首页> 外文期刊>International Journal of Plant Developmental Biology >A Simple and Efficient Protocol for Rapid Regeneration and Propagation of Taro (Cotocasia esculenta (L.) Schott.) in Vitro from Apical Meristems
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A Simple and Efficient Protocol for Rapid Regeneration and Propagation of Taro (Cotocasia esculenta (L.) Schott.) in Vitro from Apical Meristems

机译:一种从根尖分生组织快速再生和繁殖芋头(Cotocasia esculenta(L.)Schott。)的简单有效的协议。

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摘要

An efficient and simple protocol was developed for the in vitro regeneration and propagation of taro (Colocasia esculenta) cv. 'Muktakeshi'. Apical meristems (~1 cm) excised from leaf blight-resistant taro cultivar cv. 'Muktakeshi' grown in a net house were used as explants. Most multiple shoots (i.e., 3.6/explant), which formed on Murashige and Skoog (MS) medium supplemented with 5 mg L~(-1) 6-benzyladenine and 1 mg L~(-1) alpha-naphthaleneacetic acid, could be rooted by transferring the 4-week-oldshoots to MS basal medium without plant growth regulators. After 2 weeks, well developed plantlets were hardened in plastic cups in potting mixture (vermiculite + sand, 1:1, v/v). Acclimatized plants were transferred to 30-cm plastic pots containing topsoil and vermicompost (3:1, v/v) where they grew well.
机译:为芋头(Colocasia esculenta)cv的体外再生和繁殖开发了一种有效而简单的方案。 'Muktakeshi'。从抗叶枯萎的芋头栽培品种cv中切下的顶端分生组织(〜1 cm)。网箱中种植的'Muktakeshi'被用作外植体。在补充有5 mg L〜(-1)6-苄腺嘌呤和1 mg L〜(-1)α-萘乙酸的Murashige和Skoog(MS)培养基上形成的多数多芽(即3.6 /植株)可能是通过将4周的新芽转移到没有植物生长调节剂的MS基础培养基上而生根。 2周后,将发育良好的幼苗在盆栽混合物(ver石+沙子,1:1,v / v)的塑料杯中硬化。将已驯化的植物转移到30厘米长的装有表土和ver堆肥(3:1,v / v)的塑料盆中,使其生长良好。

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