Tissue culturing, rapid propagating and transplanting method of Rhododendron mucronulatum Turcz.
A technology of tissue culture rapid propagation and rhododendron, applied in the biological field, can solve the problems of low rooting rate of tissue culture seedling transplantation that have not been reported before, and achieve the effects of high proliferation rate, stable proliferation, and high survival rate of transplanting
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Embodiment 1
[0031] Seeds of Rhododendron japonica collected in Yunmeng mountain area of Beijing. Soak the seeds of Rhododendron japonica in sterile water for 30-60 minutes on the ultra-clean workbench, remove the sinking seeds, and then transfer them to 0.1% HgCl 2 The solution was sterilized for 5 minutes, rinsed 3 times with sterile water, and then washed with 0.1% HgCl 2 Sterilize for 5 minutes, rinse with sterile water 4 times, and inoculate on sterile medium containing 3% sucrose and 0.7% agar. The culture conditions are 25±1°C, dark, after about 2 weeks of germination, transfer to the condition of 12 hours of light per day for cultivation, and about 2 months, take the epicotyl section of the shoot tip for primary culture.
[0032] The primary culture medium is rhododendron culture medium supplemented with 1mg / L IBA and 5mg / L ZT, the culture conditions are 25±1°C, 12 hours of light per day, and the light intensity is 2000-3000Lux. In about 60 days, a large number of clustered buds...
Embodiment 2
[0038] The culture procedures were all carried out according to Example 1, the difference was that the source of the seeds was Yunmeng Mountain in Shandong, the explants of the primary culture were shoot tips of sterile seedlings, and the cluster bud induction medium was the improved B5 medium supplemented with 6-benzyl Aminoadenine 6-BA1mg / L, naphthaleneacetic acid NAA0.1mg / L. The subculture medium is rhododendron medium supplemented with indole butyric acid IBA 1mg / L and 6-benzylaminoadenine 6-BA 5mg / L. Rooting induction medium is rhododendron medium supplemented with naphthaleneacetic acid 2mg / L, 6-benzylaminoadenine 6-BA0.2mg / L.
Embodiment 3
[0040] The culture procedures were all carried out according to Example 1, the difference was that the source of the collection was Wuling Mountain, Hebei, and the primary culture medium was improved B 5 The medium was supplemented with 6-benzylaminoadenine 6-BA1.5mg / L and naphthaleneacetic acid NAA0.2mg / L. The subculture medium is rhododendron medium supplemented with indole butyric acid IBA 1.5mg / L and 6-benzylaminoadenine 6-BA 10mg / L. Rooting induction medium is rhododendron medium supplemented with 1.5mg / L naphthaleneacetic acid and 6-benzylaminoadenine 6-BA0.1mg / L.
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