http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20050076380-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e794269bf736289d22ca8eb80351bf0d http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_455c51cbbe5df91b3fac619197fa3b54 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G08G1-096 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G08G1-095 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01G1-04 |
filingDate | 2004-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_350a2c46815cad25b91412443cd3f92f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4817b617ac979f5b29dec5e96f2e3f03 |
publicationDate | 2005-07-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | KR-20050076380-A |
titleOfInvention | Method for cultivating phellinus linteus and apparatus for the method |
abstract | The present invention relates to a cultivation method of a situation mushroom and a cultivation apparatus used for the same. First, mulberry sawdust and oak sawdust or mulberry sawdust, oak sawdust and rice bran mixed with a medium mixed in a specially designed plastic culture vessel (cultivation bottle), and then made a tunnel for inoculation with a perforator. Assemble with the designed cap. The cap has the same internal capacity as the culture bottle, and the sterilization is made specially so that the size of individual pores is about 0.4 ~ 0.8㎛ so that the upper part of the cap has four holes and prevents invasion of bacteria and frees the air and moisture flow. The lid to which the sponge is bonded is attached. Sterilize and inoculate the culture bottle with the cap assembled, and inoculate the mycelia in the culture room, and then transfer to the cultivator to keep the culture at about 22-25 ° C and humidity at about 50-60%. In order to repeat the process, the first 4 to 5 days of supplying light to induce fruiting (incubation), after about 9 to 10 days to completely block the light and keep the humidity to induce the growth of fruiting ( Cancer culture). If it is determined that the harvest time is right, the water on the surface of the fresh mushrooms is evaporated (light cultivation) while supplying light again for about 2 to 3 days, then the cap is removed and the first harvest is performed. It is possible to increase the yield of high-quality situation mushrooms by harvesting several times, for example, a total of three times the situation mushrooms by culturing while repeating the light culture, cancer culture, and light culture again. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20190077764-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103739348-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20180112149-A |
priorityDate | 2004-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 51.