Method for preparing active anticancer fractions through conversion of total ginsenosides in panax plants by strain of fusarium sacchari
A technology of effective parts and total saponins, applied in the field of microorganisms, can solve the problems of occupying land and polluting the environment, and achieve the effects of reducing emissions, high tumor inhibition rate, and high product recovery rate.
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Embodiment 1
[0057] Transformation of Panax notoginseng Stem and Leaf Saponins by Fusarium sugarcane
[0058] Inoculate Fusarium sugarcane cultured under optimal culture conditions into an aqueous solution containing 2g of Panax notoginseng saponins (content > 80%). -1 , Conversion (hydrolysis) under natural pH conditions. Sampling starts after 3d. The results of TLC showed that the polyglycoside Rb in Panax notoginseng stem and leaf saponins 1 , Rb 3 After 13 days, almost all the polyglycosides in the product were converted. After the bacteria were filtered, they were injected into a D101 macroporous adsorption resin column, washed with water until colorless, and then washed with ethanol gradient. The 80-90% ethanol eluate was concentrated and evaporated to dryness to obtain 1.18 g of the converted product.
Embodiment 2
[0060] Transformation of Ginseng Fruits by Fusarium sugarcane
[0061] Inoculate Fusarium sugarcane cultured under optimal culture conditions into an aqueous solution containing 2 g of ginseng fruit (content > 70%). -1 , Conversion (hydrolysis) under natural pH conditions. After 13 days of transformation, filter out the bacteria, inject it into a D101 macroporous adsorption resin column, wash it with water until it is colorless, and then wash the resin column with an ethanol gradient. The 80-90% ethanol eluate was concentrated and evaporated to dryness to obtain 1.04 g of the converted product.
Embodiment 3
[0063] Transformation of American Ginsenosides by Fusarium sugarcane
[0064]Inoculate Fusarium sugarcane cultured under optimal culture conditions into an aqueous solution containing 2g American ginseng saponin (content > 90%), transform at a temperature of 30°C, a shaker rotation speed of 160r min-1, and a natural pH value (hydrolysis). After 13 days of transformation, filter out the bacteria, inject it into a D101 macroporous adsorption resin column, wash it with water until it is colorless, and then wash the resin column with an ethanol gradient. The 80-90% ethanol eluate was concentrated and evaporated to dryness to obtain 1.14 g of the converted product.
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