Biological transformation method for preparing high-activity theasaponin
A technology of biotransformation and tea saponin, applied in biochemical equipment and methods, methods based on microorganisms, microorganisms, etc., can solve the problems of low economic benefits, achieve the effects of reducing pollution emissions, mild experimental conditions, and easy-to-control products
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Embodiment 1
[0034] (1) Purification of crude tea saponin using AB-8 macroporous resin:
[0035] Soak the crude tea saponin extracted from camellia oleifera cake with ethanol solution with a mass concentration of 70%, filter the clear liquid, steam the ethanol under reduced pressure at 50°C to obtain the clear liquid of camellia oleifera saponin, and put AB-8 macroporous resin on the clear liquid The column was allowed to stand still for full adsorption, washed with deionized water and 0.1% NaOH aqueous solution at a rate of 1.5BV / h in sequence, then washed with deionized water until the pH of the washing solution was 7, eluted with ethanol solution, and the ethanol eluate was collected. Concentrate under reduced pressure at 50°C to dryness to obtain purified tea saponin;
[0036] (2) Preparation of tea saponin enzymatic hydrolysis substrate:
[0037] Put 0.3g of purified tea saponin into a porcelain bowl, add 100mL of methanol to dissolve it, add 3g of 100-200 mesh silica gel to the solu...
Embodiment 2
[0047] The experimental method is the same as in Example 1, except that the bacterial classification used when extracting the enzyme liquid is replaced by Aspergillus niger sp.848 bacteria to obtain 3-oxo-[β-D-galactopyranosyl-(1-2)-β- D-Glucopyranosyl]-21-oxo-angelyl-28-oxo-acetyl-teasapogenin A.
Embodiment 3
[0049] The experimental method is the same as in Example 1, except that the bacterial classification used when extracting the enzyme liquid is replaced by Aspergillus oryzae sp.39 bacteria to obtain 3-oxo-[β-D-galactopyranosyl-(1-2)-β- D-Glucopyranosyl]-21-oxo-angelyl-28-oxo-acetyl-teasapogenin A.
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