http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100308521-B1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B64D17-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B64D17-025 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-70 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N1-21 |
| filingDate | 1999-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2001-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2001-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-100308521-B1 |
| titleOfInvention | Genetically engineered Escherichia coli strains and the methods to produce optically pure D- or L-lactate production using the strains |
| abstract | The present invention relates to a pure E. coli (Escherichia coli) and a method for producing pure D- or L-lactic acid using the same, and more specifically, because the metabolic pathway is modified using genetic engineering techniques, the production of acetic acid and succinic acid genetically E. coli JP203, which can selectively produce only D-type lactic acid, or Escherichia coli JP204, which can selectively produce only L-type lactic acid, was obtained, and these strains were grown first in aerobic conditions. Secondly, the present invention relates to a method capable of selectively mass-producing only D- or L-lactic acid in a more efficient and higher yield by converting the culture conditions into anaerobic conditions. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-102010031152-A1 |
| priorityDate | 1999-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 464.