Technetium reduction and precipitation by sulfate-reducing bacteria

被引:97
作者
Lloyd, JR
Nolting, HF
Sole, VA
Bosecker, K
机构
[1] Univ Birmingham, Sch Biol Sci, Birmingham B15 2TT, W Midlands, England
[2] DESY, European Mol Biol Lab, Hamburg Outstn, D-2000 Hamburg, Germany
[3] Fed Inst Geosci & Nat Resources, D-3000 Hannover, Germany
基金
英国医学研究理事会; 英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
biomineralization; metal reduction; radionuclide bioaccumulation;
D O I
10.1080/01490459809378062
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Resting cells of the sulfate-reducing bacterium Desulfovibrio desulfuricans ATCC 29577 were able to precipitate the radionuclide technetium, supplied as the pertechnetate anion (TcO4-), under anaerobic conditions by two discrete mechanisms. Sulfidogenic cultures, supplied with sulfate and lactate as an electron acceptor and donor, respectively, precipitated the radionuclide as an insoluble sulfhide. Using electron microscopy in combination with energy-dispersive x-ray analysis (EDAX), the precipitate was shown to be extracellular, and contained S as the major element at a fivefold stoichiometric excess to Tc as quantified by proton-induced x-ray emission analysis (PIXE). With hydrogen supplied as the electron donor, the pertechnetate anion was utilized as an alternative electron acceptor in the absence of sulfate. The radionuclide was removed from solution, but in these cultures the precipitate was cell associated, with Tc as the major element detected by PIXE (Tc:S ratio of 2:1). Reduction of the radionuclide in lieu of sulfate was confirmed using XAS. Hydrogen uptake, couple to metal reduction, was also monitored manometrically, with 1 mol H-2 used to reduce 1 mol TcO4-. The implications of these results on Tc mobility in the environment are discussed, and possible biotechnological uses of sulfate-reducing bacteria in bioremediation programs to treat Tc-contaminated waters are highlighted.
引用
收藏
页码:45 / 58
页数:14
相关论文
共 28 条
[1]   ELECTRONIC AND STRUCTURAL INVESTIGATIONS OF TECHNETIUM COMPOUNDS BY X-RAY-ABSORPTION SPECTROSCOPY [J].
ALMAHAMID, I ;
BRYAN, JC ;
BUCHER, JJ ;
BURRELL, AK ;
EDELSTEIN, NM ;
HUDSON, EA ;
KALTSOYANNIS, N ;
LUKENS, WW ;
SHUH, DK ;
NITSCHE, H ;
REICH, T .
INORGANIC CHEMISTRY, 1995, 34 (01) :193-198
[2]   COMPARATIVE METABOLIC BEHAVIOR AND INTERRELATIONSHIPS OF TC AND S IN SOYBEAN PLANTS [J].
CATALDO, DA ;
GARLAND, TR ;
WILDUNG, RE ;
FELLOWS, RJ .
HEALTH PHYSICS, 1989, 57 (02) :281-287
[3]   THE OXFORD SUBMICRON NUCLEAR MICROSCOPY FACILITY [J].
GRIME, GW ;
DAWSON, M ;
MARSH, M ;
MCARTHUR, IC ;
WATT, F .
NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION B-BEAM INTERACTIONS WITH MATERIALS AND ATOMS, 1991, 54 (1-3) :52-63
[4]   BIOACCUMULATION AND CHEMICAL MODIFICATION OF TC BY SOIL BACTERIA [J].
HENROT, J .
HEALTH PHYSICS, 1989, 57 (02) :239-245
[5]   A DOUBLE-FOCUSING EXAFS BEAM LINE, DATA ACQUISITION AND EVALUATION SYSTEM FOR BIOLOGICAL APPLICATIONS [J].
HERMES, C ;
GILBERG, E ;
KOCH, MHJ .
NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION A-ACCELERATORS SPECTROMETERS DETECTORS AND ASSOCIATED EQUIPMENT, 1984, 222 (1-2) :207-214
[6]  
JOHANNSON SAE, 1988, PIXE NOVEL TECHNIQUE
[7]  
Kotegov K., 1968, ADV INORG CHEM RAD, V11, P1
[8]  
Lloyd JR, 1997, BIOTECHNOL BIOENG, V55, P505, DOI 10.1002/(SICI)1097-0290(19970805)55:3<505::AID-BIT6>3.0.CO
[9]  
2-G
[10]   Reduction and removal of heptavalent technetium from solution by Escherichia coli [J].
Lloyd, JR ;
Cole, JA ;
Macaskie, LE .
JOURNAL OF BACTERIOLOGY, 1997, 179 (06) :2014-2021