High-quality preservation method for cordyceps militaris strain
A technology for Cordyceps militaris mycelium and Cordyceps militaris, which is applied in the field of high-quality preservation of Cordyceps militaris strains, can solve the problems that fruit bodies are prone to bending, the ability to form fruit bodies is reduced, and strains are easily contaminated, and the quality of strains can be improved. and stability, shortening the quality evaluation time, and the effect of plump and rich ascus shells
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Embodiment 1
[0040] Example 1 Cordyceps militaris strain preservation method optimization—mycelium block method
[0041] 1. Materials and methods
[0042] 1.1 Mycelium block preparation
[0043] The Cordyceps militaris mycelium was inoculated onto the modified potato dextrose agar medium, cultured in the dark for 3 days at 23° C., and then cultured in light for 20 days (light intensity 100 lx). Cut into 3mm×3mm hyphae pieces with a sterile scalpel and place them in a sterile 1.5mL centrifuge tube for later use.
[0044] 1.2 Types of protective agents
[0045] Peptone solution: prepared with water, concentration 0.06g / mL, sterilized by high-pressure steam at 121°C for 20 minutes;
[0046] Pasteurized skimmed milk: imported milk from Germany (purchased from Aishi Chenxi brand);
[0047] Autoclaved skimmed milk: the above-mentioned skimmed milk was sterilized by high-pressure steam at 121° C. for 5 minutes.
[0048] 1.3 Preservation conditions
Embodiment 2
[0056] Example 2 Cordyceps militaris preservation method optimization—bacterial suspension method
[0057] 1. Materials and methods
[0058] 1.1 Bacterial suspension preparation
[0059] The Cordyceps militaris mycelium was inoculated onto the modified potato dextrose agar medium, cultured in the dark for 3 days at 23° C., and then cultured in light for 20 days (light intensity 100 lx). Use a sterile inoculation needle to inoculate the mycelium and spores of Cordyceps militaris into the improved potato glucose liquid medium, place at 23°C, and shake the bacteria at 150rpm for 3 days, until the content of mycelium balls in the bacterial suspension reaches more than 2000 / 100mL. After shaking the bacteria, divide the bacterial suspension into sterile 1.5mL centrifuge tubes for later use.
[0060] 1.2 Types of protective agents
[0061] Peptone solution: prepared with water, concentration 0.06g / mL, sterilized by high-pressure steam at 121°C for 20 minutes;
[0062] Pasteuriz...
Embodiment 3
[0070] Example 3 Cordyceps militaris preservation method optimization—optimization of preservation period
[0071] According to the optimized preservation scheme screened in Examples 1 and 2, the preferred strain preservation method and preservation period are further studied. Cordyceps militaris preservation method optimization - preservation period is as follows:
[0072] 1. Materials and methods
[0073] 1.1 Mycelium block preparation
[0074] The Cordyceps militaris mycelium was inoculated onto the improved PDA medium, cultured in the dark for 3 days at 23° C., and then cultured in light for 20 days (light intensity 100 lx). Cut into 3mm×3mm hyphae pieces with a sterile scalpel and place them in a sterile 1.5mL centrifuge tube for later use.
[0075] 1.2 Preparation of protection solution
[0076] Peptone solution: prepared with water, concentration 0.06%, sterilized by high-pressure steam at 121°C for 20 minutes;
[0077] 1.3 Optimization method of storage period
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