Method for culturing tetraploid dendrobium nobile
A breeding method, tetraploid technology, applied in horticultural methods, botanical equipment and methods, plant gene improvement, etc., can solve the problems of high frequency of chimeric tetraploid, difficult to guarantee germplasm, long breeding cycle, etc., to achieve Increase the output of medicinal materials, shorten the time, improve the effect of quality and output
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Embodiment 1
[0023] (1) The plants of variety A and variety B are planted and cultivated according to conventional methods;
[0024] (2) Aseptically sow the seeds of different varieties of original plants in solid medium to obtain diploid protocorms of varieties A and B. The culture is static culture on MS solid medium at a temperature of 22 ℃, light time 10 hours, light intensity 1500lux, color temperature 4000K;
[0025] (3) Transfer the obtained diploid protocorms into a mixture containing 200mg / L colchicine, 0.5mg / L NAA (naphthalene acetic acid), 1mg / L 6-BA (6-benzylaminopurine), and the pH value is 5.6± 0.2 in 1 / 2MS liquid medium for mutagenesis at 30°C for 12 hours;
[0026] (4) Rinse the above-mentioned treated explants with sterile water and transfer them to MS solid medium. The light intensity is 1500lux, the color temperature is 4000K, the photoperiod is 16 hours / day, and the culture temperature is 22°C. Continue to cultivate under the conditions until the seedlings are differe...
Embodiment 2
[0031] (1) The plants of variety A and variety B are planted and cultivated according to conventional methods;
[0032] (2) Aseptically sow the seeds of different varieties of original plants in solid medium to obtain diploid protocorms of varieties A and B. The culture is static culture on MS solid medium at a temperature of 25 ℃, light time 12 hours, light intensity 3000lux, color temperature 5000K;
[0033] (3) Transfer the obtained diploid protocorms into a mixture containing 150mg / L colchicine, 1mg / L NAA (naphthalene acetic acid), 2mg / L 6-BA (6-benzylaminopurine), and the pH value is 5.6± 0.2 in 1 / 2MS liquid medium for mutagenesis at 30°C for 12 hours;
[0034] (4) Rinse the above-mentioned treated explants with sterile water and transfer them to MS solid medium. The light intensity is 3000lux, the color temperature is 5000K, the photoperiod is 16 hours / day, and the culture temperature is 25°C. Continue to cultivate under the conditions until the seedlings are different...
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