Detection and Quantification of Dysprosium in Plant Tissues.

IF 2.3 3区 生物学 Q2 PLANT SCIENCES
Plant Direct Pub Date : 2026-04-12 eCollection Date: 2026-04-01 DOI:10.1002/pld3.70164
Edmaritz Hernández-Pagán, Kanjana Laosuntisuk, Alex T Harris, Allison N Haynes, David Buitrago, Anisa Guedira, Cyprian Rajabu, Michael W Kudenov, Colleen J Doherty
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引用次数: 0

Abstract

The growing demand for rare-earth elements (REEs), particularly dysprosium (Dy), underscores the need for sustainable extraction methods. Recovery of Dy, particularly from geographically distributed waste sources, is challenging. This gap positions phytomining, a technique using plants to accumulate metals, as a promising alternative. However, plant species differ in their ability to accumulate metals in high concentrations, necessitating efficient screening methods. In this study, we developed a high-throughput fluorescence-based assay to detect and quantify Dy uptake in plant tissues. The Dy detection method described in the present work exploits Dy's unique spectroscopic properties for sensitive and efficient analysis, enabling the detection of concentrations as low as 0.07 μM, with a detection limit of 0.2 μM in a plant matrix. By incorporating sodium tungstate (Na2WO4) as a fluorescence enhancer, we achieved robust emission intensities at 480 and 580 nm, facilitating Dy quantification in complex plant matrices. Additionally, the use of time-resolved fluorescence techniques reduces background autofluorescence from plant tissues, enhancing signal specificity. Validation of the fluorescence method with inductively coupled plasma mass spectrometry (ICP-MS) demonstrated a strong correlation in Dy levels. Greenhouse trials confirmed the method's utility for screening Dy accumulation in living plants and highlighted the potential for rapid stand-off detection. This fluorescence-based approach offers a scalable, efficient tool for identifying Dy-accumulating plants and advances phytomining as a sustainable strategy for REE recovery.

植物组织中镝的检测与定量。
对稀土元素(ree),特别是镝(Dy)的需求不断增长,强调了对可持续提取方法的需求。镝的回收,特别是从地理上分散的废物来源中回收,是具有挑战性的。这一差距使得植物采矿(一种利用植物积累金属的技术)成为一种有希望的替代方案。然而,植物物种在高浓度积累金属的能力不同,需要有效的筛选方法。在这项研究中,我们开发了一种基于荧光的高通量测定方法来检测和量化植物组织中Dy的摄取。本研究中描述的Dy检测方法利用Dy独特的光谱特性进行敏感和高效的分析,可以检测低至0.07 μM的浓度,在植物基质中检测限为0.2 μM。通过加入钨酸钠(Na2WO4)作为荧光增强剂,我们在480和580 nm处获得了强大的发射强度,有助于在复杂的植物基质中定量测定Dy。此外,使用时间分辨荧光技术减少了植物组织的背景自身荧光,增强了信号的特异性。用电感耦合等离子体质谱(ICP-MS)验证的荧光方法证实了Dy水平的强相关性。温室试验证实了该方法用于筛选活植物中Dy积累的实用性,并强调了快速隔离检测的潜力。这种基于荧光的方法提供了一种可扩展的、有效的工具,用于识别富集稀土的植物,并将植物矿开采作为稀土回收的可持续战略。
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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来源期刊
Plant Direct
Plant Direct Environmental Science-Ecology
CiteScore
5.00
自引率
3.30%
发文量
101
审稿时长
14 weeks
期刊介绍: Plant Direct is a monthly, sound science journal for the plant sciences that gives prompt and equal consideration to papers reporting work dealing with a variety of subjects. Topics include but are not limited to genetics, biochemistry, development, cell biology, biotic stress, abiotic stress, genomics, phenomics, bioinformatics, physiology, molecular biology, and evolution. A collaborative journal launched by the American Society of Plant Biologists, the Society for Experimental Biology and Wiley, Plant Direct publishes papers submitted directly to the journal as well as those referred from a select group of the societies’ journals.
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