Assessment of genetic uniformity in micro propagated plantlets of turmeric (Curcuma longa L.) through DNA markers

M. R. S. Gowda, R. Sowmya
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Abstract

Turmeric is herbaceous plant, characterized by long lance-shaped leaves sprouting from its rhizomatous underground stem. Notably, its rhizomes contain the bioactive compounds curcuminoids, renowned for its medicinal and culinary significance. However, meeting the surging demand for turmeric, particularly during off- seasons, presents a formidable challenge due to the sluggish vegetative propagation rate in Curcuma longa. Given the scarcity of sexual reproduction in turmeric, micropropagation emerges as the convenient method for obtaining disease-free seeds. In addressing the challenge of direct regeneration of the native Erode local cultivar of turmeric, this study endeavors to establish a protocol for in vitro plantlet production. Results indicate that multiple shoots were successfully induced, notably with 13.32 μM of 6-benzylaminopurine (BAP), yielding a response rate of 73.2±4.7% and an average shoot count of 6.95±0.81 per explant. Subsequently, a concentration of 17.76 μM of BAP demonstrated a response rate of 56.5%±4.7%, with an average shoot count of 5.94±0.81 per explant. Additionally, a combination of 13.32 μM BAP and 2.68 μM Naphthaleneacetic acid (NAA) resulted in 8.65±0.47 shoots per explant, with a response rate of 73.66±1.25%. Similarly, 13.32 μM BAP combined with 5.37 μM NAA yielded 7.32±0.47 shoots per explant, with a response rate of 72.33±0.47%. The acclimatization of plantlets in a greenhouse exhibited a remarkable survival rate, ranging from 90% to 98%. Importantly, all regenerated plantlets closely resembled the mother plants morphologically. Genetic uniformity assessment, employing 10 ISSR and 4 DAMD markers, indicated more than 90% uniformity among one mother plant and regenerants. This indicates a significant genetic uniformity, ensuring consistency in desired traits across the regenerated plantlets.
通过 DNA 标记评估姜黄(Curcuma longa L.)微繁殖植株的遗传一致性
姜黄是一种草本植物,其特征是从根状茎的地下茎中长出长矛状的叶子。值得注意的是,其根茎含有生物活性化合物姜黄素,因其药用和烹饪价值而闻名。然而,由于姜黄的无性繁殖速度缓慢,要满足对姜黄激增的需求,尤其是在淡季,是一项艰巨的挑战。鉴于姜黄无性繁殖的稀缺性,微繁殖成为获得无病种子的便捷方法。为应对姜黄本地埃罗德栽培品种直接再生的挑战,本研究致力于建立离体小植株生产规程。结果表明,使用 13.32 μM 的 6-苄基氨基嘌呤(BAP)可成功诱导多芽,反应率为 73.2±4.7%,每个外植体的平均芽数为 6.95±0.81。随后,浓度为 17.76 μM 的 BAP 的反应率为 56.5%±4.7%,每个外植体的平均芽数为 5.94±0.81。此外,13.32 μM BAP 和 2.68 μM 萘乙酸(NAA)的组合可使每个外植体产生 8.65±0.47 个芽,反应率为 73.66±1.25%。同样,13.32 μM BAP 与 5.37 μM NAA 结合使用时,每个外植体可产生 7.32±0.47 个芽,反应率为 72.33±0.47%。小植株在温室中适应性培养的成活率非常高,从 90% 到 98% 不等。重要的是,所有再生小植株在形态上都与母株非常相似。利用 10 个 ISSR 和 4 个 DAMD 标记进行的遗传一致性评估表明,一株母株和再生植株之间的一致性超过 90%。这表明遗传一致性很高,确保了再生小植株所需性状的一致性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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