Microorganism with knock-in at acetolactate decarboxylase gene locus

US12264348B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12264348-B2
Application numberUS-202318310636-A
CountryUS
Kind codeB2
Filing dateMay 2, 2023
Priority dateJun 6, 2020
Publication dateApr 1, 2025
Grant dateApr 1, 2025

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Abstract

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Provided herein is a genetically engineered microorganism comprising knock-in of DNA at an acetolactate decarboxylase gene locus. Replacement of the acetolactate decarboxylase gene with DNA encoding one or more native or nonnative enzymes confers certain advantages, including fermentation stability and increased production of native and nonnative products from gaseous substrates.

First claim

Opening claim text (preview).

The invention claimed is: 1. A genetically engineered C1-fixing microorganism comprising knock-in of DNA at an acetolactate decarboxylase gene locus, wherein the microorganism comprises oscillations in metabolite production and gas consumption. 2. The microorganism of claim 1 , wherein the DNA replaces the coding region of the acetolactate decarboxylase gene. 3. The microorganism of claim 1 , wherein the DNA does not replace the acetolactate decarboxylase promoter. 4. The microorganism of claim 1 , wherein the microorganism does not produce 2,3-butanediol. 5. The microorganism of claim 1 , wherein the DNA encodes one or more enzymes. 6. The microorganism of claim 5 , wherein the one or more enzymes are nonnative to the microorganism. 7. The microorganism of claim 5 , wherein the one or more enzymes are native to the microorganism. 8. The microorganism of claim 5 , wherein the one or more enzymes are under the control of an acetolactate decarboxylase promoter. 9. The microorganism of claim 1 , wherein the DNA comprises a promoter. 10. The microorganism of claim 5 , wherein the one or more enzymes are under the control of both an acetolactate decarboxylase promoter and at least one other promoter. 11. The microorganism of claim 5 , wherein the one or more enzymes comprise a thiolase, a CoA transferase, and a decarboxylase selected from acetoacetate decarboxylase or alpha-ketoisovalerate decarboxylase. 12. The microorganism of claim 11 , wherein the microorganism produces one or more of butadiene and 1-butanol. 13. The microorganism of claim 11 , wherein the microorganism further comprises a disruptive mutation in a primary-secondary alcohol dehydrogenase gene. 14. The microorganism of claim 5 , wherein the one or more enzymes enable production of 1-butanol, butyrate, butene, butadiene, methyl ethyl ketone, ethylene, acetone, isopropanol, lipids, 3-hydroxypropionate, terpenes, isoprene, fatty acids, 2-butanol, 1,2-propanediol, 1 propanol, 1 hexanol, 1 octanol, chorismate-derived products, 3 hydroxybutyrate, 1,3 butanediol, 2-hydroxyisobutyrate or 2-hydroxyisobutyric acid, isobutylene, adipic acid, 1,3 hexanediol, 3-methyl-2-butanol, 2-buten-1-ol, isovalerate, isoamyl alcohol, or monoethylene glycol. 15. The microorganism of claim 1 , wherein the microorganism is a Wood-Ljungdahl microorganism. 16. The microorganism of claim 1 , wherein the microorganism is a bacterium. 17. The microorganism of claim 1 , wherein the microorganism is a member of a genus selected from Acetobacterium, Alkalibaculum, Blautia, Butyribacterium, Clostridium, Eubacterium, Moorella, Oxobacter, Sporomusa , and Thermoanaerobacter. 18. A method of producing a product comprising culturing the microorganism of claim 1 in the presence of a gaseous substrate. 19. The method of claim 18 , wherein the gaseous substrate comprises a C1-carbon source comprising CO, CO2, and/or H2. 20. The method of claim 18 , wherein the gaseous substrate comprises syngas or industrial waste gas. 21. The method of claim 18 , wherein the product is 1-butanol, butyrate, butene, butadiene, methyl ethyl ketone, ethylene, acetone, isopropanol, lipids, 3-hydroxypropionate, terpenes, isoprene, fatty acids, 2-butanol, 1,2-propanediol, 1 propanol, 1 hexanol, 1 octanol, chorismate-derived products, 3 hydroxybutyrate, 1,3 butanediol, 2-hydroxyisobutyrate or 2-hydroxyisobutyric acid, isobutylene, adipic acid, 1,3 hexanediol, 3-methyl-2-butanol, 2-buten-1-ol, isovalerate, isoamyl alcohol, or monoethylene glycol.

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Classifications

  • polyhydric · CPC title

  • containing one or more isoprene units, i.e. terpenes (carotenes C12P23/00) · CPC title

  • Ketones · CPC title

  • Hydroxy-carboxylic acids · CPC title

  • Unsaturated compounds, i.e. alkenes, alkynes or allenes · CPC title

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What does patent US12264348B2 cover?
Provided herein is a genetically engineered microorganism comprising knock-in of DNA at an acetolactate decarboxylase gene locus. Replacement of the acetolactate decarboxylase gene with DNA encoding one or more native or nonnative enzymes confers certain advantages, including fermentation stability and increased production of native and nonnative products from gaseous substrates.
Who is the assignee on this patent?
Lanzatech Inc
What technology area does this patent fall under?
Primary CPC classification C12Y401/01001. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Apr 01 2025 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 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).