Method for rapid propagation of pelargonium by means of tissue culture
A tissue culture and geranium technology, applied in the field of plant tissue culture, can solve the problems such as the limitation of the number and speed of reproduction, and achieve the effect of maintaining the advantage of the strain, increasing the number and speed, and reducing the size
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Embodiment 1
[0036] A tissue culture rapid propagation method of Pelargonium, the steps are:
[0037] (1) Selection and disinfection of explants
[0038] Select young geranium leaves with a clean surface as explants, first soak them in 75% ethanol for 1 min, then sterilize them with sodium hypochlorite solution containing 5% available chlorine on a clean bench for 5 min, and finally rinse them with sterile water for 5 min. times, 1 min each time, to obtain sterile explants;
[0039] callus induction
[0040] Cut the sterile explant in step (1) into 0.5*0.5cm pieces, remove the leaf edge and veins, first cut a wound on the back of the leaf (the length of the wound on the back of the leaf is 0.4-0.55cm, and the wound should avoid the veins position, do not cut through, and keep the upper surface of the leaf intact), then inoculate the back of the leaf on the callus induction medium downward, and culture in the dark at 25°C for one week, then follow the cycle of "light culture 16h-dark c...
Embodiment 2
[0049] A tissue culture rapid propagation method of geranium, the difference from Example 1 lies in: step (2) callus induction: two wounds crossing 60 degrees are cut at the center position of the back of the leaf.
Embodiment 3
[0051] A tissue culture rapid propagation method of geranium, which is different from Example 1 in that: step (3) induces the differentiation medium to obtain plants, and after the young shoots are differentiated, continue to culture for 3 to 4 weeks: the culture process is specifically: According to the cycle of "light culture 12h-dark culture 12h", continue to culture at 18-25℃ for another 2-3 weeks, and then follow the cycle of "light culture 16h-dark culture 8h", continue to culture at 22-25℃ 1 to 2 weeks.
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