Plant regeneration method of vinca from hairly root
A technology for regenerating plants and periwinkles, applied in the biological field, can solve problems such as undiscovered, and achieve the effect of solving the shortage of drug sources
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Embodiment 1
[0018] Induction of Callus and Differentiation of Adventitious Buds in Vinca Hairy Roots
[0019] The explants of periwinkle hairy roots were cut into 2-3 cm long segments and cultured on callus induction medium, which was MS (Murashige and Skoog, 1962) + naphthaleneacetic acid (NAA ) 0.3mg / L+6-benzyladenine (6-BA) 2.0mg / L+3% sucrose+0.26% plant gel. After 10-20 days of light culture, the hairy roots can be covered with nodular callus, and the callus induction rate reaches 100%; the callus is inoculated on the adventitious bud induction medium for subculture 1- 2 generations, 20-25 days per generation, a large number of light green buds are produced on the surface of the callus, and the adventitious bud induction medium is MS + naphthaleneacetic acid (NAA) 0.3mg / L + 6-benzyladenine (6-BA) 2.0mg / L + 3% sucrose + 0.26% plant gel; select the callus containing green buds and continue to subculture on the above medium. After about 20 days of cultivation, the green buds will gradua...
Embodiment 2
[0022] Rooting of adventitious buds of periwinkle
[0023] The adventitious buds differentiated in Example 1 were cut and cultured in a rooting medium, the rooting medium was 1 / 2MS+3% sucrose+0.26% phytogel, the culture temperature was 25±1°C, and the light was 16 hours a day . After 8-10 days of cultivation, white root processes visible to the naked eye appear at the base of the adventitious buds. After 20 days of light cultivation, 5-10 adventitious roots can be differentiated. The differentiation rate of adventitious roots is 100%. After 30 days, 5 - In vitro plantlets 6 cm high with 3-5 pairs of leaves.
Embodiment 3
[0025] Rapid Propagation of Periwinkle Regenerated Plants
[0026] The vigorously growing periwinkle regenerated plants in Example 2 were selected and cultured in the rapid propagation medium by means of cutting and multiplication to form a periwinkle regenerated plant strain. The rapid propagation medium is MS medium + 3% sucrose + 0.26% phytogel without adding any plant growth regulating substances, the culture temperature is 25±1°C, and the light is 16 hours a day.
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