Rapid propagation method of ginger virus-free seedlings by one step
A technology of virus-free seedlings and ginger, which is applied in the field of plant tissue culture, can solve the problems of ginger yield decline, consumption of commercial ginger, and stress resistance decline, and achieve the effects of shortening the production cycle, reducing production costs, and shortening the cycle
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Embodiment 1
[0021] Ginger one-step becomes the rapid propagation method of virus-free seedling, and its steps are:
[0022] 1. Select bright yellow, shiny, full and healthy ginger with many buds and no scars, rinse it with tap water, bury it in the washed sand bed, and store it at 20°C or 21°C or 22°C or 24°C or 24°C Or germinate at 25°C. When the shoots grow to 1cm or 1.5cm or 2cm long, cut them with a blade, rinse with tap water to remove the sand;
[0023] 2. The buds are placed in an incubator and treated at 50°C for 5 minutes to complete detoxification;
[0024] 3. Soak in 75% alcohol solution by volume for 10s or 15s or 20s or 25s or 30s on the ultra-clean workbench, rinse with sterile water for 3 times, and then disinfect with 0.1% (weight ratio) mercury chloride solution for 10min or 11min or 12min, wash with sterile water 3 times or 4 times or 5 times;
[0025] 4. After draining the water, dissect the processed material under a dissecting microscope under aseptic conditions, c...
Embodiment 2
[0031] Ginger one-step becomes the rapid propagation method of virus-free seedling, and its steps are:
[0032] 1. Select bright yellow, shiny, plump and robust ginger with many buds and no scars, rinse it with tap water, bury it in a washed sand bed, and accelerate germination at 25°C. When the shoots grow to 1.5cm long, cut them with a blade, rinse with tap water to remove the sand;
[0033] 2. The buds are placed in an incubator and treated at 50°C for 5 minutes to complete detoxification;
[0034] 3. Soak in 75% alcohol solution by volume for 20 seconds on the ultra-clean workbench, rinse with sterile water for 3 times, then disinfect with 0.1% (by weight) mercury solution for 12 minutes, and rinse with sterile water for 5 times;
[0035] 4. After draining the water, dissect the processed material under a dissecting microscope under aseptic conditions, cut out the 0.2mm growth point of the meristem, and quickly inoculate it into the induction medium. The active ingredien...
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