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首页> 外文期刊>Indian Journal of Biotechnology >Micropropagation of Valeriana wallichii DC. (Indian Valerian) through nodes
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Micropropagation of Valeriana wallichii DC. (Indian Valerian) through nodes

机译:Valeriana wallichii DC的微繁殖。 (印度缬草)通过节点

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In vitro propagation method was developed for obtaining large number of plantlets of Valeriana wallichii DC. (Valerianaceae), an indigenous high value medicinal and aromatic plant species of Indian Himalayan region, using nodes of in vitro grown seedlings. High frequency shoot proliferation was induced in explains cultured on Murashige and Skoog (MS) medium supplemented with different concentrations of 6-benzyladenine (BA), kinetin (Kn), adenine sulphate (AS) and thidiazuron (TDZ). Amongst all the tested cytokinins, 3.0 mu M BA was found to be the most effective and an average. of 12.0 shoots per nodal explant were formed after 15 d of culture. Higher concentration of TDZ (3.0 mu M) was found least effective among all the cytokinins used for shoot induction. Rooting (100 %) was observed in PGR-free Murashige and Skoog medium after 12 d of incubation of microshoots. Well rooted plantlets (30-d-old) were successfully transplanted and established in mixture of soil and sand (3:1) under partially shade conditions.
机译:开发了一种体外繁殖方法,用于获得Valeriana wallichii DC的大量幼苗。 (缬草科),印度喜马拉雅地区的一种本土高价值药用和芳香植物物种,使用了体外生长的幼苗的结节。在Murashige和Skoog(MS)培养基上培养的培养基中诱导了高频芽增殖,该培养基补充了不同浓度的6-苄基腺嘌呤(BA),激动素(Kn),硫酸腺嘌呤(AS)和噻二唑(TDZ)。在所有测试的细胞分裂素中,发现3.0μM BA是最有效和平均的。培养15天后,每个结外植体中形成12.0个新芽。发现在用于芽诱导的所有细胞分裂素中,较高浓度的TDZ(3.0μM)最无效。微芽培养12天后,在不含PGR的Murashige和Skoog培养基中观察到生根(100%)。在部分遮荫条件下,将根深蒂固的小植株(30天大)成功移植并在土壤和沙子的混合物(3:1)中建立。

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