Tissue-culture fast propagation method of musella lasiocarpa plant
A technology for tissue culture, rapid propagation and ground gushing golden lotus, applied in the field of plant tissue culture, can solve the problems of limited number of sucking buds, difficult to clean and sterilize, difficult to obtain materials, etc., and achieve the effects of convenient disinfection and sterilization, and easy to obtain materials.
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Embodiment 1
[0035] A, callus induction: take the inflorescences of Trollus chinensis that are about to open in the field, peel off the outer bracts, soak them in a sodium hypochlorite solution with a mass concentration of 2% on the ultra-clean workbench for 5 minutes, and rinse them with sterile water for 3 times , then soaked in mercuric chloride solution with a mass concentration of 0.1% for 20 minutes, rinsed with sterile water for 4 times, blotted the surface moisture with sterile filter paper, and then inserted into callus induction medium: modified MS, 1.0mg L -1 6-BA, 6.0mg·L -1 NAA, 20.0g·L -1 Sucrose, cultured in the dark at 25°C for 30 days, induced callus, and the callus induction rate was 64.0%;
[0036] B. Callus adventitious bud differentiation: inoculate the callus induced in step A in the callus adventitious bud differentiation medium: modified MS, 30.0g L -1 Sucrose, at a culture temperature of 25°C and a light time of 12h·d -1 , with an illumination intensity of 40 μm...
Embodiment 2
[0041] A, callus induction: get the nasturtium inflorescence that is just about to open in the field, peel off the outer bracts, soak it with 0.2% sodium hypochlorite solution for 15 minutes on the ultra-clean workbench, rinse it with sterile water for 5 times, and then use Soak in 1% mercuric chloride solution for 5 minutes, rinse with sterile water 8 times, blot the surface moisture with sterile filter paper, insert into callus induction medium: modified MS, 2.0mg L -1 6-B A, 3.0mg·L -1 NAA, 30.0g·L -1 Sucrose, cultivated in the dark at 20°C for 50 days, induced callus, and the callus induction was 76.0%;
[0042] B. Callus adventitious bud differentiation: inoculate the callus induced in step A in the callus adventitious bud differentiation medium: modified MS, 2.0mg L -1 6-BA, 0.02mg·L -1 NAA, 20.0g·L -1 Sucrose, at a culture temperature of 20°C and a light time of 8h·d -1 , with a light intensity of 30 μmol m -2 ·s -1 Under the condition of culturing for 40 days, t...
Embodiment 3
[0047] A, callus induction: take the nasturtium inflorescences that are just about to open in the field, peel off the outer bracts, soak them in 1% sodium hypochlorite solution for 10 minutes on the ultra-clean workbench, rinse them with sterile water 4 times, and then use Soak in 0.5% mercuric chloride solution for 15 minutes, rinse with sterile water 6 times, blot the surface moisture with sterile filter paper, insert into callus induction medium: modified MS, 6.0 mg L -1 6-BA, 1.0mg·L -1 NAA, 40.0g·L -1 Sucrose, cultured in the dark at 30°C for 40 days, induced callus, and the callus induction rate was 30.0%.
[0048] B. Callus Adventitious Bud Differentiation: Inoculate the above-mentioned induced callus in callus adventitious bud differentiation medium: modified MS, 3.0mg·L -1 6-BA, 0.04mg·L -1 NAA, 40.0g·L -1 Sucrose, at a culture temperature of 30°C and a light time of 10h·d -1 , with an illumination intensity of 50 μmol m -2 ·s -1 Under the condition of culturin...
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