Kizhakke Modongal Shamsudheen, Valiyaparambath Musfir Mehaboob, K. Faizal, Palusamy Raja, G. Thiagu, A. Shajahan
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引用次数: 0
摘要
目的:我们研究的主要重点是建立一种利用根茎芽通过间接器官发生实现高山植物再生的可靠方法。材料与方法材料与方法:将根茎外植体置于添加了 0.5 至 2.5 mg/L 2,4-D 的 MS 培养基上以诱导胼胝体的形成。在含有 1.5 mg/L 2,4-D 的 MS 培养基上观察到的茧诱导效果更好,茧呈淡绿色,质地紧密。将胼胝体转移到添加了不同浓度细胞分裂素(如 BAP、Kinetin 和 TDZ)的 MS 培养基上进行芽诱导。结果结果:结果:1.0 mg/L BAP 的芽诱导率最高(91.0±3.21%),每个胼胝体的芽数最多(9.66±0.88),小植株长度最大(91.13±1.44 mm)。然后将再生最好的芽转移到不同浓度(0.25 毫克/升、0.5 毫克/升、0.75 毫克/升和 1.0 毫克/升)的 NAA 和 IBA 等助剂中进行生根。在含有 0.5 毫克/升 IBA 的 MS 培养基中,诱导出了较高的生根频率(93.00±1.73%)、最大根数(21.66±1.76)和最大根长(93.33±1.76 毫米)。结论结论我们已开发出一种可靠且易于复制的方案,用于在受控实验室环境中诱导姬松茸的胼胝体,并随后进行植株再生。随后,离体小植株成功适应了田间条件。
A Study on Callus Induction and the Successful Regeneration of Plantlets from Rhizome Explants of Alpinia galanga (L.) Willd., a Valuable Medicinal Plant
Aim:Aim: The primary focus of our study is to establish a reliable approach for plant regeneration via indirect organogenesis of Alpinia galanga , utilizing rhizome buds. Materials and Methods: Materials and Methods: The rhizome explants were placed onto MS media supplemented with 0.5 to 2.5 mg/L 2,4-D to induce callus formation. The more effective callus induction was observed on MS media containing 1.5 mg/L 2,4-D with a light green, compact nature of callus. The callus transferred to MS media supplemented with various cytokinin’s such as BAP, Kinetin and TDZ in different concentrations for shoot induction. Results: Results: The highest shoot induction frequency (91.0±3.21%), the maximum number of shoots per callus (9.66±0.88) and the highest plantlet length (91.13±1.44 mm) were observed in 1.0 mg/L BAP. The best-regenerated shoot buds were then transferred to auxins such as NAA and IBA with various concentrations (0.25 mg/L, 0.5 mg/L, 0.75 mg/L and 1.0 mg/L) for root initiation. High rooting frequency (93.00±1.73%), maximum number of roots (21.66±1.76) and maximum root length (93.33±1.76 mm) were induced in MS medium containing 0.5 mg/L IBA. Conclusion: Conclusion: We have developed a reliable and easily replicable protocol for callus induction and subsequent plant regeneration of A. galanga in controlled laboratory settings. Following this, the in vitro plantlets were successfully acclimatized to field conditions.