Cyrtopterin tissue culturing method and fast reproduction thereof
A technique of tissue culture and rhododendron orchid, applied in horticultural methods, botany equipment and methods, plant cells, etc., can solve the problems of rhododendron orchid reproduction difficulties, lack of seedlings, etc., to solve the shortage of seedlings, short production cycle, simplify The effect of the training program
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Embodiment 1
[0016] Embodiment 1 adopts Rhododendron orchid capsule seeds as explants. On the ultra-clean workbench, first wipe the capsule surface with 70% alcohol cotton balls for disinfection, then dip the capsules in alcohol and burn them for sterilization; Cut open the capsule with a scalpel, spread the tiny seeds evenly on the surface of 1 / 2MS solid medium supplemented with 0.5mg / L NAA, the pH of the medium is 5.5-5.8, and place it at a temperature of 25±2°C in complete darkness After half a year of cultivation, the seeds germinate and form small white protocorms. Transfer this small protocorm to B with 3.0~6.0mg / L 6-BA+0.2mg / L NAA+0.1% activated carbon+2% sugar 5 Solid proliferation medium, pH 5.5-5.8, placed at a temperature of 25±2°C, light time 12h / d, and light intensity 1500-2000lx, the small white protocorms will gradually turn green and form clustered protocorms with a long surface. It is covered with white hairs, and some stem nodes are elongated to form rhizomes. After 40-...
Embodiment 2
[0017] Embodiment 2 adopts the bud eye on the rhododendron orchid pseudobulb as the explant, rinses the soil on it with clear water first, dries, then packs into a triangular flask, and pours it into a triangular flask with 70% alcohol under aseptic conditions. Sterilize the pseudobulbs in a bottle for 20 seconds, then sterilize them by immersing them in 0.1% mercuric acid solution for 8 minutes, and then wash them with sterile water for 5 times, each time for 3 minutes; finally dry the water with sterile filter paper, cut out the bud eyes on the pseudocorms, and inoculate them. In the pre-prepared MS medium, the pH value of the medium is 5.5-5.8, placed at a temperature of 25±2°C, a light time of 12h / d, and a light intensity of 1500-2000lx, about 10d will start to germinate and form white small protocorms. After 30 days, the protocorm was transferred to the proliferation medium for culture, and a protocorm in cluster shape was obtained. The surface of the corm was covered with...
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