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Efficient method of micropropagation and in vitro rooting of teak (Tectona grandis L.) focusing on large-scale industrial plantations

机译:专注于大规模工业人工林的柚木微繁殖和离体生根的有效方法

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摘要

Multiple shoots of high quality were produced in vitro from nodal explants of Tectona grandis. An average of about 4 shoots/uninodal explant was obtained within 4 weeks of culture on Murashige and Skoog’s (mMS) medium modified by 50% reduction in NH4NO3 concentration, supplemented with benzylaminopurine (1.5 mg L−1); indole-3-butyric acid (0.01 mg L−1) and gibberellic acid (0.1 mg L−1). The latter was applied bothin the medium and by soaking the nodal segments for 10 s. in a gibberellic acid solution of 100 mg L−1. Hundred percent of shoots rooted cultured onmodified MS medium containing IBA (0.5 mg L−1) and putrescine (160 mg L−1). Putrescine promoted both strong and highly ramified roots and fastgrowing shoots during the rooting phase, conditioning the plantlets for a good survival and quality. Plantlets were transferred to jiffy pots for a shortacclimatization stage in greenhouse where they survived at 100%. This highly reproducible procedure can be adopted for large scale teak propagation.
机译:从巨大的Tectona grandis的外植体在体外产生了许多高质量的芽。在Murashige和Skoog's(mMS)培养基上,经NH4NO3浓度降低50%修饰,并补充了苄基氨基嘌呤(1.5 mg L-1),在培养的4周内平均获得约4枝/单节外植体;吲哚-3-丁酸(0.01 mg L-1)和赤霉素(0.1 mg L-1)。后者既可以在培养基中使用,也可以通过将节段浸泡10 s来使用。在100 mg L-1的赤霉素溶液中。百分百的新芽生根培养在含有IBA(0.5 mg L-1)和腐胺(160 mg L-1)的改良MS培养基上。腐胺在生根期能促进强壮和高度分枝的根以及速生芽,调节小苗以获得良好的存活率和品质。将小植株转移到刚孵化的花盆中,使其在温室中短暂适应环境,并在其中存活100%。这种高度可重复的程序可用于大规模柚木繁殖。

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