Semi-artificial cultivation method for amanita parvipantherina
A semi-artificial, Amanita technology, applied in the field of semi-artificial cultivation of the wild poisonous fungus Amanita japonica, and the cultivation of large fungi, can solve difficult problems and achieve the effects of low production cost, energy saving, and plant saving
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example 2
[0023] 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 Left or right, gently embed it on the surface of a 500ml Erlenmeyer flask medium, the medium is a modified SPDM medium, and the medium components are: 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, 12.00g / L agar, 180ml / L of wort supplemented with 15.5 Baume, 0.20g / L glutamic acid, 15mg / L of growth active substances, control the pH value to 5.4, culture temperature is 23 ℃, dark culture 15 days, mycelia covered the triangle flask;
[0024] Inoculate the above well-grown mycelium into the cultivation medium of a 1000ml Erlenmeyer flask, the medium being: 50% pulverized native leaf humus+50% bran, supplemented with 180ml of 15.5 Baume wort / Kg, glutamic acid 0.25g / Kg, growth active substance 15mg / Kg, adjust the pH value to 5.5, cultivate at 24°C, cult...
example 3
[0028] 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 Left or right, gently embed it on the surface of a 500ml Erlenmeyer flask medium, the medium is a modified SPDM medium, and the medium components are: 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, 12.00g / L agar, 180ml / L of wort supplemented with 15.5 Baume, 0.20g / L glutamic acid, 15mg / L of growth active substances, control the pH value to 5.4, culture temperature is 23 ℃, dark culture 15 days, mycelia covered the triangle flask;
[0029] Inoculate the above well-grown mycelium into the cultivation medium of a 1000ml Erlenmeyer flask, the medium being: 50% pulverized native leaf humus+50% bran, supplemented with 160ml of wort of 15.0 Baume / Kg, glutamic acid 0.20g / Kg, growth active substance 13mg / Kg, adjust the pH value to 5.6, culture temperature ...
example 4
[0033] 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 Left or right, gently embed it on the surface of a 500ml Erlenmeyer flask medium, the medium is a modified SPDM medium, and the medium components are: 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, 12.00g / L agar, 180ml / L of wort supplemented with 15.5 Baume, 0.20g / L glutamic acid, 15mg / L of growth active substances, control the pH value to 5.4, culture temperature is 23 ℃, dark culture 15 days, mycelia covered the triangle flask;
[0034] Inoculate the above well-grown mycelium into the culture medium of a 1000ml Erlenmeyer flask, the culture medium is: 50% pulverized native leaf humus+50% bran, supplemented with 170ml of 15.0 Baume wort / Kg, glutamic acid 0.25g / Kg, growth active substance 15mg / Kg, adjust the pH value to 5.5, cultivate at 24°C, cul...
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