Method for co-culturing amanita subfrostiana mycelium by using mycorrhizal fungus and saprobic fungus
A technology using mycorrhizal and yellow-scaled amanita, which is applied in the biological field, can solve the problems of difficult induction of mycelia, slow growth of mycelia, and limited number of distributions, and achieve simple and easy cultivation, increased growth speed, and low production costs Effect
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example 1
[0018] Pick healthy fruiting bodies that grow well and have not opened umbrellas in the field; take the internal aseptic tissue block of about 0.35cm at the junction of the cap and the stipe 2 Size, gently embedded in the induction medium, the medium components are: potato 200g / L, fructose 9g / L, protein jelly 1.00g / L, MgSO 4 1.00g / L, CaCl 2 1.00g / L, KH 2 PO 4 0.50g / L, 100ml of 16.0 Baume's wort, 10.00g / L of agar, the pH value of the control medium was 5.6, and cultured in dark at 22-23°C for 50 days, white fluffy hyphae grew on the surface of the tissue block; The silk is subcultured in the above-mentioned induction medium to obtain the mycelium used in the present invention;
[0019] The mycelium is transferred to the proliferation medium, and the components of the proliferation medium are: potato 200g / L, fructose 9g / L, protein jelly 1.00g / L, ZnSO 4 0.40g / L, MgSO 4 0.40g / L, 0.80mg / L zeatin ZT, 25g / L crushed habitat humus soil passed through a 80-mesh sieve, 25g / L enzym...
example 2
[0022] Pick healthy fruiting bodies that grow well and have not opened umbrellas in the field; take the internal aseptic tissue block of about 0.35cm at the junction of the cap and the stipe 2 Size, gently embedded in the induction medium, the medium components are: potato 200g / L, fructose 11g / L, protein jelly 1.25g / L, MgSO 4 1.00g / L, CaCl 2 1.00g / L, KH 2 PO 4 0.50g / L, 125ml of 16.0 Baume's wort, 10.00g / L of agar, the pH value of the control medium was 6.0, and cultured in dark at 22-23°C for 60 days, white fluffy hyphae grew on the surface of the tissue block; The silk is subcultured in the above-mentioned induction medium to obtain the mycelium used in the present invention;
[0023] The mycelium is transferred to the proliferation medium, and the components of the proliferation medium are: potato 200g / L, fructose 11g / L, protein jelly 1.25g / L, ZnSO 4 0.60g / L, MgSO 4 0.60g / L, 1.00mg / L zeatin ZT, 35g / L crushed habitat humus soil passed through a 80-mesh sieve, 35g / L enz...
example 3
[0026] Pick healthy fruiting bodies that grow well and have not opened umbrellas in the field; take the internal aseptic tissue block of about 0.35cm at the junction of the cap and the stipe 2 Size, gently embedded in the induction medium, the medium components are: potato 200g / L, fructose 10g / L, protein jelly 1.10g / L, MgSO 4 1.00g / L, CaCl 2 1.00g / L, KH 2 PO 4 0.50g / L, 110ml of baume wort, 110ml of agar, 10.00g / L of agar, the pH value of the control medium is 5.6, cultured in dark at 22-23°C for 55 days, white fluffy hyphae grow on the surface of the tissue block; The silk is subcultured in the above-mentioned induction medium to obtain the mycelium used in the present invention;
[0027]The mycelium is transferred to the proliferation medium, and the components of the proliferation medium are: potato 200g / L, fructose 10g / L, protein jelly 1.10g / L, ZnSO 4 0.50g / L, MgSO 4 0.50g / L, 0.90mg / L zeatin ZT, 30g / L crushed habitat humus soil passed through a 80-mesh sieve, 30g / L e...
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