Literature DB >> 9835573

Enumeration and detection of anaerobic ferrous iron-oxidizing, nitrate-reducing bacteria from diverse European sediments.

K L Straub1, B E Buchholz-Cleven.   

Abstract

Anaerobic, nitrate-dependent microbial oxidation of ferrous iron was recently recognized as a new type of metabolism. In order to study the occurrence of three novel groups of ferrous iron-oxidizing, nitrate-reducing bacteria (represented by strains BrG1, BrG2, and BrG3), 16S rRNA-targeted oligonucleotide probes were developed. In pure-culture experiments, these probes were shown to be suitable for fluorescent in situ hybridization, as well as for hybridization analysis of denaturing gradient gel electrophoresis (DGGE) patterns. However, neither enumeration by in situ hybridization nor detection by the DGGE-hybridization approach was feasible with sediment samples. Therefore, the DGGE-hybridization approach was combined with microbiological methods. Freshwater sediment samples from different European locations were used for enrichment cultures and most-probable-number (MPN) determinations. Bacteria with the ability to oxidize ferrous iron under nitrate-reducing conditions were detected in all of the sediment samples investigated. At least one of the previously described types of bacteria was detected in each enrichment culture. MPN studies showed that sediments contained from 1 x 10(5) to 5 x 10(8) ferrous iron-oxidizing, nitrate-reducing bacteria per g (dry weight) of sediment, which accounted for at most 0.8% of the nitrate-reducing bacteria growing with acetate. Type BrG1, BrG2, and BrG3 bacteria accounted for an even smaller fraction (0.2% or less) of the ferrous iron-oxidizing, nitrate-reducing community. The DGGE patterns of MPN cultures suggested that more organisms than those isolated thus far are able to oxidize ferrous iron with nitrate. A comparison showed that among the anoxygenic phototrophic bacteria, organisms that have the ability to oxidize ferrous iron also account for only a minor fraction of the population.

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Year:  1998        PMID: 9835573      PMCID: PMC90933     

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  28 in total

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4.  Phylogenetic probes for analyzing abundance and spatial organization of nitrifying bacteria.

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5.  Phylogenetic stains: ribosomal RNA-based probes for the identification of single cells.

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Authors:  N B Ramsing; H Fossing; T G Ferdelman; F Andersen; B Thamdrup
Journal:  Appl Environ Microbiol       Date:  1996-04       Impact factor: 4.792

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Authors:  A Alfreider; J Pernthaler; R Amann; B Sattler; F Glockner; A Wille; R Psenner
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Journal:  Appl Environ Microbiol       Date:  2011-10-14       Impact factor: 4.792

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Journal:  Appl Environ Microbiol       Date:  2006-01       Impact factor: 4.792

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7.  Specific detection, isolation, and characterization of selected, previously uncultured members of the freshwater bacterioplankton community.

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10.  Fe(II) oxidation is an innate capability of nitrate-reducing bacteria that involves abiotic and biotic reactions.

Authors:  Hans K Carlson; Iain C Clark; Steven J Blazewicz; Anthony T Iavarone; John D Coates
Journal:  J Bacteriol       Date:  2013-05-17       Impact factor: 3.490

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