Method for preparing coriolan
A technology of Yunzhi polysaccharide and crude polysaccharide is applied in the field of preparation of Yunzhi polysaccharide, which can solve the problems of large energy consumption, large consumption, environmental pollution and the like, and achieve the effects of reducing energy consumption, reducing production cost and improving yield.
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Embodiment 1
[0020] Weigh the net weight of Versicolor versicolor mycelium 122.13g (dried weight 16.22g), add 125mL of pure water and crush it, add water to 350mL, then add 7gNa 2 CO 3 , after 2 hours of water bath at 90°C, repeated leaching and filtration twice, and then the extract was concentrated to 1 / 5 of the original volume. 200 mL of the obtained concentrated solution was added with 3 times the volume of 95% ethanol for precipitation, left to stand for 24 hours, filtered, and the precipitated part was dried to obtain crude polysaccharide. Add 200mL of 70℃ hot water to dissolve the crude polysaccharide, add 40mL of chloroform and 8mL of n-butanol, shake vigorously for 20min to form a gel, and filter at 4000r / min in a centrifuge for 15min, collect the supernatant, remove the denatured protein in the lower layer and the chloroform in the upper layer , to obtain a solution of 130 mL. Adjust the pH to 9.0 with NaOH, add 15% H 2 o 2 20mL, and then in a water bath at 50°C for 4h, and s...
Embodiment 2
[0021] Embodiment 2: the ultraviolet absorption spectrometry of the product that embodiment 1 obtains
[0022] The ultraviolet scanner HITACHI (Japan) carried out ultraviolet scanning of 190-360nm on the sample aqueous solution to determine whether it is a protein-bound polysaccharide. The measurement results are shown in Figure 1. Yunzhi polysaccharide is a protein-containing glycopeptide complex. It can be seen from the figure above that there is no absorption at 260nm, and there is a shoulder-shaped peak at around 270-280nm, which is the characteristic absorption of protein-bound polysaccharides.
Embodiment 3
[0023] Embodiment 3: the Yunzhi polysaccharide content determination of the product that embodiment 1 obtains
[0024] Accurately weigh 20mg of standard glucose in a 500mL volumetric flask, add water to the mark, absorb 0.2, 0.4, 0.6, 0.8, 1.0, 1.2, 1.4, 1.6, 1.8mL respectively, make up to 2.0mL with water, and then add 5% Phenol 1.0mL and concentrated sulfuric acid 5.0mL, let stand for 10min, shake well, 30℃ water bath for 20min. After that, the optical density (OD) was measured at 490nm, and 2.0mL of water was used as a blank. Abscissa is glucose concentration, and ordinate is OD value, draws standard curve figure (seeing accompanying drawing 2), carries out linear regression, obtains regression equation: y=0.0146x+0.0103, R 2 = 0.9984. Draw 1.0ml of the sample solution, the operation steps are the same as above, repeat three times, the measured OD values are 0.2983, 0.2901, 0.2956, take the average value, and check the standard curve. The correction coefficient of Yunz...
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