http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S58216690-A

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Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c62268de3e92657ca5b9adcac4778225
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P13-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P13-00
filingDate 1982-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_322cdd3ad247fc4e5813480764d0945c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0a25ffa6fa85806c4478fd32e5f79acd
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publicationDate 1983-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S58216690-A
titleOfInvention Method for obtaining l-threonine
abstract PURPOSE: To prepare L-threonine with a high efficiency, by reacting a cluture of a microorganism in which only an enzyme hydrolyzing L-threnonie contained therein is slectively inactivated with an isomeric mixture of the threonine. n CONSTITUTION: A culture, microbial cell or extract therefrom of a microorganism, e.g. Psedomonas DK-2 or Bacillus DL-315, having the ability to produce D- threonine aldolase and/or L-allothreonine aldolase in kept at such a temperature as to inactivate only an enzyme hydrolyzing L-threonine selectively without deteriorating the activity of the above-mentioned enzyme for a given time, e.g. 30W 75°C, preferably 35W55°C, for 5minW48hr to inactivate only the enzyme hydrolyzing the L-threonine, and then the above-mentioned culture, microbial cell or extract therefrom is reacted with an isomeric mixture of the threonine. n COPYRIGHT: (C)1983,JPO&Japio
priorityDate 1982-06-10-04:00^^<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: 20.