Preparation method of pholiota nameko polysaccharide extract
A technology for polysaccharides and extracts from the mushroom, which is applied in the field of preparation of polysaccharides from mushrooms, can solve the problems of low extraction rate, high cost, unsuitability for large-scale production, etc., and achieves simple operation, low cost, and improved protein removal ratio. Effect
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Embodiment 1
[0036] (1) Weigh 100g of dried slippery mushroom, add 20 times (2000ml) hot water at 80°C to soak, and let it stand for 12 hours to fully swell. The beater beats three times at a high speed with an interval of 30 seconds, each time for 2 minutes, to obtain a slippery mushroom slurry.
[0037] (2) Add 0.252 g of trypsin with an activity of 2500 U / mg to the above-mentioned slippery mushroom slurry and incubate at 37° C. for 1 hour. Then add 0.168 g of cellulase with an activity of 1000 U / mg and incubate at 55° C. for 2 hours. Then the temperature was raised to 80° C. for 3 hours, and the first extract and precipitate were collected by filtration. Extract the first precipitation with an equal amount of water under ultrasonic wave at 400W for 30 minutes (every ultrasonic work is 5 seconds, with 1 second interval), and filter to get the second extract and residue. Wash the residue of the second filtration twice, each time with 10 times the amount of water added to the residue. F...
Embodiment 2
[0047] (1) Weigh 100g of dried slippery mushroom, add 20 times (2000ml) hot water at 80°C to soak, and let it sit for 12 hours to fully swell. The beater beats three times at a high speed with an interval of 30 seconds, each time for 2 minutes, to obtain a slippery mushroom slurry.
[0048] (2) Add 0.252 g of trypsin with an activity of 2500 U / mg to the above-mentioned slippery mushroom slurry and incubate at 37° C. for 1 hour. Then add 0.168 g of cellulase with an activity of 1000 U / mg and incubate at 55° C. for 2 hours. Then the temperature was raised to 80° C. for 3 hours, and the first extract and precipitate were collected by filtration. Add an equal amount of water to the first precipitation and extract under ultrasonic wave at 400W for 30 minutes (every ultrasonic work is 5 seconds, with an interval of 1 second), and then filter to get the second extraction solution and residue. Clean the residue filtered for the second time twice, each time with 10 times the amount o...
Embodiment 3
[0055] 1. Pretreatment of macroporous resin
[0056] The new resin must be treated before use to remove a small amount of oligomers, organic matter and harmful ions contained in the resin. During the test, the MG-2 macroporous adsorption resin was eluted with absolute ethanol under reflux until the eluent was evaporated to dryness and there was no residue. The resin washed with absolute ethanol was stored for future use after evaporating the solvent.
[0057] Soak the resin with ethanol-water solution to remove air bubbles and fully swell the resin. MG-2 macroporous adsorption resin is packed in ethanol wet column, continue to flow and wash with absolute ethanol on the column, check the outflowing ethanol from time to time, until it is mixed with water and does not become white turbid. Then wash away ethanol with a large amount of distilled water; then use 0.5% hydrochloric acid solution to flow wash on the column, and then use a large amount of distilled water to flow wash ...
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