Tissue culture and rapid propagation method for Acer rubrum 'Brandywine'
A tissue culture rapid propagation and red maple technology, applied in the field of plant tissue culture, can solve the problems of low seed setting rate and limited seedlings, etc., and achieve the effect of rapid growth and strong adaptability
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Embodiment 1
[0017] (1) Disinfection of explants: Rinse the collected stems with clean water for 10 minutes and gently brush off the impurities on them with a brush. Disinfect them with 75% ethanol solution for 10 seconds in an ultra-clean workbench, and then wash them with sterile water for 3 seconds. Then, sterilize with 0.1% mercuric chloride solution for 10 minutes, rinse with sterile water for 4 times, absorb the water with sterile filter paper, and set aside.
[0018] (2) Induction culture: Cut the sterilized stem section in step (1) into a 1.5cm-long stem section and inoculate it into the induction medium for bud induction culture. After inoculation, culture in total darkness at 25°C for 5 days, and then place in light for 10 hours a day with a light intensity of 2000lx and culture at a temperature of 25°C until adventitious buds form, with an average contamination rate of only 4.5 %, the average survival rate was 89.7%, and the induction rate was 85.3%. The induction medium is: WP...
Embodiment 2
[0023] (1) Disinfection of explants: Rinse the collected stems with clean water for 15 minutes and gently brush off the impurities on them with a brush. Disinfect them in 75% ethanol solution for 20 seconds in an ultra-clean workbench, and then wash them with sterile water for 5 minutes. Then, sterilize with 0.1% mercuric chloride solution for 16 minutes, rinse with sterile water for 6 times, and then use sterile filter paper to absorb the water for later use.
[0024] (2) Induction culture: Cut the sterilized stem section in step (1) into a 1.5cm-long stem section and inoculate it into the induction medium for bud induction culture. After inoculation, culture in total darkness at 27°C for 7 days, and then place in light for 14 hours a day with a light intensity of 3000 lx and culture at a temperature of 27°C until adventitious buds form, with an average contamination rate of only 5.3 %, the average survival rate was 90.4%, and the induction rate was 86.7%. The induction medi...
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