Skip to main content
Log in

Ferrous iron oxidation by anoxygenic phototrophic bacteria

  • Letter
  • Published:

From Nature

View current issue Submit your manuscript

Abstract

NATURAL oxidation of ferrous to ferric iron by bacteria such as Thiobacillus ferrooxidans or Gallionella ferruginea1, or by chemical oxidation2,3 has previously been thought always to involve molecular oxygen as the electron acceptor. Anoxic photochemical reactions4–6 or a photobiological process involving two photosystems7–9 have also been discussed as mechanisms of ferrous iron oxidation. The knowledge of such processes has implications that bear on our understanding of the origin of Precambrian banded iron formations10–14. The reducing power of ferrous iron increases dramatically at pH values higher than 2–3 owing to the formation of ferric hydroxy and oxyhydroxy compounds1,2,15 (Fig. 1). The standard redox potential of Fe3+/Fe2+ (E0 = +0.77 V) is relevant only under acidic conditions. At pH 7.0, the couples Fe(OH)3/Fe2+ (E′0 = -0.236V) or Fe(OH)3 + HCO3FeCO3 (E′0 = +0.200 V) prevail, matching redox potentials measured in natural sediments9,16,17. It should thus be possible for Fe(n) around pH 7.0 to function as an electron donor for anoxygenic photosynthesis. The midpoint potential of the reaction centre in purple bacteria is around +0.45 V (ref. 18). Here we describe purple, non-sulphur bacteria that can indeed oxidize colourless Fe(u) to brown Fe(in) and reduce CO2 to cell material, implying that oxygen-independent biological iron oxidation was possible before the evolution of oxygenic photosynthesis.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Wood, P. M. in Bacterial Energy Transduction (ed. Anthony, C.) 183–230 (Academic, London, 1988).

    Google Scholar 

  2. Stumm, W. & Morgan, J. J. Aquatic Chemistry 2nd ed (Wiley-lnterscience, New York, 1981).

    Google Scholar 

  3. Schwertmann, U. & Cornell, R. M. Iron Oxides in the Laboratory (VCH. Weinheim. 1991).

    Google Scholar 

  4. Cairns-Smith, A. G. Nature 276, 807–808 (1978).

    Article  ADS  CAS  Google Scholar 

  5. Braterman, P. S., Cairns-Smith, A. G. & Sloper, R. W. Nature 303, 163–164 (1983).

    Article  ADS  CAS  Google Scholar 

  6. François, L. M. Nature 320, 352–354 (1986).

    Article  ADS  Google Scholar 

  7. Hartman, H. in Microbial Mats: Stromatolites (eds Cohen, Y., Castenholz, R. W. & Halvorson, H. O.) 449–453 (Liss, New York, 1984).

    Google Scholar 

  8. Walker, J. C. G. Nature 329, 710–711 (1987).

    Article  ADS  CAS  Google Scholar 

  9. Cohen, Y. in Microbial Mats (eds Cohen. Y. & Rosenberg, E.) 22–36 (Am. Soc. Microbiol., Washington, 1990).

    Google Scholar 

  10. Schopf, J. W. A. Rev. Earth Planet. Sci. 3, 213–249 (1975).

    Article  ADS  Google Scholar 

  11. Schidlowski, M. in The Early History of the Earth (ed. Windley, B. F.) 525–535 (Wiley, London, 1976).

    Google Scholar 

  12. Gole, M. J. & Klein, C. J. Geol. 89, 169–183 (1981).

    Article  ADS  Google Scholar 

  13. Beukes, N. J. & Klein, C. in The Proterozoic Biosphere (eds Schopf, J. W. & Klein, C.) 147–158 (Cambridge Univ. Press, Cambridge, 1992).

    Google Scholar 

  14. Kasting, J. F., Holland, H. D. & Kump, L. R. in The Proterozoic Biosphere (eds Schopf, J, W. & Klein, C.) 159–163 (Cambridge Univ. Press, Cambridge, 1992).

    Google Scholar 

  15. Garrels, R. M. & Christ, C. L. Solutions, Minerals and Equilibria (Harper & Row, New York, 1965).

    Google Scholar 

  16. Mackenzie, F. T. & Wollast, R. in Global Chemical Cycles and their Alterations by Man (ed. Stumm, W.) 45–59 (Dahlem Konferenzen, Berlin, 1977).

    Google Scholar 

  17. Jørgensen, B. B. in Microbial Geochemistry (ed. Krumbein, W. E.) 91–124 (Blackwell, Oxford, 1983).

    Google Scholar 

  18. Dutton, P. L. & Prince, R. C. in The Photosynthetic Bacteria (eds Clayton, R. K. & Sistrom, W. R.) 525–570 (Plenum, New York, 1978).

    Google Scholar 

  19. Widdel, F. & Bak, F. in The Prokaryotes Vol. 4 (eds Balows, A., Trüper, H. G., Dworkin, M., Harder, W. & Schleifer, K.-H.) 3352–3378 (Springer. New York, 1992).

    Book  Google Scholar 

  20. Pfennig, N. Int. J. syst. Bact. 28, 283–288 (1978).

    Article  CAS  Google Scholar 

  21. Cohen, Y., Jørgensen, B. B., Revsbech, N. P. & Poplawski, R. Appl. environ. Microbiol 51, 398–407 (1986).

    CAS  PubMed  PubMed Central  Google Scholar 

  22. Pfennig, N. in Bergey's Manual of Systematic Bacteriology Vol. 3 (eds Staley, J. T., Bryant, M. P., Pfennig, N. & Holt, J. G.) 1650–1651 (Williams & Wilkins. Baltimore, 1989).

    Google Scholar 

  23. Lovley, D. R. Microbiol. Rev. 55, 259–287 (1991).

    CAS  PubMed  PubMed Central  Google Scholar 

  24. Nealson, K. H. & Myers, C. R. Appl. environ. Microbiol. 58, 439–443 (1992).

    CAS  PubMed  PubMed Central  Google Scholar 

  25. Stookey, L. L. Analyt. Chem. 42, 779–781 (1970).

    Article  CAS  Google Scholar 

  26. Lovley, D. R. & Philipps, E. J. P. Appl. environ. Microbiol. 51, 683–689 (1986).

    CAS  PubMed  PubMed Central  Google Scholar 

  27. Lowry, O. H., Rosebrough, N. J., Farr, A. L. & Randall, R. J. J. biol. Chem. 193, 265–275 (1951).

    CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Widdel, F., Schnell, S., Heising, S. et al. Ferrous iron oxidation by anoxygenic phototrophic bacteria. Nature 362, 834–836 (1993). https://doi.org/10.1038/362834a0

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/362834a0

  • Springer Nature Limited

This article is cited by

Navigation