In vitro Regeneration of Multiple Shoots in Abelmoschus esculentus (L.) Moench (Okra) via Apical Shoot Meristem Culture

Melvin A. Daniel, S. Maria Packiam, Duraipandiyan Veeramuthu
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Abstract

Introduction: To develop the efficient protocol for multiple shoot regeneration of A.esculentus by apical root culture method. Abelmoschus esculentus L., commonly known as okra, is a member of the Malvaceae family, which is widely consumed due to its high nutrient content and potential therapeutic properties. Okra contains various bioactive compounds that exhibit antibacterial properties and may be useful in treating type-2 diabetes, digestive diseases, and liver detoxification. To select the plant for the present and prepare the efficient protocol for the development of multiple shoot regeneration culture method. Methods: In this study, we developed an efficient protocol for multiple shoot regeneration of A. esculentus using the apical shoot culture method. Mature shoot apex explants of the germinated A. esculentus genotype CoBhH1 were cultured on Murashige and Skoog (MS) medium supplemented with different concentrations of cytokinins (BAP and TDZ) and auxins (IAA and NAA) to determine the optimal conditions for shoot induction. Results: The highest number of multiple shoots (27.04 shoots) was obtained with 0.8 mg/L TDZ. Excised shoots were cultured on MS medium supplemented with GA3, which induced elongation of the shoots to a maximum of 8-10 cm. Regenerated plantlets were successfully transferred to soil, with a 100% survival rate and no differences in morphology or growth characteristics compared to control plants. Rooting was achieved with 1 mg/L IBA. Conclusion: This study provides an efficient protocol for multiple shoot regeneration of A. esculentus through apical shoot culture, which has potential applications in plant breeding and genetic engineering.
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青豆多芽离体再生的研究秋葵根尖分生组织培养的研究
前言:研究金银花根尖培养法再生多芽的高效方案。秋葵(Abelmoschus esculentus L.),俗称秋葵,是一种葵科植物,因其高营养含量和潜在的治疗特性而被广泛食用。秋葵含有多种具有抗菌特性的生物活性化合物,可能对治疗2型糖尿病、消化系统疾病和肝脏排毒有用。目的:选择适宜的植株,为多芽再生培养方法的发展制定有效的方案。方法:采用顶芽培养的方法,建立了一套高效的多根再生方案。以萌发后CoBhH1基因型黄瓜茎尖成熟外植体为材料,在添加不同浓度细胞分裂素(BAP和TDZ)和生长素(IAA和NAA)的Murashige和Skoog (MS)培养基上培养,确定诱导芽的最佳条件。结果:TDZ用量为0.8 mg/L时,多芽数最多,达27.04根;在MS培养基中添加GA3,可诱导芽伸长,最大可达8-10 cm。再生植株移栽成功,成活率100%,形态和生长特征与对照植株无差异。添加1mg /L IBA可生根。结论:本研究提供了一种高效的竹叶顶茎再生方案,在植物育种和基因工程中具有潜在的应用价值。
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