In-vitro culture and planting regeneration and propagation method of Xianglei honeysuckle leaves and culture medium
A technology for in vitro culture and rooting medium, which is applied in the field of in vitro culture of Xianglei honeysuckle leaves, plant regeneration and propagation methods and medium, can solve the problems of less rooting, low proliferation coefficient and high cost of plants, and achieves seedling growth. Robust, high multiplication factor, cost-saving effect
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Embodiment 1
[0015] Induction of leaf callus:
[0016] Select the young leaves or adult leaves on the healthy plants of Xianglei honeysuckle, soak them in 75% alcohol for 30 seconds, then disinfect them with 2% NaClO for 6 minutes, rinse them with sterile water for 3 times, and put the leaves on the ultra-clean workbench cut into 1cm 2 A small piece was inoculated into the medium composition B 5 +6-BA 1.0mg / L+NAA 0.1mg / L+3% sucrose in callus induction medium for 30-40 days;
[0017] Differentiation of callus:
[0018] Transfer the induced callus to medium composition B 5 +6-BA 1.5mg / L+NAA 0.1mg / L+3% sucrose in the differentiation medium for 1 to 2 months to get clustered buds;
[0019] Strong seedling cultivation:
[0020] Separate the dense clustered buds and transfer them to hormone-free 1 / 2MS strong seedling medium for 1-2 weeks;
[0021] Rooting culture:
[0022] Transfer the rootless strong seedlings to the rooting medium whose medium composition is 1 / 4MS+NAA0.2mg / L+IBA0.4mg / L+...
Embodiment 2
[0023] Embodiment 2 Comparison experiment of the effect of Xianglei honeysuckle leaf in vitro culture and plant regeneration and multiplication method of the present invention and prior art
[0024] Under the premise that other conditions are consistent, the method of the present invention is compared with the in vitro culture method in the prior art, and the experimental parameters and results are as shown in Table 1:
[0025] Table 1
[0026]
[0027] As can be seen from Table 1, compared with the existing Xianglei honeysuckle in vitro tissue culture technology, using the method and medium of the present invention to carry out in vitro culture and regeneration of Xianglei honeysuckle, the proliferation coefficient is high, and the callus The differentiation rate reaches 70% to 80%; 11-13 rootless seedlings take root after 20-25 days of rooting culture, which takes a short time and the seedlings grow robustly, and the concentrations of hormones, sugars, and MS mother liquo...
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