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:
Jul. 05, 2011

Filed:

Feb. 26, 2010
Applicants:

Yoshimi Kikuchi, Kawasaki, JP;

Masayo Date, Kawasaki, JP;

Yukiko Umezawa, Kawasaki, JP;

Keiichi Yokoyama, Kawasaki, JP;

Hiroshi Matsui, Kawasaki, JP;

Inventors:

Yoshimi Kikuchi, Kawasaki, JP;

Masayo Date, Kawasaki, JP;

Yukiko Umezawa, Kawasaki, JP;

Keiichi Yokoyama, Kawasaki, JP;

Hiroshi Matsui, Kawasaki, JP;

Assignee:

Ajinomoto Co., Inc., Tokyo, JP;

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C12N 9/10 (2006.01); C12N 1/20 (2006.01); C12N 15/00 (2006.01); C12P 21/04 (2006.01); A61K 38/00 (2006.01); C07H 21/04 (2006.01); C07H 21/02 (2006.01); C07K 1/00 (2006.01); C12Q 1/68 (2006.01); C12Q 1/00 (2006.01);
U.S. Cl.
CPC ...
Abstract

The present invention relates to a process for secretory production of a foreign protein, in particular, transglutaminase by a coryneform bacterium. According to the present invention, a process is provided for the secretory production of a foreign protein, in particular, transglutaminase, by making a coryneform bacterium to produce an industrially useful foreign protein, in particular, transglutaminase and efficiently release the product extracellularly (i.e., secretory production). An intended foreign protein, in particular, transglutaminase, is produced by using an expression construct wherein the gene sequence of the intended foreign protein containing the pro-structure part, in particular, pro-transglutaminase gene sequence, is ligated to the downstream of a sequence encoding the signal peptide region from a coryneform bacterium, introducing this expressional genetic construct into a coryneform bacterium, culturing the thus transformed coryneform bacterium, and treating the extracellularly released protein with a protease, etc. to cleave and eliminate the pro-part.


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