Building method of rhododendron aureum leaf regeneration system
A method for establishing a method and a leaf technology, applied in the field of plant tissue culture, can solve the problems of low reproduction coefficient and long growth cycle, and achieve the effect of high reproduction coefficient and high domestication difficulty.
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Embodiment 1
[0018] (1) Disinfection of explants: Collect the delicate leaves of healthy Rhododendron spp., scrub gently with a soft brush dipped in washing powder water, rinse with tap water for 2 hours, and then place them in an ultra-clean workbench. Disinfect them with 75% ethanol for 8 seconds and then use sterile Wash 3 times with water, then sterilize with 0.1% mercury liter solution for 5 minutes, rinse 5 times with sterile water, and then dry the water drops on the surface with sterile filter paper before use.
[0019] (2) Differentiation culture: Excise the petiole of the leaf treated in step (1), lightly scratch a few times on the leaf with a sterile scalpel, and inoculate the differentiation medium in such a way that the back of the leaf is in contact with the medium for callus Tissue and cluster bud induction. After inoculation, it was first cultured in total darkness at 25°C for 20 days, then placed in light for 14 hours a day, with a light intensity of 3000lx, and placed at ...
Embodiment 2
[0024] (1) Disinfection of explants: Collect the delicate leaves of healthy Rhododendron oxderica plants, gently scrub them with a soft brush dipped in washing powder water, rinse with tap water for 3 hours, then place them in an ultra-clean workbench, first disinfect them with 75% ethanol for 10 seconds, and then use sterile Wash 5 times with water, then disinfect with 0.1% mercuric chloride solution for 8 minutes, rinse 5 times with sterile water, and then dry the water drops on the surface with sterile filter paper before use.
[0025] (2) Differentiation culture: Excise the petiole of the leaf treated in step (1), lightly scratch a few times on the leaf with a sterile scalpel, and inoculate the differentiation medium in such a way that the back of the leaf is in contact with the medium for callus Tissue and cluster bud induction. After inoculation, it was first cultured in total darkness at 27°C for 25 days, then placed in light for 15 hours a day, with an illumination int...
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