首页> 外文期刊>In Vitro Cellular and Development Biology. Plant: Journal of the Tissue Culture Association >In vitro plant regeneration of Passiflora setacea DC (Passifloraceae): the influence of explant type, growth regulators, and incubation conditions
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In vitro plant regeneration of Passiflora setacea DC (Passifloraceae): the influence of explant type, growth regulators, and incubation conditions

机译:西番莲DC(西番莲科)的体外植物再生:外植体类型,生长调节剂和培养条件的影响

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The present study aimed to establish a protocol for in vitro organogenesis of Passiflora setacea and to determine the genetic stability of regenerated plants. Three types of explants (leaf, hypocotyl, and root), four growth regulator combinations [Murashige and Skoog (MS) salts, MS + 6-benzyladenine (BA), MS + thidiazuron (TDZ), and MS + BA + TDZ], and two light regimes (16-h photoperiod and continuous darkness) were tested. After 30 d on induction medium, the percentage of explants forming shoots was evaluated. Direct and indirect organogenesis was evident from hypocotyl- and root-derived explants, whereas only indirect organogenesis was observed from leaf explants. The presence of BA was essential for shoot formation from leaf explants and improved the response of hypocotyl segments under a 16-h photoperiod compared to the cytokinin-free control. However, after transfer to shoot elongation medium, the greatest number of elongated shoots was obtained from hypocotyl segments that had been induced on BA + TDZ medium under a 16-h photoperiod, as was also observed for root explants. Flow cytometry analysis confirmed the genetic stability of the regenerants based on DNA quantity (2C = 2.57 pg) in comparison with seed-derived plantlets (2C = 2.60 pg). This is the first report on the in vitro regeneration of P. setacea.
机译:本研究旨在建立西番莲体外器官发生的协议,并确定再生植物的遗传稳定性。三种类型的外植体(叶子,下胚轴和根),四种生长调节剂组合[Murashige和Skoog(MS)盐,MS + 6-苄腺嘌呤(BA),MS +噻二唑酮(TDZ)和MS + BA + TDZ],并测试了两种光照条件(16小时光照周期和连续黑暗)。在诱导培养基上30天后,评估形成芽的外植体的百分比。从下胚轴和根来源的外植体中可以看出直接和间接的器官发生,而从叶外植体中仅观察到了间接器官发生。与无细胞分裂素的对照相比,BA的存在对于从叶外植体形成芽是必不可少的,并且可以改善在16小时光周期下下胚轴片段的反应。但是,转移到枝条伸长培养基后,从在16小时的光周期下BA + TDZ培养基上诱导的下胚轴节段中获得了最多数量的伸长枝条,这也可以从根外植体中观察到。流式细胞仪分析证实了与基于DNA的种子(2C = 2.60 pg)相比,基于DNA量(2 C = 2.57 pg)的再生子的遗传稳定性。这是关于P. setacea体外再生的第一份报告。

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