Method for preparing high-yield tremella polysaccharide by fementing tremella spores
A technology of tremella polysaccharides and tremella spores, which is applied in the field of preparation of high-yield tremella polysaccharides by fermentation of tremella spores, can solve the problems of low yield, high cost, and complicated production methods of tremella polysaccharides, and achieve high-yield extracellular polysaccharides, convenient operation, and easy realization The effect of industrialization
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specific Embodiment approach 1
[0019] Specific embodiment one: what this embodiment records is a kind of preparation method of tremella spore fermentation high-yield tremella polysaccharide, described method step is as follows:
[0020] Step 1: Purchasing Tremella fungus strain Tr21 from Xinghua Fungi Research Institute, Gutian County, Fujian Province;
[0021] Step 2: Prepare slant preservation medium: take 200 g of peeled potatoes and cut them into small pieces, add 800 mL of distilled water, boil for 20-30 min, filter with gauze to obtain the filtrate, add 20 g of glucose, 1 g of peptone, and 1 g of KH to the filtrate 2 PO 4 , 0.5 g MgSO 4 ·7H 2 0. 20 g of agar, after heating and dissolving, add water to a total volume of 1 L, and the pH is natural, and sterilize at 115° C. for 20 to 30 min; the effect of the slant preservation medium is to increase the angular area;
[0022] Step 3: Activating Tremella fungus strains: inoculate the strain of Step 1 on the slant preservation medium of Step 2, and cult...
specific Embodiment approach 2
[0028] Embodiment 2: In Embodiment 1, a method for preparing Tremella spores fermented with high-yield Tremella polysaccharides, in step 5, the plant used in the plant extract is a plant of the genus Rhizoma Lauraceae.
Embodiment 1
[0030] (1) Activation of Tremella fungus strains: inoculate Tremella fungus mother species on the slant preservation medium composed of the following composition. Cut 200g of peeled potatoes into small pieces, add 800mL of distilled water, boil for 30min, filter with gauze to get the filtrate, add 20g of glucose, 1g of peptone, KH 2 PO 4 1g, MgSO 4 ·7H 2 O 0.5g, agar 2g, add water to 1L after heating to dissolve, pH is natural, sterilize at 115°C for 25min. After inoculation, culture at 24°C for 5 days.
[0031] (2) Cultivation of liquid seeds: add 20g glucose, 2g peptone, 1g yeast extract, 3 g K 2 HPO 4 , 1.5 g MgSO 4 ·7H 2 O, adjust the pH value to 5.8 with 1mol / L HCl or NaOH, and sterilize at 115°C for 30min. Under aseptic operation conditions, rinse with 10mL sterile normal saline to activate the growth of bacteria on the slant preservation medium to make a bacterial suspension, and add the bacterial suspension according to the inoculation amount of 6% of the volum...
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