细胞外高分子物质在脱硫弧菌 UR1 通过细胞外电子传递还原铀过程中的调控作用

IF 7.7 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Environmental Research Pub Date : 2024-08-28 DOI:10.1016/j.envres.2024.119862
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引用次数: 0

摘要

利用电活性细菌将铀(VI)还原为不溶性铀(IV)的途径已成为解决人类活动造成的铀污染水的一种有效且前景广阔的方法。然而,关于胞外聚合物物质(EPS)在涉及胞外电子转移(EET)机制的铀还原过程中的作用的知识还很有限。本研究分离了一种新型铀(VI)还原菌株--Desulfovibrio vulgaris UR1,其铀去除能力高达 2.75 mM/(g 干细胞)。基于可靠的 EPS 提取方法(45 °C加热),对 D. vulgaris UR1 悬浮液中 EPS 的处理(去除或添加 EPS)突出了其在促进铀还原效率方面的关键作用。第二天,不同 EPS 含量的系统对铀(VI)的去除率差异很大:在添加 EPS 的系统中为 60.8%,在原始系统中为 48.5%,而在去除 EPS 的系统中为 22.2%。生物固体的表征证实了 D. vulgaris UR1 对铀(VI)的还原作用,主要产物是铀矿石和二氧化硫(直径为 2.88-4.32 纳米)。由于 EPS 形成了一个可渗透的屏障,这些纳米粒子在保留 EPS/ 添加 EPS 的细胞中主要固定在 EPS 中,而在去除 EPS 的细胞中则固定在细胞外质中。在 EPS 中发现了多种电活性物质,如酪氨酸/色氨酸芳香族化合物、黄素和类醌物质,这可能是通过提供更多电子快车增强铀还原的原因。此外,蛋白质组学研究发现,EPS 中大量蛋白质富集于催化活性和电子传递活性亚类中。其中,铁硫蛋白,如羟胺还原酶(P31101)、丙酮酸:铁氧还蛋白氧化还原酶(A0A0H3A501)和亚硫酸盐还原酶(P45574),在调控 D. vulgaris UR1 的 EET 中发挥了最关键的作用。这项工作强调了 EPS 在 D. vulgaris UR1 的铀还原过程中的重要性,表明 EPS 既是还原剂,又是重金属铀的渗透屏障。
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Regulatory roles of extracellular polymeric substances in uranium reduction via extracellular electron transfer by Desulfovibrio vulgaris UR1

The pathway of reducing U(VI) to insoluble U(IV) using electroactive bacteria has become an effective and promising approach to address uranium-contaminated water caused by human activities. However, knowledge regarding the roles of extracellular polymeric substances (EPS) in the uranium reduction process involving in extracellular electron transfer (EET) mechanisms is limited. Here, this study isolated a novel U(VI)-reducing strain, Desulfovibrio vulgaris UR1, with a high uranium removal capacity of 2.75 mM/(g dry cell). Based on a reliable EPS extraction method (45 °C heating), manipulation of EPS in D. vulgaris UR1 suspensions (removal or addition of EPS) highlighted its critical role in facilitating uranium reduction efficiency. On the second day, U(VI) removal rates varied significantly across systems with different EPS contents: 60.8% in the EPS-added system, 48.5% in the pristine system, and 22.2% in the EPS-removed system. Characterization of biogenic solids confirmed the reduction of U(VI) by D. vulgaris UR1, and the main products were uraninite and UO2 (2.88–4.32 nm in diameter). As EPS formed a permeable barrier, these nanoparticles were primarily immobilized within the EPS in EPS-retained/EPS-added cells, and within the periplasm in EPS-removed cells. Multiple electroactive substances, such as tyrosine/tryptophan aromatic compounds, flavins, and quinone-like substances, were identified in EPS, which might be the reason for enhancement of uranium reduction via providing more electron shuttles. Furthermore, proteomics revealed that a large number of proteins in EPS were enriched in the subcategories of catalytic activity and electron transfer activity. Among these, iron-sulfur proteins, such as hydroxylamine reductase (P31101), pyruvate: ferredoxin oxidoreductase (A0A0H3A501), and sulfite reductase (P45574), played the most critical role in regulating EET in D. vulgaris UR1. This work highlighted the importance of EPS in the uranium reduction by D. vulgaris UR1, indicating that EPS functioned as both a reducing agent and a permeation barrier for access to heavy metal uranium.

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来源期刊
Environmental Research
Environmental Research 环境科学-公共卫生、环境卫生与职业卫生
CiteScore
12.60
自引率
8.40%
发文量
2480
审稿时长
4.7 months
期刊介绍: The Environmental Research journal presents a broad range of interdisciplinary research, focused on addressing worldwide environmental concerns and featuring innovative findings. Our publication strives to explore relevant anthropogenic issues across various environmental sectors, showcasing practical applications in real-life settings.
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