http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20160051932-A

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N2310-11
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-113
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filingDate 2014-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_59800d215c5f72c26be5f4cbf9bdb003
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6c916e22a4bc6280cd1ab0f55a8a9b9f
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_42b013ea04679aa6002fa5d58619be7f
publicationDate 2016-05-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20160051932-A
titleOfInvention Use of novel α-glucosidase gene Agls6 with stable activity in high concentration organic solvent and recombinant enzyme produced therefrom
abstract The present invention relates to an α-glucosidase gene isolated from an egg-culturing microorganism existing in a larval gland and the use thereof. The present invention relates to a method for isolating a novel enzyme gene which degrades alpha-1, 4-glycosidic bond at the terminal of a non-reducing alpha-glycoside from an egg-culturing microorganism in a larva of a Hermetia illucens larvae, And can be efficiently applied in various industrial processes using vegetable high molecular polysaccharides. In addition, the decomposition effect of the novel enzyme gene according to the present invention can be used in the food fermentation industry, the paper / textile industry, the alcohol production process, the manufacture of medicines and the glycosylation of plant polysaccharides in addition to the industrial process.
priorityDate 2014-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 535.