Pleurotus eryngii polysaccharide capable of reducing accumulation of foam cell lipid and preparation method thereof
A technology for the accumulation of polysaccharides and lipids in Pleurotus eryngii, applied in food preparation, anti-toxic agents, food science, etc., can solve problems such as difficult to make innovative breakthroughs, separation and purification of active polysaccharides, and difficult structure identification, so as to reduce lipids quality accumulation, simple preparation and high yield
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Embodiment 1
[0020] Embodiment one, the preparation of polysaccharide
[0021] (1) Separation and purification of the active polysaccharides of Pleurotus eryngii was first carried out, and the dried Pleurotus eryngii fruiting mushroom powder was leached with hot water at 90°C for 3 hours, and the crude polysaccharide PE was obtained by four-fold volume ethanol precipitation;
[0022] (2) Crude polysaccharide PE passes through a dialysis membrane with a molecular cut-off of 3.5 kDa, dialyzes overnight with deionized water to remove small molecular weight impurities, redissolves in deionized water after drying the precipitate, adds trypsin to remove protein, and adds hydrogen peroxide to remove pigment , and finally add four times the volume of absolute ethanol to precipitate the polysaccharide, and obtain water-soluble Pleurotus eryngii polysaccharide (PEPE) after centrifugal drying;
[0023] (3) Separate and purify PEPE with DEAE-52 anion exchange column, use 0.05 M phosphate buffer (PBS) ...
Embodiment 2
[0025] Example 2: After derivatization of PEPE-1 and PEPE-2, two single polysaccharide components were detected by gas chromatography, and the monosaccharide composition analysis of PEPE-1 and PEPE-2 was carried out by complete acid hydrolysis (TFA hydrolysis) Post-gas chromatographic analysis method. The sample was hydrolyzed with 2 mol / L TFA 4 mL at 110°C for 4 h, the hydrolyzed sample solution was evaporated to dryness under reduced pressure, and then about 0.5 mL of methanol was added to the sample to dissolve the sample completely. ) were evaporated to dryness three times to obtain fully hydrolyzed monosaccharide components. The obtained sample acid hydrolyzate and standard monosaccharides were acetylated and then detected by gas phase. Finally, the composition and ratio of monosaccharides in the sample were estimated according to the retention time and peak area of the standard monosaccharides. The results are shown in Table 1.
[0026] Table 1 Gas phase analysis res...
Embodiment 3
[0031] Example three: Fourier transform infrared spectrum detection of PEPE-1 and PEPE-2 two single polysaccharide components, the results are shown as image 3As shown, the infrared spectra of the two single polysaccharide components of PEPE-1 and PEPE-2 show that this group of high polymers has no derivatization groups, which are polyhydroxy compounds, and the polysaccharides are in the pyranose configuration. Periodic acid can selectively oxidize and break down the dihydroxyl or trihydroxyl groups in sugar molecules to generate corresponding polysaccharide aldehydes, formaldehyde or formic acid. The reaction proceeds quantitatively, and one molecule of periodic acid is consumed for every C-C bond split. The sugar group bonded at the 1→2 position is oxidized by periodic acid, and each sugar group consumes only one molecule of periodic acid on average, and no formic acid is released; the sugar group bonded at the 1→4 position is oxidized by periodic acid, On average, each s...
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