Barron A, Sun J, Passaretti S, Sbarbati C, Barbieri M, Colombani N, Jamieson J, Bostick BC, Zheng Y, Mastrocicco M, Petitta M, Prommer H (2022) In situ arsenic immobilisation for coastal aquifers using stimulated iron cycling: lab-based viability assessment. Appl Geochem 136:105155. https://doi.org/10.1016/j.apgeochem.2021.105155
Bayer T, Tomaszewski EJ, Bryce C, Kappler A, Byrne JM (2023) Continuous cultivation of the lithoautotrophic nitrate-reducing Fe(ii)-oxidizing culture ks in a chemostat bioreactor. Environ Microbiol Rep 15(4):324–334. https://doi.org/10.1111/1758-2229.13149
Beller HR, Zhou P, Legler TC, Chakicherla A, Kane S, Letain TE, O’Day PA (2013) Genome-enabled studies of anaerobic, nitrate-dependent iron oxidation in the chemolithoautotrophic bacterium Thiobacillus denitrificans. Front Microbiol. https://doi.org/10.3389/fmicb.2013.00249
Benzerara K, Miot J, Morin G, Ona-Nguema G, Skouri-Panet F, Férard C (2011) Significance, mechanisms and environmental implications of microbial biomineralization. C R Geosci 343(2–3):160–167. https://doi.org/10.1016/j.crte.2010.09.002
Berg M, Luzi S, Trang PTK, Viet PH, Giger W, Stüben D (2006) Arsenic removal from groundwater by household sand filters: comparative field study, model calculations, and health benefits. Environ Sci Technol 40(17):5567–5573. https://doi.org/10.1021/es060144z
Berg JS, Michellod D, Pjevac P, Martinez-Perez C, Buckner CRT, Hach PF, Schubert CJ, Milucka J, Kuypers MMM (2016) Intensive cryptic microbial iron cycling in the low iron water column of the meromictic Lake Cadagno: a cryptic microbial iron cycle. Environ Microbiol 18(12):5288–5302. https://doi.org/10.1111/1462-2920.13587
Blöthe M, Roden EE (2009) Composition and activity of an autotrophic Fe(II)-oxidizing, nitrate-reducing enrichment culture. Appl Environ Microbiol 75(21):6937–6940. https://doi.org/10.1128/AEM.01742-09
Bryce C, Blackwell N, Schmidt C, Otte J, Huang Y-M, Kleindienst S, Tomaszewski E, Schad M, Warter V, Peng C, Byrne JM, Kappler A (2018) Microbial anaerobic Fe(II) oxidation—ecology, mechanisms and environmental implications: microbial anaerobic Fe(II) oxidation. Environ Microbiol 20(10):3462–3483. https://doi.org/10.1111/1462-2920.14328
Burke IT, Boothman C, Lloyd JR, Livens FR, Charnock JM, McBeth JM, Mortimer RJG, Morris K (2006) Reoxidation behavior of technetium, iron, and sulfur in estuarine sediments. Environ Sci Technol 40(11):3529–3535. https://doi.org/10.1021/es052184t
Carlson HK, Clark IC, Melnyk RA, Coates JD (2012) Toward a mechanistic understanding of anaerobic nitrate-dependent iron oxidation: balancing electron uptake and detoxification. Front Microbiol. https://doi.org/10.3389/fmicb.2012.00057
Carlson HK, Clark IC, Blazewicz SJ, Iavarone AT, Coates JD (2013) Fe(II) oxidation is an innate capability of nitrate-reducing bacteria that involves abiotic and biotic reactions. J Bacteriol 195(14):3260–3268. https://doi.org/10.1128/JB.00058-13
Chakraborty A, Picardal F (2013a) Induction of nitrate-dependent Fe(II) oxidation by Fe(II) in Dechloromonas sp. strain UWNR4 and Acidovorax sp. strain 2AN. Appl Environ Microbiol 79(2):748–752. https://doi.org/10.1128/AEM.02709-12
Chakraborty A, Picardal F (2013b) Neutrophilic, nitrate-dependent, Fe(II) oxidation by a Dechloromonas species. World J Microbiol Biotechnol 29(4):617–623. https://doi.org/10.1007/s11274-012-1217-9
Chakraborty A, Roden EE, Schieber J, Picardal F (2011) Enhanced growth of Acidovorax sp. strain 2AN during nitrate-dependent Fe(II) oxidation in batch and continuous-flow systems. Appl Environ Microbiol 77(24):8548–8556. https://doi.org/10.1128/AEM.06214-11
Chaudhuri S, Lack J, Coates J (2001) Biogenic magnetite formation through anaerobic biooxidation of Fe(II). Appl Environ Microbiol. https://doi.org/10.1128/AEM.67.6.2844-2848.2001
Chen D, Cheng K, Liu T, Chen G, Kappler A, Li X, Zeng RJ, Yang Y, Yue F, Hu S, Cao F, Li F (2023) Novel insight into microbially mediated nitrate-reducing Fe(II) oxidation by Acidovorax sp. strain BoFeN1 using dual N-O isotope fractionation. Environ Sci Technol 57(33):12546–12555. https://doi.org/10.1021/acs.est.3c02329
