Agaricus blazei bacterium exopolysaccharide preparing process
A production method and a fungus cell technology are applied in the production field of edible fungal polysaccharides, can solve the problems of falsely high output of extracellular polysaccharides, problems of quality and purity, easy agglomeration, etc., so as to be beneficial to industrial application, ensure purity, and improve yield Effect
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Embodiment 1
[0022] Agaricus brasiliensis strain: Agaricus brasiliensis 03, the strain was tissue isolated from Agaricus blazei fruiting bodies grown by mushroom farmers in Curitiba, Paraná, Brazil. Inoculate it on PDA (potato dextrose agar) slant medium. After incubating at 25~28℃ for 7-10 days, store it in a refrigerator at about 4℃ for later use. Inoculate the strain on PDA slant medium before use. Upper activation, that is, after 7-10 days of constant temperature culture at 25~30℃, the mycelium (without culture medium) is inoculated in a sterilized Erlenmeyer flask containing liquid seed culture medium and cultured statically for 5 days. 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℃. At this time, the mycelium grows white and prosperous. Use a sieve to collect the mycelium in the liquid, and remove the mycelium under aseptic conditions. Wash the bacteria three times with water, put th...
Embodiment 2
[0025] The formula of the production medium in this example is: 50 grams of sucrose, 8 grams of a 1:1 mixture of yeast extract and ammonium sulfate, K 2 HPO 4 5 grams, MgSO 4 2.5 g, the balance is water, prepared into 1000 ml of culture solution, adjusted to pH 6, and the rest of the steps from the preparation of the strain to the extraction and purification are the same as in Example 1. The extraction rate of extracellular polysaccharide in this case was 789.5 mg / L.
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