Special low-temperature cryoprotectant for cordyceps sinensis strain preservation and use method thereof
A technology of low-temperature freezing and Cordyceps strains, applied in the direction of preservation of microorganisms, methods based on microorganisms, biochemical equipment and methods, etc., can solve the problems of preservation reports, no Cordyceps fungal strains, etc.
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example 1
[0020] 1. Culture of Cordyceps militaris
[0021] The Cordyceps militaris strains were inoculated on PDA slant medium and cultured in the dark at 25 °C. When the diameter of the colony grew to 4 cm, the strains were cultured under light for 4 days to induce the color change of the strains, reduce the formation of aerial hyphae, and promote the formation of spores.
[0022] 2. Preparation of protective agent
[0023] The protective agent consists of two parts, that is, Cordyceps liquid medium, which consists of: glucose 10 g, peptone 4 g, yeast extract 1 g, water to 1000 mL, natural pH. The other part is glycerin. The Cordyceps nutrient solution was sterilized at 115 °C for 30 min, and the glycerin was sterilized at 121 °C for 20 min. Glycerin was prepared with Cordyceps nutrient solution under aseptic conditions before use, and the mass concentration of glycerin was 30%.
[0024] 3. Preparation of strain mycelium and spore suspension
[0025] Gently scrape the mycelium of...
example 2
[0029] 1. Culture of cicadae strains
[0030] Cicadae strains were inoculated on PDA plates with a diameter of 9 cm, and cultured in the dark at 25 °C. When the diameter of the colony grows to 3 cm, the bacteria are cultured under light for 3 days to promote the formation of spores.
[0031] 2. Preparation of protective agent
[0032] The protective agent is composed of two parts, that is, Cordyceps nutrient solution, which is composed of: 20 g of glucose, 8 g of peptone, 2 g of yeast extract, dilute water to 1000 mL, and natural pH. The other part is glycerin. The two parts were sterilized separately, the Cordyceps nutrient solution was sterilized at 115 °C for 30 min, and the glycerin was sterilized at 121 °C for 20 min. Glycerin was prepared with Cordyceps nutrient solution under aseptic conditions before use, and the mass concentration of glycerin was 40%.
[0033] 3. Preparation of strain mycelium and spore suspension
[0034] Gently scrape the mycelia of the culture...
example 3
[0038] 1. Cultivation of Cordyceps gunis
[0039]Cordyceps guni strains were inoculated on PDA plates with a diameter of 6 cm, and cultured in the dark at 16 °C. When the diameter of the colony grew to 3 cm, the strain was cultured under light to induce the mycelia to form spores.
[0040] 2. Preparation of protective agent
[0041] The protective agent is composed of two parts, that is, Cordyceps liquid medium, which is composed of 18 g of glucose, 5 g of peptone, 1 g of yeast extract, water to 1000 mL, and natural pH. The other part is glycerin. The two parts were sterilized separately, the Cordyceps nutrient solution was sterilized at 115 °C for 30 min, and the glycerin was sterilized at 121 °C for 20 min. Glycerin was prepared with Cordyceps nutrient solution under aseptic conditions before use, and the mass concentration of glycerin was 35%.
[0042] 3. Preparation of strain mycelium and spore suspension
[0043] Gently scrape the mycelia of the cultured plate strain...
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