Method for tissue culture and rapid propagation of narcissus pseudonarcissus by using ramentum
A fast and narcissistic technology, applied in the field of agriculture, to achieve the effect of increasing the speed of reproduction, shortening the production cycle and saving costs
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Embodiment 1
[0056] European narcissus tissue culture and rapid propagation method are carried out in several steps in the following order:
[0057] 1. Selection and sterilization of explant parts: 2-year-old Narcissus bulbs were stored at 5°C for 40 days. Choose a bulb with a strong appearance, peel off the outermost layer of dry scales and residual old roots at the base at room temperature, soak it in washing powder water for 5 minutes as usual, rinse it with running water for 30 minutes, and then soak it in 70% (volume percentage) alcohol for 1 minute. After washing 4 times with sterile water, remove the upper 1 / 3 scale leaves, and then put 0.1% (mass percentage) HgCl 2 Soak in the solution for 10 minutes, and then rinse with sterile water 4 times as a spare material for primary culture. The treated bulbs are first removed from the bulb disk, and then the scales are cut into blocks of 10mm×10mm.
[0058] 2. Callus induction culture: Inoculate the lower part of the scales into the call...
Embodiment 2
[0065] This European narcissus tissue culture and rapid propagation method, except for the following distinguishing features, all the other steps and methods are the same as in Example 1.
[0066] The explants used in the first step are 2-year-old European narcissus bulbs, which have been treated at a low temperature of 9°C for 45 days, and the inner and lower scales of the bulbs are selected.
[0067] The callus induction medium in the second step is MS+6-BA 2.0mg L -1 +2,4-D 0.3mg L -1 + sucrose 30g / L+ agar 5.6g / L, pH 5.8, culture temperature 25°C, light time 12h / d, light intensity 1000lx, culture 30d, callus induction rate 98%.
[0068] Adventitious bud or bulblet differentiation medium in step 3 is MS+6-BA 2.0mg·L -1 +NAA0.2mg·L -1 + sucrose 30g / L+ agar 5.6g / L, pH 5.8, culture temperature 25°C, light intensity 2000lx, light time 12h / d, cultured for 35 days, the induced differentiation rate was 96%.
[0069] The subculture medium of step 4 is MS+6-BA 1.5mg L -1 +NAA0.3...
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