Method for cultivating adventitious root tissue of wild panax ginseng C.A.Mey.
A wild ginseng and root tissue technology, applied in the field of plant tissue culture, can solve the problems of exogenous gene safety, low ginsenoside content, shorten breeding time, etc., and achieve the effects of fast adventitious root proliferation, high induction rate, and low cost
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[0028] 2) Preparation of standard solution
[0029] Accurately weigh 1 mg each of the standard ginsenosides Rg1, Re, Ro, Rf, Rb1, Rg2, Rh1, Rc, Rb2, Rb3, Rd, Rg3, and Rh2 that have been dried under reduced pressure for more than 24 hours, and place them in a 5mL volumetric flask. Ultrasonic dissolve methanol, then dilute to volume with methanol to make 0.2mg·mL -1 The ginsenoside mixed standard stock solution was sealed and stored in a refrigerator at 4°C.
[0030] 3) Preparation of sample solution
[0031] Accurately weigh 0.2g of dried adventitious root sample and place it in a 100mL Erlenmeyer flask with a stopper, add 20mL of methanol, bathe in 60°C water for 1h, suction filter while hot, repeat the extraction once, and combine the filtrates. The filtrate was evaporated to dryness, then dissolved in 10 mL of distilled water, extracted twice with 20 mL of n-butanol, and the n-butanol layer was collected, treated by rotary evaporation, and then dilute to 1 mL with methanol...
Embodiment 1
[0033] The first solid medium is MS basic medium with 2.0mg / L 2,4-dichlorophenoxyacetic acid, 0.5mg / L 6-furfurylaminopurine, 3% sucrose, pH 5.8, at 121 ℃, 0.1MPa pressure sterilization for 25 minutes.
Embodiment 2
[0035] The second solid medium was MS basal medium with 5.0 mg / L indolebutyric acid, 3% sucrose, pH 5.8, sterilized at 121° C. and 0.1 MPa pressure for 25 minutes for use.
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