Tissue culture and rapid propagation method for paphiopedilum dianthum
A technology of tissue culture and Papudendron longiflorum, applied in the field of plant tissue culture, to achieve the effect of simple medium formula, strong growth of seedlings, simple and easy-to-operate operation process
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Embodiment 1
[0059] Embodiment 1. Determination of self-pollination and fruit pod optimum harvesting period of P.
[0060] Experimental materials: Papudendron longifolia was obtained from the greenhouse of Vegetable and Flower Research Institute, Chinese Academy of Agricultural Sciences; various reagents or medium components used in all the examples of the present invention were obtained commercially.
[0061] Select the large and colorful Paphiopedilum longifolia for artificial cross-pollination, such as figure 1 As shown, pods were grown after pollination.
[0062] After pollination, pods were collected on the 240th day, the 270th day, the 300th day, the 330th day, the 360th day, the 390th day and the 420th day, respectively.
[0063] After the above-mentioned fruit pods were washed with tap water, they were placed in 10% sodium hypochlorite solution for disinfection for 20 minutes, sterilized with 70% alcohol for 30 seconds, then sterilized with 0.1% mercury liter for 10 minutes, and...
Embodiment 2
[0067] Embodiment 2. Determination of the optimal germination medium of Papudendron longifolium seeds
[0068] Eight different germination media were designed, and the existing MS medium in the prior art was supplemented with sucrose and carrageenan (germination medium No. 9) as a control, as shown in Table 4.
[0069] Table 4. Components and contents of 9 media
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[0072]
[0073] According to the method as described in Example 1, the seeds in the fruit pods collected on the 330th day after pollination were respectively inoculated in the 9 media in the above-mentioned Table 4 for germination and culture, and the germination of the seeds was observed.
[0074] As a result, it was found that the seeds of Paphiopedilum longum could germinate well in 8 kinds of germination media designed by the present invention, and the germination rate was significantly higher than that of the control medium, and the germination rate in No. ⑥ medium was the highest, r...
Embodiment 3
[0075] Embodiment 3. Determination of the best propagation medium for Papudendron longifolium seeds
[0076] Five different proliferation media were designed, as shown in Table 5.
[0077] Table 5. Proliferation and differentiation of the protocorm of P. longifolia on different proliferation media
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[0079]
[0080] The seedlings cultivated in Example 2 were inoculated into the above-mentioned proliferation medium, subcultured once every 4 weeks, and the proliferation of the seedlings was observed.
[0081] Proliferation culture was carried out for about 8 weeks, and it was found that the proliferation effect of seedlings in the second proliferation medium was good, protocorms grew on calluses, and the seedlings were robust.
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