Tissue Culture Rapid Propagation Method of Jinjili Begonia
A tissue culture and rapid technology, applied in the field of plant tissue culture, can solve the problems of long propagation cycle of Jinjili crabapple seeds, inability to carry out large-scale propagation, and restrictions on the promotion and application of varieties, and achieve fast propagation speed, high rooting rate, and robust growth Effect
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Embodiment 1
[0022] A method for fast propagation of Jinjili Begonia tissue culture, comprising the following steps:
[0023] 1) Selection and cleaning of explants: From April to May, the current year’s branches containing axillary buds were collected from the strong branches of the mother plant of Jinjili Begonia, soaked in soapy water for 5-15 minutes, rinsed with running water for 30-90 minutes, and then set aside;
[0024] 2) Disinfection of explants: Disinfect the cleaned explants with alcohol with a volume fraction of 65-75% on the ultra-clean workbench for 30-60 seconds, rinse with sterile water 3-5 times, each time for 2-4 minutes ; Disinfect with 0.2-0.3% mercury liter for 5-10 minutes, rinse with sterile water 3-5 times, 2-4 minutes each time;
[0025] 3) Primary culture: cut the sterilized explants into 2-4 cm long stems containing axillary buds on the ultra-clean workbench, and insert the stems into the bud induction medium at a culture temperature of 25 ± 1. The light time at...
Embodiment 2
[0029] The Jinjili Begonia tissue culture rapid propagation method comprises the following steps:
[0030] 1) Selection and cleaning of explants: From April to May, the current year's branches containing axillary buds were collected from the strong branches of the mother plant of Jinjili Begonia, soaked in soapy water for 10 minutes, rinsed with running water for 60 minutes, and then set aside;
[0031] 2) Disinfection of explants: Disinfect the cleaned explants with 70% alcohol on the ultra-clean workbench for 30 seconds, rinse with sterile water 4 times, each time for 2 minutes; then disinfect with 0.2% mercury liter for 8 minutes, without Rinse with bacterial water 5 times, 2 minutes each time;
[0032] 3) Primary culture: Cut the sterilized explants into 2cm-long stem segments containing 1 axillary bud on an ultra-clean workbench, and insert the stem segments into bud induction medium at a culture temperature of 25± 1. The light time at ℃ is 15h, and the light intensity i...
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