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:
Aug. 21, 2018

Filed:

Mar. 31, 2010
Applicant:

Fumikazu Yokoyama, Kanagawa, JP;

Inventor:

Fumikazu Yokoyama, Kanagawa, JP;

Assignee:
Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C12N 9/24 (2006.01); C12N 9/42 (2006.01); C12P 19/02 (2006.01); C12P 19/14 (2006.01); D06M 16/00 (2006.01); D21C 5/00 (2006.01); D21C 5/02 (2006.01); D21H 21/10 (2006.01); A23K 20/189 (2016.01); A23K 10/14 (2016.01);
U.S. Cl.
CPC ...
C12N 9/2437 (2013.01); A23K 10/14 (2016.05); A23K 20/189 (2016.05); C12N 9/2445 (2013.01); C12P 19/02 (2013.01); C12P 19/14 (2013.01); C12Y 302/01004 (2013.01); C12Y 302/01021 (2013.01); D06M 16/003 (2013.01); D21C 5/005 (2013.01); D21C 5/025 (2013.01); D21H 21/10 (2013.01); C12P 2203/00 (2013.01); Y02E 50/16 (2013.01); Y02W 30/648 (2015.05);
Abstract

An object is to identify endoglucanase and β-glucosidase genes by isolating genomic DNA containing cellulase genes, which are classified into endoglucanases or β-glucosidases, from, and sequencing the nucleotide sequences thereof. The inventors intensively compared the amino acid sequences of known endoglucanases and β-glucosidases with each other to find conserved region of amino acid sequences in, and various primers were designed based on the information. PCR was carried out using the various primers thus designed and genomic DNA or cDNA as a template. As a result, gene fragments of endoglucanases and β-glucosidases were obtained. Primers were designed based on the gene fragments, and PCR was carried out to amplify nine genes of endoglucanases and β-glucosidases. The nucleotide sequences thereof were sequenced, and the present invention was completed.


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