Departamento de Ingeniería Genética de Plantas, Unidad de Biotecnología e Ingeniería Genetica de Plantas, Centro de Investigación y de Estudios Avanzados del IPN, Apartado Postal 629, 36500, Irapuato, Gto., Mexico.
Plant Cell Rep. 1996 Dec;16(3-4):226-31. doi: 10.1007/BF01890873.
In this work we report a new method forin vitro chili pepper (Capsicum annuum L.) plant regeneration based on shoot formation from wounded hypocotyls. Chili pepper seeds were surface sterilized and germinated on agar (0.8%) at 25 ± 2°C in the dark. Five factors that may influence shoot regeneration were studied: age of seedlings, hypocotyl wounding site, time elapsed between wounding the hypocotyls and decapitation of seedlings, culture media and cultivars. In order to study the influence of the first three factors on shoot regeneration, the apical, middle or basal hypocotyl regions of seedlings of cv. Mulato Bajio at different stages of development (9, 15, 16, 21 and 28 d old) were wounded with a syringe needle, and the seedlings were cultured on MS semisolid medium without growth regulators at 25 ± 2°C under a 16/8 h light/dark photoperiod (daylight fluorescent lamps; 35 μmol m-(2) s-(-1)) until decapitation. The seedlings were decapitated (3 mm below the cotyledons) at different times after wounding (0, 2, 4, 10, 12 and 14 d), and each explant was evaluated for bud and shoot formation (≥ 5 mm in length) at the wounded site after 30 d of incubation. In general, seedlings at the stage of curved hypocotyl (9 d old) wounded in the apical region of hypocotyl were the best explants for shoot regeneration when inoculated on culture medium without growth regulators. Decapitation after wounding also influenced the shoot regeneration efficiency, with 10-14 d being the best period. Up to 90% shoot regeneration in cv. Mulato Bajio was obtained under these conditions. Statistically significant differences were observed for shoot formation among 21 cultivars tested. Regeneration of whole plants was achieved by rooting the shoots with indole-3-butyric acid pulses of 60 mg L(-1) for 3 h and then subculturing on MS medium without growth regulators.
在这项工作中,我们报告了一种新的基于受伤下胚轴形成芽的体外辣椒(Capsicum annuum L.)植物再生方法。辣椒种子在 25±2°C 黑暗条件下在琼脂(0.8%)上表面消毒并发芽。研究了可能影响芽再生的 5 个因素:苗龄、下胚轴受伤部位、下胚轴受伤与幼苗斩首之间的时间间隔、培养基和品种。为了研究前三个因素对芽再生的影响,用注射器针在不同发育阶段(9、15、16、21 和 28 d)的 Mulato Bajio 品种的幼苗的上胚轴、中胚轴或下胚轴区域进行受伤,并在 25±2°C 下在无生长调节剂的 MS 半固体培养基上培养,在 16/8 h 光/暗光周期(日光荧光灯;35 μmol m-2 s-1)下,直到斩首。在受伤后不同时间(0、2、4、10、12 和 14 d)斩首(距子叶 3 mm 以下),并在培养 30 天后评估每个外植体在受伤部位的芽和芽形成(≥5 mm 长)。一般来说,在弯曲下胚轴(9 d 龄)阶段,在上胚轴区域受伤的幼苗是接种无生长调节剂培养基时芽再生的最佳外植体。受伤后斩首也影响芽再生效率,10-14 d 是最佳时期。在这些条件下,Mulato Bajio 品种的芽再生率高达 90%。在所测试的 21 个品种中,观察到芽形成的统计显著差异。通过用 60 mg L-1 吲哚-3-丁酸脉冲处理 3 h 诱导芽生根,然后在无生长调节剂的 MS 培养基上继代培养,实现了整株植物的再生。