Method for preparing rare ginsenoside by using schizophyllum commune for biotransformation of ginsenoside
A technology of rare ginseng saponins and ginsenosides, applied in biochemical equipment and methods, microorganism-based methods, microorganisms, etc., can solve problems such as insecurity, and achieve the effect of improving health care and medicinal efficacy
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Embodiment 1
[0046] Schizophyllum was inoculated into the liquid fermentation medium at an inoculum of 5%, the pH of the medium was 8, and ginsenoside Rb 1 The feeding amount was 5g / L, the rotation speed of the shaker was 120 r / min, and the fermentation was carried out at 20°C for 4 days. After the fermentation, the bacterial liquid was filtered, and the mycelium was ultrasonically extracted 3 times with 80% ethanol, 30 min each time. Extract the solvent under reduced pressure at 40°C, concentrate it into an aqueous solution, and then combine the concentrated extract with the bacterial solution; separate with macroporous resin D101, elute with a gradient of 20%-90% ethanol, and detect by thin-layer chromatography , collect and merge the fraction solutions with the same Rf value as the positive reference substance of ginseng rare saponins, recover the solvent under reduced pressure, separate and prepare by preparative liquid chromatography, and obtain ginsenoside F 2 and compound K. The c...
Embodiment 2
[0048] Schizophyllum was inoculated into the liquid fermentation medium at an inoculation amount of 10%, the pH of the medium was 7, and ginsenoside Rb 2 The feeding amount was 10g / L, the rotation speed of the shaker was 140 r / min, and the fermentation was carried out at 22°C for 5 days. After the fermentation, the bacterial liquid was filtered, and the mycelium was ultrasonically extracted 4 times with 80% ethanol, 30 min each time. The solvent was recovered from the extract under reduced pressure at 50°C, and concentrated into an aqueous solution. Then the concentrated extract was combined with the bacterial solution, separated with macroporous resin D101, 20%-90% ethanol gradient elution, detected by thin layer chromatography, collected and combined with the same Rf value of the positive reference substance of ginseng rare saponins The fraction solution was recovered under reduced pressure, and separated and prepared by preparative liquid chromatography to obtain compound ...
Embodiment 3
[0050] Schizophyllum was inoculated into the liquid fermentation medium with a 15% inoculation amount, the pH of the medium was 6, the feeding amount of ginsenoside Rc was 20g / L, the rotation speed of the shaker was 160 r / min, and the fermentation was carried out at 25°C. Cultured for 6 days. After the fermentation, the bacterial liquid was filtered, and the mycelium was ultrasonically extracted 5 times with 80% ethanol, 30 min each time. The solvent was recovered from the extract under reduced pressure at 60°C, and concentrated into an aqueous solution. Then the concentrated extract was combined with the bacterial solution, separated with macroporous resin D101, 20%-90% ethanol gradient elution, detected by thin layer chromatography, collected and combined with the same Rf value of the positive reference substance of ginseng rare saponins The fraction solution was recovered under reduced pressure and the solvent was separated and prepared by preparative liquid chromatography...
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