Rapid propagation method for calatheaveitchiana
An arrowroot and beautiful technology, which is applied in the field of rapid propagation of arrowroot, can solve the problems of difficult seed formation, long growth cycle of beautiful arrowroot, and difficulty in quickly multiplying finished products, and achieves improved reproductive efficiency and seedling survival rate. High and improve the effect of traditional system coefficient
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Embodiment 1
[0029] A method for fast breeding of beautiful arrowroot, comprising:
[0030] S11. Take the female parent of the beautiful arrowroot, tube culture after disinfection, take the side buds, peel off part of the leaf sheaths, soak them in alcohol after cleaning, then soak them in disinfectant solution for disinfection, take them out and clean them after a period of time, peel off part of the leaf sheaths, and soak them again until Disinfectant solution, after a period of time, take it out for cleaning, peel off the remaining leaf sheaths, and obtain explants;
[0031] S12. Inducing and culturing adventitious buds on the explants until obtaining adventitious bud seedlings;
[0032] S13. Take the adventitious bud seedlings, divide them into individual plants, remove the leaves, keep the stem section, carry out adventitious bud proliferation and culture on the stem section, until 2~3 adventitious bud seedlings re-grow from the stem section;
[0033] S14. Repeat S13 for a certain nu...
Embodiment 2
[0038] The difference between Example 2 and Example 1 is that in the step S11, the female parent of Arrowroot is taken and disinfected by irrigation with chlorothalonil solution, and the chlorothalonil solution is chlorothalonil: solvent=1:2000 The dilution solution; the tube culture is to transplant the female parent to a clean greenhouse for cultivation, the controlled environment temperature is 15~17°C, the humidity is 80~95%, and the light intensity is not more than 10000lux; the length of the side buds is 2~5cm , in the ultra-clean workbench, peel off part of the leaf sheath, keep the innermost 2~3 layers of clean leaf sheath, cut the incision flat with a scalpel, soak in clean water and detergent for 5 minutes, rinse with clean water, wash with 75% alcohol Soak for 30s, then immerse in 0.6% sodium hypochlorite solution for disinfection for 10-12 minutes, stir continuously during the disinfection process; take out the sterilized side buds and wash them with water, peel off...
Embodiment 3
[0040] The difference between Example 3 and Example 1 is that in the S12 step, when the explants are induced to cultivate adventitious buds, the ambient temperature is controlled at 25-26°C, the light duration is 10h / d, the light intensity is 2000-3000lux, and the culture is carried out for 60 ~80d.
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