Chinese gooseberry stem tip detoxification and rapid propagation method
A technology for detoxification of kiwifruit stem tips, applied in horticultural methods, botanical equipment and methods, horticulture, etc., can solve the problems of no detoxification of kiwifruit stem tips, low reproduction coefficient, inability to meet rapid reproduction, etc. Survival after planting, improve reproduction coefficient, and meet the effect of rapid reproduction
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Embodiment 1
[0022] (1) material selection: screen strong Hongyang kiwifruit plants from the kiwifruit orchard in March, mark them well, cut the 1-2cm long terminal buds, and set them aside;
[0023] (2) Disinfection of materials: first rinse with running water under tap water for 2 hours, cut off the fully expanded leaves, then soak them in 75% ethanol for 20 seconds under a sterile operating table, rinse them with sterile water, and then use 0.1% HgCl 2 Soak for 5 minutes, then rinse 4 times with sterile water;
[0024] (3) Peel off the shoot tip: use the shoot tip with 1-2 leaf primordia aseptically stripped from the terminal bud obtained in (2) under a dissecting microscope as an explant, the shoot tip size is 0.15-0.3mm, and the shape is a protrusion State, put the shoot tip into the medium (MS+6-BA1mg / L+GA 3 0.1mg / L, agar 6g / L, sucrose 25g / L, pH5.8) for inoculation and culture, the culture conditions are temperature 25-27°C, light intensity 1500Lux, and the number of light hours per...
Embodiment 2
[0028] (1) material selection: screen strong Hongyang kiwifruit plants from the kiwifruit orchard in March, mark them well, cut the 1-2cm long terminal buds, and set them aside;
[0029] (2) Material disinfection: first rinse with running water under tap water for 2 hours, cut off the fully expanded leaves, then soak them in 75% ethanol for 30 seconds under a sterile operating table, rinse them with sterile water, and then use 0.1% HgCl 2 Soak for 6 minutes, then rinse 6 times with sterile water;
[0030] (3) Peel off the shoot tip: use the shoot tip with 1-2 leaf primordia aseptically stripped from the terminal bud obtained in (2) under a dissecting microscope as an explant, the shoot tip size is 0.15-0.3mm, and the shape is a protrusion State, put the shoot tip into the culture medium (MS+6-BA3mg / L+GA 3 0.3mg / L, agar 6g / L, sucrose 25g / L, pH5.8) for inoculation culture, the culture conditions are temperature 25-27 ℃, light intensity is 2000Lux, and the number of light hours ...
Embodiment 3
[0034] (1) material selection: screen strong Hongyang kiwifruit plants from the kiwifruit orchard in March, mark them well, cut the 1-2cm long terminal buds, and set them aside;
[0035] (2) Material disinfection: first rinse with running water under tap water for 2 hours, cut off the fully expanded leaves, then soak them in 75% ethanol for 25 seconds under a sterile operating table, rinse them with sterile water, and then use 0.1% HgCl 2 Soak for 5.5min, then rinse 5 times with sterile water;
[0036] (3) Peel off the shoot tip: use the shoot tip with 1-2 leaf primordia aseptically stripped from the terminal bud obtained in (2) under a dissecting microscope as an explant, the shoot tip size is 0.15-0.3mm, and the shape is a protrusion State, put the shoot tip into the culture medium (MS+6-BA2mg / L+GA 3 0.2mg / L, agar 6g / L, sucrose 25g / L, pH 5.8) for inoculation and culture, the culture conditions are temperature 25-27°C, light intensity 1800Lux, and the number of light hours p...
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