Method for producing polysaccharides by fermenting yellow serofluid with edible and medicinal fungi
A technology of medicinal fungus and yellow pulp water, which is applied in the direction of microorganism-based methods, biochemical equipment and methods, fermentation, etc., can solve the problems of being unable to recycle, can only be discharged at will, and the unit content is low, so as to achieve high promotion and utilization Value, production cost reduction, high yield effect
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Embodiment 1
[0024] Embodiment 1: (the method utilizing mushroom (135) bacterial classification to produce fungal polysaccharide)
[0025] Follow these steps:
[0026] (1) Pretreatment of the yellow pulp water: the yellow pulp water produced during the processing of soybean products is concentrated with a Sehan brand 0.2MPa reverse osmosis membrane until the solid content reaches 30%, and then set aside;
[0027] (2) Preparation of culture medium: including,
[0028] 1) Seed medium: glucose 1.5%, K 2 HPO 4 0.5%, MgSO 4 0.2%, make up to 100% with pretreated yellow pulp water, pH 6, sterilized, and set aside;
[0029] 2) Production medium: glucose 1.5%, K 2 HPO 4 0.5%, MgSO 4 0.2%, make up to 100% with pretreated yellow pulp water, pH 6, sterilized, and set aside;
[0030] (3) Strain activation: Inoculate the cultivated strains of shiitake mushrooms on the PDA slant medium, cultivate them at 25-28°C for 10 days, store them in a refrigerator at 4°C, and store them for later use; ...
Embodiment 2
[0036] Embodiment 2: (the method that utilizes oyster mushroom (No. brown level 1) bacterial classification to produce fungal polysaccharide)
[0037] In this example, step (2) 2) production medium formula is: sucrose 0.5%, K 2 HPO 4 0.4%, MgSO 40.05%; Step (3) bacterial classification activation: Pleurotus ostreatus cultivated bacterial classification is inoculated on the PDA slant medium, cultivates 9 days in 25-28 ℃; The inoculation cultivation of step (4) seed liquid: the activated bacterial classification inoculation amount is 2%; step (5) inoculation culture of production medium: shake culture at 25-28°C for 7 days; step (6) extract fungal polysaccharides from mycelium: ultrasonic extraction time is 60 minutes, and the temperature is raised to 95 After leaching for 60 minutes at ℃; step (7) extracting fungal polysaccharides from the fermentation filtrate: the ultrasonic extraction time of the fermentation filtrate is 20 minutes; the remaining process steps are the sam...
Embodiment 3
[0039] Embodiment 3: (the method utilizing Hericium erinaceus (Su monkey 19) bacterial classification to produce fungal polysaccharide)
[0040] In this example, step (2) 2) production medium formula is: brown sugar 0.8%, K 2 HPO 4 0.3%, MgSO 4 0.08%; step (3) bacterial classification activation: Hericium erinaceus cultivation bacterial classification is inoculated on the PDA slant medium, cultivates 8 days in 25-28 ℃; The inoculation cultivation of step (4) seed liquid: activation bacterial classification inoculum 3%; step (5) inoculation culture of production medium: shake culture at 25-28°C for 7 days; step (6) extract fungal polysaccharides from mycelium: ultrasonic extraction time is 40 minutes, and the temperature is raised to Extract at 100°C for 60 minutes; step (7) extract fungal polysaccharides from the fermentation filtrate: the ultrasonic extraction time of the fermentation filtrate is 25 minutes; the remaining process steps are the same as in Example 1;
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