A kind of high-efficiency and rapid propagation method of Coleus coleus
A high-efficiency, colorful leaf technology, applied in the field of plant tissue culture, can solve the problems of slow formation of adventitious buds, less than 5%, and deformed seedlings
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Embodiment 1
[0023] ① Selection of explants: From March to April, select a robust and good-looking Coleus saponifera grass as the mother plant, and take new sword-shaped buds at the base as explants for future use.
[0024] ② Disinfection of explants: On the ultra-clean workbench, put the sword-shaped buds into sterile empty bottles, use 0.1% mercury liter as the disinfectant, disinfect for 6 minutes, and then rinse with sterile water twice. The sterility rate is 90%.
[0025] ③Callus induction and adventitious bud differentiation: Peel off the wrapped leaves of the sterilized sword-shaped buds, insert them into the induction and differentiation medium; 1 stem segment / cup, 26±1°C, 1000~2000lux culture, light 12h / d, Transplant once every 2 months.
[0026]Differentiation induction medium: MS+2mg / L 6-BA+2mg / L CPPU+0.01 mg / L NAA+30g / L sucrose+6.5g / L agar, pH6.0. After 23 days of culture, the base began to expand. After 48 days of culture, the expanded base began to differentiate into sword...
Embodiment 2
[0032] ① Selection of explants: From March to April, select a robust and good-looking Coleus saponifera grass as the mother plant, and take new sword-shaped buds at the base as explants for future use.
[0033] ② Disinfection of explants: On the ultra-clean workbench, put the sword-shaped buds into sterile empty bottles, use 0.1% mercury liter as the disinfectant, disinfect for 8 minutes, and then rinse with sterile water twice. The sterility rate is 95%.
[0034] ③Callus induction and adventitious bud differentiation: Peel off the wrapped leaves of the sterilized sword-shaped buds, insert them into the induction and differentiation medium; 1 stem segment / cup, 26±1°C, 1000~2000lux culture, light 12h / d, Transplant once every 2 months.
[0035] Differentiation induction medium: MS+2mg / L 6-BA+3mg / L CPPU+0.01 mg / L NAA+30g / L sucrose+6.5g / L agar, pH6.0. After 21 days of culture, the base began to expand. After 46 days of culture, the expanded base began to differentiate into swor...
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