Literature DB >> 26682861

Coexistence of Microaerophilic, Nitrate-Reducing, and Phototrophic Fe(II) Oxidizers and Fe(III) Reducers in Coastal Marine Sediment.

Katja Laufer1, Mark Nordhoff1, Hans Røy2, Caroline Schmidt1, Sebastian Behrens1,3, Bo Barker Jørgensen2, Andreas Kappler4,2.   

Abstract

Iron is abundant in sediments, where it can be biogeochemically cycled between its divalent and trivalent redox states. The neutrophilic microbiological Fe cycle involves Fe(III)-reducing and three different physiological groups of Fe(II)-oxidizing microorganisms, i.e., microaerophilic, anoxygenic phototrophic, and nitrate-reducing Fe(II) oxidizers. However, it is unknown whether all three groups coexist in one habitat and how they are spatially distributed in relation to gradients of O2, light, nitrate, and Fe(II). We examined two coastal marine sediments in Aarhus Bay, Denmark, by cultivation and most probable number (MPN) studies for Fe(II) oxidizers and Fe(III) reducers and by quantitative-PCR (qPCR) assays for microaerophilic Fe(II) oxidizers. Our results demonstrate the coexistence of all three metabolic types of Fe(II) oxidizers and Fe(III) reducers. In qPCR, microaerophilic Fe(II) oxidizers (Zetaproteobacteria) were present with up to 3.2 × 10(6) cells g dry sediment(-1). In MPNs, nitrate-reducing Fe(II) oxidizers, anoxygenic phototrophic Fe(II) oxidizers, and Fe(III) reducers reached cell numbers of up to 3.5 × 10(4), 3.1 × 10(2), and 4.4 × 10(4) g dry sediment(-1), respectively. O2 and light penetrated only a few millimeters, but the depth distribution of the different iron metabolizers did not correlate with the profile of O2, Fe(II), or light. Instead, abundances were homogeneous within the upper 3 cm of the sediment, probably due to wave-induced sediment reworking and bioturbation. In microaerophilic Fe(II)-oxidizing enrichment cultures, strains belonging to the Zetaproteobacteria were identified. Photoferrotrophic enrichments contained strains related to Chlorobium and Rhodobacter; the nitrate-reducing Fe(II) enrichments contained strains related to Hoeflea and Denitromonas. This study shows the coexistence of all three types of Fe(II) oxidizers in two near-shore marine environments and the potential for competition and interrelationships between them.
Copyright © 2016, American Society for Microbiology. All Rights Reserved.

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Year:  2015        PMID: 26682861      PMCID: PMC4771319          DOI: 10.1128/AEM.03527-15

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


  66 in total

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6.  The anaerobic degradation of organic matter in Danish coastal sediments: iron reduction, manganese reduction, and sulfate reduction.

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9.  Anaerobic Fe(II)-oxidizing bacteria show as resistance and immobilize as during Fe(III) mineral precipitation.

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  15 in total

1.  Microaerophilic Fe(II)-Oxidizing Zetaproteobacteria Isolated from Low-Fe Marine Coastal Sediments: Physiology and Composition of Their Twisted Stalks.

Authors:  K Laufer; M Nordhoff; M Halama; R E Martinez; M Obst; M Nowak; H Stryhanyuk; H H Richnow; A Kappler
Journal:  Appl Environ Microbiol       Date:  2017-03-31       Impact factor: 4.792

2.  Genomic Insights into Two Novel Fe(II)-Oxidizing Zetaproteobacteria Isolates Reveal Lifestyle Adaption to Coastal Marine Sediments.

Authors:  Nia Blackwell; Casey Bryce; Daniel Straub; Andreas Kappler; Sara Kleindienst
Journal:  Appl Environ Microbiol       Date:  2020-08-18       Impact factor: 4.792

3.  Growth and Population Dynamics of the Anaerobic Fe(II)-Oxidizing and Nitrate-Reducing Enrichment Culture KS.

Authors:  Claudia Tominski; Helene Heyer; Tina Lösekann-Behrens; Sebastian Behrens; Andreas Kappler
Journal:  Appl Environ Microbiol       Date:  2018-04-16       Impact factor: 4.792

4.  Insights into Carbon Metabolism Provided by Fluorescence In Situ Hybridization-Secondary Ion Mass Spectrometry Imaging of an Autotrophic, Nitrate-Reducing, Fe(II)-Oxidizing Enrichment Culture.

Authors:  Claudia Tominski; Tina Lösekann-Behrens; Alexander Ruecker; Nikolas Hagemann; Sara Kleindienst; Carsten W Mueller; Carmen Höschen; Ingrid Kögel-Knabner; Andreas Kappler; Sebastian Behrens
Journal:  Appl Environ Microbiol       Date:  2018-04-16       Impact factor: 4.792

5.  Proteome Response of a Metabolically Flexible Anoxygenic Phototroph to Fe(II) Oxidation.

Authors:  Casey Bryce; Mirita Franz-Wachtel; Nicolas C Nalpas; Jennyfer Miot; Karim Benzerara; James M Byrne; Sara Kleindienst; Boris Macek; Andreas Kappler
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6.  Cryptic Cycling of Complexes Containing Fe(III) and Organic Matter by Phototrophic Fe(II)-Oxidizing Bacteria.

Authors:  Chao Peng; Casey Bryce; Anneli Sundman; Andreas Kappler
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7.  Biological rejuvenation of iron oxides in bioturbated marine sediments.

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8.  Meta-omics Reveal Gallionellaceae and Rhodanobacter Species as Interdependent Key Players for Fe(II) Oxidation and Nitrate Reduction in the Autotrophic Enrichment Culture KS.

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Journal:  Appl Environ Microbiol       Date:  2021-07-13       Impact factor: 4.792

9.  Evidence for the Existence of Autotrophic Nitrate-Reducing Fe(II)-Oxidizing Bacteria in Marine Coastal Sediment.

Authors:  Katja Laufer; Hans Røy; Bo Barker Jørgensen; Andreas Kappler
Journal:  Appl Environ Microbiol       Date:  2016-09-30       Impact factor: 4.792

10.  Zetaproteobacteria Pan-Genome Reveals Candidate Gene Cluster for Twisted Stalk Biosynthesis and Export.

Authors:  Elif Koeksoy; Oliver M Bezuidt; Timm Bayer; Clara S Chan; David Emerson
Journal:  Front Microbiol       Date:  2021-06-18       Impact factor: 5.640

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