Cultivating method for cordyceps militaris by using manyprickle acathopanax root
A cultivation method and technology of Acanthopanax senticosus, applied in the fields of botanical equipment and methods, fertilizer mixtures, gardening, etc., can solve the problems of inconvenient medicines and large dosages, and achieve the reduction of taking methods, enhancement of supplementary efficacy, and shortening of growth. effect of cycles
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specific Embodiment approach 1
[0011] Specific implementation mode 1: The cultivation method of Acanthopanax senticosus Cordyceps militaris in this embodiment is carried out according to the following steps: 1. Inoculate the Cordyceps militaris strain Yufeng No. 2 on the PDA solid medium and culture it in the dark in a biochemical incubator at 28°C for 5 days , To obtain the activated strain; 2. Cut the activated strain into a 1cm×1cm colony and inoculate it into 300ml liquid seed culture medium. After incubating for 24 hours, it is placed under the condition of 23℃ and 120r / min. Cultivate in the dark for 6 days to obtain a bacterial suspension, and then add 200ml of sterile water to obtain a liquid strain; 3. Inoculate 5ml of the liquid strain into a culture flask containing Acanthopanax senticosus solid medium, and place it at a temperature of 22℃, Incubate in the dark for 10 to 14 days at a humidity of 55% to 60% to obtain mycelium, then move to the light and place at a temperature of 23°C, a humidity of 5...
specific Embodiment approach 2
[0019] Specific embodiment two: this embodiment is different from specific embodiment one in that the PDA solid medium in step one is composed of 200g potato liquid, 20g glucose, 18g agar and 1000ml water, and the pH is natural; Preparation: 200g peeled potatoes, cut into pieces and boiled for 30 minutes, filtered with gauze to make up to 1000ml, pH natural, autoclaved at 121°C for 30 minutes. Other steps and parameters are the same as in the first embodiment.
specific Embodiment approach 3
[0020] Specific embodiment three: This embodiment is different from specific embodiment one in that in step two, each L of liquid seed culture medium consists of 200g potato liquid, 20g glucose, 1g magnesium sulfate, 1g potassium dihydrogen phosphate and the balance of water. Composition, natural pH; preparation of the potato liquid: 200g peeled potatoes, cut into pieces, boiled for 30 minutes, filtered with gauze to make up to 1000ml, pH natural, autoclaved at 121°C for 30 minutes. Other steps and parameters are the same as in the first embodiment.
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Abstract
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