A kind of method for tissue culture and rapid propagation of Lemonia dichotome
A kind of technology of two pieces of chicory, tissue culture, applied in the field of plant reproduction, can solve problems such as unreported
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Embodiment 1
[0017] a. Disinfection treatment of explants: Use the leaves of the wild Didymostigma obtusum (Clarke) W.T.Wang plant in Nankun Mountain, Shihe Wonderland Scenic Area, Guangdong Province as explants, rinse the explants with clean water first, and then use Mass fraction 1%NaClO solution was sterilized for 10 minutes, rinsed with sterile water 5 times, and the explants after disinfection were obtained;
[0018] b. Induction of the first generation of adventitious buds: inoculate the sterilized explants on the induction medium, and inoculate them at a temperature of 25±1°C and a light intensity of 50 μmol·m -2 ·s -1 , light time 12h·d -1 Under the condition of culturing for 30 days, the leaf explants were induced to form adventitious buds. The induction medium used was: TDZ2.0μmol, NAA0.2μmol, sucrose 30g, agar 5.5g per liter, and the rest was MS medium, pH 5.6, the induction coefficient is 44.6, and the induction medium per liter is prepared as follows: dissolve 2.0 μmol of TD...
Embodiment 2
[0024] a. Disinfection treatment of explants: Use the leaves of the wild Didymostigma obtusum (Clarke) W.T.Wang plant in Nankun Mountain, Shihe Wonderland Scenic Area, Guangdong Province as explants, rinse the explants with clean water first, and then use Mass fraction 1%NaClO solution was sterilized for 11 minutes, rinsed with sterile water 5 times, and the explants after disinfection were obtained;
[0025] b. Induction of the first generation of adventitious buds: inoculate the sterilized explants on the induction medium, and inoculate them at a temperature of 25±1°C and a light intensity of 50 μmol·m -2 ·s -1 , light time 12h·d -1 Under the condition of culturing for 30 days, the leaf explants were induced to form adventitious buds. The induction medium used was: each liter contained TDZ3. 5.6, each liter of induction medium is prepared as follows: dissolve 2.0 μmol of TDZ, 0.2 μmol of NAA, 30 g of sucrose, and 5.5 g of agar in 1L of MS medium, and sterilize at 121°C for...
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