Method for embryogenic cells of anthurium scherzerianum to quickly proliferate and regenerate plant
An embryogenic cell and plant regeneration technology, applied in the fields of botanical equipment and methods, plant regeneration, horticultural methods, etc., can solve the problems of long cycle, low proliferation rate, complex plant regeneration steps, etc., and achieve shortened time and simplified operation. effect of the process
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Embodiment 1
[0028] (1) Embryogenic induction of embryogenic callus: Take young leaves of young seedlings of Anthurium cultivar Alabama, after surface disinfection treatment, cut the leaves into 5 mm fragments, and inoculate them on embryogenic callus induction medium cultured in a dark environment at a temperature of 26°C for 4 weeks to obtain yellow embryogenic callus;
[0029] (2) Establishment of embryogenic cell suspension culture line: In a metal mesh with a pore size of 1.0 mm, the embryogenic callus was broken with tweezers, and sieved through the metal mesh to form embryogenic cell clusters with a diameter of no more than 1.0 mm; 0.1 g The embryogenic cell mass was inoculated in a 100ml Erlenmeyer flask with 20ml of embryogenic cell suspension medium, and cultured at a temperature of 26°C, with light of 900 lux, and shaking at 100 rpm; when subcultured, the proliferated The embryogenic cell mass was broken, and 0.1 g of the embryogenic cell mass was transferred to a 100 ml Erlenme...
Embodiment 2
[0035] The difference between this example and Example 1 is that the stems of the young seedlings of the anthurium cultivar 'Alabama' are treated with surface disinfection, cut into 10 mm sections, and then inoculated in somatic embryo induction medium to cultivate the obtained body. Cell embryo, all the other are identical with embodiment 1. Under this condition, the embryogenic callus induction rate of Anthurium anthurium reached 95.1%.
Embodiment 3
[0037] The difference between this example and Example 1 or 2 is that the embryogenic cell suspension medium in step (2) contains 2.0 mg / L of 6-BA and 2.0 mg / L of 2,4-D, and the rest are the same as in Example 1 or 2 for the same. Under this condition, the suspension culture of embryogenic cells can proliferate 2.82 times per week and more than 63 times per month.
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