Method for detoxification of lily through somatic embryogenesis
An embryogenesis and somatic cell technology, applied in horticultural methods, botanical equipment and methods, plant regeneration, etc., can solve the problems of complicated shoot tip culture operation, easy browning of shoot tip, incomplete detoxification, etc. Cultivation time, good detoxification effect, and the effect of mass reproduction
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Embodiment 1
[0024] The method for lily detoxification through the somatic embryogenesis pathway comprises the following steps:
[0025] 1) Embryogenic callus induction: Lily scales cultivated under sterile conditions were used as explants, inoculated on solid medium for embryogenic callus induction, and cultured for 28 days to induce embryogenic callus.
[0026] Among them, the composition of embryogenic callus induction medium is: MS medium + PIC 1 ~ 3mg L -1 +Agar 7g·L -1 + sucrose 30g·L -1 , PH value is 5.8. PIC is one of the plant growth regulators, its full name in English is Picloram, and its Chinese name is picloram.
[0027] The embryogenic callus induction medium is to add 7g·L -1 Agar and 30g·L -1 Sucrose, maintain a pH of 5.8, and add the following ingredients:
[0028] PIC (mg·L -1 ) BA (mg·L -1 ) NAA (mg·L -1 ) Effect Recipe 1 1 0 0 Fewer calluses formed at the base of the scales, accompanied by a small amount of differentiation into smal...
Embodiment 2
[0035] In this example, step 1) and step 2) are the same as in Example 1, and step 3) is the subculture of spherical somatic embryos in a bioreactor: inoculate the spherical somatic embryos obtained in step 2) in Example 1 The first-generation subculture was carried out in a bioreactor added with liquid proliferation medium, and the mass-volume concentration of spherical somatic embryos inoculated in each bioreactor was 0.5-5% (w / v), that is, each Add 100ml of liquid proliferation medium to a bioreactor to inoculate 0.5~5g of spherical somatic cell embryos. In this embodiment, 1 g of spherical somatic cell embryos was inoculated in each bioreactor, and the air flow of the bioreactor was adjusted to 20 ml min after inoculation. -1 , the temperature was kept at 24±2°C, and cultured for 14 days under dark and light culture conditions to obtain the first generation of subcultured somatic cell embryos.
[0036] The newly produced spherical somatic embryos were screened out from th...
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