Beyenal Haluk, Sani Rajesh K, Peyton Brent M, Dohnalkova Alice C, Amonette James E, Lewandowski Zbigniew
Center for Biofilm Engineering and Department of Civil Engineering, Montana State University, Bozeman, Montana 59717-3980, USA.
Environ Sci Technol. 2004 Apr 1;38(7):2067-74. doi: 10.1021/es0348703.
Hexavalent uranium [U(VI)] was immobilized using biofilms of the sulfate-reducing bacterium (SRB) Desulfovibrio desulfuricans G20. The biofilms were grown in flat-plate continuous-flow reactors using lactate as the electron donor and sulfate as the electron acceptor. U(VI)was continuously fed into the reactor for 32 weeks at a concentration of 126 microM. During this time, the soluble U(VI) was removed (between 88 and 96% of feed) from solution and immobilized in the biofilms. The dynamics of U immobilization in the sulfate-reducing biofilms were quantified by estimating: (1) microbial activity in the SRB biofilm, defined as the hydrogen sulfide (H2S) production rate and estimated from the H2S concentration profiles measured using microelectrodes across the biofilms; (2) concentration of dissolved U in the solution; and (3) the mass of U precipitated in the biofilm. Results suggest that U was immobilized in the biofilms as a result of two processes: (1) enzymatically and (2) chemically, by reacting with microbially generated H2S. Visual inspection showed that the dissolved sulfide species reacted with U(VI) to produce a black precipitate. Synchrotron-based U L3-edge X-ray absorption near edge structure (XANES) spectroscopy analysis of U precipitated abiotically by sodium sulfide indicated that U(VI) had been reduced to U(IV). Selected-area electron diffraction pattern and crystallographic analysis of transmission electron microscope lattice-fringe images confirmed the structure of precipitated U as being that of uraninite.
利用硫酸盐还原菌(SRB)脱硫弧菌G20的生物膜固定六价铀[U(VI)]。生物膜在平板连续流反应器中生长,以乳酸作为电子供体,硫酸盐作为电子受体。将U(VI)以126微摩尔的浓度连续加入反应器中32周。在此期间,可溶性U(VI)从溶液中被去除(占进料的88%至96%)并固定在生物膜中。通过估计以下参数来量化硫酸盐还原生物膜中U的固定动力学:(1)SRB生物膜中的微生物活性,定义为硫化氢(H2S)产生速率,并根据使用微电极测量的生物膜上的H2S浓度分布来估计;(2)溶液中溶解的U的浓度;(3)生物膜中沉淀的U的质量。结果表明,U通过两个过程固定在生物膜中:(1)酶促过程和(2)化学过程,即与微生物产生的H2S反应。目视检查表明溶解的硫化物与U(VI)反应产生黑色沉淀。对硫化钠非生物沉淀的U进行基于同步加速器的U L3边缘X射线吸收近边结构(XANES)光谱分析表明,U(VI)已还原为U(IV)。选区电子衍射图和透射电子显微镜晶格条纹图像的晶体学分析证实沉淀的U的结构为晶质铀矿。