Detoxifying fast breeding technique for edible lily
A technology for eating lilies and lilies, applied in applications, plant cells, horticulture, etc., can solve the problems of affecting economic value, susceptibility to viruses, low reproduction coefficient, etc.
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Embodiment 1
[0025] A virus-free and rapid propagation technology for edible lily, which includes in sequence: taking edible lily micro-shoot tips, starting, and substituting strong seedlings to obtain virus-free lily tissue-cultured seedlings, and inducing regeneration of scales through strong seedlings , the regenerated scales induce clustered buds, the clustered buds are subcultured, and then the regenerated scales are induced after the strong seedlings, and the regenerated scales are then induced to induce adventitious buds, and the cycle is alternated to carry out batch propagation, wherein the virus-free lily group Seedling cultivation comprises the following steps:
[0026] The first step is to take edible lily bulbs and undergo sand culture for 7-10 days, peel off the outer scales, clean and disinfect, peel off the growth points under the dissecting microscope, and cut off the stem tips with a size of 0.1-0.2mm;
[0027] In the second step, the micro-shoot tips were inoculated and ...
Embodiment 2
[0032] A technology for detoxification and rapid propagation of edible lily. On the basis of Example 1, regenerating scales to induce adventitious buds, including in sequence: taking edible lily micro shoot tips, starting and substituting strong seedlings to obtain detoxified lily tissue culture After the seedlings are tested as virus-free, the regenerated scales are induced through the strong seedlings, and the regenerated scales are used to induce adventitious buds. Circulation, carry out batch propagation, wherein, described detoxification lily tissue culture seedling cultivation step comprises:
[0033] The first step is to take edible lily bulbs and undergo sand culture for 7-10 days, peel off the outer scales, clean and disinfect, peel off the growth point under the dissecting microscope, and cut off the stem tips with a size of 0.1-0.2mm as the starting point for propagation Material;
[0034] In the second step, the micro-shoot tips were inoculated on the starting med...
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