Tissue-culturing quick propagation method of wild rhizoma panacis japonici
A technology of tissue culture and bamboo ginseng, which is applied in the field of plant tissue culture, can solve the problems of slow propagation speed of bamboo ginseng seeds, achieve the effects of saving rare and endangered plants, short production cycle, and overcoming generational variation
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Embodiment 1
[0030] Embodiment 1: the tissue culture rapid propagation method of this wild bamboo ginseng, concrete steps are as follows:
[0031] 1) Selection and sterilization of explants: take the stems of wild bamboo ginseng, and use them as explants for tissue culture after surface sterilization;
[0032] 2) Callus induction culture: under sterile conditions, inoculate the cut stems (1cm long) on the induced callus medium of MS+2,4-D 1.0mg / L+sucrose 30g / L, and form by induction embryogenic callus;
[0033] 3) Callus proliferation culture: embryogenic callus is cultured on the proliferation medium of 1 / 2MS+2,4-D 1.0mg / L+KT 0.2mg / L+sucrose 20g / L to form embryogenic callus ;
[0034] 4) Embryoid body differentiation culture: embryogenic callus was cultured on the differentiation medium of 1 / 2MS+2,4-D 1.0mg / L+KT 1.0mg / L+sucrose 20g / L, and the embryogenic callus Surface differentiation of embryoid bodies;
[0035] 5) Embryoid body proliferation culture: the embryoid body with embryog...
Embodiment 2
[0040] Embodiment 2: the tissue culture rapid propagation method of this wild bamboo ginseng, concrete steps are as follows:
[0041] 1) Selection and sterilization of explants: take the leaves of wild bamboo ginseng, and use them as explants for tissue culture after surface sterilization;
[0042] 2) Callus induction and proliferation culture: under sterile conditions, inoculate leaf slices (1cm×1cm) in MS+2,4-D 1.0mg / L+KT 0.1mg / L+sucrose 30g / L to induce callus On tissue culture medium, embryogenic callus is formed by induction;
[0043] 3) Callus proliferation culture: embryogenic callus is cultured on the proliferation medium of 1 / 2MS+2,4-D 1.0mg / L+KT 1.0mg / L+sucrose 20g / L to form embryogenic callus ;
[0044] 4) Embryoid body differentiation culture: embryogenic callus was cultured on the differentiation medium of 1 / 2MS+2,4-D 0.2mg / L+KT 0.2mg / L+sucrose 20g / L, and the embryogenic callus Surface differentiation of embryoid bodies;
[0045] 5) Embryoid body proliferation ...
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