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:
Oct. 27, 2009

Filed:

Sep. 06, 2005
Applicants:

Yoko Asakura, Kawasaki, JP;

Jun Nakamura, Kawasaki, JP;

Sohei Kanno, Kawasaki, JP;

Mikiko Suga, Kawasaki, JP;

Eiichiro Kimura, Kawasaki, JP;

Hisao Ito, Kawasaki, JP;

Kazuhiko Matsui, Kawasaki, JP;

Tsuyoshi Ohsumi, Tokyo, JP;

Tsuyoshi Nakamatsu, Kawasaki, JP;

Osamu Kurahashi, Kawasaki, JP;

Inventors:

Yoko Asakura, Kawasaki, JP;

Jun Nakamura, Kawasaki, JP;

Sohei Kanno, Kawasaki, JP;

Mikiko Suga, Kawasaki, JP;

Eiichiro Kimura, Kawasaki, JP;

Hisao Ito, Kawasaki, JP;

Kazuhiko Matsui, Kawasaki, JP;

Tsuyoshi Ohsumi, Tokyo, JP;

Tsuyoshi Nakamatsu, Kawasaki, JP;

Osamu Kurahashi, Kawasaki, JP;

Assignee:

Ajinomoto Co., Inc., Tokyo, JP;

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
C12P 13/14 (2006.01); C12Q 1/48 (2006.01); C12Q 1/32 (2006.01); C12Q 1/68 (2006.01); C12N 9/02 (2006.01); C12N 9/10 (2006.01); C12N 1/21 (2006.01); C12P 21/00 (2006.01); C12N 15/00 (2006.01); C07K 14/00 (2006.01); C07H 21/00 (2006.01);
U.S. Cl.
CPC ...
Abstract

A method of producing coryneform bacteria having an improved amino acid or nucleic acid-productivity comprises the steps of introducing a mutation in a promoter sequence of amino acid- or nucleic acid-biosynthesizing genes on a chromosome of a coryneform bacterium so that it is close to a consensus sequence or introducing a change in the promoter sequence of amino acid- or nucleic acid-biosynthesizing genes on the chromosome of a coryneform bacterium by gene recombination so that it is close to a consensus sequence, obtaining mutants of the coryneform amino acid- or nucleic acid-producing microorganism, culturing the mutants and select a mutant capable of producing the intended amino acid or nucleic acid in a large amount. This method allows one of skill in the art to construct a mutant capable of enriching or controlling the expression of an intended gene without using a plasmid and to promote production of amino acids in a high yield, by the recombination or mutation.


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