Rapid rhizoma polygonati propagation technology method
A fast and technical technology, applied in the field of bioengineering, can solve the problems of insufficient seed source, high production cost, long production cycle, etc., and achieve the effect of large reproduction coefficient, low production cost and low pollution rate.
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Embodiment 1
[0015] The mature fruit picked back, rubbed off the exocarp, layered with fine sand and placed in a refrigerator at 3°C for 30 days, and then treated with 200ppmGA 3 Soak for 24 hours, put it into an incubator at 26°C for constant temperature cultivation, the germination rate reaches 70%, and then soak it in 200ppm KT for 12 hours, the germination rate can reach 90%. Most can be sown to outdoor seedlings.
[0016] Remove the fibrous roots of the germinated small underground rhizomes, wash them in running water for one day and one night, treat them with 8% calcium hypochlorite for 30 minutes, disinfect them with 70% ethanol three times in an ultra-quiet bench, and disinfect them with 0.1% mercury chloride for 8 minutes. Rinse with water for 5 times, cut small rhizome buds longitudinally, inoculate into solid medium of MS plus 6-BA1.0mg / L\2,4-D0.5mg / L\sucrose 30g / L\agar 7g / L, PH5.8 Cultivate under the conditions of temperature 26℃, light time 16h\light intensity 1500Lx, and c...
Embodiment 2
[0018] The refrigerated seeds were treated with 400ppmGA 3 Soak for 12 hours, put it in an incubator at 26°C for constant temperature cultivation, and the germination rate is about 40%. After the radicle grows, soak it in 300ppm KT for 12 hours, and the germination rate is about 80%.
[0019] After the callus was induced completely according to the S1 method, the difference was that it was first transferred to MS plus TDZ1.5mg / L\2,4-D1.0mg / L\sucrose 30g / L\agar 7g / L medium for 15 Transfer to MS and add 6-BA1.0mg / L\NAA2.0mg / L\sucrose 30g / L\agar 7g / L on the differentiation medium culture induction again, the cluster bud of every piece of callus reaches 8.9; S2.
[0020] Compared with S1 and S2, the germination rate of seed treatment S1 increased by 30% compared with S2, and the bud germination rate increased by 10%. In the process of tissue culture, according to the results of differentiation culture, S2 had 2.4 more shoots per callus on average than S1.
[0021] The above spe...
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