Brick-red xerocomus silwoodensis test tube sporocarp primordium inducing method
A technology of boletus velvet cap and test tube, which is applied in the field of induction of fruiting body primordium of boletus velvet cap in test tube, and can solve the problem of slow growth of mycelium, incomplete understanding of the symbiotic mechanism of symbiotic tree species in mycelium growth and development, etc. problem, to achieve the effect of easy operation, increased cultivation cost, and low production cost
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example 1
[0018] Pick mature fruiting bodies in the field that grow robustly, have no pests, have not fully opened umbrellas, have thicker stipe, and thicker caps; bring the fruiting bodies back to the laboratory, and use alcohol cotton balls on the ultra-clean table to wipe the surface of the caps lightly and the stipe part, use a scalpel blade to gently remove the epidermis in the middle of the cap, take a cross from the middle of the cap, divide the fruiting body into four, take the internal sterile tissue block at the junction of the stipe and the cap, and cut into 0.25cm 2 small pieces;
[0019] Gently embed the cut small tissue pieces on the surface of a 18×180 mm test tube slant induction medium, the medium components are: 80.00 g / L of potato, 35 g / L of enzymatically decomposed pine needle powder, 15 g of fermented corn compound powder / L, CaCl 2 1.00g / L, KH 2 PO 4 0.60g / L, 80ml / L of wort juice of 16.0 Baume, 12.00 g / L of agar, the control pH value is 5.40; The preparation me...
example 2
[0022] Pick mature fruiting bodies in the field that grow robustly, have no pests, have not fully opened umbrellas, have thicker stipe, and thicker caps; bring the fruiting bodies back to the laboratory, and use alcohol cotton balls on the ultra-clean table to wipe the surface of the caps lightly and the stipe part, use a scalpel blade to gently remove the epidermis in the middle of the cap, take a cross from the middle of the cap, divide the fruiting body into four, take the internal sterile tissue block at the junction of the stipe and the cap, and cut into 0.35cm 2 small pieces;
[0023] The cut small tissue pieces were gently embedded on the surface of a 18×180 mm test tube slant induction medium. The medium components were: potato 90.00 g / L, enzymatic pine needle powder 38 g / L, fermented corn compound powder 17 g / L L. CaCl 2 1.00g / L, KH 2 PO 4 0.60g / L, 85ml / L of wort juice of 16.0 Baume, 12.00 g / L of agar, the control pH value is 5.60; The preparation method of descri...
example 3
[0026]Pick mature fruiting bodies in the field that grow robustly, have no pests, have not fully opened umbrellas, have thicker stipe, and thicker caps; bring the fruiting bodies back to the laboratory, and use alcohol cotton balls on the ultra-clean table to wipe the surface of the caps lightly and the stipe part, use a scalpel blade to gently remove the epidermis in the middle of the cap, take a cross from the middle of the cap, divide the fruiting body into four, take the internal sterile tissue block at the junction of the stipe and the cap, and cut into 0.49cm 2 small pieces;
[0027] The cut small tissue pieces were gently embedded on the surface of a 18×180 mm test tube slant induction medium. The medium components were: potato 100 g / L, enzymatic pine needle powder 40 g / L, fermented corn compound powder 20 g / L. L. CaCl 2 1.00g / L, KH 2 PO 4 0.60g / L, 90ml / L of wort juice of 16.0 Baume, 12.00 g / L of agar, the control pH value is 5.40; The preparation method of describe...
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