Method for producing 3-hydroxypropionic acid and other products

US9428778B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9428778-B2
Application numberUS-201414575927-A
CountryUS
Kind codeB2
Filing dateDec 18, 2014
Priority dateSep 27, 2009
Publication dateAug 30, 2016
Grant dateAug 30, 2016

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

This invention relates to metabolically engineered microorganism strains, such as bacterial strains, in which there is an increased utilization of malonyl-CoA for production of a chemical product, which includes 3-hydroxypropionic acid.

First claim

Opening claim text (preview).

What is claimed is: 1. A method for producing a product having malonyl-CoA as a substrate in a microbial production pathway of the product, the method comprising combining a carbon source and a microorganism cell culture to produce said product, wherein a) said cell culture comprises an inhibitor of a fatty acid synthase or said microorganism is genetically modified for reduced enzymatic activity of an enzyme wherein the enzyme is selected from the group consisting of beta-ketoacyl-ACP synthase (fabH, fabF, fabB), beta-ketoacyl-ACP reductase (fabG), beta-hydroxyacyl-ACP dehydratase (fab A), and enoyl-ACP reductase (fabI); and either: b1) said microorganism is genetically modified for overexpression of udhA or pntAB; or b2) said microorganism is genetically modified for overexpression of accA, accB, accC, accD, or any combination thereof. 2. The method of claim 1 , wherein said carbon source has a ratio of carbon-14 to carbon-12 of about 1.0×10 −14 or greater. 3. The method of claim 1 , wherein said carbon source is glucose, sucrose, fructose, dextrose, lactose, or a combination thereof. 4. The method of claim 1 , wherein said inhibitor of the fatty acid synthase is selected from the group consisting of thiolactomycin, triclosan, cerulenin, thienodiazaborine, and isoniazid. 5. The method of claim 1 , wherein said reduced enzymatic activity of the enzyme occurs via introduction of a heterologous nucleic acid sequence comprising an inducible promoter operably linked to a sequence coding for the enzyme or a heterologous nucleic acid sequence coding for the enzyme with reduced activity. 6. The method of claim 5 , wherein said beta-ketoacyl-ACP synthase has temperature sensitive enzyme activity or said enoyl-ACP reductase has temperature sensitive enzyme activity. 7. The method of claim 1 , wherein said overexpression of udhA or pntAB occurs by introduction of a heterologous nucleic acid sequence coding for a polypeptide having at least 90% homology with a sequence selected from the group consisting of SEQ ID NO. 776 and SEQ ID NO. 778. 8. The method of claim 1 , wherein said microorganism is further genetically modified for increased intracellular bicarbonate levels by introduction of a heterologous nucleic acid sequence coding for a polypeptide having cyanase and/or carbonic anhydrase activity. 9. The method of claim 8 , wherein said heterologous nucleic acid sequence is selected from a sequence having at least 90% homology with SEQ ID NO. 337. 10. The method of claim 1 , wherein said overexpression of accA, accB, accC, accD, or any combination thereof occurs by introduction of a heterologous nucleic acid sequence coding for a polypeptide having at least 90% homology with a sequence selected from the group consisting of SEQ ID NO. 768, SEQ ID NO.769, SEQ ID NO.770, SEQ ID NO.771, SEQ ID NO.772, SEQ ID NO.773, SEQ ID NO.774, and SEQ ID NO. 775. 11. The method of claim 1 , wherein said microorganism is further genetically modified to decrease activity of lactate dehydrogenase, phosphate acetyltransferase, pyruvate oxidase, pyruvate-formate lyase, or a combination thereof. 12. The method of claim 1 , wherein said microorganism cell culture comprises increased intracellular bicarbonate levels by supplementation with bicarbonate or carbonate. 13. The method of claim 1 , wherein the product comprises an alkyl carboxylate. 14. The method of claim 13 , wherein the alkyl carboxylate is selected from the group consisting of: a methyl ester of a carboxylic acid, an ethyl ester of a carboxylic acid, and mixtures thereof. 15. The method of claim 14 , wherein the methyl ester of a carboxylic acid comprises a methyl ester of 3-hydroxypropionic acid and the ethyl ester of a carboxylic acid comprises an ethyl ester of 3-hydroxypropionic acid. 16. The method of claim 13 , wherein the alkyl carboxylate is selected from the group consisting of methyl carboxylates and ethyl carboxylates, and mixtures thereof. 17. The method of claim 16 , wherein the methyl carboxylate is a methyl ester of 3-hydroxypropionic acid and the ethyl carboxylate is an ethyl ester of 3-hyrdroxypropionic acid.

Assignees

Inventors

Classifications

  • Biofuels, e.g. bio-diesel · CPC title

  • A61L15/24Primary

    Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives thereof {(A61L15/225 takes precedence)} · CPC title

  • Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression · CPC title

  • Homopolymers or copolymers of acrylic acid esters · CPC title

  • using catalysts, e.g. selective catalysts · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9428778B2 cover?
This invention relates to metabolically engineered microorganism strains, such as bacterial strains, in which there is an increased utilization of malonyl-CoA for production of a chemical product, which includes 3-hydroxypropionic acid.
Who is the assignee on this patent?
Cargill Inc, Univ Colorado Regents
What technology area does this patent fall under?
Primary CPC classification A61L15/24. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Aug 30 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).