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Callus Induction and Plant Regeneration from Leaf Segments of Unique Tropical Woody Plant Parasponia andersonii Planch

机译:独特热带木本植物Parasponia andersonii Planch叶节的愈伤组织诱导和植株再生

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The purpose of the present study was to develop effective methods for callus induction, shoot regeneration, and rooting for Parasponia andersonii . Leaf explants of P. andersonii were placed on Lloyd and McCown’s (WPM) medium supplemented with various concentrations of TDZ and NAA for callus induction. Callus induction was observed on media containing 0.1 - 0.2 mg/l TDZ with 0.05 mg/l NAA. Maximum shoot regeneration was observed when the calluses were cultured on MS supplemented with TDZ and IBA. Shoots cultured on WPM medium supplemented with 0.5 mg/l IBA had the maximum rooting percentage (100) in 3 weeks. Rooted plants were transplanted to a potting mixture containing vermiculite (50%) and peat (50%) (v/v). After 2 months, more than 20% of plants survived and were transferred to the greenhouse. Thus, a new effective method has been developed for P. andersonii micropropagation that can be used in studies of plant- Rhizobium symbiosis and for the generation of transgenic Parasponia plants.
机译:本研究的目的是开发有效的方法来诱导愈伤组织的愈伤组织诱导,枝条再生和生根。将P. andersonii的叶子外植体放在Lloyd和McCown(WPM)培养基中,该培养基中添加了不同浓度的TDZ和NAA以诱导愈伤组织。在含有0.1-0.2 mg / l TDZ和0.05 mg / l NAA的培养基上观察到愈伤组织诱导。当愈伤组织在补充了TDZ和IBA的MS上培养时,观察到最大的芽再生。在补充有0.5 mg / l IBA的WPM培养基上培养的芽在3周内具有最大的生根百分比(100)。将生根的植物移植到含有ver石(50%)和泥炭(50%)(v / v)的盆栽混合物中。 2个月后,超过20%的植物存活下来并转移到温室中。因此,已经开发了一种用于安德森疟原虫微繁殖的新的有效方法,该方法可用于植物根瘤菌共生研究和转基因副孢子虫植物的产生。

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