Induction method for embryogenesis and plant regeneration of in vitro haploid of macleaya cordata anther
A technology of embryogenesis and regeneration, which is applied in the field of plant tissue culture, can solve the problem that the reproduction method cannot meet the market demand, and achieve the effect of low pollution rate and high callus induction rate
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Embodiment 1
[0031] (1) The preparation of the medium, including the basic medium and the components and proportions of the medium in each stage of tissue culture:
[0032] 1) Basic medium: There are two kinds of basic medium, BLCG and MS, in which 30g / L sucrose, 7g / L agar, and pH5.8 are added respectively;
[0033]2) Embryogenic callus medium: BLCG+2,4-D0.5mg / L+6-BA0.5mg / L;
[0034] 3) Embryoid body induction medium: MS+2,4-D0.5mg / L+6-BA0.5mg / L;
[0035] 4) Somatic embryo germination and seedling growth medium: MS+GA 3 0.5mg / L;
[0036] (2) Anther tissue somatic embryogenesis:
[0037] 1) Collection and disinfection of explants: Take the emerald-green bods that are in the full flowering stage, 2-12 mm in length, and fall back to the flower buds (the anther part where most of the microspore cells are in the single-nucleated marginal stage is observed under a microscope, see the attached figure 1 ), cleaned with distilled water, and rinsed with sterile water on an ultra-clean workbench;...
Embodiment 2
[0043] This embodiment adopts embryogenic callus culture medium: 2, 4-D takes 1.0, 1.5mg / L, 2.0, 2.5, 3.0mg / L respectively; the rest of the implementation steps are the same as in Example 1, all of which can achieve the results of Example 1. Effect.
Embodiment 3
[0045] This embodiment adopts embryoid body induction medium: 2, 4-D take 0.8, 1.0 mg / L respectively; the rest of the implementation steps and techniques are the same as in Example 1, and the effect of Example 1 can be achieved.
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