http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H09135689-A

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filingDate 1995-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2801371ff4525b9a00fe6410bc7e53e1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5cf275e9d93880ef75f2d2d35158b671
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publicationDate 1997-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H09135689-A
titleOfInvention Yeast mannose-1-phosphate transferase gene and method for producing mannose-1-phosphate-containing acidic sugar chain and phosphate-containing acidic sugar chain using the same
abstract (57) Abstract: Yeast (Saccharomyces cerevisiae) mannose-1-phosphate transferase gene, yeast cells transformed with plasmid DNA into which the gene has been introduced are cultured in a medium, A method for producing a mannose-1-phosphate-containing acidic sugar chain, which comprises obtaining a mannose-1-phosphate transferase and allowing it to act on a neutral core sugar chain in vivo or in vitro, and the mannose- 1- A method for producing a phosphoric acid-containing acidic sugar chain, which comprises removing a mannose portion by acid-treating a phosphoric acid-containing acidic sugar chain. [Effects] According to the present invention, an acidic sugar chain obtained by adding mannose-1-phosphate to the same neutral core sugar chain as that of high-mannose produced by mammalian cells such as human is produced by a genetic engineering method using yeast. A large amount and high purity can be produced. Furthermore, to produce a large amount of a useful acidic sugar chain identical to the human-derived phosphate-containing core sugar chain, which can function as a marker for glycoprotein transport to lysosomes in mammalian cells such as humans, in high purity. You can
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Total number of triples: 405.