Anaerobic redox cycling of iron by freshwater sediment microorganisms

Summary The potential for microbially mediated anaerobic redox cycling of iron (Fe) was examined in a first‐generation enrichment culture of freshwater wetland sediment microorganisms. Most probable number enumerations revealed the presence of significant populations of Fe(III)‐reducing (approximate...

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Published inEnvironmental microbiology Vol. 8; no. 1; pp. 100 - 113
Main Authors Weber, Karrie A., Urrutia, Matilde M., Churchill, Perry F., Kukkadapu, Ravi K., Roden, Eric E.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Science Ltd 01.01.2006
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Summary:Summary The potential for microbially mediated anaerobic redox cycling of iron (Fe) was examined in a first‐generation enrichment culture of freshwater wetland sediment microorganisms. Most probable number enumerations revealed the presence of significant populations of Fe(III)‐reducing (approximately 108 cells ml−1) and Fe(II)‐oxidizing, nitrate‐reducing organisms (approximately 105 cells ml−1) in the freshwater sediment used to inoculate the enrichment cultures. Nitrate reduction commenced immediately following inoculation of acetate‐containing (approximately 1 mM) medium with a small quantity (1% v/v) of wetland sediment, and resulted in the transient accumulation of NO2− and production of a mixture of gaseous end‐products (N2O and N2) and NH4+. Fe(III) oxide (high surface area goethite) reduction took place after NO3− was depleted and continued until all the acetate was utilized. Addition of NO3− after Fe(III) reduction ceased resulted in the immediate oxidation of Fe(II) coupled to reduction of NO3− to NH4+. No significant NO2− accumulation was observed during nitrate‐dependent Fe(II) oxidation. No Fe(II) oxidation occurred in pasteurized controls. Microbial community structure in the enrichment was monitored by denaturing gradient gel electrophoresis analysis of polymerase chain reaction‐amplified 16S rDNA and reverse transcription polymerase chain reaction‐amplified 16S rRNA, as well as by construction of 16S rDNA clone libraries for four different time points during the experiment. Strong similarities in dominant members of the microbial community were observed in the Fe(III) reduction and nitrate‐dependent Fe(II) oxidation phases of the experiment, specifically the common presence of organisms closely related (≥ 95% sequence similarity) to the genera Geobacter and Dechloromonas. These results indicate that the wetland sediments contained organisms such as Geobacter sp. which are capable of both dissimilatory Fe(III) reduction and oxidation of Fe(II) with reduction of NO3− to NH4+. Our findings suggest that microbially catalysed nitrate‐dependent Fe(II) oxidation has the potential to contribute to a dynamic anaerobic Fe redox cycle in freshwater sediments.
Bibliography:istex:8B2A95EDC0BBEFD00BBE760A57515C6C92E53CD1
ArticleID:EMI873
ark:/67375/WNG-60F1QZQH-K
Present address: University of California, Department of Plant and Microbial Biology, Berkeley, CA 94720‐3102, USA.
ObjectType-Article-1
SourceType-Scholarly Journals-1
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USDOE
AC05-76RL01830
PNNL-SA-43700
ISSN:1462-2912
1462-2920
DOI:10.1111/j.1462-2920.2005.00873.x