长石菖蒲液体培养根茎诱导和快速再生方案:一步培养

P. Borpuzari, N. Bisht
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引用次数: 3

摘要

本实验旨在利用东北地区重要竹种长石菖蒲的节培养进行离体再生。在不同浓度的BAP和Kn培养基中培养单个辅芽进行破芽和芽再生。采集期和外植体类型是影响芽断的主要因素。在BAP 1.0 + Kn 1.0的液体基础培养基Murashigs and Skoogs (MS)中实现了植株的单步再生,培养3周内再生苗数最多,可达6 ~ 8个。在继代培养中,接种的完整节和切节培养均产生芽和根茎。在含有BAP 1.0 + Kn 1.0的培养基中,连续继代培养可产生同时生根和根茎,培养时间延长至11周。在非实验室条件下,90%的健康生根苗建立了培养反应。整个实验在培养培养12周内完成。在FRCBR, Aizwal田间一年后观察到离体植株生长良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhanced rhizome induction and fast regeneration protocol in liquid culture of Dendrocalamus longispathus Kurz: A single step culture
The present experimental study was aimed for in-vitro regeneration through nodal culture of Dendrocalamus longispathus an important bamboo species of north-eastern region. Single auxillary buds were cultured in different concentration of BAP and Kn incorporated media for bud breaking and shoot regeneration. Effect of collection period and type of explants is a major impact on bud breaking. Single step plantlet regeneration has been achieved in the liquid basal medium Murashigs and Skoogs (MS) with BAP 1.0 + Kn 1.0 shows best regeneration of 6 to 8 numbers of shoots within 3 weeks of culture. Both inoculated intact node and cut node cultures produced shoots and rhizomes during subcultures. Increased incubation period up to 11 weeks with serial sub culture produced simultaneous roots and rhizomes in the cultured media containing BAP 1.0 + Kn 1.0. Culture response of 90% healthy rooted plantlets has been established outside the lab condition. The whole experiment completed within 12 weeks of culture incubation. Good growth of established in-vitro plantlets in field of FRCBR, Aizwal is observed after one year.
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