Method for improving tissue culture multiplication effect of sweetgum and culture medium
A technology of subculture multiplication and multiplication cultivation, applied in horticultural methods, botanical equipment and methods, horticulture, etc., can solve the problems of long tissue culture seedling cultivation cycle, low survival rate of old tree spikes, high cost of seedlings, etc., and achieve shortening Subculture proliferation culture cycle, improve the effect of subculture proliferation, improve the effect of material utilization
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Embodiment 1
[0032] (1) Initial bud induction culture: Select a good single plant with good plant type, stable discoloration, good discoloration effect, and no pests in the forest of Liquidambar sweetgum, carry out pile cutting or circumcision to promote germination in the previous year, collect the year's growth, and grow to Germination strips of 35-40 cm were used as explants, which were inoculated into the first-generation induction medium modified B5+6-BA 2.5mg·L after routine disinfection -1 +NAA 0.5mg·L -1 + sucrose 30g·L -1 + Agar 4.5g·L -1 The initial buds were induced, and the induction rate was 91.2%;
[0033] (2) Proliferation medium: two kinds of medium were prepared for the proliferation of shoots, and the medium for subculture ① was formulated with improved B5+BA 1.0mg·L -1 +NAA 0.1mg·L -1 +PVP 3.0g·L -1 + sucrose 30g·L -1 + Agar 4.5g·L -1 ; The formula of subculture proliferation medium ② adopts improved B5+KT 2.0mg·L -1 +NAA 0.01mg·L -1 +IBA 0.5mg·L -1 +PVP3.0g·L ...
Embodiment 2
[0036] (1) Initial bud induction culture: Select a good single plant with good plant type, stable discoloration, good discoloration effect, and no pests in the forest of Liquidambar sweetgum, carry out pile cutting or circumcision to promote germination in the previous year, collect the year's growth, and grow to Germination strips of 30-35 cm are used as explants, and after routine disinfection, they are inoculated into the first-generation induction medium modified B5+6-BA 2.5 mg·L -1 +NAA 0.5mg·L -1 + sucrose 30g·L -1 + Agar 4.5g·L -1 The initial buds were induced, and the induction rate was 90.7%.
[0037] (2) Proliferation medium: two kinds of medium were prepared for the proliferation of shoots, and the medium for subculture ① was formulated with improved B5+BA 2.0mg·L -1 +NAA 0.18mg·L -1 +PVP 6.0g·L -1 + sucrose 30g·L -1 + Agar 4.5g·L -1 ; Subculture proliferation medium ② formula adopts improved B5+KT 3.0mg·L -1 +NAA 0.01mg·L -1 +IBA 0.5mg·L -1 +PVP 3.0g·L -...
Embodiment 3
[0040] (1) Initial bud induction culture: Select a good single plant with good plant type, stable discoloration, good discoloration effect, and no pests in the forest of Liquidambar sweetgum, carry out pile cutting or circumcision to promote germination in the previous year, collect the year's growth, and grow to Germination strips of 30-40 cm were used as explants, and after routine disinfection, they were inoculated into the first-generation induction medium to improve B5+6-BA 2.5 mg·L -1 +NAA 0.5mg·L -1 + sucrose 30g·L -1 + Agar 4.5g·L -1 The initial buds were induced, and the induction rate was 91.5%.
[0041] (2) Subculture proliferation medium: prepare 2 kinds of subculture proliferation medium for subculture bud proliferation culture, subculture proliferation medium ① formula adopts improved B5+BA2.0mg·L -1 +NAA0.16mg·L -1 +PVP 3.0g·L -1 + sucrose 30g·L -1 + Agar 4.5g·L -1 ; Subculture Proliferation Medium ② formula adopts improved B5+KT 2.5mg L -1 +NAA0.01mg·L ...
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