Tissue culture propagation method of alum root kimono
A technology of kimono and alum root, which is applied in the field of tissue culture and propagation of the important ornamental plant alum root "kimono", which can solve the problems of limited and large difference in variety characteristics, and achieve the effect of improving the reproduction coefficient
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Embodiment 1
[0024] The tissue culture of alum root "kimono" is carried out according to the following steps:
[0025] 1. Preparation of culture medium: configure induction medium MS medium MS+1mg / L KT+0.2mg / L TDZ+1mg / LIBA, sucrose 28g / L, agar 7g / L, pH6.0; configure differentiation culture: MS +1mg / L6-BA+0.5mg / LKT+0.1mg / L IBA, sucrose 28g / L, agar 7g / L, pH6.0; prepare strong seedling and rooting medium: MS+0.3mg / L IBA+0.5mg / LNAA, sucrose 30g / L, agar 7g / L, adjust pH 6.0;
[0026] 2. Specific operation steps:
[0027] (1) Collection of explants: alum root "kimono" is one of the more popular alum root varieties on the market, and the alum root "kimono" used in the present invention is purchased from the Yunnan Provincial Academy of Agricultural Sciences. The disease-free leaves were picked from the mother plant of Kimono;
[0028] (2) Callus induction: the leaves obtained after the sterilization process were blotted dry on the surface with sterile filter paper on the ultra-clean table, cut...
Embodiment 2
[0032] Put the alum root seedlings that need to be cultured in the greenhouse for 1 month, water them with water every day, take the disease-free leaves of the alum root "kimono", wash them under running water for 12 hours, and then set aside;
[0033] 1) Sterilization of explants: take the prepared leaves on a sterile ultra-clean table, disinfect with 75% alcohol for 20 seconds, rinse with sterile water for 3-5 times, disinfect with 0.1% mercuric chloride for 9 minutes, use Rinse with sterile water 3-5 times for later use;
[0034] 2) Callus induction: the induction medium is MS+1mg / L KT+0.2mg / L TDZ+1mg / L IBA, sucrose 28g / L, agar 7g / L, pH6.0, dark culture for 5 days and light culture 30-40 days, the light and dark time is 12h / 12h. The terminal buds obtained after the sterilization process were blotted dry on the surface with sterile filter paper on the ultra-clean table, cut into small pieces of 1cm*1cm with sterile curved scissors, inoculated into the induction medium, and ...
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