Culture method for inhibiting browning of bolete mycelium
A cultivation method and mycelium technology, which are applied in the directions of botanical equipment and methods, horticulture, and application, can solve the problems of easy browning of culture medium and mycelium, high price, and natural yield decline, and reduce browning. factors, the effect of shortening the culture period and reducing the degree of browning
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example 1
[0017] Mature fruiting bodies picked in the field with good growth, no pests, unopened umbrellas, thicker stipe, and thicker caps;
[0018] Bring the fruiting body back to the laboratory, wipe the surface of the cap and the stipe with an alcohol cotton ball on the ultra-clean table to remove the surface sediment or soil, divide the fruiting body into two from the middle of the cap, and dissect it Take the internal tissue block at the junction of the stipe and the cap with a knife, and cut into about 0.3-0.50cm 2 small pieces;
[0019] Gently embed the small tissue pieces cut above into the surface of the test tube slant induction medium (induction 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 0.40g / L, KNO 3 0.40g / L, V B1 0.10mg / L, wort juice 150 ml / L, glutamic acid 0.16 g / L, agar 13.00g / L, control the pH value to be about 5.4), culture temperature is 22~23℃, dark culture for 7 days, around the bacteria block...
example 2
[0023] Mature fruiting bodies picked in the field with good growth, no pests, unopened umbrellas, thicker stipe, and thicker caps;
[0024]Bring the fruiting body back to the laboratory, wipe the surface of the cap and the stipe with an alcohol cotton ball on the ultra-clean table to remove the surface sediment or soil, divide the fruiting body into two from the middle of the cap, and dissect it Take the internal tissue block at the junction of the stipe and the cap with a knife, and cut into about 0.3-0.50cm 2 small pieces;
[0025] Gently embed the small tissue pieces cut above into the surface of the test tube slant induction medium (induction medium: potato 200.00g / L, glucose 20.00g / L, MgSO 4 1.30g / L, CaCl 2 1.20g / L, KH 2 PO 4 0.60g / L, NH 4 NO 3 0.40g / L, KNO 3 0.40g / L, V B1 0.30mg / L, wort 150 ml / L, glutamic acid 0.20 g / L, agar 15.00 g / L, control the pH value to be about 5.4), culture temperature is 22~23℃, dark culture for 8 days, around the bacteria block The w...
example 3
[0029] Mature fruiting bodies picked in the field with good growth, no pests, unopened umbrellas, thicker stipe, and thicker caps;
[0030] Bring the fruiting body back to the laboratory, wipe the surface of the cap and the stipe with an alcohol cotton ball on the ultra-clean table to remove the surface sediment or soil, divide the fruiting body into two from the middle of the cap, and dissect it Take the internal tissue block at the junction of the stipe and the cap with a knife, and cut into about 0.3-0.50cm 2 small pieces;
[0031] Gently embed the small tissue pieces cut above into the surface of the test tube slant induction medium (induction medium: potato 200.00g / L, glucose 20.00g / L, MgSO 4 1.20g / L, CaCl 2 0.80g / L, KH 2 PO 4 0.40g / L, NH 4 NO 3 0.40g / L, KNO 3 0.40g / L, V B1 0.20mg / L, wort juice 150 ml / L, glutamic acid 0.13g / L, agar 10.00g / L, control the PH value to be about 5.4), culture temperature is 22~23℃, dark culture for 12 days, around the bacteria block...
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