A kind of myrtle tissue culture rapid propagation technique
A technique of tissue culture, rapid propagation and myrtle, applied in the field of plant tissue culture, can solve problems such as no reports, and achieve the effect of solving the problem of supplying high-quality myrtle seedlings
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Embodiment 1
[0017] (1) Collection and processing of explants: Select the full-bodied branches of the year's visceral buds from an excellent single plant of myrtle, soak in washing powder water for 15 minutes after removing leaves, rinse with tap water for 1 hour after brushing, and cut into 1-3 cm long strips The stems of axillary buds were first sterilized with 75% ethanol for 8 seconds, then washed 3 times with sterile water, then sterilized with 0.1% mercuric chloride solution for 20 minutes, washed 5 times with sterile water, and then set aside.
[0018] (2) Primary culture: Inoculate the above-mentioned stem segments on the primary culture medium, culture in total darkness at 28°C for 40 days, and then place under light for 10 hours a day with a light intensity of 2000lx until adventitious buds are induced. The primary medium is: MS+6-BA1.2mg / L+NAA0.4mg / L+CPPU0.05mg / L+Ad1.0mg / L+sucrose 25g / L+agar 4g / L, with a pH of 5.7.
[0019] (3) Proliferation culture: Transfer the above-mentioned...
Embodiment 2
[0023] (1) Collection and processing of explants: Select the full-bodied branches of the year's visceral buds from an excellent single plant of myrtle, soak in washing powder water for 30 minutes after removing leaves, rinse with tap water for 2 hours after brushing, and cut into 1-3 cm long strips The stems of axillary buds were first sterilized with 75% ethanol for 20 seconds, then washed 5 times with sterile water, then sterilized with 0.1% mercuric chloride solution for 15 minutes, rinsed 6 times with sterile water, and then set aside.
[0024] (2) Primary culture: Inoculate the above-mentioned stem segments on the primary culture medium, culture them in total darkness at 25°C for 30 days, and then place them under light for 11 hours a day with a light intensity of 2000 lx until adventitious buds are induced. The primary medium is: MS+6-BA1.0mg / L+NAA0.2mg / L+CPPU0.1mg / L+Ad2.0mg / L+sucrose 25g / L+agar 4g / L, with a pH of 5.8.
[0025] (3) Proliferation culture: Transfer the abo...
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