Cheng K, Li H, Yuan X, Yin Y, Chen D, Wang Y, Li X, Chen G, Li F, Peng C, Wu Y, Liu T (2022) Hematite-promoted nitrate-reducing Fe(II) oxidation by Acidovorax sp. strain BoFeN1: roles of mineral catalysis and cell encrustation. Geobiology 20(6):810–822. https://doi.org/10.1111/gbi.12510
Coby AJ, Picardal F, Shelobolina E, Xu H, Roden EE (2011) Repeated anaerobic microbial redox cycling of iron. Appl Environ Microbiol 77(17):6036–6042. https://doi.org/10.1128/AEM.00276-11
Coker VS, Pattrick RAD, van der Laan G, Lloyd JR (2006) Formation of magnetic minerals by non-magnetotactic prokaryotes. In: Schüler D (ed) Magnetoreception and magnetosomes in bacteria. Springer, Berlin, pp 275–300
Dippon U, Pantke C, Porsch K, Larese-Casanova P, Kappler A (2012) Potential function of added minerals as nucleation sites and effect of humic substances on mineral formation by the nitrate-reducing Fe(II)-oxidizer Acidovorax sp. BoFeN1. Environ Sci Technol 46(12):6556–6565. https://doi.org/10.1021/es2046266
Dixit S, Hering JG (2003) Comparison of Arsenic(V) and Arsenic(III) Sorption onto Iron Oxide Minerals: Implications for Arsenic Mobility. Environ Sci Technol 37(18):4182–4189. https://doi.org/10.1021/es030309t
Dopffel N, Jamieson J, Bryce C, Joshi P, Mansor M, Siade A, Prommer H, Kappler A (2022) Temperature dependence of nitrate-reducing Fe(II) oxidation by Acidovorax strain BoFeN1—evaluating the role of enzymatic vs. abiotic Fe(II) oxidation by nitrite. FEMS Microbiol Ecol 97(12):fiab155. https://doi.org/10.1093/femsec/fiab155
Du Z, Zhang Y, Xu A, Pan S, Zhang Y (2022) Biogenic metal nanoparticles with microbes and their applications in water treatment: a review. Environ Sci Pollut Res 29:3213–3229. https://doi.org/10.1007/s11356-021-17042-z
Ehrenreich A, Widdel F (1994) Anaerobic oxidation of ferrous iron by purple bacteria, a new type of phototrophic metabolism. Appl Environ Microbiol 60(12):4517–4526. https://doi.org/10.1128/AEM.60.12.4517-4526.1994
Emmerich M, Bhansali A, Lösekann-Behrens T, Schröder C, Kappler A, Behrens S (2012) Abundance, distribution, and activity of Fe(II)-oxidizing and Fe(III)-reducing microorganisms in hypersaline sediments of Lake Kasin, Southern Russia. Appl Environ Microbiol 78(12):4386–4399. https://doi.org/10.1128/AEM.07637-11
Eswayah AS, Smith TJ, Gardiner PHE (2016) Microbial transformations of selenium species of relevance to bioremediation. Appl Environ Microbiol 82(16):4848–4859. https://doi.org/10.1128/AEM.00877-16
Etique M, Jorand FPA, Zegeye A, Grégoire B, Despas C, Ruby C (2014) Abiotic process for Fe(II) oxidation and green rust mineralization driven by a heterotrophic nitrate reducing bacteria (Klebsiella mobilis). Environ Sci Technol 48(7):3742–3751. https://doi.org/10.1021/es403358v
Flemming H-C, Wuertz S (2019) Bacteria and archaea on earth and their abundance in biofilms. Nat Rev Microbiol 17(4):247–260. https://doi.org/10.1038/s41579-019-0158-9
Fuller CC, Davis JA, Waychunas GA (1993) Surface chemistry of ferrihydrite: part 2. Kinetics of arsenate adsorption and coprecipitation. Geochim Cosmochim Acta 57(10):2271–2282. https://doi.org/10.1016/0016-7037(93)90568-H
Gadd GM (2010) Metals, minerals and microbes: geomicrobiology and bioremediation. Microbiology 156(3):609–643. https://doi.org/10.1099/mic.0.037143-0
Galani A, Noutsopoulos C, Anastopoulou P, Varouxaki A, Mamais D (2022) Reductive Cr(VI) removal under different reducing and electron donor conditions—a soil microcosm study. Water 14(14):2179. https://doi.org/10.3390/w14142179
Grimm H, Lorenz J, Straub D, Joshi P, Shuster J, Zarfl C, Muehe EM, Kappler A (2024) Nitrous oxide is the main product during nitrate reduction by a novel lithoautotrophic iron(II)-oxidizing culture from an organic-rich paddy soil. Appl Environ Microbiol. https://doi.org/10.1128/aem.01262-24
He S, Tominski C, Kappler A, Behrens S, Roden EE (2016) Metagenomic analyses of the autotrophic Fe(II)-oxidizing, nitrate-reducing enrichment culture KS. Appl Environ Microbiol 82(9):2656–2668. htt
Comments (0)