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
[0030] Seeds of Rhododendron japonica collected in Yunmeng mountain area of Beijing were soaked in sterile water for 30 to 60 minutes on a super-clean workbench, and the sunken seeds were removed, then sterilized in 0.1% HgCl2 solution for 5 minutes, and rinsed with sterile water. Rinse 3 times with sterile water, then sterilize with 0.1% HgCl2 for 5 minutes, rinse 4 times with sterile water, 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.
[0031] 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 were induced, with about 30 bud ...
Embodiment 2
[0037] The culture procedures were all carried out according to Example 1, except that the source of the seeds was Yunmeng Mountain in Shandong, the explants of the primary culture were the shoot tips of sterile seedlings, and the cluster bud induction medium was improved. The B5 medium was supplemented with 6- Benzylaminoadenine 6-BA1mg / L, NAA0.1mg / L. The subculture medium is rhododendron medium supplemented with indole butyric acid IBA 1mg / L and 6-benzylaminoadenine 6-BA 5mg / L. The rooting induction medium is rhododendron medium supplemented with naphthalene acetic acid 2mg / L, 6-benzylaminoadenine 6-BA0.2mg / L.
Embodiment 3
[0039] The culture procedures were all carried out according to Example 1, except that the source of the seeds was Wuling Mountain, Hebei, and the primary culture medium was improved. The B5 medium was supplemented with 6-benzylaminoadenine 6-BA1.5mg / L, and Nai Acetate 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. The rooting induction medium is rhododendron medium supplemented with 1.5 mg / L of naphthalene acetic acid and 0.1 mg / L of 6-benzylaminoadenine 6-BA.
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