Method for extracting purified active lentinan from leftover materials of edible fungi
A technology for mushroom polysaccharide and leftover material is applied in the field of extracting and purifying active mushroom polysaccharide, which can solve the problems of affecting the quality and quality of purified active mushroom polysaccharide, loss of purified active mushroom polysaccharide, lack of a better extraction method, etc., and achieves prevention of loss and simple equipment. , to ensure the effect of purity
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Embodiment 1
[0027] Step 1. Material preparation: select the leftovers of edible fungi, and remove the leftovers of edible fungi with damage, corrosion, etc.;
[0028] Step 2, material preparation: weigh 2g of the prepared edible fungus leftovers, cut the 2g edible fungi leftovers into small pieces, add a certain weight of water, and then homogenize with a tissue masher;
[0029] Step 3. Heating the homogeneous solution: take 18mL of the homogeneous solution and put it into a 0.9L beaker, then add 27mL of distilled water, heat to boil, then boil on low heat for 0.9 hours;
[0030] Step 4. Filtration: After heating, filter the liquid in the cup with 8 layers of gauze to remove the residue, and transfer the supernatant to another beaker;
[0031] Step 5. Concentrate the supernatant: pour the supernatant into a round-bottomed flask, concentrate on a rotary concentrator, and stop when the volume of the concentrate reaches 95mL;
[0032] Step 6, concentrate centrifugation: centrifuge the conce...
Embodiment 2
[0038] Step 1. Material preparation: select the leftovers of edible fungi, and remove the leftovers of edible fungi with damage, corrosion, etc.;
[0039] Step 2, material preparation: weigh 2g of the prepared edible fungus leftovers, cut the 2g edible fungi leftovers into small pieces, add a certain weight of water, and then homogenize with a tissue masher;
[0040] Step 3. Heating the homogeneous solution: Take 20mL of the homogeneous solution and put it into a 1L beaker, then add 30mL of distilled water, heat to boil, then boil on low heat for 1 hour;
[0041] Step 4. Filtration: After heating, filter the liquid in the cup with 8 layers of gauze to remove the residue, and transfer the supernatant to another beaker;
[0042] Step 5. Concentrate the supernatant: pour the supernatant into a round-bottomed flask, concentrate on a rotary concentrator, and stop when the volume of the concentrate reaches 100mL;
[0043] Step 6, concentrate centrifugation: centrifuge the concentra...
Embodiment 3
[0049] Step 1. Material preparation: select the leftovers of edible fungi, and remove the leftovers of edible fungi with damage, corrosion, etc.;
[0050] Step 2, material preparation: weigh 2g of the prepared edible fungus leftovers, cut the 2g edible fungi leftovers into small pieces, add a certain weight of water, and then homogenize with a tissue masher;
[0051]Step 3. Heating the homogeneous solution: Take 22mL of the homogeneous solution and put it into a 1.1L beaker, then add 33mL of distilled water, heat to boil, then boil on low heat for 1.1 hours;
[0052] Step 4. Filtration: After heating, filter the liquid in the cup with 8 layers of gauze to remove the residue, and transfer the supernatant to another beaker;
[0053] Step 5. Concentrate the supernatant: pour the supernatant into a round-bottomed flask, concentrate on a rotary concentrator, and stop when the volume of the concentrate reaches 105 mL;
[0054] Step 6, concentrate centrifugation: centrifuge the conc...
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