In-vitro rapid propagation method of double-petal Jasminum sambac
A jasmine and in vitro technology, applied in the field of artificial propagation and cultivation of plants, can solve the problems of weakening plant vigor, carrying viruses, restricting the breeding process of jasmine, etc., and achieves the effects of reducing production costs, stabilizing hereditary traits, and saving the land occupied by seedlings.
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Embodiment 1
[0029] Induction and cultivation of embodiment 1 axillary buds
[0030] 1. Take the young stems of double-lobe jasmine, shake and wash them with 0.1% Amway washing liquid on a shaker for 15-20 minutes, rinse them with running water for 60 minutes, and then rinse them with 75% alcohol for 30 seconds on an ultra-clean workbench. After washing 4 times with water, wash with 0.1% HgCl 2 Sterilize for 50-60 minutes (add a few drops of Tween 80 to mercuric chloride), rinse with sterile water for 4-5 times, and finally dry the water on the surface of the seeds with sterile filter paper.
[0031] 2. Inoculate the sterilized double-lobe jasmine stems directly into the axillary bud induction medium: add 30 g / L sucrose (edible sugar) to the basic medium of WPM, appropriate pH value; culture temperature 28 ± 1 ° C, light intensity 1000 ~3000lx, light time 10~16h, carry out light cultivation.
[0032] 3. Cultivate the stem tips of aseptic seedlings for about 20 days after the germination ...
Embodiment 2
[0033] Rooting, transplanting of induction of embodiment 2 clustering buds and test-tube plantlets
[0034] 1. After culturing for 30 days, wait for the sprouts to grow to 6-8 cm, re-inoculate the sprouts into the cluster bud induction medium of the present invention, and carry out proliferation culture. Cluster bud induction medium is to take WPM medium as basic medium, and add plant growth hormone ZT1mg / L and IBA0.5mg / L, sucrose (edible sugar) 30g / L, carry out proliferation culture. After culturing for more than 30 days, the induction rate reaches 98%, and most of the sprouts can induce clustered buds to reach 3-5.
[0035] 2. Select the test-tube seedlings that grow robustly, soak them in a sterilized solution containing NAA450mg / L for 10min, then inoculate them on 1 / 2MS basic medium, and use 15g / L sucrose (edible sugar) to induce rooting . After 40 days of cultivation, the rooting rate reached 86%, and the average root number reached 18.5.
[0036] 3. After rooting and ...
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