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首页> 外文期刊>Applied Biochemistry and Biotechnology >Preconditioning of Axillary Buds in Thidiazuron-Supplemented Liquid Media Improves In Vitro Shoot Multiplication in Nyctanthes arbor-tristis L.
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Preconditioning of Axillary Buds in Thidiazuron-Supplemented Liquid Media Improves In Vitro Shoot Multiplication in Nyctanthes arbor-tristis L.

机译:噻唑隆补充液体培养基中腋芽的预处理可改善夜蛾(Nyctanthes arbor-tristis L)的离体芽繁殖。

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摘要

An efficient tissue culture technology has been designed for mass multiplication of Nyctanthes arbor-tristis L. by preculturing nodal explants in thidiazuron (TDZ)-supplemented liquid Murashige and Skoog (MS) media. Direct inoculation of nodal segments on semi-solid MS medium augmented with various concentrations of TDZ (0.1 to 0.9 μM) produced shoots but with low regeneration response and few shoots per explant. Hence, nodal explants were pretreated with greater concentrations of TDZ (5 to 100 μM) in liquid MS media for different durations (4, 8, 12, and 16 days) with the aim of improving shoot regeneration response from cultured explants. After pretreatment, explants were transferred to agar-solidified hormone-free MS medium. Best response in terms of percent regeneration (94%), number of shoots per explant (20.00 ± 1.15), and greatest shoot length (7.23 ± 0.83 cm) were obtained with nodal segments pretreated in75 μM TDZ for 8 days. Similarly, root induction was obtained from pulse-treated microshoots for 24 h with 200 μM indole-3-butyric acid (IBA) followed by their transfer to 1/2 MS medium which produced an average of 5.50 ± 0.92 roots per microshoot. The rooted plantlets were transplanted to soil with 80% success rate.
机译:通过在补充噻地隆(TDZ)的液态Murashige和Skoog(MS)液体中预先培养结节外植体,已设计了一种有效的组织培养技术,用于大量种植夜蛾(Nyctanthes arbor-tristis L.)。将节点节段直接接种在各种浓度的TDZ(0.1至0.9μM)增强的半固体MS培养基上可产生枝条,但再生响应低,每个外植体的枝条很少。因此,节点外植体在液体MS培养基中用更高浓度的TDZ(5至100μM)预处理了不同的持续时间(4、8、12和16天),目的是改善培养的外植体的芽再生响应。预处理后,将外植体转移至琼脂固化的无激素MS培养基中。在75μMTDZ中预处理了8天的节段,获得了关于再生百分数(94%),每个外植体的芽数(20.00±1.15)和最大芽长度(7.23±0.83 cm)的最佳响应。同样,用200μM吲哚-3-丁酸(IBA)脉冲处理24小时后,根系诱导获得根诱导,然后将其转移至1/2 MS培养基中,每个微芽平均产生5.50±0.92根。将生根的小苗移植到土壤中,成功率为80%。

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