Fast reproduction of European wild black cherry tissue
A technology for tissue culture rapid propagation and black cherry, which is applied in horticultural methods, botanical equipment and methods, cultivation and other directions, can solve problems such as inability to achieve large-scale industrial production, yellowing, and difficulty in woody plants, and achieve good economical results. Socio-ecological benefits, increased market share, consistent effects of genetic traits
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Embodiment 1
[0030] Embodiment 1: this European black cherry wood tissue culture rapid propagation method, concrete steps are as follows:
[0031] 1), selection and sterilization of explants: cut semi-lignified shoots of potted wild black cherry seedlings, cut off the terminal buds and stems with axillary buds, and soak the explants in 75% alcohol for 0.5-10 minutes , sterilized with 2% sodium hypochlorite aqueous solution by volume for 10-15 minutes, and then rinsed with sterile water for 3-5 times. After surface sterilization, it was used as explants for tissue culture.
[0032] 2), induction culture: under aseptic conditions, after the explant terminal bud and the stem section with axillary buds after surface sterilization are removed, the terminal buds and the buds of the stem section with axillary buds are cut off. Inoculate upward on the induction medium of MS+BA0.25~1.0mg / L+NAA0.05~0.5mg / L to induce terminal buds and axillary buds to sprout, and then differentiate into cluster buds...
Embodiment 2
[0037] Embodiment 2: this European black cherry wood tissue culture rapid propagation method, concrete steps are as follows:
[0038] 1), selection and sterilization of explants: cut semi-lignified shoots of potted wild black cherry seedlings, cut off the terminal buds and stems with axillary buds, and soak the explants in 75% alcohol for 0.5-10 minutes , sterilized with 2% sodium hypochlorite aqueous solution by volume for 10-15 minutes, and then rinsed with sterile water for 3-5 times. The surface was sterilized and used as explants for tissue culture.
[0039] 2), induction culture: under aseptic conditions, after the explant terminal bud and the stem section with axillary buds after surface sterilization are removed, the terminal buds and the buds of the stem section with axillary buds are cut off. Inoculate upward on the induction medium of MS+BA0.75mg / L+NAA0.1mg / L to induce the germination of terminal buds and axillary buds, and then differentiate into cluster buds.
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