http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H0220295-A

Outgoing Links

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classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-465
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P21-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P21-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G69-08
filingDate 1988-07-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_81b977f26f7acb97cc9f6342cc407a27
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publicationDate 1990-01-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0220295-A
titleOfInvention Production of free epsilon-polylysine
abstract PURPOSE: To easily supply a free ε-polylysine to a field of agricultural chemicals, pharmaceuticals, etc., in high efficiency at a low cost by treating an ε-polylysine solution with a basic anion exchange resin and precipitating the treated solution with an organic solvent or freeze-drying the solution. n CONSTITUTION: An ε-polylysine-producing microbial strain such as Streptomyces albulus is cultured and the microbial cells are separated from the obtained cultured liquid to obtain a solution. The solution is treated with an ultrafiltration membrane having a fractionation molecular weight of ≥3,000 and the permeated ε-polylysine-containing liquid is treated with an ultrafiltration membrane having a fractionation molecular weight of ≤1000. The fraction left on the membrane is collected to obtain an ε-polylysine solution (A). The solution A is treated with a basic anion exchange resin such as Amberlite 1RA-402 and the treated solution is precipitated with an organic solvent or freeze-dried or spray-dried to obtain free ε-polylysine. n COPYRIGHT: (C)1990,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0557954-A3
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2006067850-A
priorityDate 1988-07-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 22.