首页> 外文期刊>Plant Biosystems >Plantlet regeneration from cotyledon, cotyledon petiole, and hypocotyl explants via somatic embryogenesis pathway in roquette (Eruca sativa Mill).
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Plantlet regeneration from cotyledon, cotyledon petiole, and hypocotyl explants via somatic embryogenesis pathway in roquette (Eruca sativa Mill).

机译:通过体细胞胚发生途径从小球(子叶草)中的子叶,子叶柄和下胚轴外植体再生植株。

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摘要

A high-efficiency plant regeneration protocol based on somatic embryo formation for Huining Roquette, an interesting ecotype of Eruca sativa Mill, was established for future transgenic applications. On Murashige and Skoog (MS) medium containing 2,4-dichlorophenoxyacetic acid (2,4-D), alone or in combination with 6-benzylaminopurine (BA) or kinetin (KT), the cotyledon explants, cotyledon petioles, and hypocotyls all produced embryogenic callus (ECs) or somatic embryos (SEs) to different extents. After transferring onto hormone-free MS medium, the ECs or SEs from the different explants and media, all of them developed shoots with a frequency of 6-48%, and then produced roots with a frequency of 2-29%. As regards the probability of shoot differentiation, cotyledon explants appeared similar to hypocotyls, but superior to cotyledon petioles; 2,4-D+KT worked more effectively than 2,4-D alone and 2,4-D+BA for callus induction and shoot differentiation. The optimal hormone combinations for plant regeneration of cotyledon, cotyledon petiole, and hypocotyl explants were 1.0 mg/l 2,4-D+0.1 mg/l KT, 0.8 mg/l 2,4-D+0.3 mg/l BA, and 1.0 mg/l 2,4-D+0.3 mg/l KT, respectively. MS medium with 60-80 g/l sucrose was the most effective for improving SE maturation and germination.
机译:建立了以体细胞胚形成为基础的高效植物再生方案,用于将来的转基因应用惠宁罗凯特(一种有趣的生态型苜蓿)。在含有2,4-二氯苯氧基乙酸(2,4-D),单独或与6-苄基氨基嘌呤(BA)或激动素(KT)结合的Murashige和Skoog(MS)培养基上,子叶外植体,子叶柄和下胚轴都产生不同程度的胚性愈伤组织(EC)或体细胞胚(SE)。将来自不同外植体和培养基的EC或SE转移到无激素的MS培养基上后,它们的芽均以6-48%的频率发生,然后产生根系,频率为2-29%。至于芽分化的可能性,子叶外植体看起来类似于下胚轴,但优于子叶叶柄。 2,4-D + KT比单独使用2,4-D和2,4-D + BA更有效地诱导愈伤组织和芽分化。子叶,子叶柄和下胚轴外植体的植物再生的最佳激素组合为1.0 mg / l 2,4-D + 0.1 mg / l KT,0.8 mg / l 2,4-D + 0.3 mg / l BA和1.0 mg / l 2,4-D + 0.3 mg / l KT。含60-80 g / l蔗糖的MS培养基最有效地改善SE的成熟和发芽。

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