Method of Tissue Culture and Rapid Propagation of Anomasia emei
A technique for fast propagation by tissue culture of Clematis Emei, applied in the field of plant tissue culture, can solve the problems of slow natural reproduction and growth, harsh growth conditions, no germination ability, etc., and achieves excellent medicinal properties, low production cost, and simple and easy method. row effect
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Embodiment 1
[0037] Materials Emei clematis, collected from Mount Emei, Sichuan. Propagate Emei golden clematis according to the following steps.
[0038] 1. Take the wild Amethyst emei plant, and cut off a 0.5cm long section containing an axillary bud.
[0039] 2. Rinse with tap water for 2-3 hours, clean with a soft brush, rinse with distilled water, place in an ultra-clean workbench, soak in 75% alcohol for 30 seconds, clean with sterile water, and disinfect the surface in 0.1% mercury solution for 15 minutes , wash with sterile water 4-5 times, 2 minutes each time.
[0040] 3. The sterilized explants were inoculated into the induction medium for cultivation; the induction medium was: MS medium + sucrose 30g / L + agar 8g / L + activated carbon 2.0g / L + 1.5mg / L6-BA + 0.5mg / LNAA , the pH value is 5.8; the culture period is 30-40 days; the culture conditions are: the light intensity is 2000lux, 16h / d, and the culture temperature is 22-25°C. After 7 days of cultivation, germination begins. ...
Embodiment 2
[0045] Materials Emei clematis, collected from Mount Emei, Sichuan. Propagate Emei golden clematis according to the following steps.
[0046] 1. Take the wild Amethyst emei plant and cut off a 0.5cm long section containing a terminal bud.
[0047] 2. Rinse with tap water for 2-3 hours, clean with a soft brush, rinse with distilled water, place in an ultra-clean workbench, soak in 75% alcohol for 30 seconds, clean with sterile water, and disinfect the surface in 0.1% mercury solution for 15 minutes , wash with sterile water 4-5 times, 2 minutes each time.
[0048] 3. The sterilized explants were inoculated into the induction medium for cultivation; the induction medium was: MS medium + sucrose 30g / L + agar 8g / L + activated carbon 2.0g / L + 1.5mg / L6-BA + 0.5mg / LNAA , the pH value is 5.8; the culture period is 30-40 days; the culture conditions are: the light intensity is 2000lux, 16h / d, and the culture temperature is 22-25°C. After about 7 days of cultivation, germination begi...
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