Twig cuttage breeding method for ginseng fruit
A technology of young branch cutting and ginseng fruit, applied in the field of young branch cutting propagation of ginseng fruit, can solve the problems of low reproduction coefficient, difficulty in seed reproduction and the like, and achieve the effect of being beneficial to healing
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Embodiment 1
[0022] 1. Selection and sterilization of explants: cut terminal buds or stems with axillary buds from potted plants or field plants as explants, and use them as explants for detoxification tissue culture after sterilization;
[0023] 2. Stem tip culture: Under aseptic conditions, the sterilized terminal buds or stem segments with axillary buds are extracted under a 40-fold binocular dissecting microscope, and a 0.2mm-sized shoot tip with 1 leaf primordium is extracted and inoculated in On the induction medium (MS+BA 1mg / L+IAA 0.1mg / L+sucrose 30g / L), after 20 days of culture under the culture condition, the shoots were induced to form from the shoot tip, and after another 20 days of culture, the stem continued to elongate. Seedlings with about 3 nodes and a height of 5 cm;
[0024] 3. Micro-cutting culture: cut the induced seedlings into 3 sections and transfer them to the micro-cutting medium (MS+BA 0.5mg / L+NAA 0.1mg / L+sugar 30g / L), and cultivate them under the culture conditi...
Embodiment 2
[0031] 1. Selection and sterilization of explants: cut terminal buds or stems with axillary buds from potted plants or field plants as explants, and use them as explants for detoxification tissue culture after sterilization;
[0032] 2. Stem tip culture: Under aseptic conditions, the sterilized terminal buds or stem segments with axillary buds are extracted under a 40-fold binocular dissecting microscope to extract 0.3mm-sized shoot tips with 2 leaf primordia, and inoculate them in On the induction medium, after culturing under culture conditions for 30 days, shoots were induced from the shoot tip to form shoots, and after culturing for another 30 days, the stems continued to grow, and were cultivated into seedlings with about 5 nodes and a height of 7 cm;
[0033] 3. Micro-cuttage culture: cut the induced seedlings into 5 sections and transfer them to the micro-cuttage medium, and cultivate them for 45 days under culture conditions, and then cultivate them into 5-section, 7cm-...
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