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In vitro Shoot and Callus Induction in Brahmi

机译:婆罗门的离体芽和愈伤组织诱导

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Plants of Brahmi Bacopa monnieri (L.) Pennell were regenerated by taking explants isolated from field-grown mature plants. This was achieved by culturing on MS solid medium with and without growth hormones. The best medium for initiation and development was MS+4 mg/l BAP +75 mg/l Adenine sulphate where the percentage of establishment was found to be very high (100%). In the multiplication stage MS +4mg/l BAP medium was found to be best in terms of average number of shoots (5.25). In the rooting stageMS+1.5mg/l NAA was found to bethe best medum in terms of average number of roots (7.5). The medium MS + 1 mg/2, 4-0 was the best medium for callus induction. This protocol can be used to generate cost-effective protocol for large-scale in vitro multiplication of brahmi.
机译:Brahmi Bacopa monnieri(L.)Pennell的植物是通过从田间生长的成熟植物中分离出的外植体进行再生的。这是通过在有或没有生长激素的MS固体培养基上培养来实现的。起始和发育的最佳培养基是MS + 4 mg / l BAP +75 mg / l腺嘌呤硫酸盐,其中建立的百分比很高(100%)。在繁殖阶段,发现MS + 4mg / l BAP培养基的平均芽数最好(5.25)。在生根阶段,就平均根数(7.5)而言,发现MS + 1.5mg / l NAA是最好的培养基。 MS + 1 mg / 2,4-0培养基是诱导愈伤组织的最佳培养基。此协议可用于生成经济高效的协议,以进行婆罗门的大规模体外繁殖。

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