Method for simultaneously extracting polysaccharide and flavone from phellinus igniarius sporophore cultivation waste
A technology of cultivation waste and Phellinus japonica, applied in the direction of medical formula, plant raw materials, medical raw materials derived from fungi, etc., can solve problems such as polluting the environment and endangering Phellinus chinensis production, achieve great economic value, high yield, and increase additional value effect
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Embodiment 1
[0030] A method for simultaneously extracting polysaccharides and flavonoids from Phellinus Phellinus cultivation waste, specifically comprising the following steps:
[0031] Step (1): drying and pulverizing the Phellinus Phellinus cultivation waste;
[0032] Step (2): Mix Phellinus japonica cultivation waste dry powder with alkaline ethanol solution (ethanol with a volume fraction of 80%, adjust pH=10 with sodium hydroxide) at a mass ratio of 1:10;
[0033] Step (3): ultrasonically treat the mixture in step (2) for 20 minutes (100 Hz, 1000W), and filter to obtain filtrate I and residue;
[0034] Step (4): Add deionized water 8 times the weight of the residue to the residue in step (3), mix well, adjust the pH value to 4, add a compound enzyme accounting for 0.2% of the weight of the mixture (the compound enzyme is cellulase : Glucose oxidase = 2:1 mixture, the same below), enzymatic hydrolysis at 45°C for 40 minutes, centrifugation of the enzymatic solution (6000 rpm, 10 min...
Embodiment 2
[0038] A method for simultaneously extracting polysaccharides and flavonoids from Phellinus Phellinus cultivation waste, specifically comprising the following steps:
[0039] Step (1): drying and pulverizing the Phellinus Phellinus cultivation waste;
[0040] Step (2): Mix Phellinus Phellinus cultivation waste dry powder with alkaline ethanol solution (volume fraction 85% ethanol, pH=11) at a mass ratio of 1:20;
[0041] Step (3): ultrasonically treat the mixture in step (2) for 30 minutes (200 Hz, 800 W), and filter to obtain filtrate I and residue;
[0042] Step (4): Add deionized water 10 times the weight of the residue to the residue in step (3), mix well, adjust the pH value to 4.5, add a compound enzyme accounting for 0.3% of the weight of the mixture, and enzymatically hydrolyze at 45°C for 50 minutes , the enzymatic hydrolyzate was centrifuged (6000 rpm, 10 minutes), and supernatant II and precipitate were separated;
[0043] Step (5): Filtrate I in step (3), remove ...
Embodiment 3
[0046]A method for simultaneously extracting polysaccharides and flavonoids from Phellinus Phellinus cultivation waste, specifically comprising the following steps:
[0047] Step (1): drying and pulverizing the Phellinus Phellinus cultivation waste;
[0048] Step (2): Mix Phellinus Phellinus cultivation waste dry powder with alkaline ethanol solution (90% ethanol by volume, pH=12) at a mass ratio of 1:30;
[0049] Step (3): ultrasonically treat the mixture in step (2) for 30 minutes (400 Hz, 200 W), and filter to obtain filtrate I and residue;
[0050] Step (4): Add deionized water 12 times the weight of the residue to the residue in step (3), mix well, adjust the pH value to 5.0, and add a compound enzyme accounting for 0.4% of the weight of the mixture (the compound enzyme is cellulase: Glucose oxidase = 2.5:1 mixture), enzymolysis at 50°C for 60 minutes, centrifugation of the enzymolysis solution (6000 rpm, 10 minutes), and separation of supernatant II and precipitate;
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