Ophiocordyceps sinensis and its application
A Chinese technology of hairy spores and spores, applied in the field of artificial cultivation of fruiting bodies of Cordyceps sinensis, can solve the problems not mentioned, and achieve the effect of promoting artificial cultivation
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[0018] Example 1: Isolation and identification of Ophiocordyceps sinensis KD11-2
[0019] 1. Obtainment of KD11-2 strain: Fresh Cordyceps was collected from Yala Township, Lucheng Town, Kangding City, Ganzi Prefecture, Sichuan Province, and transported to our laboratory through cryopreservation. In a sterile operating room or ultra-clean workbench, remove the soil and plaque around the cordyceps, and disinfect the surface with 75% alcohol; use a sterile scalpel to remove the skin of the sclerotium and sub-seats, and remove the sclerotia and sub-seats. Partially cut into small pieces (be careful to avoid the intestines of the worms), and planted on PPDA solid plate medium, cultured at 9-16℃; the isolated and non-polluting typical colony of Cordyceps sinensis was confirmed to be Cordyceps sinensis after molecular identification , Get this strain, and number it as KD11-2.
[0020] 2. Features of KD11-2 strain:
[0021] Morphological characteristics: On the PPDA solid medium, the colon...
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[0027] Example 2:
[0028] Experimental location: Guangdong Provincial Institute of Biological Resources Application in Guangzhou, the following cultures were all under normal oxygen concentration.
[0029] The KD11-2 strains of Trichosporum chinensis and other strains of Trichosporum chinensis (KD1223) were respectively connected to sterile solid PPDA medium. After 60 days of dark culture at 9°C, the colonies were picked and transferred to sterile liquid PPDA medium , At 9 ℃, 100rpm shaking culture (dark culture) for 65 days, select the same size of mycelial ball, diameter of 2-3 mm, and the light brown fermentation culture of the bacterial liquid as the liquid strain for the fruiting body of Cordyceps Cultivation and production.
[0030] In a sterile room or ultra-clean workbench, the liquid strains diluted 5 times with sterile water (30mL diluted liquid strains per 100g cultivation medium) are inserted into the sterile cultivation medium. Place the inoculated culture flask in th...
Example Embodiment
[0032] Example 3:
[0033] Experimental location: Guangdong Provincial Institute of Biological Resources Application in Guangzhou, the following cultures were all under normal oxygen concentration.
[0034] The T. chinensis KD11-2 strain and other T. chinensis strains (KD1223) were respectively connected to a sterile solid PPDA medium. After 45 days of dark culture at 16°C, the colonies were selected to be inoculated into the sterile liquid PPDA medium. At 16°C, 100 rpm shaking culture (dark culture) for 40 days, and the fermentation culture of the mycelial ball with uniform size and 2-3 mm in diameter was selected as the liquid strain for the cultivation and production of Cordyceps sinensis fruiting bodies.
[0035] In a sterile room or ultra-clean workbench, insert liquid strains diluted 10-fold with sterile water (30mL diluted liquid strains per 100g of cultivation medium) into the sterile cultivation medium. Place the inoculated culture flask in the dark at 13°C for 40 days. Aft...
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