Tissue culture rapid-propagation method of fire axillary bud of North American crabapple tableland
A tissue culture rapid propagation and plateau technology, which is applied in horticultural methods, botanical equipment and methods, horticulture, etc., can solve the problems of restricting popularization of cultivation and inability to carry out large-scale propagation, and achieve good practicability, speed up propagation and effect of scale
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Embodiment 1
[0023] A rapid propagation method of plateau fire Begonia tissue culture, comprising the following steps:
[0024] 1) Selection and pretreatment of explants: In April, select tender branches about 5 cm long from the mother plant of Plateau Fire Begonia, soak them in soapy water for 10 minutes, brush off surface stains with a soft brush, rinse them with running water for 2 hours, and set aside .
[0025] 2) Disinfection of explants: Soak the explants in 75% alcohol for 30 seconds on the ultra-clean workbench, rinse them with sterile water for 3 times, and then disinfect them with 0.1% mercury liter for 9 minutes. Bacterial water was washed 4 times, and the surface moisture was blotted dry with sterile filter paper for later use.
[0026] 3) Primary culture: After the explants were sterilized, they were cut into about 2 cm stem segments with one axillary bud, and inoculated on the primary medium for cultivation ( figure 1 ). The temperature of the culture room is 25±2°C, the ...
Embodiment 2
[0032] A rapid propagation method of plateau fire Begonia tissue culture, comprising the following steps:
[0033] 1) Selection and pretreatment of explants: In April, select tender branches about 5 cm long from the mother plant of Plateau Fire Begonia, soak them in soapy water for 10 minutes, brush off surface stains with a soft brush, rinse them with running water for 2 hours, and set aside .
[0034] 2) Disinfection of explants: Soak the explants in 75% alcohol for 30 seconds on the ultra-clean workbench, rinse them with sterile water for 4 times, and then disinfect them with 0.1% mercury liter for 9 minutes. Wash with sterile water for 5 times, and blot the surface moisture with sterile filter paper for later use.
[0035] 3) Primary culture: After the explants were sterilized, they were cut into about 2 cm stem segments with one axillary bud, and inoculated on the primary medium for cultivation ( figure 1 ). The temperature of the culture room is 25±2°C, the light time...
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