Method for rapid propagation of pinellia ternate by tissue culture
A technology of tissue culture and Pinellia species, applied in the field of rapid propagation of Pinellia japonicus, can solve the problems of non-value-added coefficient, value-added effect data description, and the reproduction coefficient needs to be improved. The effect of increasing and multiplying quickly
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Embodiment 1
[0041] (1) Seed pretreatment: From June to July or October to November every year, collect mature Vitex pinellia seeds, remove the exocarp, and bathe in 35-degree water for 3-4 days.
[0042](2) Germination: On the ultra-clean workbench, take a sterile petri dish with two layers of sterile filter paper, moisten it with sterile water, put the sterilized seeds on the petri dish, and the seed disinfection method is 0.1 Sterilize with % potassium permanganate for 25 minutes, then 75% ethanol for 5 minutes, and finally 0.1% mercury liter for 10 minutes, rinse with sterile water for 4-5 times, each time for about 3 minutes, avoid light, accelerate germination at 25°C, and wait for the hypocotyl length to be 2- At 3 cm, stem segments were taken for callus induction.
[0043] (3) Callus induction: when the length of the hypocotyl is about 1.5cm, the hypocotyl is cut into small sections of about 0.6cm, and transferred to a solid medium.
[0044] Medium formula: MS+2,4-D0.5mg / L+6-BA0.5...
Embodiment 2
[0051] This embodiment is different in that: callus differentiation medium: MS+TDZ 0.5mg / L+agar 0.7mg / L+sucrose 30g / L, pH5.8; other operating steps are the same as in Example 1 .
Embodiment 3
[0053] the embodiment
[0054] Induction medium: MS+2,4-D 0.4mg / L+6-BA 0.4mg / L+NAA 0.1mg / L+agar 0.7mg / L+sucrose 30g / L, pH5.8;
[0055] Callus proliferation medium: MS+2,4-D 0.4mg / L+6-BA 0.8mg / L+NAA 0.1mg / L+glucose 30g / L, pH5.8;
[0056] Callus differentiation medium: MS+2,4-D 0.4mg / L+6-BA 0.8mg / L+NAA 0.1mg / L+agar 0.7mg / L+sucrose 30g / L, pH5.8;
[0057] Liquid accelerated medium: MS+2,4-D 0.4mg / L+6-BA 0.8mg / L+NAA 0.1mg / L+glucose 30g / L, pH5.8;
[0058] Solid strong seedling medium: MS+2,4-D 0.4mg / L+6-BA 0.8mg / L+NAA 0.1mg / L+glucose 30g / L, pH5.8;
[0059] Other operation steps are all identical with described embodiment 1.
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