http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100635450-B1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61G2200-32 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61G7-05715 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61G7-05784 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-74 |
| filingDate | 2005-01-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2006-10-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2006-10-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-100635450-B1 |
| titleOfInvention | Transformation Methods and Foreign Protein Expression Vectors for Lactobacillus Species |
| abstract | The present invention relates to a lactic acid bacteria foreign protein expression vector and a method for transforming Lactobacillus strains using the same, and more specifically to the conditions of electroporation (electroporation) for high transformation efficiency of Lactobacillus ashdophyllus PCR primers were prepared to quickly select transformants, and the lactic acid bacterium vector pKU :: slpA- GFP capable of expressing GFP proteins in cells was prepared, which was then prepared by Lactobacillus acidophilus ATCC 43121 ( Lactobacillus acidophilus). ATCC 43121) to suggest the possibility of GFP as a reporter gene. When the lactic acid bacteria are transformed using the transformation method and the expression vector of the present invention, the recombinant protein can be stably expressed in the cell without changing the original properties. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100959696-B1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101127164-B1 |
| priorityDate | 2005-01-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 39.