Use of thiamine and nicotine adenine dinucleotide for butanol production

• US 9,012,190 B2
• Filed: 06/15/2011
• Issued: 04/21/2015
• Est. Priority Date: 06/15/2011
• Status: Active Grant

• Current Assignee: Gevo Incorporated
• Original Assignee: Butamax Advanced Biofuels LLC (International Flavors & Fragrances Incorporated)
• Inventors: Dauner, Michael, Jahic, Mehmedalija
• Primary Examiner(s): FRONDA, CHRISTIAN L
• Application Number:
  US13/160,766
• Publication Number:
  US 20120323047A1
• Time in Patent Office: 1,406 Days
• Field of Search: None
• US Class Current: 435/160
• CPC Class Codes: C12N 1/16 Yeasts; Culture media therefor
• CPC Class Codes: C12N 15/52 Genes encoding for enzymes or proenzymes
• CPC Class Codes: C12N 9/0016 with NAD or NADP as acceptor (1.4.1)
• CPC Class Codes: C12N 9/1085 transferring alkyl or aryl groups other than methyl groups (2.5)
• CPC Class Codes: C12P 7/16 Butanols
• CPC Class Codes: C12Y 104/01021 Aspartate dehydrogenase (1.4.1.21)
• CPC Class Codes: C12Y 205/01072 Quinolinate synthase (2.5.1.72)
• CPC Class Codes: Y02E 50/10 Biofuels, e.g. bio-diesel

Abstract

The invention relates generally to the field of industrial microbiology and alcohol production. More specifically, the invention relates to the use of thiamine, biosynthetic precursors of thiamine, nicotinic acid, nicotinamid, nicotinic acid riboside, nicotinamid riboside, or other biosynthetic precursors of nicotine adenine dinucleotide (NAD) to improve butanol production. Butanol production can be improved by providing sufficient amounts of thiamine, biosynthetic precursors of thiamine, nicotinic acid, nicotinamid, nicotinic acid riboside, nicotinamid riboside, or other biosynthetic precursors of nicotine adenine dinucleotide (NAD) in the production media.

Claims

1. A commercial method for producing isobutanol comprising:

a. providing a production culture comprising recombinant cells, wherein the recombinant cells comprise an engineered isobutanol biosynthetic pathway, wherein the engineered isobutanol biosynthetic pathway comprises heterologous polynucleotides encoding polypeptides that catalyze the following substrate to product conversions of the pathway;

a) pyruvate to acetolactate, catalyzed by an acetolactate synthase;

b) acetolactate to 2,3-dihydroxyisovalerate, catalyzed by an acetohydroxy acid reductoisomerase;

c) 2,3-dihydroxyisovalerate to a-ketoisovalerate, catalyzed by a acetohydroxy acid dehydratase;

d) a-ketoisovalerate to isobutyraldehyde, catalyzed by a branched-chain keto acid decarboxylase; and

e) isobutyraldehyde to isobutanol, catalyzed by a branched-chain alcohol dehydrogenase,

wherein the recombinant cells comprise at least one genetic modification that eliminates pyruvate decarboxylase activity,

and wherein the recombinant cells are capable of producing isobutanol, and production media comprising

1. thiamine or a biosynthetic precursor thereof;

2. optionally nicotinic acid, nicotinamid, or a biosynthetic precursor of NAD; and

3. a production feed derived from biomass comprising a fermentable carbon source;

wherein the production media contains less than 1 g/L of multi-component media additives; and

b. contacting the production culture with the production media in a fermentation vessel to form a production broth under conditions whereby isobutanol is produced.

2. The method of claim 1, wherein the production media is substantially free of multi-component media additives.

3. The method of claim 1, wherein the production broth contains at least about 5 mg/L thiamine or a biosynthetic precursor thereof.

4. The method of claim 1, wherein the thiamine or a biosynthetic precursor thereof is present in an amount sufficient to provide at least about 30% of the rate, titer, or specific productivity observed in media that contains about 10 g/L yeast extract.

5. The method of claim 1, wherein the recombinant cells are yeast.

6. The method of claim 5, wherein the yeast is crabtree positive or crabtree negative.

7. The method of claim 1, wherein the recombinant cell comprises a modification of an endogenous gene encoding a thiamine pyrophosphate-dependent (TPP) gene.

8. The method of claim 7, wherein the TPP-dependent gene is a pyruvate decarboxylase gene.

9. The production broth of claim 1, wherein the broth comprises isobutanol.