Agaricus blazei bacterium exopolysaccharide preparing process
A production method and the technology of velvet fungus cells, which are applied in the field of edible fungal polysaccharide production, can solve problems such as falsely high output of exopolysaccharides, quality and purity problems, and easy agglomeration, so as to be beneficial to industrial applications, ensure purity, and increase production Effect
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Embodiment 1
[0022] Agaricus brasiliensis strain: Agaricus brasiliensis 03, which was isolated from Agaricus brasiliensis fruiting bodies grown by mushroom farmers in Curitiba, Paraná, Brazil. Inoculate it on PDA (Potato Dextrose Agar) slant medium, culture it at a constant temperature of 25-28°C for 7-10 days, and store it in a refrigerator at about 4°C for later use. The strain is inoculated on PDA slant medium before use Upper activation, that is, after 7-10 days of constant temperature cultivation at 25-30°C, the mycelium (without medium) was inoculated in a sterilized Erlenmeyer flask containing liquid seed medium and cultured statically for 5 days. The liquid seed medium The formula is (weight %): glucose 2%, yeast extract 0.2%, K 2 HPO 4 0.2%; MgSO 4 0.05%, the balance is water, pH6, and the culture temperature is 28-30°C. At this time, the mycelium grows white and vigorous. Use a sieve to filter and collect the mycelium in the liquid. Wash the bacteria 3 times with water, put th...
Embodiment 2
[0025] The formulation of the production medium in this example is: 50 grams of sucrose, 8 grams of yeast extract and ammonium sulfate 1:1 mixture, K 2 HPO 4 5 g, MgSO 4 2.5 grams, with the balance being water, was prepared into 1000 milliliters of culture solution, and the pH was adjusted to 6. All the other steps from strain preparation to extraction and purification were the same as in Example 1. The exopolysaccharide extraction yield of this example was 789.5mg / L.
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