Tissue culture method of tissue culture seedling of moringa oleifera
A technology for tissue culture and tissue culture seedlings, applied in horticultural methods, botany equipment and methods, horticulture, etc., can solve the problems of yellowing and easy breaking of seedlings, and achieve the goal of improving the degree of lignification, shortening the cycle, and saving costs Effect
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Embodiment 1
[0036] A tissue culture rapid propagation method of Moringa, comprising the following steps:
[0037] (1) Experimental material must be selected: the Moringa oleifera tissue culture seedlings whose growth is neat, plant height is 3.5-4.5cm, subculture cycle is 21-25 days, leaf color is green or tender green are selected as culture material;
[0038] (2) Specific experimental steps:
[0039] (2.1) Cutting of the material: remove the leaves, keep the top buds and heart leaves, leave the petiole 0.1-0.2 cm, cut into 0.5-0.8 cm stem segments, each segment with 1-2 axillary buds;
[0040] (2.2) subculture of Moringa oleifera; terminal buds and stem sections are inoculated separately, and evenly inoculated into No. 8 subculture medium (LM-8);
[0041] Among them, the improved MS (KNO 3 0.95-1.43g / L, NH 4 NO 3 0.81-1.24g / L, MgSO 4 ·7H 2 O 0.19-0.28g / L, KH 2 PO 4 0.09-0.13g / L, CaCl 2 2H 2 O 0.22-0.44g / L, Na 2 EDTA·2H 2 O0.002-0.04g / L, FeSO 4 ·7H 2 O 0.015-0.03g / L, MnSO ...
Embodiment 2
[0048] A tissue culture rapid propagation method of Moringa, comprising the following steps:
[0049] (1) Experimental material must be selected: the Moringa oleifera tissue culture seedlings whose growth is neat, plant height is 3.5-4.5cm, subculture cycle is 21-25 days, leaf color is green or tender green are selected as culture material;
[0050] (2) Specific experimental steps:
[0051] (2.1) Cutting of the material: remove the leaves, keep the top buds and heart leaves, leave the petiole 0.1-0.2 cm, cut into 0.5-0.8 cm stem segments, each segment with 1-2 axillary buds;
[0052] (2.2) subculture of Moringa oleifera; terminal buds and stem sections are inoculated separately, and evenly inoculated into No. 8 subculture medium (LM-8);
[0053] Among them, step (2.2) improved MS (KNO 3 0.95-1.43g / L, NH 4 NO 3 0.81-1.24g / L, MgSO 4 ·7H 2 O 0.19-0.28g / L, KH 2 PO 4 0.09-0.13g / L, CaCl 2 2H 2 O 0.22-0.44g / L, Na 2 EDTA·2H 2 O 0.002-0.04g / L, FeSO 4 ·7H 2 O 0.015-0.03g...
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