Trichoderma pseudokoningii exocellular polysaccharide, preparation method and application thereof
A technology of Trichoderma cells and polysaccharides, applied in the field of microorganisms, can solve problems such as increasing the spleen index, and achieve the effect of enhancing the phagocytic activity of macrophages
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Embodiment 1
[0037] The preparation of embodiment 1 Trichoderma pseudoconii exopolysaccharide
[0038](1) Preparation of crude polysaccharide: Trichoderma pseudoconii CGMCC No.1443 was inoculated on PDA medium, activated at 28°C for 2 days, inserted into liquid medium from the plate, and cultured with shaking at 28°C and 130rpm for 6 days. Filter with four layers of gauze to remove hyphae and spores, centrifuge at 4000rpm for 15min, decolorize the supernatant through a 3520 resin column, collect the eluate, and concentrate under reduced pressure at 48°C to 1 / 4 of the original volume. The concentrate was deproteinized by the Sevag method (chloroform:n-butanol=4:1, V / V). Add 3 times the volume of 95% ethanol and let it stand overnight at 4°C, centrifuge at 5000rpm for 15 minutes, collect the precipitate, wash with ether, acetone, and 95% ethanol in sequence, dissolve the precipitate in distilled water, dialyze for 48 hours, concentrate to 1 / 4 of the original volume, and freeze Dried to obta...
Embodiment 2
[0041] Example 2 Purification of Trichoderma pseudoconii exopolysaccharide
[0042] Sephadex G-75 Sephadex column chromatography was used. Weigh 20g of Sephadex G-75 and suspend it in a large volume of water, let it settle naturally for 4 hours, remove suspended fine particles by pouring method, after repeated several times, add enough water to gradually raise the temperature to boiling, and keep it warm for 3 hours. Cool, vacuumize, and continuously load into a chromatographic column (2.5×80 cm) under gentle stirring, and pass 2-3 times of column bed volume of water to stabilize the column head. Accurately weigh 1.0 g of Trichoderma extracellular crude polysaccharide, dissolve it in 5 ml of water, put it on the column, and carry out elution with distilled water at room temperature at a flow rate of 0.4 ml / min, 15 min / tube. Use the phenol-sulfuric acid chromogenic method to track and detect tube by tube, and measure the light absorption value at 490nm. The elution volume was...
Embodiment 3
[0043] Example 3 Purity identification of Trichoderma pseudoconii exopolysaccharide
[0044] The purity and molecular weight of the polysaccharide samples were measured by high-performance gel filtration (HPGPC). According to the relationship between the molecular weight of polysaccharides on the gel column and the elution volume, a standard curve was first prepared with a series of standard dextran (Dextran) with different molecular weights. , and then compare it with the standard curve according to the elution volume of the sample (because the flow rate is constant, so the retention time is actually used). The purity of the sample was judged according to its peak shape, and the molecular weight of the sample was obtained from the standard curve.
[0045] The HPLC chromatograph used is composed of Waters 515 HPLC pump and Waters 2410 differential detector; the chromatographic column is two columns of Waters Ultrahydrogel 2000 and Ultrahydrogel 500 connected in series. The mo...
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