Plate fruiting method for morchella
A technology of Morchella and flat plate, applied in chemical instruments and methods, botanical equipment and methods, mushroom cultivation and other directions, can solve the problems of high labor intensity, poor yield stability, and no fruiting on flat plates, and achieves increased sclerotia. Number, simple operation, the effect of speeding up the formation time of primordium
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Embodiment 1
[0047] (1) Prepare 1 L of PDA medium, sterilize with high temperature and moist heat, add 50 mL of soil filtrate (1 g / mL) filtered by a cell strainer, add 25 mL of medium improver, and mix to obtain an improved PDA medium. Pour 20mL of the modified PDA medium into each plate, a total of 20 plates, and place them on the ultra-clean table to solidify naturally, as the test group;
[0048] (2) PDA medium is set as the control group: each plate is poured into 20mL PDA medium, totally 20 plates; wherein the plates used by the control group and the experimental group are exactly the same;
[0049] (3) picking an equivalent amount of Morchella importuna mycelium and inoculating them on PDA medium and improved PDA medium respectively;
[0050] (4) The experimental group and the control group were placed in a fungal incubator for dark culture, and the culture temperature was 18°C;
[0051] (5) Observe the growth of hyphae and the appearance time of sclerotia.
[0052] The improved me...
Embodiment 2
[0055] (1) Prepare 1 L of PDA medium, sterilize with high temperature and moist heat, add 50 mL of soil filtrate (1 g / mL) filtered by a cell strainer, add 25 mL of medium improver, and mix to obtain an improved PDA medium. Each petri dish is poured into the improved PDA culture medium 20mL after processing, altogether 40 petri dishes are placed on the ultra-clean platform to solidify naturally; each petri dish is inoculated with the mycelium of the same amount of Morchella spp. as in Example 1;
[0056] (2) Place 40 plates in a fungal incubator for dark cultivation;
[0057] Among them, 20 plates were set as the control group, and the culture temperature was set to 18°C;
[0058] The other 20 plates are set as the experimental group, and the set temperature is: 0~12h after inoculation, keep the temperature at 24°C; 12~36h, keep the temperature at 16°C; 36~72h, keep the temperature at 18°C; after 72h, keep the temperature at 16°C ;
[0059] (3) Observe the growth of mycelia, ...
Embodiment 3
[0063] (1) Prepare 1L of PDA medium, sterilize with high temperature and moist heat, add 50mL of soil filtrate (1g / mL) filtered by a cell filter, add 25mL of medium improver, pour 20mL of the improved PDA medium into each plate, and add 40 petri dishes are placed on the ultra-clean bench to solidify naturally; each petri dish is inoculated with the mycelia of the morel stalks of the same amount as in Example 1;
[0064] (2) Placed in a fungal incubator for cultivation, the cultivation temperature is 18°C;
[0065] Wherein, 20 plates were set as a control group, and the control group was cultured in the dark;
[0066] The other 20 plates were set as the experimental group, and the experimental group was also cultured in the dark, but it needed to be supplemented with light at key nodes. 12 hours after inoculation, 200 lux white light treatment for 1 hour; 36 hours after inoculation, 200 lux white light treatment for 1 hour; 72 hours after inoculation , 100 Lux illuminance whit...
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