Hydrogenophilus bacterium mutant having improved crotonyl-coa production capability

A genetically modified Hydrogenophilus bacterium efficiently produces crotyl alcohol, butadiene, and butanol from carbon dioxide, addressing greenhouse gas emissions and chemical production inefficiencies.

WO2025220580A1 Publication Date: 2025-10-23UTILIZATION OF CARBON DIOXIDE INST CO LTD +1
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Patent Information

Application Number
PCT/JP2025/014249
Authority / Receiving Office
WO · WO
Patent Type
Applications
Current Assignee / Owner
Priority Date
2024-04-14
Filing Date
2025-04-09
Publication Date
2025-10-23

AI Technical Summary

Technical Problem

Current methods for producing chemicals like butadiene and butanol from petroleum are inefficient and contribute to greenhouse gas emissions, while using biomass for chemical production disrupts food and feed supplies and causes environmental destruction.

Method used

A mutant Hydrogenophilus bacterium with disrupted genes for enzymes that catalyze side reactions in the crotonyl-CoA pathway, allowing for high-efficiency production of crotyl alcohol, butadiene, and butanol using carbon dioxide as a carbon source.

Benefits of technology

The mutant bacterium addresses global warming by efficiently converting carbon dioxide into valuable chemicals and biofuels, meeting the demand for chemical products while reducing reliance on petroleum.

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Abstract

Provided is a Hydrogenophilus bacterium mutant in which at least one of the below-mentioned enzyme genes (a) to (d) is disrupted, wherein the enzyme genes are located on the chromosome of a Hydrogenophilus bacterium and catalyze any one of reactions in the pathway for generating 3-hydroxybutyryl-CoA from crotonyl-CoA. The mutant is improved in terms of crotonyl-CoA production capability and can therefore be used for the efficient production of useful substances generated via crotonyl-CoA. (a) A gene that encodes a polypeptide having a 3-hydroxybutyryl-CoA dehydratase activity; (b) a gene that encodes a polypeptide having an enoyl-CoA hydratase activity; (c) a gene that encodes a polypeptide having a 3-hydroxyacyl-CoA dehydrogenase activity; and (d) a gene that encodes a polypeptide having a methylglutaconyl-CoA hydratase activity.
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