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:
Apr. 17, 2018

Filed:

Mar. 10, 2015
Applicant:

Honda Motor Co., Ltd., Minato-Ku, Tokyo, JP;

Inventors:

Migiwa Suda, Wako, JP;

Jiro Okuma, Wako, JP;

Asuka Yamaguchi, Wako, JP;

Yoshitsugu Hirose, Wako, JP;

Yasuhiro Kondo, Wako, JP;

Assignee:
Attorneys:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
C12N 1/21 (2006.01); C12N 9/24 (2006.01); C12N 15/55 (2006.01); C12P 19/02 (2006.01); C12N 9/42 (2006.01); C12P 19/14 (2006.01); C12N 15/10 (2006.01); C40B 30/02 (2006.01);
U.S. Cl.
CPC ...
C12N 9/2437 (2013.01); C12N 15/102 (2013.01); C12N 15/1034 (2013.01); C12N 15/1089 (2013.01); C12P 19/02 (2013.01); C12P 19/14 (2013.01); C12Y 302/01004 (2013.01); C40B 30/02 (2013.01);
Abstract

A method for selectively obtaining a natural variant of an enzyme having activity includes (1) a step of detecting an ORF sequence of a protein having enzyme activity from a genome database including base sequences of metagenomic DNA of environmental microbiota; (2) a step of obtaining at least one PCR clone including the ORF sequence having a full length, a partial sequence of the ORF sequence, or a base sequence encoding an amino acid sequence which is formed by deletion, substitution, or addition of at least one amino acid residue in an amino acid sequence encoded by the ORF sequence, by performing PCR cloning on at least one metagenomic DNA of the environmental microbiota by using a primer designed based on the ORF sequence; (3) a step of determining a base sequence and an amino acid sequence which is encoded by the base sequence for each PCR clone obtained in the step (2); and (4) a step of selecting a natural variant of an enzyme having activity by measuring enzyme activity of proteins encoded by each PCR clone obtained in the step (2).


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