Culture medium for culturing lilium pumilum tissues
A tissue culture, lily lily technology, applied in the field of plant biology, can solve the problems of disease infection quality, degradation, limited reproduction number, etc.
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Embodiment 1
[0016] The material of embodiment 1. Lilium tenifolia and screening statistical method
[0017] The lily lily used in the experiment was collected from Daqingshan, a suburb of Hohhot, and the collected bulbs were planted in the experimental nursery of our company. Samples were taken according to the progress of the experiment, at different periods, and supplemented at any time. The explants are the bulbs of Lilium microphylla.
[0018] Using MS as the basic medium, using 3.5g / L carrageenan as the solidifying agent, 3% edible sugar instead of sucrose as the carbon source, tap water instead of distilled water, and adding different ratios of cytokinin and auxin to the culture medium filter.
Embodiment 2
[0019] Example 2. Screening of the optimal medium for each stage of Lilium microphylla tissue culture
[0020] 1. Selection of induction differentiation medium
[0021] Set the concentration of 6-BA to five concentration gradients of 0.2mg / L, 0.5mg / L, 1.0mg / L, and 2.0mg / L, and set the concentration of NAA to 0.1mg / L, 0.2mg / L, 0.3mg / L, Four concentration gradients of 0.5mg / L were used in different combinations. When inoculating, each bottle was inoculated with a piece of bulb, and the occurrence of adventitious buds of the scale on different media was observed.
[0022] It can be seen from Table 1 that all seven hormone combinations can induce lily scales to differentiate into small bulbs, but the differentiation rates of each combination are different. No. 1 MS+6-BA 0.1mg / L+NAA 0.1mg / L is the medium for lily scales It is the best induction medium, not only has a high induction rate, but also has a large number of new shoots per explant and the highest differentiation rate, wh...
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