Method for propagating stonegarlic quickly and efficiently
A fast technology for Lycoris safflower, applied in the field of artificial propagation and cultivation of plants, can solve the degradation of Lycoris safflower bulbs, restrict the breeding process of Lycoris safflower, affect the resistance of Lycoris safflower and the quality of bulbs, etc. problems, to achieve the effects of saving seedling area, reducing production costs, and stabilizing genetic traits
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example 1
[0021] Induction and cultivation of example 1 adventitious buds
[0022] 1. Take the underground bulb of Lycoris safflower, peel off the outer scales, cut off the root, and cut off about 1 / 2 to 2 / 3 of the upper half of the bulb. Divide the bulbs with bulb discs into 4-8 pieces, shake and wash with 0.1% Amway washing liquid on the shaker for 15-20 minutes, rinse with running water for 60 minutes, and then rinse with 75% alcohol on the ultra-clean workbench for 30 seconds After washing with sterile water for 4 times, disinfect with 1% sodium hypochlorite solution for 20-30 minutes (add a few drops of Tween 80 to the sodium hypochlorite solution), rinse with sterile water for 4-5 times, and finally dry the surface of the seeds with sterile filter paper moisture.
[0023] 2. Inoculate the small pieces of sterilized Lycoris safflower bulbs directly into the adventitious bud induction medium: add in the MS basic medium, 3.0 mg / L of 6-benzyl adenine (6-BA), naphthalene acetic acid (...
example 2
[0024] Rooting, transplanting of induction of example 2 clustering buds and test-tube plantlets
[0025] 1. After cultivating for 30 days, when the sprouts grow to 2-3cm, the sprouts are reinoculated into the clump bud proliferation medium of the present invention, and the proliferation culture is carried out. The cluster bud induction medium is based on the MS medium as the basic medium, and adds 5.0 mg / L of the plant growth hormone 6-benzyl adenine (6-BA), 2,4-dichlorophenoxyacetic acid (2,4- D) 1.0mg / L, naphthaleneacetic acid (NAA) 0.5mg / L, sucrose 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 7-8 clustered buds.
[0026] 2. Choose robust test-tube plantlets, then inoculate them on 1 / 2 MS basic medium, indole butyric acid (IBA) 1.0mg / L, sucrose 60g / L, and carry out rooting induction. After 40 days of cultivation, the rooting rate reached 86%, and the average root number rea...
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