Method for establishing tea regeneration system
A method of establishment, tea technology, applied in the field of establishment of tea regeneration system, can solve the problems of long growth cycle, low reproduction coefficient, etc., and achieve the effect of high reproduction coefficient and high difficulty in solving
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Embodiment 1
[0013] (1) Disinfection of explants: Collect the delicate leaves of healthy tea plants, gently scrub them with a soft brush dipped in washing powder water, rinse them with tap water for 5 hours, place them in an ultra-clean workbench, disinfect them with 75% ethanol for 8 seconds, and then wash them with sterile water 7 times, then sterilized with 0.1% mercuric chloride solution for 8 minutes, rinsed with sterile water 8 times, and then dried the water droplets on the surface with sterile filter paper before use.
[0014] (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 26°C for 20 days, then placed in light for 12 hours a day, with a light intensity of 3000lx, and pla...
Embodiment 2
[0019] (1) Disinfection of explants: Collect the delicate leaves of healthy tea plants, gently scrub with a soft brush dipped in washing powder water, rinse with tap water for 6 hours, then place them in an ultra-clean workbench, first disinfect with 75% ethanol for 10 seconds, and then use sterile water 12 times, then sterilized with 0.1% mercuric chloride solution for 10 minutes, rinsed with sterile water for 8 times, and then dried the water droplets on the surface with sterile filter paper before use.
[0020] (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 28°C for 25 days, then placed in the light for 18 hours a day, with a light intensity of 3500lx, and placed ...
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