Subshrubby peony bark tissue culture and rapid propagation method
A technology for tissue culture rapid propagation and Paeonia suffruticosa, applied in the field of plant tissue culture, can solve the problems of restricting rapid propagation and breeding of new varieties, low reproduction coefficient, long growth cycle, etc. The effect of protecting wild resources and fast reproduction
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Embodiment 1
[0012] (1) Induction culture: After the collected stems are washed with clear water to remove surface attachments, soak in laundry detergent for 7 minutes, then rinse with running water for 2 hours, disinfect with 75% ethanol solution in an ultra-clean workbench for 12 seconds, and then wash with sterile water 5 times, and then sterilized with 0.1% mercuric chloride solution for 12 minutes, rinsed with sterile water for 5 times, sucked out the water with sterile filter paper, and inoculated into the induction medium for bud induction culture. After inoculation, first cultivate in total darkness at 26°C for 8 days, then place it under light for 13 hours a day, with a light intensity of 2200 lx, and place it under the condition of 26°C for 26 days to differentiate adventitious buds, and after 40 days Adventitious buds were produced, and the induction rate was 85%. The induction medium is: MS+1.2mg / L 6-BA+0.5mg / L NAA+22g / L sucrose+4.2g / L agar, with a pH of 5.2.
[0013] (2) Prol...
Embodiment 2
[0017] (1) Induction culture: After the collected stems are washed with clear water to remove surface attachments, soak in laundry detergent for 9 minutes, then rinse with running water for 4 hours, disinfect with 75% ethanol solution in an ultra-clean workbench for 32 seconds, and then wash with sterile water 6 times, and then sterilized with 0.1% mercuric chloride solution for 17 minutes, rinsed with sterile water for 7 times, sucked out the water with sterile filter paper, and inoculated into the induction medium for bud induction culture. After inoculation, culture in total darkness at 30°C for 9 days, then place in light for 15 hours a day with a light intensity of 3100lx, and culture at a temperature of 30°C for 22 days to differentiate adventitious buds. After 39 days, the Adventitious buds were produced, and the induction rate was 88.0%. The induction medium is: MS+3.2mg / L 6-BA+0.6mg / L NAA+27g / L sucrose+4.8g / L agar, with a pH of 5.2.
[0018] (2) Proliferation culture...
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