4.5 Article

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

Journal

AMERICAN MINERALOGIST
Volume 93, Issue 4, Pages 540-547

Publisher

MINERALOGICAL SOC AMER
DOI: 10.2138/am.2008.2467

Keywords

Fe(III)-reduction; magnetite; biogenic transformation; ferrihydrite; diffraction; goethite; Geobacter

Funding

  1. Biotechnology and Biological Sciences Research Council [BB/E004601/1] Funding Source: researchfish
  2. Engineering and Physical Sciences Research Council [EP/D058767/1] Funding Source: researchfish
  3. Natural Environment Research Council [NE/B503309/1] Funding Source: researchfish
  4. BBSRC [BB/E004601/1] Funding Source: UKRI
  5. EPSRC [EP/D058767/1] Funding Source: UKRI

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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.

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