Cephalotaxus hainanensis embryo culturing and seedling breeding method
An embryo culture and torreya technology, applied in the field of rapid plant propagation, can solve problems such as inability to apply and popularize, low seedling emergence rate, inability to emerge seedlings, etc.
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Embodiment 1
[0014] (1) Collection and selection of explants: collection and selection of mature seeds;
[0015] (2) Seed cleaning, sterilization and seed embryo acquisition: flush the mature seeds with water for 1h, and clean them with distilled water, dry them with filter paper, put them into 0.5% sodium hypochlorite solution for vacuum filtration sterilization for 8min, and then sterilize them with sterile water Rinse 3 times repeatedly;
[0016] (3) Seed embryo inoculation and cultivation: On a sterile operating table, use a sterilized dissecting microscope to peel off the seed shell with scissors and tweezers, pick the seed embryo with the tip of the knife and inoculate it on the following medium for culture: 0.5MS (Murashige and Skoog Stock medium)+0.01mg·L -1 6-BA (6-benzylpurine) + 0.2% agar + 1% sucrose + 1% coconut milk, pH 5.0; culture in dark for 2 days and then place in light for 16 h·d -1 1. Continue to cultivate for 15 days under a cold light lamp with an illumination inte...
Embodiment 2
[0020] (1) Collection and selection of explants: collection and selection of mature seeds;
[0021] (2) Seed cleaning, sterilization and seed embryo acquisition: flush the mature seeds with water for 3h, and clean them with distilled water, dry them with filter paper, put them into 2.0% sodium hypochlorite solution for vacuum filtration sterilization for 3min, and then sterilize them with sterile water Repeated washing 6 times;
[0022] (3) Seed embryo inoculation and cultivation: On the aseptic operating table, use a sterilized dissecting microscope to peel off the seed shell with scissors and tweezers, pick the seed embryo with the tip of the knife and inoculate it on the following medium for culture: 1MS (Murashige and Skoog Stock medium)+0.1mg L -1 6-BA(6-Benzylpurine)+100mg·L -1 Inositol + 0.6% agar + 5% sucrose + 5% coconut milk, pH 6.0; cultured in dark for 2 days and then placed in light cycle 16h·d -1 1. Continue to cultivate for 25 days under a cold light lamp wit...
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