Method of tissue culture and rapid propagation of healthy sugarcane seedlings
A technology for tissue culture, rapid propagation and seedlings, applied in the field of plant tissue culture, can solve the problems of incomplete removal of RSD, difficult production, long production years, etc., and achieve the effects of improving perennial rooting, improving survival rate, and low mutation rate.
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Embodiment 1
[0023] The rapid propagation method of sugarcane healthy seedling is implemented according to the following steps:
[0024] 1) Selection and treatment of sugarcane materials: take the fine sugarcane variety Yuncane 06-407 as the material, take mature sugarcane stems in January, cut into two bud stem segments, and scrub the outer surface in clean water to remove the residues of diseases and insect pests attached to the surface dirt or dirt. Seeds are soaked in 2% lime water for 30 minutes, soaked in a constant temperature water bath at 52°C for 30 minutes, planted in a 5.5-6cm thick bagasse substrate, and cultivated in a constant temperature and humidity incubator at 38°C for 5-6 days. After the axillary buds emerge That's it.
[0025] 2) Selection and treatment of axillary buds: take axillary buds with a height of 5-6 cm, and use them as explants after sterilization under sterile conditions.
[0026] 3) Axillary bud induction culture: inoculate the explants i...
Embodiment 2
[0034] The rapid propagation method of sugarcane healthy seedling is implemented according to the following steps:
[0035] 1) Selection and treatment of sugarcane materials: take the fine sugarcane variety Yuncane 05-51 as the material, take mature sugarcane stems in January, cut into two bud stem segments, and scrub the outer surface in clean water to remove the residues of diseases and insect pests attached to the surface dirt or dirt. Seeds are soaked in 2% lime water for 30 minutes, soaked in a constant temperature water bath at 52°C for 30 minutes, planted in a bagasse substrate about 6cm thick, and cultivated in a constant temperature and humidity incubator at 38°C for 5-6 days. .
[0036] 2) Selection and treatment of axillary buds: take axillary buds with a height of 5-6 cm, and use them as explants after sterilization under sterile conditions.
[0037] 3) Axillary bud induction culture: inoculate the explants in the differentiation medium: MS+6-BA1....
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