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filingDate 2010-02-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_72dfba2013117b16e673caa2bdaec5be
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3bb0a6cae1c6e0481156573a8f7718d6
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publicationDate 2011-08-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20110093120-A
titleOfInvention Recombinant Expression Vectors for Production of Beta-Agares
abstract The present invention includes a promoter of a streptomyces griseus- derived trypsin gene ( sprT ) and a beta-agarase gene ( dagA ) derived from Streptomyces coelicolor , to transform prokaryotes. signal of agar Reds recombinant expression vector and Streptomyces draw three-house (Streptomyces griseus) derived trypsin gene (sprT) promoter, Streptomyces draw three-house (Streptomyces griseus) derived trypsin gene (sprT) of the - first-type beta that A type 2 beta capable of transforming prokaryotes, including a portion of a peptide coding region and a beta-agarase gene ( dagA ) derived from Streptomyces coelicolor ( dagA ), wherein the signal peptide code is removed Agarase Recombinant Expression Vector. When the beta-agarase recombinant expression vector of the present invention is introduced into a heterologous strain, strains that do not produce beta-agarase can produce high-activity beta-agarase with high efficiency, and thus host a more manageable strain. When the recombinant expression vector of the present invention is introduced as a strain, it is possible to economically mass-produce beta-agares, and thus, the mass-produced beta-agares decomposes agar (agar), which is present in nature, to reduce reducing sugar. It can be very useful for energy, medicine and food fields.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20140061272-A
priorityDate 2010-02-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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