Tissue culture method of Aralia Cordata Thunb seedlings
A tissue culture, soil angelica technology, applied in horticultural methods, botanical equipment and methods, applications, etc., can solve the problems of high cost and long production cycle, and achieve the effects of low cost, low production cost and easy operation.
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Embodiment 1
[0018] A method for tissue culture of edible soil angelica seedlings, comprising the steps of:
[0019] (1) Explant treatment: Take the leaves of Angelica sinensis as explants, wash off the dust on the surface with water, soak in 70% alcohol for 20-30s, rinse with sterile water 2-3 times, and then use 0.1% mercury chloride The solution was soaked and disinfected for 7-10 minutes, then rinsed with sterile water for 3-5 times, and finally dried the surface moisture of the explants with sterile filter paper;
[0020] (2) Primary culture of explants: Cut the treated explants into small pieces of 1.0 cm×1.0 cm with a scalpel and inoculate them in MS +TDZ0.1 mg / L+6-BA0.1 mg / L+ NAA0.5mg / L + sucrose 30g / L + agar 6.5g / L, cultured in medium with pH 5.8, culture temperature 25±2℃, light time 12h·d-1, light intensity 2000~3000lx, cut edge at 21d Start to induce clusters of small buds at the place, the induction rate is 100%, and the proliferation rate is counted after 50 days of cultivat...
Embodiment 2
[0024] A tissue culture method for edible soil angelica seedlings, including the method steps of embodiment 1, the difference is: the explants of the primary culture are inoculated in MS+TDZ0.1 mg / L+6-BA0.5mg / L+ NAA0.5mg / L + sucrose 30g / L + agar 6.5g / L medium. On the 13th day, a large number of small buds germinated on the edge of the leaves and on the surface of the explants, and the buds were scattered on the explants. The buds were strong and light green, and the induction rate was 66.7%. After culturing for 50 days, the proliferation rate was counted, and the number of seedlings induced by a single leaf was 35-50.
Embodiment 3
[0026] A tissue culture method for edible soil angelica seedlings, comprising the method steps of Example 1, the difference is that the explants of the primary culture are inoculated in MS+6-BA0.1mg / L+NAA0.05mg / L+sucrose 30g / L+ agar 6.5g / L medium. On the 19th day, small buds began to be induced at the edge of the incision, and the induction rate was 100%. After culturing for 50 days, the proliferation rate was counted, and the number of seedlings induced by a single leaf was 40-60.
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