Method for extracting triple helix Dictyophora phalloidea polysaccharide
A technology of bamboo fungus polysaccharide and an extraction method, which is applied in the fields of biopolymers and medicinal chemistry, can solve problems such as fuzzy understanding of molecular internal structure, and achieve the effects of easy implementation, wide application prospect and clear structure.
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Embodiment 1
[0021] Pulverize the Dictyophora in a tissue grinder, degrease in a Soxhlet extractor with ethanol, ethyl acetate and acetone in sequence, and then extract with water at 20°C, 40°C, 60°C, and 80°C for three hours to obtain four kinds of The polysaccharide solution was processed as follows, and centrifuged to obtain the extract. After deproteinization by Sevage method, H 2 o 2 Oxidation decolorization, dialyzed with water and twice distilled water respectively, concentrated, graded precipitation with ethanol, freeze-dried to obtain triple helix Dictyophora polysaccharides ZS-1, ZS-2, ZS-3 and ZS-4. Freeze-dried to obtain pure polysaccharide.
Embodiment 2
[0023] Pulverize the Dictyophora in a tissue grinder, degrease in a Soxhlet extractor with ethanol, ethyl acetate and acetone in sequence, and then extract with water at 20°C, 40°C, 60°C, and 80°C for three hours to obtain four kinds of The polysaccharide solution was processed as follows, and centrifuged to obtain the extract. After deproteinization by Sevage method, H 2 o 2 Oxidative decolorization, dialyzed with clean water and twice distilled water respectively, concentrated, ultrafiltered, and freeze-dried to obtain triple helix Dictyophora polysaccharides ZS-1, ZS-2, ZS-3 and ZS-4. Freeze-dried to obtain pure polysaccharide.
[0024] The yields of the four polysaccharides ZS-1, ZS-2, ZS-3 and ZS-4 obtained in the above two examples are 0.444%, 0.364%, 0.243% and 0.388%, respectively.
[0025] The present invention uses GC to measure the monosaccharide composition of the four obtained products respectively, and finds that ZS-1 and ZS-2 are heteropolysaccharides, while ...
Embodiment 3
[0027] Embodiment 3: Measure the monosaccharide composition of each sugar
[0028] Use 2M sulfuric acid to hydrolyze and seal the polysaccharide, seal the tube and react at 100°C for six hours, use barium carbonate to neutralize the excess acid in the hydrolyzate, centrifuge to obtain the supernatant, freeze-dry, and use the method of sugar nitrile acetate derivatives to process the sample After the treatment, the monosaccharide composition was determined by gas phase.
[0029] Derivatization method: take 10 mg of solid sugar sample, 10 mg of hydroxylamine hydrochloride and 7 mg of internal standard, add 0.5 ml of pyridine, put it in a water bath at 90 ° C, heat and react for 30 minutes, take it out and cool it to room temperature, add 0.5 ml of acetic anhydride, and continue at 90 ° C The reaction was carried out for acetylation for 30 minutes, and the reaction product was directly analyzed by gas chromatography. The model of the gas chromatograph is Agilent GC6890N (Agilent...
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