Method for culturing of edible fungi
A cultivation method and technology for edible fungi, which are applied in the directions of botanical equipment and methods, application, and horticulture, can solve the problems of high energy consumption, high bacterial infection rate, small inoculation amount, etc., and achieve sufficient oxygen supply and uniform distribution of bacterial species. , the effect of short germinative time
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Embodiment 1
[0029] Embodiment 1: mushroom cultivation method
[0030] (1) Prepare a liquid primary seed medium. The formula is (w / v): 3% soluble starch, 2% sucrose, 0.1% yeast extract, 0.3% potassium dihydrogen phosphate, 0.1% magnesium sulfate, prepared with water, pH 6.0. After preparation, it is divided into 500ml Erlenmeyer flasks, each bottle is 100ml, sterilized at 0.1MPa for 30 minutes, and cooled for later use.
[0031] (2) Preparation of liquid primary species. Pick the mushroom block (together with part of the culture medium) into the sterilized and cooled primary seed culture medium, and cultivate it in a shaker flask at 180 rpm for 6 days at 25°C.
[0032] (3) Preparation of cultivar medium. The formula is (w / v): 20% potato extract (20 grams of potatoes are boiled and filtered to make 100 milliliters of potato juice), 2% sucrose, 0.2% corn flour, 0.1% fine wood chips, and the pH is natural. Put 60 liters of culture medium in a 100 liter fermenter, and after sterilizing the...
Embodiment 2
[0038] Embodiment 2: Grifola frondosa cultivation method.
[0039] (1) Preparation of liquid primary seed medium. The formula is (w / v): 20% of potato extract (20 grams of peeled potatoes are boiled in water for 20 minutes and then filtered, and the filtrate is made into 100 mL of first-class medium), 2% of sucrose, 0.25% of potassium dihydrogen phosphate, sulfuric acid Magnesium 0.05%, Peptone 0.05%, pH Natural. Divide into 500ml Erlenmeyer flasks, 100ml per bottle. Sterilize at 0.1MPa for 30 minutes, cool down for use.
[0040] (2) Preparation of liquid primary species. Pick the frondosa frondosa mother species bacterial block (together with part of the culture medium) into the sterilized and cooled first-grade species culture medium, and cultivate it in a shaker flask at 160 rpm for 5 days at 27°C.
[0041] (3) Preparation of cultivar medium. The formula is (w / v): 20% of potato extract, 2% of sucrose, 0.5% of corn flour, 0.5% of peptone, and natural pH. Pack 45 liters ...
Embodiment 3
[0047] Embodiment 3: black fungus cultivation method.
[0048] (1) Preparation of liquid primary seed medium. The formula is (w / v): 20% of potato extract (20 grams of peeled potatoes are boiled in water for 20 minutes and then filtered, and the filtrate is made into 100 mL of first-class medium), 2% of sucrose, 0.25% of potassium dihydrogen phosphate, sulfuric acid Magnesium 0.05%, pH natural. Divide into 500ml Erlenmeyer flasks, 100ml per bottle. Sterilize at 0.1MPa for 30 minutes, cool down for use.
[0049] (2) Preparation of liquid primary species. Pick the black fungus mother species bacterium block (together with part of the culture medium) into the sterilized and cooled primary species culture medium, and culture it in a shaker flask at 180 rpm at 23°C for 7 days.
[0050] (3) Preparation of cultivar medium. The formula is (w / v): 20% of potato extract, 2% of sucrose, 0.5% of corn flour, 0.5% of bean cake powder, and 0.1% of fine sawdust. Put 30 liters of culture m...
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