Engineering an increase in ethanol production by altering cofactor specificity

US10767196B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10767196-B2
Application numberUS-201214361948-A
CountryUS
Kind codeB2
Filing dateNov 30, 2012
Priority dateNov 30, 2011
Publication dateSep 8, 2020
Grant dateSep 8, 2020

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present invention provides for the manipulation of cofactor usage in a recombinant host cell to increase the formation of desirable products. In some embodiments, the invention provides for a recombinant microorganism comprising a mutation in one or more native enzymes such that their cofactor specificity is altered in such a way that overall cofactor usage in the cell is balanced for a specified pathway and there is an increase in a specific product formation within the cell. In some embodiments, endogenous enzymes are replaced by enzymes with an alternate cofactor specificity from a different species.

First claim

Opening claim text (preview).

What is claimed is: 1. A recombinant cellulolytic Clostridium host cell comprising at least one heterologous nucleic acid sequence encoding a bifunctional alcohol-acetaldehyde dehydrogenase, wherein the bifunctional alcohol-acetaldehyde dehydrogenase is AdhE; wherein the bifunctional AdhE is encoded by a heterologous nucleic acid identical to a polynucleotide that encodes the polypeptide of SEQ ID NO:21, wherein the bifunctional AdhE uses NADPH as a cofactor instead of NADH; wherein the recombinant Clostridium host cell further comprises a genetic modification that leads to the down-regulation of the native enzyme lactate dehydrogenase; and wherein the recombinant Clostridium host cell has an increased production of ethanol compared to a wildtype cellulolytic Clostridium cell without the heterologous nucleic acid and the down-regulation of the native enzyme lactate dehydrogenase. 2. The recombinant cellulolytic Clostridium host cell of claim 1 , wherein the recombinant host cell further comprises a genetic modification that leads to the down-regulation of the native alcohol dehydrogenase and/or acetaldehyde dehydrogenase. 3. The recombinant cellulolytic Clostridium host cell of claim 1 , wherein the host cell is selected from the group consisting of Clostridium thermocellum, Clostridium cellulolyticum, Clostridium clariflavum , and Clostridium phytofermentans. 4. The recombinant cellulolytic Clostridium host cell of claim 1 , wherein the heterologous nucleic acid encoding the bifunctional alcohol-acetaldehyde dehydrogenase is at least about 99% identical to the polynucleotide of SEQ ID NO 20. 5. The recombinant cellulolytic Clostridium host cell of claim 1 , wherein the heterologous nucleic acid encoding the bifunctional alcohol-acetaldehyde dehydrogenase is identical to SEQ ID NO: 20. 6. The recombinant cellulolytic Clostridium host cell of claim 1 , wherein the host cell is Clostridium thermocellum. 7. A composition comprising the host cell from claim 1 and a carbon-containing feedstock, wherein the feedstock is selected from the group consisting of woody biomass, grasses, sugar-processing residues, municipal waste, agricultural wastes and any combination thereof. 8. The composition of claim 7 , wherein the feedstock comprises recycled wood pulp fiber, sawdust, hardwood, softwood, rice straw, rice hulls, barley straw, corn cobs, cereal straw, wheat straw, canola straw, oat straw, oat hulls, corn fiber, stover, succulents, agave, cane bagasse, switchgrass, miscanthus, paper sludge, municipal waste or any combination thereof. 9. A method of producing ethanol comprising: (a) providing the host cell of claim 1 ; (b) culturing the host cell in the presence of a carbon containing feedstock for sufficient time to produce ethanol; and, optionally (c) extracting the ethanol.

Assignees

Inventors

Classifications

  • acting on the aldehyde or oxo group of donors (1.2) · CPC title

  • C12P7/06Primary

    Ethanol, i.e. non-beverage · CPC title

  • acting on CH-OH groups as donors (1.1) · CPC title

  • Alcohol dehydrogenase (1.1.1.1) · CPC title

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

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What does patent US10767196B2 cover?
The present invention provides for the manipulation of cofactor usage in a recombinant host cell to increase the formation of desirable products. In some embodiments, the invention provides for a recombinant microorganism comprising a mutation in one or more native enzymes such that their cofactor specificity is altered in such a way that overall cofactor usage in the cell is balanced for a spe…
Who is the assignee on this patent?
Enchi Corp, Dartmouth College, Ut Battelle Llc
What technology area does this patent fall under?
Primary CPC classification C12P7/06. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Sep 08 2020 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).