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Structure, Morphology and Growth of Biogenic Greigite (Fe3S4)

Published online by Cambridge University Press:  15 February 2011

B. R. Heywood
Affiliation:
School of Chemistry, University of Bath, Bath BA2 7AY, UK.
S. Manna
Affiliation:
School of Chemistry, University of Bath, Bath BA2 7AY, UK.
R. B. Frankelb
Affiliation:
Department of Physics, California Polytechnic State University, San Luis Obispo, CA 93407, USA.
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Abstract

Several species of aquatic bacteria are known to exploit the earth's geomagnetic field as a means of directing their motion towards suitable habitats. A feature common to these bacteria is the presence of discrete intracellular magnetic inclusions, magnetosomes, aligned in chains along the long axis of the organism. The size and orientation of the individual magnetic particles imparts a permanent magnetic dipole moment to the cell which is, in turn, responsible for the magnetotactic response. In all species examined to date the magnetic particles have been found to be well-ordered, single domain, membrane-bounded crystals with reproducible, species-specific morphologies. Until recently, however, only crystals of the mixed valence iron oxide, magnetite (Fe3O4), were identified in these magnetotactic bacteria. We have now identified three species of bacteria from sulphidic environments which contain crystals of the mixed valence ferrimagnetic iron sulphide, greigite (Fe3S4). High resolution electron microscopical studies of the biogenic greigite crystals showed that they also exhibit the narrow size range (50–90nm) and unique crystallographic habits (e.g. cubo-octahedral, rectangular prismatic) which characterized and distinguished the inclusions in other magnetotactic species. Thus, it would appear that the bio-precipitation of iron sulphides in magnetotactic bacteria is a highly regulated process which is directed and controlled at the molecular level. These findings are not only important to our understanding of biomineralization in unicellular organisms but may also be significant to studies of paleomagnetism. Furthermore, the controlled synthesis of greigite presents an interesting challenge to material scientists and solid state chemists.

Type
Research Article
Copyright
Copyright © Materials Research Society 1991

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References

REFERENCES

1. Mann, S., Sparks, N. H. C., Frankel, R. B., Bazylinski, D. A. and Jannasch, H. W. Nature 343, 258261 (1990).Google Scholar
2. Farina, M., Motta de Esquivel, D. and Lins de Barros, H. G. P. Nature 343, 256258 (1990).Google Scholar
3. Heywood, B.R., Bazylinski, D. A., Garratt-Reed, A., Mann, S. and Frankel, R. B. Naturwissenschaften in press (1990)Google Scholar
4. Mann, S., Frankel, R. B. and Blakemore, R. P. Nature 310 405407 (1984)Google Scholar
5. Berner, R. A. J. Geol. 72 293306 (1964)Google Scholar
6. Horiuchi, S., Wada, H. and Moori, T. J Crystal Growth 24–25 624626 (1974)Google Scholar
7. Hallberg, R. O. N. Jahrbuch Mineral Monatsohefte 481–500 (1972)Google Scholar
8. Freke, A. M. D. J Biochem. Microbiol. Tech. Eng. 111 (1), 2939 (1961)Google Scholar
9. Sparks, N. H. C., Mann, S., Bazylinski, D. A., Lovely, D. R., Jannasch, H. W. and Frankel, R. B. Earth and Planetary Science Lett. 98, 1422 (1990)Google Scholar
10. Cutter, G. A. and Velinsky, D. J. Marine Chemistry 23, 311327 (1988)Google Scholar
11. Snowball, I. and Thompson, R. J Quaternary Science 3 (2), 121125 (1988)Google Scholar
12. Russell, M. J., Hall, A. J. and Turner, D. Terra Nova 1, 238241 (1989)CrossRefGoogle Scholar
13. Doss, B. Beil Band Abt. 33, 662713 (1912)Google Scholar
14. Williams, S. A. Amer Minerol 53, 20872088 (1968)Google Scholar
15. Mann, S. and Frankel, R. B. in Biomineralization: Chemical and Biochemical Perspectives (eds. Mann, S., Webb, J. and Willliams, R. J. P.) 389426 (VCH Weinheim, 1989).Google Scholar
16. Mann, S., Heywood, B. R., Rajam, S., Walker, J. B. A., Davey, R. J. and Birchall, J D. Advanced Materials 2, 257261 (1990)Google Scholar
17. Yamaguichi, S. and Wada, H. J Applied Physics 41 (4), 18731874 (1970)Google Scholar
18. Gorby, Y. A., Beveridge, T. J. and Blakemore, R. P. JBacteriol 170, 834841 (1988)Google Scholar
19. Swain, L. D. and Boyan, B. D. J Dent Res, 67, 526530 (1988)Google Scholar
20. Frankel, R. B. Ann. Rev. Biophys. Bioeng. 13, 85103 (1984)CrossRefGoogle Scholar