http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100429001-B1

Outgoing Links

Predicate Object
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P7-42
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N9-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-70
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Y301-01075
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-55
filingDate 2001-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2004-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2004-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-100429001-B1
titleOfInvention A Gene Coding for Intracellular Polyhydroxyalkanoate(PHA) Depolymerase from Alcaligenes latus
abstract The present invention provides a gene encoding an intracellular PHA degrading enzyme derived from Alcaligenes latus , an amino acid sequence of an electric gene, a recombinant expression vector comprising an electric gene, and an optically pure (R) -hydride using the same. A method for mass production of oxycarboxylic acids. Since the intracellular PHA degrading enzyme derived from Alkali generatus of the present invention is superior to the PHA degrading enzyme derived from other microorganisms, using a recombinant microorganism including an electric gene and a PHA biosynthetic enzyme system effectively and economically optically Pure (R) -hydroxycarboxylic acid can be prepared, and the synthesis of PHA and decomposition into (R) -hydroxycarboxylic acid are simultaneously released into the culture solution, greatly simplifying the overall process and allowing continuous processing. In addition, an increase in overall yield can be expected.
priorityDate 2001-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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