Method for quickly growing seedling of wild buckwheat rhizome by tissue culture
A tissue culture, golden buckwheat technology, applied in horticultural methods, botanical equipment and methods, horticulture and other directions, can solve the problems of golden buckwheat tissue culture seedling refining and transplanting technology research, the stem should not be induced to root, and the browning phenomenon deepens. , to achieve the effect of maintaining genetic stability, shortening the breeding cycle, and easy to obtain materials
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Embodiment 1
[0029]The young golden buckwheat stems introduced from Jiangsu and cultivated in the experimental base of the Institute of Medicinal Plants for many years were used as explants, cut into 2-3cm sections, treated with 70% alcohol for 30 seconds, rinsed with sterile water twice, and then Soak in 0.1% mercury liter solution for 12 minutes, shake constantly during the period, and finally rinse with sterile water 5 times, 1 minute each time. The explants treated above were cut into 30 single-bud stem segments, inoculated in MS medium containing 2.0mg / L 6-BA+0.5mg / LTDZ+0.2mg / L NAA+30% sucrose, at 25 ±2°C, 1500-3000Lux, culture under 12-16h / d light to induce and proliferate adventitious buds, and obtain clustered seedlings (such as figure 1 ), subcultured once every 30 days, and a large number of adventitious sprouts were obtained after subcultured 3 times. Select robust rootless seedlings of about 2-3 cm, and transfer them to a rooting medium to induce rooting. The formula of the ro...
Embodiment 2
[0031] The young golden buckwheat stems introduced from Guizhou and cultivated in the experimental base of the Institute of Medicinal Plants for many years were used as explants, cut into 2-3cm long sections, treated with 70% alcohol for 30 seconds, and washed twice with sterile water , and then soaked in 0.1% mercuric chloride solution for 10 minutes, shaking constantly during the period, and finally rinsed with sterile water 5 times, 1 minute each time. The explants treated above were cut into 30 single-bud stem segments, inoculated in MS medium containing 1.0mg / L6-BA+0.5mg / L NAA+30% sucrose, at 25±2°C, 1500- 3000Lux, culture under 12-16h / d light to induce adventitious buds, after 2 weeks axillary buds germinate to form sterile seedlings. The obtained sterile seedlings are further cut into single-bud stem segments, and transferred to the bud proliferation medium obtained by screening. The composition of the culture medium is: MS+2.0mg / L 6-BA+0.2mg / L TDZ+0.5mg / L NAA+30% sucr...
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