Wang Pingping, Dong Faqin, Wang Xuhui, Liu Mingxue, Nie Xiaoqin, Zhou Lei, Huo Tingting, Zhang Wei, Wei Hongfu
The Key Laboratory of Solid Waste Treatment and Resource, Ministry of Education, Southwest University of Science and Technology Mianyang Sichuan 621010 China
School of Environment and Resource, Southwest University of Science and Technology Mianyang Sichuan 621010 China.
RSC Adv. 2018 Aug 31;8(54):30692-30700. doi: 10.1039/c8ra05715j. eCollection 2018 Aug 30.
Understanding the mechanisms for electron shuttles (ESs) in microbial extracellular electron transfer (EET) is important in biogeochemical cycles, bioremediation applications, as well as bioenergy strategies. In this work, we adapted electrochemical techniques to probe electrochemically active and redox-active . This approach detected flavins and humic-like substances of , which were involved in electron transfer to the electrode. A combination of three-dimensional excitation-emission (EEM) florescence spectroscopy methods identified a mixture of riboflavin and humic-like substances in supernatants during sustained incubations. The reductive behaviour of U(vi) by in the presence of riboflavin (RF) and anthraquinone-2-sulfonate (AQS) was also investigated in this study. The results indicated that RF and AQS significantly accelerated electron transfer from cells to U(vi), thus enhancing reductive U(vi). The precipitate was further evidenced by SEM, FTIR, XPS and XRD, which demonstrated that chernikovite [H(UO)(PO)·8HO] became the main product on the cell surface of . In a contrast, U(iv) mainly existed amorphously on the cell surface of with added RF and AQS. This work has significant implications in elucidating RF and AQS as electron shuttles that are efficient in reduction of uranium in geological environments.
了解微生物细胞外电子转移(EET)中电子穿梭体(ESs)的机制在生物地球化学循环、生物修复应用以及生物能源策略中都很重要。在这项工作中,我们采用电化学技术来探测具有电化学活性和氧化还原活性的物质。这种方法检测到了参与向电极电子转移的黄素和类腐殖质物质。三维激发-发射(EEM)荧光光谱法相结合,确定了在持续培养过程中上清液中存在核黄素和类腐殖质物质的混合物。本研究还考察了在核黄素(RF)和蒽醌-2-磺酸盐(AQS)存在下,[物质名称缺失]对U(vi)的还原行为。结果表明,RF和AQS显著加速了电子从细胞向U(vi)的转移,从而增强了U(vi)的还原。通过扫描电子显微镜(SEM)、傅里叶变换红外光谱(FTIR)、X射线光电子能谱(XPS)和X射线衍射(XRD)进一步证实了沉淀物,结果表明磷铀矿[H(UO)(PO)·8HO]成为[微生物名称缺失]细胞表面的主要产物。相比之下,在添加RF和AQS的情况下,U(iv)主要以无定形形式存在于[微生物名称缺失]的细胞表面。这项工作对于阐明RF和AQS作为在地质环境中有效还原铀的电子穿梭体具有重要意义。