http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105002205-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-15 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N1-21 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-60 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-53 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-77 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P7-04 |
| filingDate | 2015-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2019-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2019-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-105002205-B |
| titleOfInvention | The genetic engineering bacterium and its construction method of a kind of high yield isoamyl alcohol and application |
| abstract | The invention discloses a kind of genetic engineering bacterium of high yield isoamyl alcohol and its construction method and applications.It is to express α-ketoisovaleric acid decarboxylase gene kivd and alcohol dehydrogenase gene adh3 in corynebacterium glutamicum, and obtain the genetic engineering bacterium of high yield isoamyl alcohol, the nucleotide sequence of the α-ketoisovaleric acid decarboxylase gene kivd is as shown in SEQ ID NO.1, and the nucleotide sequence of the alcohol dehydrogenase gene adh3 is as shown in SEQ ID NO.2.The fermented culture 12h of recombinant bacterium of the invention, the yield of isoamyl alcohol may be up to 497mg/L, be that reporter engineering bacteria synthesizes the highest recombinant bacterium of isoamyl alcohol ability at present. |
| priorityDate | 2015-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 2005.