A method for rapidly inducing regenerated plants from the true leaves of Australian soybean
A technology for regenerating plants and Australian soybeans, which is applied to the field of rapidly inducing regenerated plants from true leaves of Australian soybeans, can solve the problems of delayed production, high production costs, and no seeds, and achieves the effects of healthy differentiation buds, short differentiation time, and strong root systems.
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Embodiment 2
[0027] In this example, KT and IAA are used as the main auxin for callus induction differentiation and proliferation culture redifferentiation as controls, including the following steps:
[0028] 1. Disinfection of mature embryos: Select full-bodied Australian soybean seeds with intact seed coats, soak them in distilled water for 12 hours at room temperature, so that the seeds can fully absorb water and swell, remove the seed coats, and select complete seed embryos; on the ultra-clean workbench, Soak in 0.5% potassium permanganate solution for 6 minutes, rinse with sterile water 3 to 5 times, 3 minutes each time; then disinfect with 3.0% sodium hypochlorite solution for 8 minutes, rinse with sterile water 3 to 5 times, 5 minutes each time.
[0029] 2. Start culture: inoculate the mature embryos treated in step (1) into the start medium N 6 Cultured for 15-20 days. The sucrose in the medium is 30 g / L, the agar is 6 g / L, and the pH value is 5.8-5.9. During this period, the cul...
Embodiment 3
[0038] In this example, 1 / 2 N 6 No N spraying for rooting medium and transplanting 6 The macroelement mother solution is used as a contrast, comprising the following steps:
[0039] 1. Disinfection of mature embryos: Select full-bodied Australian soybean seeds with intact seed coats, soak them in distilled water for 12 hours at room temperature, so that the seeds can fully absorb water and swell, remove the seed coats, and select complete seed embryos; on the ultra-clean workbench, Soak in 0.5% potassium permanganate solution for 6 minutes, rinse with sterile water 3 to 5 times, 3 minutes each time; then disinfect with 3.0% sodium hypochlorite solution for 8 minutes, rinse with sterile water 3 to 5 times, 5 minutes each time.
[0040] 2. Start culture: inoculate the mature embryos treated in step (1) into the start medium N 6 Cultured for 15-20 days. The sucrose in the medium is 30 g / L, the agar is 6 g / L, and the pH value is 5.8-5.9. During this period, the culture tempera...
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