Method for rapidly propagating small leopard amanita mycelium
A technology of mycelium and amanita, which is applied in the field of rapid indoor cultivation of wild poisonous fungus Amanita amanita mycelium, can solve the problems of slow growth of mycelium in the early stage and difficulty in multiplying, so as to shorten the growth cycle and reduce production costs. Low, easy-to-operate effect
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example 1
[0020] Pick young fruiting bodies with good growth, no pests, and unopened umbrellas in the field; bring the fruiting bodies back to the laboratory, and use alcohol cotton balls on the ultra-clean table to gently wipe the surface of the cap and the stipe;
[0021] Slightly remove the epidermis and the surrounding part of the cap with a sterile blade, and cut the remaining middle part of the cap and the stipe into pieces of about 0.10-0.25cm 2 Small squares, gently embedded in the surface of the induction medium, the medium is 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), add wort juice (15.0 Baume) 150ml, control the pH value to 5.4, culture temperature is 22℃, culture in dark for 40 days, the tissue blocks are raised in many places, and the surface grows lumps , dense fluffy white hyphae;
[0022] Pick out the well-growing myceli...
example 2
[0024] Pick young fruiting bodies with good growth, no pests, and unopened umbrellas in the field; bring the fruiting bodies back to the laboratory, and use alcohol cotton balls on the ultra-clean table to gently wipe the surface of the cap and the stipe;
[0025] Slightly remove the epidermis and the surrounding part of the cap with a sterile blade, and cut the remaining middle part of the cap and the stipe into pieces of about 0.10-0.25cm 2 Small squares, gently embedded in the surface of the induction medium, the medium is 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 B1 0.10mg / L, agar 12.00g / L), supplemented wort juice (15.5 Baume) 165ml, controlled PH value to 5.6, culture temperature was 23°C, cultured in dark for 42 days, the tissue pieces bulged in many places, and the surface grew lumps , dense fluffy white hyphae;
[0026] Pick out the well-growing my...
example 3
[0028] Pick young fruiting bodies with good growth, no pests, and unopened umbrellas in the field; bring the fruiting bodies back to the laboratory, and use alcohol cotton balls on the ultra-clean table to gently wipe the surface of the cap and the stipe;
[0029] Slightly remove the epidermis and the surrounding part of the cap with a sterile blade, and cut the remaining middle part of the cap and the stipe into pieces of about 0.10-0.25cm 2 Small squares, gently embedded in the surface of the induction medium, the medium is 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), add wort juice (16.0 Baume) 180ml, control PH value to 5.4, culture temperature is 24°C, culture in dark for 38 days, the tissue blocks bulge in many places, and the surface grows lumps , dense fluffy white hyphae;
[0030] Pick out the well-growing mycelia in the...
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