ArticleFrontiers in microbiology2015
Fe biomineralization mirrors individual metabolic activity in a nitrate-dependent Fe(II)-oxidizer.
Article in Frontiers in microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.
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Who cites it
17 citing papers in PubMed.
- Article
- Endogenous iron biomineralization in the mouse spleen of metabolic diseases.Fundamental research · 2026Article
- Therapeutic and antioxidant potential of bionanofactory Ochrobactrum sp.-mediated magnetite and zerovalent iron nanoparticles against acute experimental toxoplasmosis.PLoS neglected tropical diseases · 2023Article
- Underestimation about the Contribution of Nitrate Reducers to Iron Cycling Indicated byMolecules (Basel, Switzerland) · 2022Article
- Elucidating heterogeneous iron biomineralization patterns in a denitrifying As(iii)-oxidizing bacterium: implications for arsenic immobilization.Environmental science. Nano · 2022Article
- Controlling pore-scale processes to tame subsurface biomineralization.Re/views in environmental science and bio/technology · 2022Review
- Oligotrophic Growth of Nitrate-Dependent FeFrontiers in microbiology · 2022Article
- Forced Biomineralization: A Review.Biomimetics (Basel, Switzerland) · 2021Review
- Disinfection of water and wastewater by biosynthesized magnetite and zerovalent iron nanoparticles via NAP-NAR enzymes of Proteus mirabilis 10B.Environmental science and pollution research international · 2019Article
- Extreme Arsenic Bioaccumulation Factor Variability in Lake Titicaca, Bolivia.Scientific reports · 2019Article
- Draft Genome Sequences of the Nitrate-Dependent Iron-Oxidizing ProteobacteriaMicrobiology resource announcements · 2018Article
- NanoSIMS imaging of extracellular electron transport processes during microbial iron(III) reduction.FEMS microbiology ecology · 2018Article
- Identifying and Quantifying the Intermediate Processes during Nitrate-Dependent Iron(II) Oxidation.Environmental science & technology · 2018Article
- Nitrate-Dependent Iron Oxidation: A Potential Mars Metabolism.Frontiers in microbiology · 2018Article
- Novel Mechanism for Surface Layer Shedding and Regenerating in Bacteria Exposed to Metal-Contaminated Conditions.Frontiers in microbiology · 2018Article
- Preservation of Archaeal Surface Layer Structure During Mineralization.Scientific reports · 2016Article
- Article
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Microbial biomineralization sometimes leads to periplasmic encrustation, which is predicted to enhance microorganism preservation in the fossil record. Mineral precipitation within the periplasm is, however, thought to induce death, as a result of permeability loss preventing nutrient and waste transit across the cell wall. This hypothesis had, however, never been investigated down to the single cell level. Here, we cultured the nitrate reducing Fe(II) oxidizing bacteria Acidovorax sp. strain BoFeN1 that have been previously shown to promote the precipitation of a diversity of Fe minerals (lepidocrocite, goethite, Fe phosphate) encrusting the periplasm. We investigated the connection of Fe biomineralization with carbon assimilation at the single cell level, using a combination of electron microscopy and Nano-Secondary Ion Mass Spectrometry. Our analyses revealed strong individual heterogeneities of Fe biomineralization. Noteworthy, a small proportion of cells remaining free of any precipitate persisted even at advanced stages of biomineralization. Using pulse chase experiments with (13)C-acetate, we provide evidence of individual phenotypic heterogeneities of carbon assimilation, correlated with the level of Fe biomineralization. Whereas non- and moderately encrusted cells were able to assimilate acetate, higher levels of periplasmic encrustation prevented any carbon incorporation. Carbon assimilation only depended on the level of Fe encrustation and not on the nature of Fe minerals precipitated in the cell wall. Carbon assimilation decreased exponentially with increasing cell-associated Fe content. Persistence of a small proportion of non-mineralized and metabolically active cells might constitute a survival strategy in highly ferruginous environments. Eventually, our results suggest that periplasmic Fe biomineralization may provide a signature of individual metabolic status, which could be looked for in the fossil record and in modern environmental samples.
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