Semi-artificial cultivation method for amanita parvipantherina
A kind of semi-artificial and amanita technology, which is applied in the field of large-scale fungus cultivation and semi-artificial cultivation of wild poisonous fungus Amanita japonica, which can solve difficult problems and achieve the effects of low production cost, saving workshops and energy
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example 1
[0019] Pick out the mycelium that grows well, remove the medium on it, and cut it into 4 to 6 parts, each part is 0.25cm 2 Gently embed it on the surface of a 500ml Erlenmeyer flask medium, the medium is a modified SPDM medium (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 0.10mg / L, agar 12.00g / L), supplemented wort juice (15.5 baume) 180ml, glutamic acid 0.20g / L, growth active substance 15mg / L, control the pH value of 5.4, culture temperature is 23 ℃, dark Cultivate for 15 days, and the hyphae will cover the triangle flask;
[0020] Inoculate the above well-growing mycelium into the cultivation medium (50% crushed original mulch + 50% bran) of a 1000ml Erlenmeyer flask, add 150ml of wort juice (16.5 Baume) and 0.10 glutamic acid g / L, growth active substance 10mg / L, adjust PH value to 5.4, culture temperature is 23°C, culture in dark for 28 days, the hyphae basically cover the ...
example 2
[0024] Pick out the mycelium that grows well, remove the medium on it, and cut it into 4 to 6 parts, each part is 0.25cm 2 Gently embed it on the surface of a 500ml Erlenmeyer flask medium, the medium is a modified SPDM medium (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 0.10mg / L, agar 12.00g / L), supplemented wort juice (15.5 baume) 180ml, glutamic acid 0.20g / L, growth active substance 15mg / L, control the pH value of 5.4, culture temperature is 23 ℃, dark Cultivate for 15 days, and the hyphae will cover the triangle flask;
[0025] Inoculate the above well-grown mycelium into the cultivation medium (50% crushed in situ humus + 50% bran) of a 1000ml Erlenmeyer flask, supplemented with 180ml of wort (15.5 baume) and 0.25 glutamic acid g / L, growth active substance 15mg / L, adjust PH value to 5.5, culture temperature is 24°C, culture in dark for 30 days, mycelia basically cover th...
example 3
[0029] Pick out the mycelium that grows well, remove the medium on it, and cut it into 4 to 6 parts, each part is 0.25cm 2 Gently embed it on the surface of a 500ml Erlenmeyer flask medium, the medium is a modified SPDM medium (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 0.10mg / L, agar 12.00g / L), supplemented wort juice (15.5 baume) 180ml, glutamic acid 0.20g / L, growth active substance 15mg / L, control the pH value of 5.4, culture temperature is 23 ℃, dark Cultivate for 15 days, and the hyphae will cover the triangle flask;
[0030] Inoculate the above well-growing mycelium into the cultivation medium (50% crushed original mulch + 50% bran) of a 1000ml Erlenmeyer flask, add 160ml of wort juice (15.0 Baume) and 0.20 glutamic acid g / L, growth active substance 13mg / L, adjust PH value to 5.6, culture temperature is 22, dark culture for 25 days, mycelia basically covered the triang...
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