Subculture method of Cornus walteri Wanger. tissue culture seedlings
A technology of subculture and tissue culture seedlings, which is applied in the field of plant tissue culture, can solve the problems of slow elongation, no high branches, and low multiplication coefficient, and achieve the goal of promoting internode elongation, increasing multiplication coefficient, and stabilizing multiplication coefficient Effect
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Embodiment 1
[0016] The subculture method of a kind of hairy tissue culture seedling of the present invention, comprises the following steps:
[0017] (1) Proliferation culture: Cut the aseptic tissue-cultured seedlings of Trichosanthemi that meet the subculture requirements, cut the bud clusters <1cm into small clusters on the ultra-clean workbench and inoculate them in DKW+6-BA 0.25mg / L+IBA0. In the proliferation medium of 1mg / L + sucrose 30g / L + agar powder 6.5g / L, the culture condition is 25°C, the light intensity is 1800lx, and the light is 14h per day. After one subculture proliferation cycle, clustered buds are formed, with an average proliferation coefficient of 10.27 ;
[0018] (2) Elongation culture: cut the sterile tissue cultured shoots of the hairy tree that meet the subculture requirements, and cut the strong bud branches ≥ 1 cm in the tissue cultured seedlings into ≥ 0.5 cm and containing at least one pair of buds on the ultra-clean workbench. Stem section, inoculated in DK...
Embodiment 2
[0020] The subculture method of a kind of hairy tissue culture seedling of the present invention, comprises the following steps:
[0021] (1) Proliferation culture: Cut the aseptic tissue-cultured seedlings of Trichosanthes spp. that meet the subculture requirements, cut the bud clusters <1cm into small clusters on the ultra-clean workbench and inoculate them in DKW+6-BA1mg / L+IBA0.5mg / In the proliferation medium of L + sucrose 30g / L + agar powder 6.5g / L, the culture condition is 25°C, the light intensity is 2000lx, and the light is 14h per day. After 2 subculture proliferation cycles, clustered buds are formed, with an average proliferation coefficient of 12.33;
[0022] (2) Elongation culture: cut the sterile tissue cultured shoots of the hairy tree that meet the subculture requirements, and cut the strong bud branches ≥ 1 cm in the tissue cultured seedlings into ≥ 0.5 cm and containing at least one pair of buds on the ultra-clean workbench. Stem section, inoculated in DKW+6...
Embodiment 3
[0024] The subculture method of a kind of hairy tissue culture seedling of the present invention, comprises the following steps:
[0025] (1) Proliferation culture: cut the aseptic tissue-cultured seedlings of Trichosanthemi that meet the subculture requirements, cut the bud clusters <1cm into small clusters or single buds on the ultra-clean workbench and inoculate them in DKW+6-BA 0.5mg / L In the proliferation medium of +IBA0.8mg / L+sucrose 30g / L+agar powder 6.5g / L, the culture condition is 25℃, the light intensity is 1800lx, and the light is 14h per day. Proliferation coefficient 14.18;
[0026] (2) Elongation culture: cut the sterile tissue cultured shoots of the hairy tree that meet the subculture requirements, and cut the strong bud branches ≥ 1 cm in the tissue cultured seedlings into ≥ 0.5 cm and containing at least one pair of buds on the ultra-clean workbench. Stem section, inoculated in DKW+6-BA1mg / L+NAA0.5mg / L+GA 3 In the elongation medium of 1mg / L+sucrose 30g / L+aga...
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