Time-resolved synchrotron powder X-ray diffraction study of magnetite formation by the Fe(III)-reducing bacterium Geobacter sulfurreducens

被引:60
作者
Coker, Victoria S. [1 ]
Bell, Anthony M. T. [2 ]
Pearce, Carolyn I. [1 ]
Pattrick, Richard A. D. [1 ]
van der Laan, Gerrit [1 ,2 ,3 ]
Lloyd, Jonathan R. [1 ]
机构
[1] Univ Manchester, Sch Earth Atmospher & Environm Sci, Manchester M13 9PL, Lancs, England
[2] Daresbury Lab, STFC, Warrington WA4 4AD, Cheshire, England
[3] Diamond Light Source, Didcot OX11 0DE, Oxon, England
基金
英国工程与自然科学研究理事会; 英国自然环境研究理事会; 英国生物技术与生命科学研究理事会;
关键词
Fe(III)-reduction; magnetite; biogenic transformation; ferrihydrite; diffraction; goethite; Geobacter;
D O I
10.2138/am.2008.2467
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
The Fe(III)-reducing bacterium Geobacter sulfurreducens produces nanometer-sized magnetite by transferring electrons from organic matter or hydrogen to ferrihydrite, resulting in the reductive transformation of the ferrihydrite to magnetite, and the generation of ATP for growth. Electron transfer can occur by direct contact between the cell surface and the mineral or via a soluble "electron shuttle," for example a quinone-containing humic species. The minerals produced at different stages of ferrihydrite reduction during two experiments, one with and one without the humic analog anthraquinone-2, 6-disulphonate (AQDS), were measured using high-resolution synchrotron powder X-ray diffraction. Amorphous 2-line ferrihydrite converts to goethite, then to a mixture of goethite and magnetite, and finally to magnetite. Samples with and without AQDS showed the same general mineralogical trends, and the rate of reaction was faster in the presence of AQDS. In addition, two transient minerals structurally similar to goethite and magnetite were observed to form as intermediates between ferrihydrite and goethite and goethite and magnetite, but only in samples produced in the absence of the electron shuttle. These transient minerals were named proto-goethite and proto-magnetite. Proto-goethite has a shorter c-axis [4.467(20) angstrom] than crystalline goethite, a function of size (<2 nm) where quantum properties prevail. Proto-magnetite is identified by long tetrahedral (2.113 angstrom) and short octahedral (1.943 angstrom) Fe-O bonds compared to stoichiometric magnetite, possibly indicative of a coordination crossover caused by charge density [Fe(II)] migration to tetrahedral sites. Fe(II) in solution or sorbed to the mineral surface is considered to be the catalyst causing the mineral transformations. The Fe(II) is thought to form predominantly from the reductive dissolution of 2-line ferrihydrite by G. sulfurreducens.
引用
收藏
页码:540 / 547
页数:8
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