous NAD-linked methanol dehydrogenase.

14. The method of claim 13 , wherein the heterologous NAD-linked methanol dehydrogenase is a heterologous Bacillus methanolicus NAD-linked methanol dehydrogenase.

15. The cell-free method of claim 2 , wherein the recombinant cells are derived from recombinant bacteria.

16. The cell-free method of claim 15 , wherein the recombinant bacteria are recombinant Escherichia coli.

17. The cell-free method of claim 1 , wherein

(i) the methane monooxygenase has EC number 1.14.13.25 or 1.14.18.3,

(ii) the methanol dehydrogenase has EC number 1.1.1.244, 1.1.2.7, or 1.1.99.37,

(iii) the hexulose-6-phosphate synthase has EC number 4.1.2.43,

(iv) the 6-phospho-3-hexuloisomerase has EC number 5.3.1.27,

(v) the 6-phosphofructokinase has EC number 2.7.1.11,

(vi) the fructose bisphosphate aldolase has EC number 4.1.2.13,

(vii) the triose phosphate isomerase has EC number 5.3.1.1,

(viii) the transketolase has EC number 2.2.1.1,

(xi) the ribulose-5-phosphate 3-isomerase has EC number 5.3.1.6, or the ribulose-5-phosphate 3-epimerase has EC number 5.1.3.1,

(xii) the glyceraldehyde 3-phosphate dehydrogenase has EC number 1.2.1.12,

(xiii) the phosphoglycerate kinase has EC number 2.7.2.3,

(xiv) the phosphoglycerate mutase has EC number 5.4.2.11 or 5.4.2.12,

(xv) the enolase has EC number 4.2.1.11, and

(xvi) the pyruvate kinase has EC number 2.7.1.40.

18. The cell-free method of claim 1 , wherein the pressure in the bioreactor is at least 1 bar.

19. The cell-free method of claim 18 , wherein the pressure in the bioreactor is at least 2 bar.

20. The cell-free method of claim 1 , wherein the pyruvate is produced at a production rate of at least 10 g/L-h.

21. The cell-free method of claim 1 , wherein the bioreactor comprises a gas phase and an aqueous phase.

22. The cell-free method of claim 21 , wherein the bioreactor further comprises an organic solvent.

23. The cell-free method of claim 22 , wherein the organic solvent is selected from the group consisting of pentane, hexane, heptane, octane, nonane, and decane.

24. The cell-free method of claim 1 , wherein the methane monooxygenase is obtained from a methanotroph.

25. The cell-free method of claim 24 , wherein the methanotroph is a Methylococcus capsulatus Bath methanotroph.

26. The method of claim 1 , wherein the methanol dehydrogenase is a heterologous NAD-linked methanol dehydrogenase.

27. The method of claim 26 , wherein the heterologous NAD-linked methanol dehydrogenase is a heterologous Bacillus methanolicus NAD-linked methanol dehydrogenase.

28. The cell-free method of claim 1 , wherein the recombinant cells are recombinant bacteria.

29. The cell-free method of claim 28 , wherein the recombinant bacteria are recombinant Escherichia coli.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 25, 2014
From: BLAKE, WILLIAM JEREMY; SWARTZ, JAMES R.
To: GREENLIGHT BIOSCIENCES, INC.
Reel/Frame 032295/0533 →
Continuity (2)
Provisional Application 61740972 · Dec 21, 2012
Related Publication 20140193869A1 · Jul 10, 2014