IP Library Granted Patent US 8,309,323
Granted Patent B2
US 8,309,323 · App. 12/742,906 · Granted Nov 13, 2012

Dimethyloctane as an advanced biofuel

Assignee: Synthetic Genomics, Inc.
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Quick Facts
Patent No.
US 8,309,323
App. No.
12/742,906
Granted
Nov 13, 2012
Kind
B2
Abstract

This invention describes genes, metabolic pathways, microbial strains and methods to produce 2,6-dimethyloctane as an advanced biofuel from renewable feedstocks.

Claims (24)

1. A method for producing a fuel or fuel additive, wherein said method comprises:

(i) providing a culture medium, wherein the culture medium comprises a carbon source;

(ii) contacting said culture medium with a recombinant microorganism comprising a biosynthetic pathway capable of converting a carbon source to geraniol acetate, wherein the recombinant microorganism comprises an exogenous gene encoding a geraniol acetyl transferase and at least one additional exogenous gene encoding an enzyme of the pathway;

(iii) recovering said geraniol acetate from the culture medium; and

(iv) converting said geraniol acetate to said fuel or fuel additive.

2. The method of claim 1 , wherein the at least one additional exogenous gene encodes an enzyme selected from the group consisting of:

a 1-deoxy-xylulose 5-phosphate synthase; a 1-deoxy-D-xylulose-5-phosphate reductoisomerase; a 4-diphosphocytidyl-2-C-methyl-D-erythritol synthase; a 4-diphosphocytidyl-2-C-methyl-D-erythritol kinase; a 2-C-methyl-D-erythritol-2,4-cyclodiphosphate synthase; a 1-hydroxy-2-methyl-2-(E)-butenyl-4-diphosphate synthase; a 1-hydroxy-2-methyl-2-(E)-butenyl-4-diphosphate reductase; an acetyl-CoA acetyltransferase; a 3-hydroxy-3-methyl-glutaryl-CoA synthase; a branched chain aminotransferase or leucine aminotransferase; a 2-oxoisovalerate dehydrogenase; an isovaleryl-CoA dehydrogenase; a 3-methylcrotonyl-CoA carboxylase; a 3-methylglutaconyl-CoA hydratase; a 3-hydroxy-3-methyl-glutaryl-CoA reductase; a mevalonate kinase; a phosphomevalonate kinase; a mevalonate-5-diphosphate decarboxylase; an isopentenyl diphosphate isomerase; a geranyl diphosphate synthase; and a geraniol synthase.

3. The method of claim 2 , wherein at least one additional exogenous gene encodes a 3 hydroxy-3-methyl-glutaryl-CoA reductase.

4. The method of claim 3 , wherein at least one additional exogenous gene encodes a truncated 3-hydroxy-3-methyl-glutaryl-CoA reductase.

5. The method of claim 2 , wherein at least one additional exogenous gene encodes an isopentyl diphosphate isomerase.

6. The method of claim 2 , wherein at least one additional exogenous gene encodes a geraniol synthase.

7. The method of claim 2 , wherein the recombinant microorganism further comprises an exogenous gene encoding a mutant farnesyl pyrophosphate synthase.

8. The method of claim 7 , wherein said microorganism comprises a gene replacement of an endogenous farnesyl pyrophosphatase synthase gene with a gene encoding a mutant farnesyl pyrophosphate synthase.

9. The method of claim 1 , wherein the fuel or fuel additive is a dimethyloctane, or a derivative or isomer thereof.

10. The method of claim 9 , wherein step (iv) comprises:

hydrogenating the geraniol acetate, wherein the hydrogenating comprises the step of contacting the geraniol acetate with hydrogen gas and a catalyst, which results in the formation of 2,6-dimethyloctane.

11. The method of claim 1 , wherein the microorganism is an archaea, a bacterium, a yeast, a fungus, a thraustochytrid, or a photosynthetic microorganism.

12. The method of claim 1 , where the carbon source is selected from the group consisting of carboxylic acids, alcohols, sugar alcohols, aldehydes, amino acids, carbohydrates, saturated or unsaturated fatty acids, ketones, peptides, proteins, lignocellulosic material, carbon dioxide, and coal.

13. A method for producing geraniol acetate, wherein said method comprises:

(i) providing a culture medium, wherein the culture medium comprises a carbon source;

(ii) contacting said culture medium with a recombinant microorganism comprising a biosynthetic pathway capable of converting a carbon source to geraniol acetate, wherein the recombinant microorganism comprises an exogenous gene encoding a geraniol acetyl transferase and at least one additional exogenous gene encoding an enzyme of the pathway; and

(iii) recovering said geraniol acetate from the culture medium.

14. The method of claim 13 , wherein the at least one additional exogenous gene encodes an enzyme selected from the group consisting of:

a 1-deoxy-xylulose 5-phosphate synthase; a 1-deoxy-D-xylulose-5-phosphate reductoisomerase; a 4-diphosphocytidyl-2-C-methyl-D-erythritol synthase; a 4-diphosphocytidyl-2-C-methyl-D-erythritol kinase; a 2-C-methyl-D-erythritol-2,4-cyclodiphosphate synthase; a 1-hydroxy-2-methyl-2-(E)-butenyl-4-diphosphate synthase; a 1-hydroxy-2-methyl-2-(E)-butenyl-4-diphosphate reductase; an acetyl-CoA acetyltransferase; a 3-hydroxy-3-methyl-glutaryl-CoA synthase; a branched chain aminotransferase or leucine aminotransferase; a 2-oxoisovalerate dehydrogenase; an isovaleryl-CoA dehydrogenase; a 3-methylcrotonyl-CoA carboxylase; a 3-methylglutaconyl-CoA hydratase; a 3-hydroxy-3-methyl-glutaryl-CoA reductase; a mevalonate kinase; a phosphomevalonate kinase; a mevalonate-5-diphosphate decarboxylase; an isopentenyl diphosphate isomerase; a geranyl diphosphate synthase; and a geraniol synthase.

Assignments (4)
CHANGE OF NAME Recorded Apr 7, 2022
From: SYNTHETIC GENOMICS, INC.
To: VIRIDOS, INC.
Reel/Frame 059631/0684 →
RELEASE OF SECURITY INTEREST Recorded Nov 10, 2020
From: OXFORD FINANCE LLC
To: SYNTHETIC GENOMICS, INC.; GENOVIA BIO, LLC; GREEN RESOURCES, LLC; SGI-DNA, INC.; SYNTHETIC GENOMICS VACCINES, INC.
Reel/Frame 054372/0822 →
SECURITY INTEREST Recorded Mar 20, 2019
From: SYNTHETIC GENOMICS, INC.
To: OXFORD FINANCE LLC
Reel/Frame 048655/0406 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 4, 2010
From: ROESSLER, PAUL G.; VERRUTO, JOHN; MARTIN, KEVIN V.; WATTS, KEVIN; PICATAGGIO, STEPHEN
To: SYNTHETIC GENOMICS, INC.
Reel/Frame 024787/0571 →
Continuity (2)
Provisional Application 60987683 · Nov 13, 2007
Related Publication 20110160501A1 · Jun 30, 2011