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Ferrous iron oxidation by anoxygenic phototrophic bacteria

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Widdel, Friedrich, Schnell, Sylvia, Heising, Silke, Ehrenreich, Armin, Assmus, Bernhard, Schink, Bernhard·1993·Nature

DOI 10.1038/362834a0

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PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT
Lowry, O. H., Rosebrough, N., Farr, A. L., & Randall, R. (1951) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)52451-6 · Cited by 316,394
Bergey's Manual of Systematic Bacteriology
(1990) · Annals of Internal Medicine · doi:10.7326/0003-4819-112-5-391_3 · Cited by 15,633
Ferrozine---a new spectrophotometric reagent for iron
Stookey, L. L. (1970) · Analytical Chemistry · doi:10.1021/ac60289a016 · Cited by 4,712
Bergey's Manual of Systematic Bacteriology
(1989) · Annals of Internal Medicine · doi:10.7326/0003-4819-111-5-448_7 · Cited by 2,940
Solutions, minerals and equilibria
Holland, H. D. (1966) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(66)90075-5 · Cited by 2,425
Solutions, Minerals and Equilibria
Garrels, R. M., & Christ, C. L. (1965) · Medical Entomology and Zoology · Cited by 2,128
Gram-Negative Mesophilic Sulfate-Reducing Bacteria
Widdel, F., & Bak, F. (1992) · Springer eBooks · doi:10.1007/978-1-4757-2191-1_21 · Cited by 1,567
Self-citation
Organic Matter Mineralization with Reduction of Ferric Iron in Anaerobic Sediments
Lovley, D. R., & Phillips, E. J. (1986) · Applied and Environmental Microbiology · doi:10.1128/aem.51.4.683-689.1986 · Cited by 1,430
Photosynthetic bacteria
Evans, M. C. W. (1979) · Nature · doi:10.1038/279561a0 · Cited by 1,269
The Proterozoic Biosphere
(1992) · Cambridge University Press eBooks · doi:10.1017/cbo9780511601064 · Cited by 902

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Stumm, W. & Morgan, J. J. Aquatic Chemistry 2nd ed (Wiley-lnterscience, New York, 1981).
Cohen, Y. in Microbial Mats (eds Cohen. Y. & Rosenberg, E.) 22–36 (Am. Soc. Microbiol., Washington, 1990).
Schidlowski, M. in The Early History of the Earth (ed. Windley, B. F.) 525–535 (Wiley, London, 1976).
Jørgensen, B. B. in Microbial Geochemistry (ed. Krumbein, W. E.) 91–124 (Blackwell, Oxford, 1983).

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Authors: Widdel, F., Schnell, S., Heising, S., Ehrenreich, A., Assmus, B., & Schink, B.
Affiliations: Max Planck Institute for Marine Microbiology (DE)
University of Konstanz (DE)
ORCID: Schnell, Sylvia
Heising, Silke
Ehrenreich, Armin
Schink, Bernhard
Venue: Nature
Publisher: Springer Science and Business Media LLC
Published: 1993-04
Volume: 362
Issue: 6423
Pages: 834-836
ISSN: 0028-0836 (ISSN-L)
1476-4687
DOI: 10.1038/362834a0
OpenAlex: W2070567272
Cited by: 735
References: 30
Citations by year: 2026: 10 · 2025: 24 · 2024: 24 · 2023: 28 · 2022: 31 · 2021: 29 · 2020: 27 · 2019: 31 · 2018: 18 · 2017: 29 · 2016: 29 · 2015: 33 · 2014: 34 · 2013: 43 · 2012: 30
FWCI: 8.56
Type: journal article
Language: en
Open access: green
nbn-resolving.de
Licence: www.springer.com/tdm (tdm)
Locations: Nature (publishedVersion)
KOPS (University of Konstanz) (submittedVersion)
MPG.PuRe (Max Planck Society) (submittedVersion)
Topics: Physical Sciences › Earth and Planetary Sciences › Paleontology › Paleontology and Stratigraphy of Fossils
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
Physical Sciences › Materials Science › Metals and Alloys › Metal Extraction and Bioleaching
Keywords: ferrous iron oxidation, anoxygenic photosynthesis, purple non-sulfur bacteria, iron oxidation, redox potential, banded iron formations, iron oxyhydroxide, carbon dioxide reduction, Acidithiobacillus ferrooxidans, Gallionella ferruginea

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