Rapid preparation method of termitomyces robustus strain
A production method and technology of fir fir are applied in the directions of botanical equipment and methods, fertilizer mixtures, horticulture, etc., and can solve the problems of difficulty in propagation, slow growth of mycelium, difficulty in mass production, etc., and achieve shortened cultivation period and low production cost. , the effect of simple culture medium
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example 1
[0018] Mature fruiting bodies picked in the field with good growth, no pests, unopened umbrellas, thicker stipe, and thicker caps;
[0019] Bring the fruiting body back to the laboratory, wipe the surface of the cap and the stipe with an alcohol cotton ball on the ultra-clean table to remove the surface sediment or soil, divide the fruiting body into two from the middle of the cap, and dissect it Take the internal tissue block at the junction of the stipe and the cap with a knife, and cut into about 0.20-0.40cm 2 small pieces;
[0020] Gently embed the above-cut small tissue pieces on the surface of the mother seed medium on the inclined plane of the test tube. The mother seed medium is: potato 200.00g / L, glucose 20.00g / L, MgSO 4 1.00g / L, CaCl 2 1.00g / L, KH 2 PO 4 0.50g / L, NH 4 NO 3 0.35g / L, KNO 3 0.35g / L, vitamin B 1 2.50mg / L, agar 12.00g / L, control pH value 4.5, culture temperature 26°C, dark culture for 15 days, a small amount of white hyphae sprouted on the o...
example 2
[0024] Mature fruiting bodies picked in the field with good growth, no pests, unopened umbrellas, thicker stipe, and thicker caps;
[0025] Bring the fruiting bodies back to the laboratory, use alcohol cotton balls on the ultra-clean table, lightly wipe the surface of the cap and the stipe and other parts, remove the surface sediment or soil, divide the fruiting bodies from the middle of the cap in two, and dissect Take the internal tissue block at the junction of the stipe and the cap with a knife, and cut into about 0.20-0.40cm 2 small pieces;
[0026] Gently embed the above-cut small tissue pieces on the surface of the mother seed medium on the inclined plane of the test tube. The mother seed medium is: potato 200.00g / L, glucose 20.00g / L, MgSO 4 1.00g / L, CaCl 2 0.50g / L, KH 2 PO 4 0.60g / L, NH 4 NO 3 0.45g / L, KNO 3 0.45g / L, vitamin B 12.00mg / L, agar 12.00g / L, control pH value 4.5, culture temperature 25°C, dark culture for 18 days, a small amount of white hyphae...
example 3
[0030] Mature fruiting bodies picked in the field with good growth, no pests, unopened umbrellas, thicker stipe, and thicker caps;
[0031] Bring the fruiting body back to the laboratory, wipe the surface of the cap and the stipe with an alcohol cotton ball on the ultra-clean table to remove the surface sediment or soil, divide the fruiting body into two from the middle of the cap, and dissect it Take the internal tissue block at the junction of the stipe and the cap with a knife, and cut into about 0.20-0.40cm 2 small pieces;
[0032] Gently embed the above-cut small tissue pieces on the surface of the mother seed medium on the inclined plane of the test tube. The mother seed medium is: potato 200.00g / L, glucose 20.00g / L, MgSO 4 1.00g / L, CaCl 2 0.80g / L, KH 2 PO 4 0.40g / L, NH 4 NO 3 0.40g / L, KNO 3 0.40g / L, vitamin B 1 2.20mg / L, agar 12.00g / L, control PH value to 4.0, culture temperature is 24°C, culture in dark for 17 days, a small amount of white hyphae sprouted...
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