| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5929f2d6f4dba84be8dd3a8ba633db12 |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K2319-02 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N9-52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-74
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-625
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-00 |
| classificationIPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-19
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-43 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-62
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-74
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N1-21
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N1-00 |
| filingDate |
1986-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7fd475778651324700cdb9341b2010cf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_88f64f0ba18cc5b2ff771a56a2975af4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c529ad53d42ef0e73dc0a7fbe1996af7 |
| publicationDate |
1988-05-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
JP-S63102684-A |
| titleOfInvention |
Gene and use thereof |
| abstract |
PURPOSE:To obtain a DNA to code serrapeptase polypeptide useful for producing a large amount of serrapeptase by genetic engineering technology, prepared from chromosome DNA of a bacterium belonging to the genus Serratia capable of producing serrapeptase. CONSTITUTION:Chrmosome DNA is prepared from a cell of a bacteria (e.g. Serratia marcescens) capable of producing serrapeptase and scissored with a restriction enzyme. The prepared chromosome DNA fragment is linked to a vector (e.g. pBR322 or pUC12) by then use of DNA ligase. A host cell is transformed with the recombinant DNA. The prepared transformant is selected based on drug resistance of used vector as an index and then DNA having base sequence shown by formula I [X1 and X2 are T or G] and/or formula II (Y1 is T or G; Y2 is A, G, T or C; Y3 is T or G) is screened by the use of a prove to give a clone to hybridize the DNA. |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2008505129-A |
| priorityDate |
1985-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |