Table of Contents
Journal of Biophysics
Volume 2011 (2011), Article ID 860382, 10 pages
http://dx.doi.org/10.1155/2011/860382
Research Article

CsmA Protein is Associated with BChl a in the Baseplate Subantenna of Chlorosomes of the Photosynthetic Green Filamentous Bacterium Oscillochloris trichoides belonging to the Family Oscillochloridaceae

1A.N. Belozersky Institute of Physico-Chemical Biology, Building A, M.V. Lomonosov Moscow State University, Moscow 119991, Russia
2Department of Biophysics, M.V. Lomonosov Moscow State University, Moscow 119991, Russia

Received 29 April 2011; Revised 30 June 2011; Accepted 5 July 2011

Academic Editor: Eaton Edward Lattman

Copyright © 2011 Anastasiya Zobova et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. B. K. Pierson and R. W. Castenholz, “The family Chloroflexaceae,” in The Prokaryotes, A. Balows, H. G. Trüper, M. Dworkin, W. Harder, and K. H. Schleifer, Eds., pp. 3754–3774, Springer, Heidelberg, Germany, 2nd edition, 1992. View at Google Scholar
  2. H. G. Trüper and N. Pfennig, “The family Chloroflexaceae,” in The Prokaryotes, A. Balows, H. G. Trüper, M. Dworkin, W. Harder, and K. H. Schleifer, Eds., pp. 3583–3592, Springer, New York, NY, USA, 2nd edition, 1992. View at Google Scholar
  3. O. I. Keppen, T. P. Tourova, B. B. Kuznetsov, R. N. Ivanovsky, and V. M. Gorlenko, “Proposal of Oscillochloridaceae fam. nov. on the basis of a phylogenetic analysis of the filamentous anoxygenic phototrophic bacteria, and emended description of Oscillochloris and Oscillochloris trichoides in comparison with further new isolates,” International Journal of Systematic and Evolutionary Microbiology, vol. 50, no. 4, pp. 1529–1537, 2000. View at Google Scholar · View at Scopus
  4. R. E. Blankenship and K. Matsuura, “Antenna complexes from green photosynthetic bacteria,” in Light-Harvesting Antennas in Photosynthesis, B. R. Green and W. W. Parson, Eds., pp. 195–217, Kluwer Academic Publishers, Dordrecht, 2003. View at Google Scholar
  5. J. M. Olson, “Chlorophyll organization and function in green photosynthetic bacteria,” Photochemistry and Photobiology, vol. 67, no. 1, pp. 61–75, 1998. View at Google Scholar · View at Scopus
  6. D. A. Bryant, A. M. G. Garcia Costas, J. A. Maresca et al., “Candidatus Chloracidobacterium thermophilum: an aerobic phototrophic acidobacterium,” Science, vol. 317, no. 5837, pp. 523–526, 2007. View at Publisher · View at Google Scholar · View at Scopus
  7. J. Oelze and J. R. Golecki, “Membranes and chlorosomes of green bacteria: structure, composition and development,” in Anoxygenic Photosynthetic Bacteria, R. E. Blankenship, M. T. Madigan, and C. E. Bauer, Eds., Kluwer Academic Publishers, Dordrecht, 1995. View at Google Scholar
  8. A. A. Krasnovsky and M. I. Bystrova, “Self-assembly of chlorophyll aggregated structures,” BioSystems, vol. 12, no. 3-4, pp. 181–194, 1980. View at Google Scholar · View at Scopus
  9. K. Matsuura, M. Hirota, K. Shimada, and M. Mimuro, “Spectral forms and orientation of bacteriochlorophylls c and a in chlorosomes of the green photosynthetic bacterium Chloroflexus aurantiacus,” Photochemistry and Photobiology, vol. 57, no. 1, pp. 92–97, 1993. View at Google Scholar
  10. L. A. Staehelin, J. R. Golecki, R. C. Fuller, and G. Drews, “Visualization of the supramolecular architecture of chlorosomes (Chlorobium type vesicles) in freeze-fractured cells of Chloroflexus aurantiacus,” Archives of Microbiology, vol. 119, no. 3, pp. 269–277, 1978. View at Google Scholar · View at Scopus
  11. L. A. Staehelin, J. R. Golecki, and G. Drews, “Supramolecular organization of chlorosomes (Chlorobium Vesicles) and of their membrane attachment sites in Chlorobium limicola,” Biochimica et Biophysica Acta, vol. 589, no. 1, pp. 30–45, 1980. View at Google Scholar · View at Scopus
  12. M. F. Hohmann-Marriott, R. E. Blankenship, and R. W. Roberson, “The ultrastructure of Chlorobium tepidum chlorosomes revealed by electron microscopy,” Photosynthesis Research, vol. 86, no. 1-2, pp. 145–154, 2005. View at Publisher · View at Google Scholar · View at Scopus
