c-Type cytochrome-dependent formation of U(IV) nanoparticles by Shewanella oneidensis

Autor: Daad A. Saffarini, John M. Zachara, Matthew J. Marshall, Alexander S. Beliaev, Jeffrey S. McLean, David W. Kennedy, Barry Lai, Samantha B. Reed, Alice Dohnalkova, Vanessa L. Bailey, Margaret F. Romine, Maxim I. Boyanov, David E. Culley, Cody J. Simonson, James K. Fredrickson, Kenneth M. Kemner, Zheming Wang, Liang Shi
Jazyk: angličtina
Rok vydání: 2006
Předmět:
Shewanella
Cytochrome
QH301-705.5
Iron
Mineralogy
chemistry.chemical_element
Metal Nanoparticles
Cytochrome c Group
Glycocalyx
Redox
Microbiology
General Biochemistry
Genetics and Molecular Biology

Metal
Uraninite
Bioremediation
Extracellular polymeric substance
Tissue Distribution
Shewanella oneidensis
Biology (General)
chemistry.chemical_classification
General Immunology and Microbiology
biology
General Neuroscience
Polysaccharides
Bacterial

Phosphorus
Periplasmic space
Electron acceptor
Uranium
biology.organism_classification
Uranium Compounds
Eubacteria
Biodegradation
Environmental

Membrane
chemistry
Environmental chemistry
visual_art
Synopsis
biology.protein
visual_art.visual_art_medium
Environmental science
General Agricultural and Biological Sciences
Bacterial outer membrane
Oxidation-Reduction
Bacterial Outer Membrane Proteins
Nuclear chemistry
Research Article
Zdroj: PLoS Biology, Vol 4, Iss 9, p e268 (2006)
PLoS Biology
PLoS Biology, Vol 4, Iss 8, p e282 (2006)
ISSN: 1545-7885
1544-9173
Popis: Modern approaches for bioremediation of radionuclide contaminated environments are based on the ability of microorganisms to effectively catalyze changes in the oxidation states of metals that in turn influence their solubility. Although microbial metal reduction has been identified as an effective means for immobilizing highly-soluble uranium(VI) complexes in situ, the biomolecular mechanisms of U(VI) reduction are not well understood. Here, we show that c-type cytochromes of a dissimilatory metal-reducing bacterium, Shewanella oneidensis MR-1, are essential for the reduction of U(VI) and formation of extracelluar UO 2 nanoparticles. In particular, the outer membrane (OM) decaheme cytochrome MtrC (metal reduction), previously implicated in Mn(IV) and Fe(III) reduction, directly transferred electrons to U(VI). Additionally, deletions of mtrC and/or omcA significantly affected the in vivo U(VI) reduction rate relative to wild-type MR-1. Similar to the wild-type, the mutants accumulated UO 2 nanoparticles extracellularly to high densities in association with an extracellular polymeric substance (EPS). In wild-type cells, this UO 2-EPS matrix exhibited glycocalyx-like properties and contained multiple elements of the OM, polysaccharide, and heme-containing proteins. Using a novel combination of methods including synchrotron-based X-ray fluorescence microscopy and high-resolution immune-electron microscopy, we demonstrate a close association of the extracellular UO 2 nanoparticles with MtrC and OmcA (outer membrane cytochrome). This is the first study to our knowledge to directly localize the OM-associated cytochromes with EPS, which contains biogenic UO 2 nanoparticles. In the environment, such association of UO 2 nanoparticles with biopolymers may exert a strong influence on subsequent behavior including susceptibility to oxidation by O 2 or transport in soils and sediments.
Microorganisms that catalyze changes in oxidation states of metals can be used to decontaminate environments of radionuclides. Here, c-type cytochromes on the outer membrane of a dissimilatory metal reducing bacterium are shown to be essential for the reduction of uranium(VI).
Databáze: OpenAIRE