The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jun. 04, 2019

Filed:

Dec. 03, 2015
Applicant:

Hubei University of Technology, Wuhan, Hubei, CN;

Inventors:

Yajie Tang, Wuhan, CN;

Kaizhi Jia, Wuhan, CN;

Yanghua Xu, Wuhan, CN;

Quan Zhang, Wuhan, CN;

Hongmei Li, Wuhan, CN;

Assignee:
Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
C12N 15/70 (2006.01); C12N 15/74 (2006.01); C12N 9/88 (2006.01); C12N 15/81 (2006.01); G01N 30/50 (2006.01); G01N 30/80 (2006.01); G01N 27/447 (2006.01);
U.S. Cl.
CPC ...
C12N 9/88 (2013.01); C12N 15/81 (2013.01); C12Y 404/01011 (2013.01); G01N 27/447 (2013.01); G01N 30/50 (2013.01); G01N 30/80 (2013.01);
Abstract

Embodiment of the present invention discloses a kind of methionine lyase and its encoding gene and biosynthetic method. According to the present invention, the gene encoding methionine lyase as shown in SEQ ID No. 1 is separated from the genome of. Embodiment of the present invention further provides an efficient biosynthetic method of methionine lyase, comprising: (1) cloning gene (shown in SEQ ID No.1) encoding methionine degradation enzyme into a yeast expression vector to construct recombinant yeast expression vector; (2) transforming the recombinant yeast expression vector intoto obtain expression strain; (3) inducing the expression strain to express the methionine lyase, collecting induced strains, purifying expressed recombinant methionine lyase. Purity of recombinant methionine lyase prepared according to the present invention is above 90%, and its efficiency of degradating methionine can reach 0.53±0.0030 μM MTL·h·mg protein.


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