Strawberry detoxification tissue culture method under LED condition
A tissue culture and strawberry technology, which is applied in the field of strawberry detoxification tissue culture under LED conditions, can solve the problems of high heat generation, short life of fluorescent tubes, unsatisfactory luminous efficiency, etc., and achieve the effect of improving efficiency and reducing costs
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Embodiment 1
[0043] A method for detoxifying tissue culture of strawberries under LED conditions, carried out as follows:
[0044] 1), the selection of culture conditions, with LED (light-emitting diode) as tissue culture light source, the ratio of red light (630 ± 20nm) and blue light (460 ± 20nm) in LED is 2~5:1~2, and light intensity 1500~2000Lx, the light time is 12~16h / d, and the culture temperature is 25±2℃.
[0045] 2), the preparation of culture medium, including each component of basic culture medium and culture medium of each stage of tissue culture and the contained weight per liter are:
[0046](1) Basic medium: MS basic medium for induction, proliferation, and seedling growth medium; 1 / 2 MS basic medium for rooting medium; among them, sucrose or white sugar 20-40g / L, agar 7-9g / L, pH 5.6~5.8;
[0047] (2) Induction medium: MS+BA0.1~2.0mg / L+NAA0.01~0.5mg / L;
[0048] (3) Proliferation medium: MS+BA0.1~2.0mg / L+NAA0.01~0.5mg / L;
[0049] (4) Strong seedling medium: MS+BA0.1~1.0m...
Embodiment 2
[0070] In this example, LED (light emitting diode) was used as the light source for tissue culture, the ratio of red light and blue light in LED was 3:1, the light intensity was 2000Lx, the light time was 16h / d, and the culture temperature was 25±2°C. Induction medium: MS+BA1.0mg / L+NAA0.2mg / L; Proliferation medium: MS+BA 0.5mg / L+NAA 0.1mg / L; Strong seedling medium: MS+BA 0.1mg / L+NAA0 .05mg / L; rooting medium: 1 / 2MS+IBA 0.5mg / L.
[0071] All the other steps, technique, condition are all the same as embodiment 1.
Embodiment 3
[0073] In this example, LED (light emitting diode) was used as the light source for tissue culture, the ratio of red light and blue light in LED was 2:1, the light intensity was 1500Lx, the light time was 16h / d, and the culture temperature was 25±2°C. Induction medium: MS+BA1.0mg / L+NAA0.2mg / L; Proliferation medium: MS+BA 0.5mg / L+NAA 0.1mg / L; Strong seedling medium: MS+BA 0.1mg / L+NAA0 .05mg / L; rooting medium: 1 / 2MS+IBA 0.5mg / L.
[0074] All the other steps, technique, condition are all the same as embodiment 1.
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