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细菌胞外聚合物与针铁矿的相互作用:宏观和光谱学联合研究。

Reactions between bacterial exopolymers and goethite: A combined macroscopic and spectroscopic investigation.

机构信息

State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China; State Key Laboratory of Soil Erosion and Dryland Farming on Loess Plateau, Institute of Soil and Water Conservation, Chinese Academy of Sciences and Ministry of Water Resources, Yangling 712100, China.

State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China.

出版信息

Water Res. 2012 Nov 1;46(17):5613-5620. doi: 10.1016/j.watres.2012.07.046. Epub 2012 Aug 13.

Abstract

The adsorption to goethite of extracellular polymeric substances (EPS) isolated from Pseudomonas putida was investigated using batch adsorption experiments, electrophoretic mobility (EM) measurements, Fourier transform infrared (FTIR) spectroscopy, isothermal titration calorimetry (ITC) and X-ray absorption fine structure (XAFS) spectroscopy. The adsorption of EPS decreased the point of zero charge of goethite from 7.6 to 3.2, suggesting the formation of negatively charged inner-sphere surface complexes. The adsorption isotherms of EPS on goethite conformed to the Langmuir equation. The adsorption energy constant (K) of EPS on goethite was in the sequence of EPS phosphate-containing moieties > nitrogen-containing moieties > carbon-containing moieties, indicating those containing phosphate were the most strongly adsorbed. FTIR showed ligand exchange of phosphate groups of EPS with surface hydroxyls on goethite. Extended X-ray absorption fine structure (EXAFS) and X-ray absorption near edge structure (XANES) spectroscopy results further demonstrated phosphate groups of EPS can form monodentate inner-sphere complexes at lower pH 3.0, while form bidentate inner-sphere complexes at higher pH 9.0. The oxidation state of iron in goethite was not changed after the reaction with EPS at different pH values. The information obtained in this study is of fundamental significance for the understanding of the interaction mechanisms between bacteria and minerals in soil and aquatic environments.

摘要

采用批量吸附实验、电泳迁移率(EM)测量、傅里叶变换红外(FTIR)光谱、等温热滴定(ITC)和 X 射线吸收精细结构(XAFS)光谱研究了从假单胞菌中分离出的胞外聚合物(EPS)对针铁矿的吸附作用。EPS 的吸附降低了针铁矿的零电荷点从 7.6 至 3.2,表明形成了带负电荷的内球表面配合物。EPS 在针铁矿上的吸附等温线符合朗缪尔方程。EPS 在针铁矿上的吸附能常数(K)的顺序为 EPS 含磷部分 > 含氮部分 > 含碳部分,表明含磷部分吸附最强。FTIR 表明 EPS 中的磷酸基团与针铁矿表面的羟基发生了配体交换。扩展 X 射线吸收精细结构(EXAFS)和 X 射线吸收近边结构(XANES)光谱结果进一步表明,在较低 pH 值 3.0 下,EPS 的磷酸基团可以形成单齿内球配合物,而在较高 pH 值 9.0 下形成双齿内球配合物。在不同 pH 值下与 EPS 反应后,针铁矿中铁的氧化态没有变化。本研究获得的信息对于理解土壤和水生环境中细菌与矿物之间的相互作用机制具有重要的基础意义。

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