Method of obtaining saline cistanche phenylethanol glycoside kind compound using bio-conversion technique
A technology of biotransformation and cistanche, applied in chemical instruments and methods, sugar derivatives, sugar derivatives, etc., to achieve the effect of short cultivation period and low production cost
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Embodiment 1
[0015] Example 1: Addition of two amino acid precursors for biotransformation
[0016] (1) In the improved MS medium, add 20-50 g of sucrose or glucose, 0.1-4 mg of indole acetic acid (IAA) and 0.1-4 mg of 6-benzylaminopurine (BA) per liter of culture medium to make a basic medium .
[0017] (2) Add 50-500 mg of phenylalanine and 50-400 mg of tyrosine per liter of culture medium to the basic medium, then adjust the pH value to 5.5-7.0 with acid or alkali to make a synthetic medium, Sterilized at 125°C under 0.1Mpa pressure and cooled before use.
[0018] (3) Inoculate the Cistanche deserticola callus cells on the synthetic medium described in step (2), and the inoculation amount is about 20%. After culturing at 25° C. for one week in the dark, the cells are harvested, freeze-dried, extracted with a solvent to obtain a crude extract, and purified to obtain phenylethanol glycosides.
Embodiment 2
[0019] Example 2: Addition of Cucumber Juice Precursors for Bioconversion
[0020] The cucumber juice in this example can be obtained by the following method: select fresh cucumber, stir and pulverize it, centrifuge at 4000r.p.m, 20°C for 30min, take the supernatant and filter it, and store it at 4°C for later use.
[0021] (1) In the improved MS medium, 20-50 g of sucrose or glucose, 0.1-4 mg of indole acetic acid (IAA) and 0.1-4 mg of kinetin were added per liter of culture medium to make a basic medium.
[0022] (2) Add 40 to 200 ml of cucumber juice per liter of culture medium to the basic medium, then adjust the pH value to 5.5 to 7.0 with acid or alkali to make a synthetic medium, and sterilize at 125°C under a pressure of 0.1Mpa After cooling, it is ready to use.
[0023] (3) Inoculate the Cistanche deserticola callus cells on the synthetic medium described in step (2), and the inoculation amount is about 30%. After culturing at 25° C. for one week in the dark, the ce...
Embodiment 3
[0024] Example 3: Addition of caffeic acid precursor for biotransformation
[0025] (1) In the improved MS medium, add 20-50 g of sucrose or glucose, 0.1-4 mg of indole acetic acid (IAA) and 0.1-4 mg of 6-benzylaminopurine (BA) per liter of culture medium to make a basic medium .
[0026] (2) Add 5 to 100 ml of caffeic acid per liter of culture medium to the basic medium, then adjust the pH value to 5.5 to 7.0 with acid or alkali to make a synthetic medium, and sterilize at 125°C under a pressure of 0.1Mpa After cooling, it is ready to use.
[0027] (3) Inoculate the Cistanche deserticola callus cells on the synthetic medium described in step (2), and the inoculation amount is about 50%. After culturing at 25° C. for one week in the dark, the cells are harvested, freeze-dried, extracted with a solvent to obtain a crude extract, and purified to obtain phenylethanol glycosides.
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