Cerasus campanulata somatic cell embryogenesis method
A technology of embryogenesis and somatic cells, applied in the field of plant cultivation, to achieve the effects of complete structure, fast seedling growth and short cycle
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Embodiment 1
[0033] Example 1 Induction of embryogenic callus
[0034]Immature embryos were used to induce embryogenic callus. The immature fruits collected in spring are first washed with running water for 2 hours, then sterilized with alcohol for 30 seconds on an ultra-clean bench, rinsed with sterilized distilled water, and then treated with 0.1% mercury chloride or 84 disinfectant for 7-20 minutes, and rinsed with distilled water , the immature fruit is cut open with a scalpel in the ultra-clean workbench, and two cotyledons and immature embryos are taken out and placed on the induction medium, such as figure 2 As indicated, the inoculated material was placed in an incubator at 23°C for dark cultivation. The immature embryo starts to start about half a month after being placed on the induction medium, such as image 3 , Figure 4 , Figure 5 and Figure 6 As shown in , some have direct somatic embryogenesis, some have red radicles that begin to elongate, some have white protrusio...
Embodiment 2
[0036] Embodiment 2 Embryogenic callus proliferation stage
[0037] In the embryogenic callus proliferation stage, the proliferation medium was used, and the proliferation medium continued to use MS basic medium, and placed in an incubator at 23°C for dark culture, such as Figure 7 shown. Embryoid body generation, on the embryogenic callus proliferation medium, after several subcultures, as Figure 8 and Figure 9 As shown, white, spherical embryoid bodies were produced on yellow-green callus.
Embodiment 3
[0038] The development and maturation of embodiment 3 embryoid bodies
[0039] After the development and maturation of the embryoid body, after the formation of the spherical embryo, transfer it to the cultivation medium for cultivation under light, and light for 12 hours d -1 , the illuminance is 1200 lx, and the room temperature is 22-27°C. Such as Figure 10 As shown, the seedlings developed into plantlets on the MS medium, transferred to the growth medium, continued to cultivate, and grew into complete plantlets, such as Figure 11 shown.
[0040] The somatic embryogenesis technology of Fujian mountain cherry of the present invention provides a method for the large-scale vegetative propagation of Fujian mountain cherry with a short cycle, high reproduction rate and low cost, and effectively solves the problem that the existing stands of Fujian mountain cherry are extremely rare and the seeds are mature. It is very easy to burst, the collection, storage and germination...
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