Application of n-acetylglucosamine in promoting the development of blastospores of Cordyceps sinensis and the formation of mycelium
A technology of acetylglucosamine and Cordyceps sinensis, which is applied to microorganism-based methods, fungi, microorganisms and other directions, can solve the problems of long time for developing and forming mycelium, low efficiency of artificial cultivation of Cordyceps sinensis, etc., and achieves shortened time, mycelium The effect of increasing the formation rate
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Embodiment 1
[0021] Prepare Cordyceps sinensis liquid culture medium, with 30g boiled potato filtrate (30g potato is boiled with water, then filter, take filtrate, be 30g boiled potato filtrate, the same below), 1.5g peptone, 3g maltose, 0.08 g magnesium sulfate, 0.25 g potassium dihydrogen phosphate, 3 mg vitamin B 1 Put it into a conical flask, and dilute to 150ml with water. After autoclaving, place in a culture room at 12±2°C to pre-cool, insert blastospores into every 150mL liquid medium ( figure 1 ) to make the final concentration 10 5 each / mL, and add N-acetylglucosamine (without adding N-acetylglucosamine as a control) to make the final concentration 5mg / l, place it on a shaker with a rotation speed of 100 rpm, and store it at 12±2°C , cultivate under dark conditions, cultivate the 2nd day, take out 1mL culture bacterium liquid, microscopic examination finds that blastospore begins to germinate, cultivate the 8th day, take out 1mL culture bacterium liquid, the mycelia of blastosp...
Embodiment 2
[0023] Prepare Cordyceps sinensis liquid culture medium, 30g boiled potato filtrate, 1.5g peptone, 3g maltose, 0.08g magnesium sulfate, 0.25g potassium dihydrogen phosphate, 3mg vitamin B 1 Put it into a conical flask, and dilute to 150ml with water. After autoclaving, place in a culture room at 12±2°C for pre-cooling, insert blastospores into every 150mL of liquid medium to make the final concentration of 10 7 each / mL, and add N-acetylglucosamine (without adding N-acetylglucosamine as a control) to make the final concentration 5mg / l, place it on a shaker with a rotation speed of 100 rpm, at 12°C, in the dark On the second day of cultivation, take out 1mL culture liquid, and microscopic examination reveals that blastospores begin to germinate. On the eighth day of cultivation, take out 1mL culture liquid, and the mycelia formation rate of blastospores reaches 54% under a microscope. The mycelium formation rate increased by 127.94% compared with the control without adding the ...
Embodiment 3
[0025] Prepare Cordyceps sinensis liquid culture medium, 30g boiled potato filtrate, 1.5g peptone, 3g maltose, 0.08g magnesium sulfate, 0.25g potassium dihydrogen phosphate, 3mg vitamin B 1 Put it into a conical flask, and dilute to 150ml with water. After autoclaving, place in a culture room at 12±2°C for pre-cooling, insert blastospores into every 150mL of liquid medium to make the final concentration of 10 5 each / mL, and add N-acetylglucosamine (without adding N-acetylglucosamine as a control) to make the final concentration 50mg / l, place it on a shaker with a rotation speed of 100 rpm, and store it at 12±2°C , cultivated under dark conditions, cultured on the second day, took out 1mL of the culture liquid, microscopic examination found that blastospores began to germinate, cultured on the eighth day, took out 1mL of culture liquid, and examined under a microscope that the hyphae formation rate of blastospores reached 51.11 %, the rate of mycelium formation was 107.17% hig...
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