Artificially cultured Grifulaumbelleta strain, Amillariella mellea and sclerotium production method for Grifulaumbelleta strain
A production method, the technology of Armillaria armillaria, applied in botany equipment and methods, fertilizer mixtures, horticulture, etc., can solve the problems of restricting Polyporus umbilicalis, difficulties in artificial cultivation provenance, and rising artificial cultivation costs, so as to achieve rapid formation of sclerotia , to meet the effect of large-scale production and low production cost
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Embodiment 1
[0025] 1) Inoculate the strain of Polyporus spp. in a sterile environment, the volume ratio of the strain of Polyporus spp. to the culture medium is 25:100, cultivate it at 20°C for 20 days to make a first-class strain, and form a large number of sclerotia on the inclined surface of the test tube;
[0026] 2) After sterilizing with the formula of the primary medium, cool the upright test tube at 25°C, transfer Armillaria armillaria, the volume ratio of the strain to the medium is 25:100, and the culture conditions are the same as that of Polyporus sp., to obtain Armillaria armillaria kind;
[0027] 2. Prepare a secondary culture medium with a water content of 60% by weight ratio of 20% corn squid and 80% eucalyptus wood chips. The corn squid is pre-soaked in water for 12-16 hours before use; then put the secondary medium into Seal the jar with a polypropylene film and autoclave for 90 minutes at 121°C; cool down to below 25°C and inoculate the first-grade strains of Polyporus...
Embodiment 2
[0031] 1) Inoculate the strain of Polyporus spp. in a sterile environment, the volume ratio of the strain of Polyporus spp. to the culture medium is 20:100, cultivate it at 27°C for 20 days to make a first-grade strain, and form a large number of sclerotia on the inclined surface of the test tube;
[0032] 2) After sterilizing with the formula of the primary medium, cool the upright test tube at 25°C, transfer to Armillaria armillaria, the volume ratio of the strain to the medium is 20:100, and the culture conditions are the same as that of Polyporus sp.;
[0033]2. Prepare the secondary culture medium with 55% water content with 60% corn squid, 40% broad-leaved maple and elm with a diameter of 0.1-2cm and 3-5cm long small wood section. Soak in water for 1 hour to pre-wet; then put the secondary culture medium into a can bottle and seal it with a polypropylene film, and autoclave for 90 minutes at 121°C; cool down to below 25°C, and inoculate the pigs obtained in step "1" at th...
Embodiment 3
[0037] 1) Inoculate the strain of Polyporus spp. in a sterile environment, the volume ratio of the strain of Polyporus spp. to the culture medium is 16:100, cultivate it at 25°C for 18 days to make a first-class strain, and form a large number of sclerotia on the inclined surface of the test tube;
[0038] 2) After sterilizing with the first-grade medium formula, cool the upright test tube at 25°C, transfer to Armillaria armillaria, the volume ratio of strain to medium is 16:100, and the culture conditions are the same as that of Polyporus sp.;
[0039] 2. Prepare a secondary medium with a water content of 58% by weight ratio of 30% corn squash and 70% chestnut sawdust. Corn squash needs to be soaked in water and pre-wetted 12-16 hours in advance; then put the secondary medium into canned bottles And seal it with a polypropylene film, and sterilize under high pressure at 121°C for 90 minutes; after cooling to below 25°C, simultaneously inoculate the first-class strains of Polyp...
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