Divergent impacts of antibiotics on ferrihydrite biotransformation by Shewanella oneidensis: electron transfer regulation and iron redox cycling

IF 5.6 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Xinyue Li, Jianxin Chen, Xiyuan Chen, Yuxin Wang, Jieyu Li, Xiangchun Guo, Yan Shi, Kejing Zhang and Zhang Lin
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Abstract

Antibiotics, as ubiquitous environmental pollutants, disrupt iron biogeochemical cycles. However, their role in regulating ferrihydrite (Fh) transformation mediated by dissimilatory iron-reducing bacteria, and their coupled conversion, remains poorly understood. This study investigates the influence of antibiotics on Fh biotransformation by Shewanella oneidensis MR-1, focusing on the regulation of microbe–mineral interfacial electron transfer. Among seven representative antibiotics, sulfamethoxazole enhanced Fe(II) production by promoting microbial electron flux, thereby accelerating Fh transformation toward magnetite. Conversely, chloramphenicol suppressed Fe(II) generation by competing for microbial electrons via nitro group reduction and inhibiting extracellular electron transfer, kinetically trapping mineral transformation at the goethite stage. Sulfamethoxazole was reductively degraded by biogenic Fe(II) via N–O bond cleavage, facilitating green rust formation and further promoting magnetite nucleation, whereas chloramphenicol was predominantly hydrolyzed by microbes or on mineral surfaces without contributing to Fe(III) reduction. These findings reveal that antibiotics can serve as either electron mediators or competitors, directly coupling their degradation to iron redox cycling and controlling mineral transformation pathways. This work provides novel insights into the environmental persistence of antibiotics and their previously overlooked role in mineral transformation, with critical implications for managing antibiotic-contaminated ecosystems.

Abstract Image

抗生素对希瓦氏菌水合铁生物转化的不同影响:电子转移调控和铁氧化还原循环
抗生素作为无处不在的环境污染物,破坏了铁的生物地球化学循环。然而,它们在调节由异化铁还原菌介导的水合铁(Fh)转化中的作用,以及它们的耦合转化,仍然知之甚少。本研究探讨了抗生素对希瓦氏菌MR-1 Fh生物转化的影响,重点研究了微生物-矿物界面电子转移的调控。在7种代表性抗生素中,磺胺甲恶唑通过促进微生物电子通量来促进铁(II)的产生,从而加速铁向磁铁矿的转化。相反,氯霉素通过硝基还原和抑制胞外电子转移争夺微生物电子来抑制Fe(II)的产生,从而在针铁矿阶段动态捕获矿物转化。磺胺甲恶唑被生物源铁(II)通过N-O键解理还原降解,促进绿锈形成并进一步促进磁铁矿成核,而氯霉素主要被微生物或矿物表面水解而不参与铁(III)的还原。这些发现表明,抗生素既可以作为电子介质,也可以作为竞争对手,直接将其降解与铁氧化还原循环结合起来,控制矿物转化途径。这项工作为抗生素的环境持久性及其先前被忽视的矿物质转化作用提供了新的见解,对管理抗生素污染的生态系统具有重要意义。
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来源期刊
Environmental Science: Nano
Environmental Science: Nano CHEMISTRY, MULTIDISCIPLINARY-ENVIRONMENTAL SCIENCES
CiteScore
12.20
自引率
5.50%
发文量
290
审稿时长
2.1 months
期刊介绍: Environmental Science: Nano serves as a comprehensive and high-impact peer-reviewed source of information on the design and demonstration of engineered nanomaterials for environment-based applications. It also covers the interactions between engineered, natural, and incidental nanomaterials with biological and environmental systems. This scope includes, but is not limited to, the following topic areas: Novel nanomaterial-based applications for water, air, soil, food, and energy sustainability Nanomaterial interactions with biological systems and nanotoxicology Environmental fate, reactivity, and transformations of nanoscale materials Nanoscale processes in the environment Sustainable nanotechnology including rational nanomaterial design, life cycle assessment, risk/benefit analysis
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