A coronoid cystic strain
A technology of coronoid loose capsule strains and seeds, applied in the direction of fungi, microorganisms, biochemical equipment and methods, etc., can solve the problems of weak adaptability, slow fermentation start, unstable aroma, etc., and achieve the effect of strong adaptability
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Embodiment 1
[0021] The culture method of coronoid loose capsule bacterial strain CGMCC10610 comprises the following steps:
[0022] Preparation of medium: Weigh 200g of peeled potatoes, cut into pieces, add water to boil, filter with gauze, then add 20% agar powder under heating conditions, continue heating and stirring, after the agar powder is dissolved, add glucose, stir Evenly, after cooling, add water to 1000mL, bandage, sterilize at 121°C for 20 minutes, and pour it into a plate after cooling; culture steps: under sterile conditions, streak the coronoid cystic strain CGMCC10610 on the plate, and the streaking is over Afterwards, the plates were inverted and placed in a constant temperature incubator at 28°C for 5 days.
Embodiment 2
[0024] The culture method of coronoid loose capsule bacterial strain CGMCC10610 comprises the following steps:
[0025] Preparation of medium: Weigh 200g of peeled potatoes, cut into pieces, add water to boil, filter with gauze, then add 15g of agar powder under heating conditions, continue heating and stirring, after the agar powder is dissolved, add glucose, and stir Evenly, after cooling, add water to 1000mL, bandage, sterilize at 121°C for 20 minutes, and pour it into a plate after cooling; culture steps: under sterile conditions, streak the coronoid cystic strain CGMCC10610 on the plate, and the streaking is over Afterwards, the plates were inverted and placed in a constant temperature incubator at 28°C for 7 days.
Embodiment 3
[0027] The preparation method for preparing the seed liquid of Saccharomyces coronoidis for dark tea comprises the following steps:
[0028] (1) Inoculate the coronoid cystic strain CGMCC10610 on a PDA plate, and culture it in a constant temperature incubator at 28°C until the plate is covered with colonies. Under aseptic conditions, add 10 mL of sterile distilled water to the plate covered with colonies, Scrape the yellow hyphae on the plate into sterile distilled water, use a syringe to absorb the turbid liquid in the plate, put it into a 50mL centrifuge tube, add sterile small glass beads, and centrifuge in a centrifuge for 5min (rotation: 3000r / min). After filtering through absorbent cotton, the spore suspension was obtained, and finally the concentration of the spore suspension was adjusted to 5.0×10 6 a / mL;
[0029] (2) get the tea raw material extract that concentration is 4%, as liquid culture medium after sterilization treatment, under aseptic condition, inoculate sp...
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