Rapid propagation and seedling growing method for Shuhua camellia tissue culture
A camellia bunch and tissue culture technology, applied in the field of plant tissue culture, can solve the problems of difficulty in meeting new varieties, difficult rooting of camellia tissue culture, long production cycle, etc., to shorten the time to market, meet the requirements of fast-growing seedlings in factories, and simplify the production process. Effects of production steps
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Embodiment 1
[0026] (1) Selection and disinfection of explants:
[0027] In the morning when the weather is fine, a new variety of Shuhua camellia "Xiaofenyu" (variety right number: 20120001) is selected, and the terminal buds that are free from diseases and insect pests, plump and just germinated but not yet unfolded are used as explants.
[0028] (2) Pretreatment and disinfection of explants:
[0029] Gently scrub the explants with detergent for 2-3 times, wrap them in gauze, and rinse them under running water for 20-30 minutes. Soak in 1000mg / L cephradine solution for 1 hour, and rinse with clean water. After washing, disinfect with 75% alcohol for 90 seconds, then disinfect with 0.1% mercury liter for 10 minutes, and finally wash with sterile water for 3 to 5 times, and set aside.
[0030] (3) Induction culture:
[0031] Under sterile conditions, peel off the scales and 2-3 layers of leaves wrapped in the outer layer of the terminal bud after disinfection, and then inoculate on the ...
Embodiment 2
[0035] (1) Selection of explants:
[0036] On a sunny morning, a new Shuhua camellia variety "Meiyu" (variety right number: 20120054) free from diseases and insect pests, plump and newly germinated but not yet unfolded terminal buds was selected as explants.
[0037] (2) Pretreatment and disinfection of explants:
[0038] Gently scrub the explants with detergent for 2-3 times, wrap them in gauze, and rinse them under running water for 20-30 minutes. Soak in 2000mg / L cephradine solution for 1 hour, and rinse with clean water. After washing, disinfect with 75% alcohol for 90 seconds, then disinfect with 0.1% mercury liter for 12 minutes, and finally wash with sterile water for 3 to 5 times, and set aside.
[0039] (2) Induction culture: Under sterile conditions, peel off the scales and 2-3 layers of leaves wrapped by the outer layer of the explant, and then inoculate it on the induction medium. The culture conditions are: the temperature is 24±1°C, the light intensity is 1500...
Embodiment 3
[0043] The rooting solution is 0.5 mg / L naphthaleneacetic acid (NAA), and the others are the same as in Example 1.
[0044] The rooting rate of aseptic seedlings cultivated in this implementation is 91%, and the survival rate of transplanting is 90%. Requirements for industrialized seedling cultivation.
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