4.8 Article

U(VI) Reduction to Mononuclear U(IV) by Desulfitobacterium Species

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 44, Issue 12, Pages 4705-4709

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/es903636c

Keywords

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Funding

  1. U.S. DOE Office of Science (OS), Biological and Environmental Research Division (BER)
  2. Environmental Remediation Sciences Program [ER64782]
  3. U.S. Department of Energy Basic Energy Sciences (BES) Division [DE-AC0-206CH11357]
  4. NSF IGERT
  5. NSF

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The bioreduction of U(VI) to U(IV) affects uranium mobility and fate in contaminated subsurface environments and is best understood in Gram-negative model organisms such as Geobacter and Shewanella spp. This study demonstrates that U(VI) reduction is a common trait of Gram-positive Desulfitobacterium spp. Five different Desulfitobacterium isolates reduced 100 mu M A U(VI) to U(IV) in <10 days, whereas U(VI) remained soluble in abiotic and heat-killed controls. U(VI) reduction in live cultures was confirmed using X-ray absorption near-edge structure (XANES) analysis. Interestingly, although bioreduction of U(VI) is almost always reported to yield the uraninite mineral (UO2), extended X-ray absorption fine structure (EXAFS) analysis demonstrated that the U(IV) produced in the Desulfitobacterium cultures was not UO2. The EXAFS data indicated that the U(IV) product was a phase or mineral composed of mononuclear U(IV) atoms closely surrounded by light element shells. This atomic arrangement likely results from inner-sphere bonds between U(IV) and C/N/0- or P/S-containing ligands, such as carbonate or phosphate. The formation of a distinct U(IV) phase warrants further study because the characteristics of the reduced material affect uranium stability and fate in the contaminated subsurface.

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