Method for tissue culture and rapid propagation of cortex acanthopanacis
A technique of tissue culture rapid propagation and Acanthopanax bark, applied in horticultural methods, botany equipment and methods, horticulture, etc., can solve the problems of low germination rate of Acanthopanax bark seeds and inability to meet large-scale production
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Embodiment 1
[0015] (1) Bud induction culture: Take the budd stem segment of Acanthopanax senticosus tree as explants, cut off the leaves, and cut into 2cm-long segments with 1 axillary bud, soak in detergent solution for 4min, and then use soft hair Brush gently on the surface of the explants to remove dust and part of the bacteria on the surface, then rinse with tap water for 3 hours and place in an ultra-clean workbench, disinfect with 75% ethanol for 4 seconds, wash with sterile water 4 times, and then use 0.1 Disinfected with% mercury solution for 15 minutes, rinse with sterile water 5 times and wipe off the water droplets on the surface with sterile filter paper, and then inoculate the bud induction medium for bud induction. After inoculation, cultivate in the dark at 26℃ for 2 days. Then it was cultivated for 28 days under the condition of 9 hours of light every day and light intensity of 1300lx. The bud induction rate and growth situation were counted. The bud induction rate was 88%....
Embodiment 2
[0020] (1) Bud induction culture: take the budd stem segment of Acanthopanax senticosus tree as explants, cut off the leaves, and cut into 6cm long segments with 5 axillary buds, soak in detergent solution for 12 minutes, and then use soft hair Brush gently on the surface of the explant to remove the dust and part of the bacteria on the surface, then rinse with tap water for 2 hours, then place it in an ultra-clean workbench, disinfect with 75% ethanol for 18 seconds, wash with sterile water 8 times, and then use 0.1 Disinfected with% mercury solution for 20 minutes, rinse with sterile water 5 times and wipe off the surface water droplets with sterile filter paper, then inoculate the bud induction medium for bud induction. After inoculation, cultivate in the dark at 26℃ for 4 days. Then irradiate for 12 hours every day and culture for 33 days under the condition of 2500lx light intensity. Statistics of its bud induction rate and growth situation show that the bud induction rate ...
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