Method for producing methacrylyl-CoA

US10323264B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10323264-B2
Application numberUS-201414905155-A
CountryUS
Kind codeB2
Filing dateJul 25, 2014
Priority dateAug 1, 2013
Publication dateJun 18, 2019
Grant dateJun 18, 2019

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.

The invention provides a method for producing methacrylyl-CoA that converts 3-hydroxyisobutyryl-CoA into methacrylyl-CoA using an enzyme having dehydratase activity as a method for producing methacrylyl-CoA using an enzyme catalyst. In this production method, conversion rate of 3-hydroxyisobutyryl-CoA into methacrylyl-CoA by the enzyme having dehydratase activity is 50% or higher. In this production method, furthermore, the enzyme having dehydratase activity derives from a microorganism belonging to the genus Pseudomonas or Rhodococcus.

First claim

Opening claim text (preview).

What is claimed is: 1. A method for producing methacrylyl-CoA and converting methylacryl-CoA to methacrylic acid or methacrylate ester, the method comprising: converting 3-hydroxyisobutyryl-CoA to methacrylyl-CoA in an aqueous medium in the presence of a dehydratase at a conversion rate of 50% or higher; and converting methacrylyl-CoA to methacrylic acid or methacrylate ester at a pH of 4 to 10, wherein the dehydratase is selected from a group consisting of: (a) a protein having the amino acid sequence shown in SEQ ID NO: 1 or 3; (b) a protein that is at least 80% identical to a protein having the amino acid sequence shown in SEQ ID NO: 1 or 3, and possessing dehydratase activity; (c) a protein encoded by the nucleotide sequence of SEQ ID NO: 2 or 4; (d) a protein encoded by DNA that is at least 80% identical to SEQ ID NO: 2 or 4, and possessing dehydratase activity. 2. The method according to claim 1 , wherein 3-hydroxyisobutyryl-CoA is converted to methacrylyl-CoA at a temperature of 5˜80° C. 3. The method according to claim 1 , wherein 3-hydroxyisobutyryl-CoA is converted to methacrylyl-CoA for a duration of from 1 minute to 1 week. 4. The method according to claim 1 , wherein the aqueous medium comprises 1 mM or greater of an osmolyte. 5. The method according to claim 1 , wherein 3-hydroxyisobutyryl-CoA is converted to methacrylyl-CoA in the presence of a transformant for expressing a gene for encoding a dehydratase. 6. The method according to claim 5 , wherein the gene encoding a dehydratase is derived from a microorganism. 7. The method according to claim 6 , wherein the microorganism belongs to the genus Pseudomonas or the genus Rhodococcus. 8. The method according to claim 1 , wherein the dehydratase has the amino acid sequence shown in SEQ ID NO: 1 or 3. 9. A method for producing methacrylyl-CoA, the method comprising: converting 3-hydroxyisobutyryl-CoA to methacrylyl-CoA in the presence of a transformant for expressing a gene encoding a dehydratase derived from a microorganism at a conversion rate of 50% or higher through reactions of a 3-hydroxyisobutyryl-CoA solution, which is prepared in an aqueous medium comprising 1 mM or greater of an osmolyte, at a pH of 4-10 and a temperature of 5-80° C. for a duration of from 1 minute to 1 week, wherein the dehydratase is selected from a group consisting of: (a) a protein having the amino acid sequence shown in SEQ ID NO: 1 or 3; (b) a protein that is at least 80% identical to a protein having the amino acid sequence shown in SEQ ID NO: 1 or 3, and possessing dehydratase activity; (c) a protein encoded by the nucleotide sequence of SEQ ID NO: 2 or 4; (d) a protein encoded by DNA that is at least 80% identical to SEQ ID NO: 2 or 4, and possessing dehydratase activity. 10. The method according to claim 9 , wherein the dehydratase has the amino acid sequence shown in SEQ ID NO: 1 or 3.

Assignees

Inventors

Classifications

  • Propionic acid; Butyric acids · CPC title

  • C12P19/32Primary

    having a condensed ring system containing a six-membered ring having two N-atoms in the same ring, e.g. purine nucleotides, nicotineamide-adenine dinucleotide · CPC title

  • Lyases (4.) · 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 US10323264B2 cover?
The invention provides a method for producing methacrylyl-CoA that converts 3-hydroxyisobutyryl-CoA into methacrylyl-CoA using an enzyme having dehydratase activity as a method for producing methacrylyl-CoA using an enzyme catalyst. In this production method, conversion rate of 3-hydroxyisobutyryl-CoA into methacrylyl-CoA by the enzyme having dehydratase activity is 50% or higher. In this produ…
Who is the assignee on this patent?
Mitsubishi Chem Corp
What technology area does this patent fall under?
Primary CPC classification C12P19/32. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jun 18 2019 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 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).