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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Embodiment 1
[0018] Example 1: Isolation and identification of Ophiocordyceps sinensis KD11-2 in China
[0019] 1. Acquisition of KD11-2 strain: Fresh Cordyceps sinensis was collected from Yala Township, Lucheng Town, Kangding City, Ganzi Prefecture, Sichuan Province, and transported to our laboratory through cryogenic preservation. In the aseptic operating room or ultra-clean workbench, peel off the soil and bacterial film around Cordyceps sinensis, disinfect the body surface with 75% alcohol; Part of it was cut into small pieces (pay attention to avoid the intestinal tract of the worm), planted on PPDA solid plate medium, and cultured at 9-16°C; the isolated typical colony of Cordyceps sinensis without pollution was confirmed as Cordyceps sinensis after molecular identification , to obtain the strain, and its number as KD11-2.
[0020] 2. Characteristics of KD11-2 strain:
[0021] Morphological characteristics: On the PPDA solid medium, the colony is earthy yellow, the surface of the c...
Embodiment 2
[0028] Experimental location: Guangdong Institute of Applied Bioresources located in Guangzhou City, the following cultivations are all under normal oxygen concentration.
[0029] Put the Mortierella chinensis KD11-2 strain and other Mortierella chinensis strains (KD1223) into the sterile solid PPDA medium respectively, and after culturing in the dark at 9°C for 60 days, pick the colonies and put them into the sterile liquid PPDA medium , at 9°C, 100rpm shaking culture (dark culture) for 65 days, select the fermentation culture with uniform mycelial ball size, 2-3 mm in diameter, and light brown bacterial liquid as a liquid strain, which is used for the production of fruiting bodies of Cordyceps sinensis Cultivated production.
[0030] In a sterile room or an ultra-clean workbench, use sterile water to dilute 5-fold liquid strains (inject 30 mL of diluted liquid strains per 100 g of cultivation medium) into sterile cultivation medium. Place the inoculated culture bottle at 9°C ...
Embodiment 3
[0033] Experimental location: Guangdong Institute of Applied Bioresources located in Guangzhou City, the following cultivations are all under normal oxygen concentration.
[0034] The Mortierella sinensis KD11-2 strain and other Mortierella sinensis strains (KD1223) were respectively inserted into sterile solid PPDA medium, and after dark culture at 16°C for 45 days, the colonies were selected and inoculated into sterile liquid PPDA medium. At 16°C, shake culture at 100 rpm (dark culture) for 40 days, and select the fermentation culture with uniform mycelial ball size and a diameter of 2-3 mm as a liquid strain for the cultivation and production of fruiting bodies of Cordyceps sinensis.
[0035] In a sterile room or ultra-clean workbench, inject 10-fold liquid strains diluted with sterile water (according to every 100 g of cultivation medium, insert 30 mL of diluted liquid strains) into the sterile cultivation medium. Place the inoculated culture bottle at 13°C for dark cultur...
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