http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H05153992-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ccafce13eb770568b261a9cac7d3dd17 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P19-18 |
filingDate | 1991-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_755a2d89e757f9c5b9778596d8fb4044 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f45be2594cf944e178b883b16688f9c3 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_88d9807560f060e11408215fbb2ac147 |
publicationDate | 1993-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-H05153992-A |
titleOfInvention | Method for producing mannosyl-transferring oligosaccharide |
abstract | (57) [Summary] [Object] To provide an industrial method for producing a mannosyl-transferring oligosaccharide which forms a sugar chain of a complex carbohydrate and is expected to be used as a drug or a diagnostic agent. [Structure] Manno-oligosaccharide, preferably mannotriose, as a donor substrate and N-acetylglucosamine or di-N-acetylchitobiose as an acceptor substrate, preferably in a molar ratio of 1: 0.5 to 1: 5. Dissolve to a high-concentration solution of 10% or more, pH 4-9, temperature 5 Reacting β-D-mannanase under the condition of -50 ° C, The mannose residue is transferred by the transglycosylation reaction of β-D-mannanase to obtain mannosyl N-acetylglucosamine or mannosyl di-N-acetylchitobiose. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002051795-A |
priorityDate | 1991-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 100.