Composite accelerator for Cordyceps cultivation and preparation method thereof
A compound accelerator, Cordyceps technology, applied in the directions of botanical equipment and methods, biocides, animal repellants, etc., can solve the problems of Cordyceps yield limitation, long cultivation period, low cordycepin content, etc., to promote the growth of Cordyceps, Low cost and the effect of increasing economic benefits
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Embodiment 1
[0021] (1) Inoculate the spore suspension of mucormyces CICC 3115 in YPG liquid medium sterilized at 115°C for 15 minutes. The culture temperature is 30°C, the initial pH is 6.0, the rotation speed is 150r / min, and the time is 60h.
[0022] (2) After the mucor culture is completed, the mycelium is filtered out and cleaned, and then the filtered mycelium is frozen and ultrasonically crushed. The ratio of mycelium weight to water volume (m / v) is 1:5, and the ultrasonic crushing condition is 30s each time, 60s interval, 30 cycles, after the hyphae are broken, let stand at 35°C for 6h to obtain the broken self-solution.
[0023] (3) Add octacosanol, inositol, and fructooligosaccharides (1 to 3 fructosyl groups through β(2—1) glycosidic bonds and kestose) and copper gluconate were mixed uniformly to obtain a embryo material composite accelerator; among them, octacosanol was added according to the mass volume ratio of the mucor mycelia broken self-solution at 1%, and inositol Add a...
Embodiment 2
[0026] (1) Inoculate the spore suspension of mucormyces CICC 3115 in YPG liquid medium sterilized at 115°C for 15 minutes. The culture temperature is 30°C, the initial pH is 6.0, the rotation speed is 150r / min, and the time is 60h.
[0027] (2) After the mucormycetes culture is over, filter out the mycelium and wash it. Then freeze and sonicate the filtered mycelia. The ratio of mycelium weight to water volume (m / v) is 1:4. , Standing for 6h, obtained broken self-solution.
[0028] (3) Add octacosanol, inositol, fructooligosaccharides (kestose), and copper gluconate to the mucor broken self-solution obtained in step (2) and mix evenly to obtain a composite accelerator for blank material; Wherein octacosanol is added according to the mass volume ratio 1.5% of the self-solution broken with Mucor mycelium, inositol is added according to the mass volume ratio of 3.0% of the self-solution broken with Mucor mycelia, and fructooligosaccharide is added according to the mass volume ra...
Embodiment 3
[0031](1) Inoculate the spore suspension of mucormyces CICC 3115 in YPG liquid medium sterilized at 115°C for 15 minutes. The culture temperature is 30°C, the initial pH is 6.0, the rotation speed is 150r / min, and the time is 60h.
[0032] (2) After the mucormycetes culture is over, filter out the mycelium and wash it. Then freeze and sonicate the filtered mycelia. The ratio of mycelium weight to water volume (m / v) is 1:3. , Standing for 6h, obtained broken self-solution.
[0033] (3) Add octacosanol, inositol, fructooligosaccharides (kestose), and copper gluconate to the mucor broken self-solution obtained in step (2) and mix evenly to obtain a composite accelerator for blank material; Wherein octacosanol is added according to the mass volume ratio 2.0% of the self-solution broken with Mucor mycelium, inositol is added according to the mass volume ratio of 4.5% of the self-solution broken with Mucor mycelium, and fructooligosaccharide is added according to the mass volume ra...
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