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filingDate 2012-10-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c798fea6f3881a16eae91e4a42c8b6de
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publicationDate 2013-04-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2013051608-A1
titleOfInvention Composite sugar chain hydrolase
abstract [Problem] The present invention provides: a novel endo-β-N-acetylglucosaminidase (Endo-Om); and a gene for the endo-β-N-acetylglucosaminidase (Endo-Om). [Solution] The present invention provides a novel endo-β-N-acetylglucosaminidase (Endo-Om) using a transformant produced by cloning an endo-β-N-acetylglucosaminidase (Endo-Om) gene originated from a methanol-utilizing yeast Ogataea minuta IFO10746 strain. The Endo-Om according to the present invention has a specific activity 13-fold higher than that of known Endo-M and a Vmax value 55-fold higher than that of the known Endo-M, and is useful for the analysis of the structures of sugar chains, including composite sugar chains, in glycoproteins and the modification of the sugar chains. Also provided are an endo-β-N-acetylglucosaminidase (Endo-Cp), an endo-β-N-acetylglucosaminidase (Endo-Pa) and an endo-β-N-acetylglucosaminidase (Endo-Zr) which are produced from Candida parapolymorpha DL-1 ATCC26012 strain, Pichia anomala ATCC36904 strain and Zygosaccharomyces rouxii ATCC2623 strain, respectively, on the basis of an Endo-Om gene sequence, and each of which has a similar level of composite sugar chain cleavage activity and a similar level of composite sugar chain transfer activity to those of Endo-Om.
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priorityDate 2011-10-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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