Taillefert Martial, Beckler Jordon S, Carey Elizabeth, Burns Justin L, Fennessey Christine M, DiChristina Thomas J
School of Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, GA 30332-0340, USA.
J Inorg Biochem. 2007 Nov;101(11-12):1760-7. doi: 10.1016/j.jinorgbio.2007.07.020. Epub 2007 Jul 25.
The mechanism of Fe(III) reduction was investigated using voltammetric techniques in anaerobic incubations of Shewanella putrefaciens strain 200 supplemented with Fe(III) citrate or a suite of Fe(III) oxides as terminal electron acceptor. Results indicate that organic complexes of Fe(III) are produced during the reduction of Fe(III) at rates that correlate with the reactivity of the Fe(III) phase and bacterial cell density. Anaerobic Fe(III) solubilization activity is detected with either Fe(III) oxides or Fe(III) citrate, suggesting that the organic ligand produced is strong enough to destabilize Fe(III) from soluble or solid Fe(III) substrates. Results also demonstrate that Fe(III) oxide dissolution is not controlled by the intrinsic chemical reactivity of the Fe(III) oxides. Instead, the chemical reaction between the endogenous organic ligand is only affected by the number of reactive surface sites available to S. putrefaciens. This report describes the first application of voltammetric techniques to demonstrate production of soluble organic-Fe(III) complexes by any Fe(III)-reducing microorganism and is the first report of a Fe(III)-solubilizing ligand generated by a metal-reducing member of the genus Shewanella.
在补充有柠檬酸铁或一组铁(III)氧化物作为末端电子受体的腐败希瓦氏菌菌株200的厌氧培养中,使用伏安技术研究了铁(III)还原的机制。结果表明,在铁(III)还原过程中会产生铁(III)的有机络合物,其产生速率与铁(III)相的反应性和细菌细胞密度相关。用铁(III)氧化物或柠檬酸铁都检测到厌氧铁(III)溶解活性,这表明产生的有机配体足够强,能够使可溶性或固体铁(III)底物中的铁(III)不稳定。结果还表明,铁(III)氧化物的溶解不受铁(III)氧化物固有化学反应性的控制。相反,内源性有机配体之间的化学反应仅受腐败希瓦氏菌可用反应性表面位点数量的影响。本报告描述了伏安技术首次应用于证明任何铁(III)还原微生物产生可溶性有机 - 铁(III)络合物,并且是希瓦氏菌属金属还原成员产生铁(III)溶解配体的首次报告。