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 method of rapid propagation of healthy sugarcane seedlings is implemented according to the following steps:
[0024] 1) Selection and treatment of sugarcane material: Take the sugarcane seed Yuncane 06-407 as the material, take the mature sugarcane stem in January, cut into two buds, and scrub the outer surface in clean water to remove the pest residues attached to the surface Dirt or dirt. Soak the seeds with 2% lime water for 30 minutes, soak them in a constant temperature water bath at 52°C for 30 minutes, plant them in a 5.5-6cm thick bagasse matrix, and cultivate them in a constant temperature and humidity incubator at 38°C for 5-6 days. After the axillary buds are unearthed That's it.
[0025] 2) Selection and treatment of axillary buds: Take 5-6cm high axillary buds and sterilize them under aseptic conditions as explants.
[0026] 3) Axillary bud induction culture: inoculate the explants in the differentiation medium and change the medium once ever...
Embodiment 2
[0034] The method of rapid propagation of healthy sugarcane seedlings is implemented according to the following steps:
[0035] 1) Selection and treatment of sugarcane material: Take the sugarcane seed Yuncane 05-51 as the material, take the mature sugarcane stem in January, cut into two buds, and scrub the outer surface in clean water to remove the pest residues attached to the surface Dirt or dirt. Soak the seeds with 2% lime water for 30 minutes, soak them in a constant temperature water bath at 52°C for 30 minutes, plant them in a bagasse matrix of about 6 cm thick, and cultivate them in a constant temperature and humidity incubator at 38°C for 5-6 days. After the buds are unearthed .
[0036] 2) Selection and treatment of axillary buds: Take 5-6cm high axillary buds and sterilize them under aseptic conditions as explants.
[0037] 3) Axillary bud induction culture: inoculate the explants in the differentiation medium: MS+6-BA1.0mg / L+KT0.5mg / L+sucrose 30g / L medi...
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