Tissue culture rapid propagation method for purple pitcher plant
A technique for tissue culture and rapid propagation of bottle grass, applied in the field of tissue culture and rapid propagation of purple bottle grass
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Embodiment 1
[0023] ① Selection of explants: Select a robust purple Sarracenia that is free from diseases and insect pests as the mother plant, take its stem segment with terminal buds as the explant, remove the leaves and outer bracts, and set aside.
[0024] ②Disinfection of explants: On the ultra-clean workbench, put the stems with terminal buds into sterile empty bottles, use 0.1% mercury liter as the disinfectant, disinfect for 10 minutes, and then rinse with sterile water twice. The sterility rate was 71.4%.
[0025] ③Callus induction and adventitious bud differentiation: Insert the sterilized stem segment with terminal buds into the induction and differentiation medium; 1 stem segment / cup, 26±1°C, 300~1800lux culture, light 12h / d, 1 transfer per month. Differentiation medium: MS 改 +2.5mg / L 6-BA+0.05mg / LNAA+30g / L sucrose+5.5g / L agar, pH6.0. The terminal buds began to germinate after 20 days of cultivation, and after 30 days of cultivation, the terminal buds grew, and new shoots / le...
Embodiment 2
[0030] ① Selection of explants: Select a robust purple Sarracenia that is free from diseases and insect pests as the mother plant, take its stem segment with terminal buds as the explant, remove the leaves and outer bracts, and set aside.
[0031] ② Disinfection of explants: On the ultra-clean workbench, put the stems with terminal buds into sterile empty bottles, use 0.1% mercury liter as the disinfectant, disinfect for 8 minutes, and then rinse with sterile water for 3 times. The sterility rate was 76.3%.
[0032] ③Callus induction and adventitious bud differentiation: Insert the sterilized stem segment with terminal buds into the induction and differentiation medium; 1 stem segment / cup, 26±1°C, 300~1800lux culture, light 12h / d, 1 transfer per month. Differentiation medium: MS 改 +3mg / L 6-BA+0.1mg / LNAA+30g / L sucrose+5.5g / L agar, pH6.0. The terminal buds began to germinate after 22 days of cultivation, and after 30 days of cultivation, the terminal buds grew, and new shoots...
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