In Vitro Rapid Propagation of Yulu Using Leaves as Explants
A technology of explants and leaves, applied in the fields of botanical equipment and methods, horticultural methods, plant regeneration, etc., can solve the problems that hinder the large-scale application of tissue culture in vitro rapid propagation, the low induction and differentiation rate of callus clump buds, and the inconvenience. With market-oriented production conditions and other problems, it can achieve the effects of low cost, good growth status, and short regeneration cycle.
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Embodiment 1
[0012]N1 Yulu leaves were selected as explants for rapid propagation in vitro.
[0013]1. Explant inoculation and callus induction: Take the young leaves of the N1 Yulu plant, put them in a sterile ultra-clean table, soak them in 75% (volume / volume) alcohol for 60s, and rinse them with sterile water for 2 to 3 times Then, quickly pour it into 3% (mass / volume) sodium hypochlorite solution and soak for 8 minutes, pour off the sodium hypochlorite solution, and rinse with sterile water for 4 to 5 times. Cut the treated Yulu leaves into approximately 1 cm sections; Containing 6-BA 0.5mg / L, NAA 0.1mg / L, KT 1mg / L, sucrose 3.0% (mass / volume), agar 6.0% (mass / volume), on MS solid medium with pH 5.8, light The intensity is 2000 Lux, the light time is 12 hours a day, the culture temperature is 25°C, and the subculture is performed once every 50 days. Differentiation can be induced when the yellow-green granular callus grows.
[0014]2. Induction of clump buds: transfer the callus to the differentiat...
Embodiment 2
[0017]Select OB1 Yulu leaves as explants for rapid propagation in vitro.
[0018]1. Explant inoculation and callus induction: Take the young leaves of OB1 Yulu plant, put them in a sterile ultra-clean table, soak in 75% (volume / volume) alcohol for 45s, and rinse with sterile water for 2 to 3 times Then, quickly pour it into 1.5% (mass / volume) sodium hypochlorite solution and soak for 10 minutes, pour off the sodium hypochlorite solution, and rinse with sterile water for 4 to 5 times. Cut the treated Yulu leaves into approximately 1 cm sections; Containing 6-BA 0.5mg / L, NAA 0.1mg / L, KT 1mg / L, sucrose 3.0% (mass / volume), agar 6.0% (mass / volume), on MS solid medium with pH 6.0, light The intensity is 1500 Lux, the light time is 14 hours a day, the culture temperature is 24 ℃, and the subculture is performed once every 50 days. Differentiation can be induced when the yellow-green granular callus grows.
[0019]2. Induction of clump buds: transfer the callus to the differentiation medium: MS+K...
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