http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20180128567-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b24d7429ccc24e1c2b64ac892258df3b |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N1-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N1-38 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N1-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N1-12 |
| filingDate | 2017-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9b812edf934b3bccf95fcab85a70e042 |
| publicationDate | 2018-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-20180128567-A |
| titleOfInvention | The Mass Production Method of Odontella Aurita |
| abstract | (A) adjusting the pH of the seawater to 7.5 to 8.0 using a neutralizing agent; (b) adding F / 2 medium to the seawater to form a culture medium; (c) inoculating a microalgae Odontella Aurita 1-2 L seed culture into a 10-20 L incubator; (d) dividing the 10 to 20 L culture medium cultured for 10 to 14 days into 100 to 200, culturing for 3 to 4 months, and performing primary scale-up; (e) inoculating the 10 to 20 L culture solution into a 200 to 400 L incubator and culturing for 10 to 14 days to perform a secondary scale-up; (f) recovering 50% from the culture medium in which the secondary scale-up has been completed, and continuously culturing the culture medium for 1 to 2 months after the culture medium is filled, wherein the culture in each of the above steps is performed at 15 to 20 ° C 0.0 > m3 / min < / RTI > to 0.05, and culturing the cells so that the cell density is 16 x 10 4 to 20 x 10 4 cells / mL. |
| priorityDate | 2017-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 29.