Chinese caterpillar fungus cultivation method and its special-purpose culture medium
A technology of Cordyceps sinensis and its cultivation method, applied in the direction of fungi, etc., which can solve the problems of inapplicable medium and cultivation conditions, slow growth rate, low production yield, etc., achieve good social and economic benefits, fast growth rate, and low cost Effect
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Embodiment 1
[0020] Example 1. Production of Cordyceps Mycelium
[0021] Cordyceps special medium: milk powder 50.0g, sucrose 20.0g, peptone 5.0g, yeast extract 1.0g, soybean oil 3.0g, potato 200g, dilute to 1000ml with water.
[0022] Control medium: 200 g potatoes, 20.0 g glucose, and dilute to 1000 ml with water.
[0023] 1. Preparation of culture medium
[0024] Potato processing: Peel the potatoes, cut into small pieces and boil for half an hour, then filter with gauze and add water to make up to 1000 ml.
[0025] Take 1000 ml of potato juice, add milk powder, sucrose, peptone, yeast extract, and soybean oil according to the above medium formula, dissolve, and finally dilute to 1000 ml with water.
[0026] 2. Production of Cordyceps Mycelium
[0027] Isolate the strain from natural Cordyceps sinensis, purify it, and carry out molecular biological identification to confirm that it is a true strain of Cordyceps sinensis. At the initial pH value of 6.0, the Cordyceps strains were inoculated ...
Embodiment 2
[0029] Example 2. Production of Cordyceps Mycelium
[0030] Special culture medium for Cordyceps: 50.0 g corn flour, 20.0 g sucrose, 3.0 g yeast extract, 3.0 g soybean oil, 200 g potato, and dilute to 1000 ml with water.
[0031] Control medium: 200 g potatoes, 20.0 g glucose, and dilute to 1000 ml with water.
[0032] Medium preparation: boil corn flour for half an hour, add potatoes and boil for half an hour, then filter with gauze, add sucrose, peptone, yeast extract, soybean oil according to the above formula, and finally dilute to 1000 ml with water.
[0033] Isolate the strain from natural Cordyceps sinensis, purify it, and carry out molecular biological identification to confirm that it is a true strain of Cordyceps sinensis. At the initial pH value of 6.0, the Cordyceps strains were inoculated into the above-mentioned Cordyceps special medium at an inoculum of 15%, and the bottled volume was 1 / 5 of the volume of the flask, and then at 18℃, rotating at 100rpm, 24 Shaking cu...
Embodiment 3
[0035] Example 3. Production of Cordyceps Mycelium
[0036] Cordyceps special medium: 50.0 grams of soybean meal, 20.0 grams of glucose, 5.0 grams of peptone, 3.0 grams of soybean oil, 200 grams of potatoes, and dilute the volume to 1000 ml with water.
[0037] Control medium: 200 g potatoes, 20.0 g glucose, and dilute to 1000 ml with water.
[0038] The medium was prepared in the same way as in Example 2.
[0039]Isolate the strain from natural Cordyceps sinensis, purify it, and carry out molecular biological identification to confirm that it is a true strain of Cordyceps sinensis. At the initial pH value of 6.0, the Cordyceps strains were inoculated into the above-mentioned Cordyceps special medium at an inoculum of 15%, and the bottled volume was 1 / 5 of the volume of the flask, and then at 18℃, rotating at 100rpm, 24 Shaking culture was performed for 25-30 days under dark conditions for 25-30 days to obtain Cordyceps mycelium, and the mycelium yield reached 21.5g / L. At the same...
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