Detoxication and tissue culture rapid propagation method of chewing cane axillary buds
A technology of tissue culture rapid propagation and fruit cane, applied in horticultural methods, botanical equipment and methods, horticulture, etc., can solve the problems of pollution, incomplete virus removal, low survival rate, etc., and achieve high survival rate and fast speed , The effect of easy inoculation operation
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Embodiment 1
[0024] A method for detoxifying tissue culture and rapid propagation of fruit cane is carried out as follows:
[0025] 1) Selection and sterilization of explants: From July to November, take the axillary buds of fruit cane, soak them in 75% alcohol for 0.5 to 1.0 minutes, then treat them with 0.1% mercury solution for 3 to 4 minutes, then rinse with sterile water for 3 ~5 times.
[0026] 2) Axillary bud induction culture: The axillary buds treated in step 1) are harvested under aseptic conditions, 2~3mm axillary buds are picked, the leaf sheaths are carefully removed, and the axillary bud induction medium (MS+6-BA 0.5mg / L+ IBA 0.02mg / L+activated carbon 1g / L+sucrose 30g / L+arginine 100mg / L+inositol 100mg / L+agar 5g / L) to induce bud formation.
[0027] 3) Differentiation culture: transfer the induced buds formed in step 2) to differentiation medium (MS+TDZ 0.003mg / L+IBA 0.02mg / L+sucrose 30g / L+arginine 100mg / L+ inositol 100mg / L+agar 5g / L) cluster buds are induced.
[0028] 4) Proliferat...
Embodiment 2
[0034] A method for detoxifying tissue culture and rapid propagation of fruit cane is carried out as follows:
[0035] 1) Selection and sterilization of implants: From July to November, take the axillary buds of fruit cane, soak them in 75% alcohol for 0.5 to 1.0 minutes, then treat them with 0.1% mercury solution for 3 to 4 minutes, then rinse with sterile water for 3 ~5 times.
[0036] 2) Axillary bud induction culture: the axillary buds treated in step 1) are harvested under aseptic conditions, 2~3mm axillary buds are picked, the leaf sheaths are carefully removed, and the axillary bud induction medium (MS+6-BA 0.8mg / L+IBA 0.04mg / L+active charcoal 1.8g / L+arginine 150mg / L+inositol 130mg / L) to induce bud formation.
[0037] 3) Differentiation culture: transfer the induced buds formed in step 2) to differentiation medium (MS+TDZ 0.008mg / L+IBA0.04mg / L+sucrose 35g / L+arginine 120mg / L+inositol 130mg / L) , Induce clump buds.
[0038] 4) Proliferation culture: cut the clump buds formed in ...
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