Culture medium for culturing lilium pumilum tissues
A technology of tissue culture and lily lily, applied in the field of plant biology, can solve the problems of limited reproduction number, disease infection quality, degradation, etc.
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Embodiment 1
[0016] Example 1. Materials and screening statistical methods of lily
[0017] The thin-leaf lily used in the experiment was collected from Daqingshan, a suburb of Hohhot, and the bulbs collected were planted in the company's experimental nursery. According to the progress of the experiment, samples were taken at different times and supplemented at any time. The explant is the bulb of lily.
[0018] Use MS as the basic medium, 3.5g / L carrageenan as the curing agent, 3% edible white sugar instead of sucrose as the carbon source, tap water instead of distilled water, and add different ratios of cytokinin and auxin for the medium. Of screening.
Embodiment 2
[0019] Example 2. Selection of the best culture medium for each stage of tissue culture of Lilium tenuiflora
[0020] 1. Selection of differentiation medium
[0021] Set the concentration of 6-BA to 0.2mg / L, 0.5mg / L, 1.0mg / L, and 2.0mg / L. The concentration of NAA is set to 0.1mg / L, 0.2mg / L, 0.3mg / L, Four concentration gradients of 0.5 mg / L were used in different combinations. One bulb was connected to each bottle during inoculation, and the occurrence of adventitious buds on different media was observed.
[0022] It can be seen from Table 1 that the 7 hormone combinations can induce lily scales to differentiate into small bulbs, but the differentiation rate of each combination is different. MS+6-BA 0.1mg / L+NAA 0.1mg / L is the thin-leaf lily scale medium It is the best induction medium. It not only has a high induction rate, but also has a large number of new buds per explant and the highest differentiation rate, which can reach 60.0%.
[0023] The specific statistical formula is:
[00...
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