Method for improving biological activity of sargassum fusiforme polysaccharide
A hijiki polysaccharide and biologically active technology, applied in the field of chemical engineering, to achieve the effect of lowering cholesterol content, less impact, and mild action conditions
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Embodiment 1-1
[0043]Weigh 1g of Sargassum polysaccharide (SFP) and dissolve it in 100mL citric acid-sodium citrate buffer (pH 6.0), add pectinase (30,000 U / g, 437.4 mg) and glucoamylase (100,000 U / g mL, 39.8μL) (activity ratio is 3.3:1), and then diluted to 250mL with the same acetic acid-sodium acetate buffer solution, so that the final concentration of polysaccharide in the resulting system is 4mg / ml, and the final concentration of enzyme is 68.4U / mL. The system was placed in a water bath at 54.2° C., oscillating (frequency 220 r / min) for 3 hours. Then heat in a water bath above 90°C for 15 minutes to inactivate the enzyme, filter, and concentrate the clear liquid (filtrate) by rotary steaming (60-70°C) to 1 / 4 of the original volume, dialyze for 48 hours with a dialysis bag with a molecular weight cut-off of 3500Da, and dialyze the The solution (the solution left in the dialysis bag) was concentrated by rotary evaporation (concentrated at 60-70°C to 25% of the volume of the dialysate) and...
Embodiment 1-2
[0050] The shaking reaction time was changed to 4 hours, and the rest was the same as that in Example 1-1 to obtain 882 mg of hijiki enzymatic polysaccharide (ESFP1-2), and the degradation rate of the polysaccharide obtained under this condition was 18.7%.
Embodiment 1-3
[0052] The shaking reaction time was changed to 1h, the activity ratio of pectinase and glucoamylase was 3:1, and the rest was the same as in Example 1-1 to obtain 913 mg of hijiki enzymatic polysaccharide (ESFP1-3). The polysaccharide obtained under this condition The degradation rate is 13.8%.
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