Tissue culture method of Eucommia ulmoides Oliv.
A tissue culture and culture medium technology, applied in the field of plant tissue culture, can solve the problems of inability to meet large-scale production of Eucommia seedlings, unfavorable promotion of fine Eucommia varieties, and low seed germination rate.
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Embodiment 1
[0016] (1) Bud induction culture: use the stem section of Eucommia ulmoides No. 5 with buds as explants, cut off the leaves, cut into 3.0-5.0 long segments with 2-3 axillary buds, and soak them in washing powder solution for 5 minutes , and then gently scrub the surface of the explant with a soft brush to remove the dust and some bacteria on the surface, then rinse it with tap water for 1 hour and place it in an ultra-clean workbench, first disinfect it with 75% ethanol for 5 seconds, and then wash it with sterile water for 3 seconds sterilized with 0.1% mercuric chloride solution for 10 minutes, rinsed with sterile water for 4 times, and then dried the water droplets on the surface with sterile filter paper, then inoculated into bud induction medium for bud induction. Cultivate in the dark for 3 days, then place it under light for 10 hours every day, and cultivate for 30 days under the condition of light intensity of 1500lx, count its bud induction rate and growth situation, a...
Embodiment 2
[0021] (1) Bud induction culture: take Huazhong No. 5 Eucommia eucommia stem with buds as explants, cut off the leaves, cut into 3.0-5.0 long segments with 2-3 axillary buds and soak them in washing powder solution for 10 minutes , and then gently scrub the surface of the explant with a soft brush to remove the dust and some bacteria on the surface, then rinse it with tap water for 2 hours and place it in an ultra-clean workbench, first disinfect it with 75% ethanol for 15 seconds, and then wash it with sterile water for 5 seconds sterilized with 0.1% mercuric chloride solution for 15 minutes, rinsed with sterile water for 4 times, and then dried the water droplets on the surface with sterile filter paper, then inoculated into bud induction medium for bud induction. Cultivate in the dark for 3 days, then place it under light for 10 hours every day, and cultivate for 30 days under the condition of light intensity of 1500lx, count its bud induction rate and growth situation, and ...
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