Swordlike atractylodes rhizome tissue culture and rapid propagation method
A technology of tissue culture rapid propagation and Atractylodes atractylodes, which is applied in the field of plant tissue culture, can solve the problems of Atractylodes atractylodis species mixing, restricting rapid breeding, new variety selection, and degeneration of varieties, so as to expand the speed and scale of reproduction, protect wild Atractylodes atractylodes resources, The effect of mitigating real problems
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Embodiment 1
[0016] (1) Induction culture: After the collected stems are washed with clear water to remove surface attachments, soak in laundry detergent for 5 minutes, then rinse with running water for 1 hour, disinfect with 75% ethanol solution for 10 seconds in an ultra-clean workbench, and then wash with sterile water 3 times, and then sterilized with 0.1% mercuric chloride solution for 10 minutes, rinsed with sterile water for 4 times, sucked out the water with sterile filter paper, and then inoculated into the induction medium for bud induction culture. After inoculation, first cultivate in total darkness at 25°C for 7 days, then place it under light for 12 hours a day, with a light intensity of 2000lx, and place it at a temperature of 25°C for 25 days to differentiate adventitious buds, and after 45 days Adventitious buds were produced, and the induction rate was 83.62%. The induction medium is: MS+1.0mg / L 6-BA+0.3mg / L NAA+20g / L sucrose+4.0g / L agar, with a pH of 5.5.
[0017] ...
Embodiment 2
[0021] (1) Induction culture: After the collected stem segments are washed with clear water to remove surface attachments, soak in laundry detergent for 8 minutes, then rinse with running water for 3 hours, disinfect with 75% ethanol solution in an ultra-clean workbench for 30 seconds, and then wash with sterile water 5 times, and then sterilized with 0.1% mercuric chloride solution for 15 minutes, rinsed with sterile water for 6 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 28°C for 10 days, then place in light for 14 hours a day, with a light intensity of 3000lx, and culture at a temperature of 28°C for 21 days to differentiate adventitious buds. Adventitious buds were produced, and the induction rate was 87.93%. The induction medium is: MS+3.0mg / L 6-BA+0.5mg / L NAA+25g / L sucrose+4.5g / L agar, with a pH of 5.8.
[0022] (2) Proliferation culture: ...
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