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:
Nov. 08, 2005

Filed:

May. 25, 2000
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;

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
C12P013/14 ; C07H021/04 ; C12Q001/32 ; C12N015/74 ; C12N001/20 ;
U.S. Cl.
CPC ...
Abstract

A method of producing coryneform bacteria having improved amino acid or nucleic acid productivity comprising 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 to make it close to a consensus sequence, or introducing a change in a promoter sequence of amino acid- or nucleic acid-biosynthesizing genes on a chromosome of a coryneform bacterium by gene recombination to make it close to a consensus sequence, to obtain mutants of the coryneform amino acid- or nucleic acid-producing microorganism, culturing the mutants and selecting a mutant capable of producing the intended amino acid or nucleic acid in a large amount. This method allows the construction of 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 recombination or mutation.


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