Spathiphyllum somatic embryo inducing and plant regenerating method
A technology for somatic embryos and plant regeneration, which is applied in the fields of botanical equipment and methods, plant regeneration, and horticultural methods. The time limit is relatively large and other problems, so as to achieve the effect of improved induction efficiency, easy acquisition, and convenient material acquisition.
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Embodiment 1
[0018] Embodiment 1: the present embodiment is carried out through the following steps:
[0019] (1) Somatic embryo induction. Heliconia S. cannifolium The stem segments or terminal buds were disinfected and inoculated into clustered bud induction medium to obtain sterile test-tube plantlets, and then transferred to test-tube plantlet proliferation medium at a temperature of 24-30 °C and a light intensity of 1000-1400 lux, 10-14 hours of light per day, subculture once every 3-4 weeks, and the test-tube plantlets continue to proliferate. The leaves of young test-tube plantlets were cut into 1-10 mm wide strips, inoculated in somatic embryo induction medium, and cultured in a dark environment at a temperature of 24-30 °C for 2-4 weeks to obtain somatic embryos;
[0020] (2) Proliferation of somatic embryos: The obtained somatic embryos were subcultured in the somatic embryo induction medium, and cultured in a dark environment at a temperature of 24-30 °C for 2-4 weeks, the so...
Embodiment 2
[0024] Embodiment 2: The difference between this embodiment and Example 1 is that in step (1), the petiole of the test-tube plantlet is cut into 1-10 mm sections, and then inoculated in somatic embryo induction medium to obtain somatic embryos; the rest are the same as Example 1 is the same.
Embodiment 3
[0025] Example 3: The difference between this example and Example 1 or 2 is that the somatic embryo induction medium in step (1) uses MS medium as the basic medium, and each liter of medium contains 0.05-0.25 mg of thiophene Benuron, 0.5-2.0 mg of 2,4-dichlorophenoxyacetic acid, 20-40 grams of sucrose and 6-9 grams of agar, with a pH value of 5.6-6.0; somatic embryo proliferation medium in step (2) MS medium is used as the basic medium, and each 1 liter of medium contains 0.05-0.25 mg of thidiazuron, 0.5-1.0 mg of 2,4-dichlorophenoxyacetic acid, 20-40 grams of sucrose and 6~ The agar of 9 grams, pH value is 5.6~6.0; All the other are identical with embodiment 1 or 2.
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