  13. Y. Saga and H. Tamiaki, “Transmission electron microscopic study on supramolecular nanostructures of bacteriochlorophyll self-aggregates in chlorosomes of green photosynthetic bacteria,” Journal of Bioscience and Bioengineering, vol. 102, no. 2, pp. 118–123, 2006. View at Publisher · View at Google Scholar · View at Scopus
  14. J. Pšenčik, T. P. Ikonen, P. Laurinmäki et al., “Lamellar organization of pigments in chlorosomes, the light harvesting complexes of green photosynthetic bacteria,” Biophysical Journal, vol. 87, no. 2, pp. 1165–1172, 2004. View at Publisher · View at Google Scholar · View at Scopus
  15. J. Pšenčik, J. B. Arellano, T. P. Ikonen et al., “Internal structure of chlorosomes from brown-colored Chlorobium species and the role of carotenoids in their assembly,” Biophysical Journal, vol. 91, no. 4, pp. 1433–1440, 2006. View at Publisher · View at Google Scholar · View at Scopus
  16. T. P. Ikonen, H. Li, J. Pšenčik et al., “X-ray scattering and electron cryomicroscopy study on the effect of carotenoid biosynthesis to the structure of Chlorobium tepidum chlorosomes,” Biophysical Journal, vol. 93, no. 2, pp. 620–628, 2007. View at Publisher · View at Google Scholar · View at Scopus
  17. S. Ganapathy, G. T. Oostergetel, P. K. Wawrzyniak et al., “Alternating syn-anti bacteriochlorophylls form concentric helical nanotubes in chlorosomes,” Proceedings of the National Academy of Sciences of the United States of America, vol. 106, no. 21, pp. 8525–8530, 2009. View at Publisher · View at Google Scholar · View at Scopus
  18. P. D. Gerola and J. M. Olson, “A new bacteriochlorophyll a-protein complex associated with chlorosomes of green sulfur bacteria,” Biochimica et Biophysica Acta, vol. 848, no. 1, pp. 69–76, 1986. View at Google Scholar · View at Scopus
  19. N-U Frigaard, H. Li, A. G. M. Chew, J. A. Maresca, and D. A. Bryant, “Chlorobium tepidum: insights into the physiology and biochemistry of green sulfur bacteria from the complete genome sequence,” Photosynthesis Research, vol. 78, no. 2, pp. 93–117, 2003. View at Publisher · View at Google Scholar · View at Scopus
  20. J. Pšenčik, A. M. Collins, L. Liljeroos et al., “Structure of chlorosomes from the green filamentous bacterium Chloroflexus aurantiacus,” Journal of Bacteriology, vol. 191, no. 21, pp. 6701–6708, 2009. View at Publisher · View at Google Scholar · View at Scopus
  21. G. A. Montaňo, H. M. Wu, S. Lin, D. C. Brune, and R. E. Blankenship, “Isolation and characterization of the B798 light-harvesting baseplate from the chlorosomes of Chloroflexus aurantiacus,” Biochemistry, vol. 42, no. 34, pp. 10246–10251, 2003. View at Publisher · View at Google Scholar · View at Scopus
  22. R. J. van Dorssen, H. Vasmel, and J. Amesz, “Pigment organization and energy transfer in the green photosynthetic bacterium Chloroflexus aurantiacus II. The chlorosome,” Photosynthesis Research, vol. 9, no. 1-2, pp. 33–45, 1986. View at Publisher · View at Google Scholar · View at Scopus
  23. D. E. Tronrud, J. Wen, L. Gay, and R. E. Blankenship, “The structural basis for the difference in absorbance spectra for the FMO antenna protein from various green sulfur bacteria,” Photosynthesis Research, vol. 100, no. 2, pp. 79–87, 2009. View at Publisher · View at Google Scholar · View at Scopus
  24. R. G. Feick and R. C. Fuller, “Topography of the photosynthetic apparatus of Chloroflexus aurantiacus,” Biochemistry, vol. 23, no. 16, pp. 3693–3700, 1984. View at Google Scholar · View at Scopus
  25. G. Niedermeier, J. A. Shiozawa, F. Lottespeich, and R. G. Feick, “The primary structure of two chlorosome proteins from Chloroflexus aurantiacus,” FEBS Letters, vol. 342, no. 1, pp. 61–65, 1994. View at Publisher · View at Google Scholar
  26. Y. Sakuragi, N-U Frigaard, K. Shimada, and K. Matsuura, “Association of bacteriochlorophyll a with the CsmA protein in chlorosomes of the photosynthetic green filamentous bacterium Chloroflexus aurantiacus,” Biochimica et Biophysica Acta, vol. 1413, no. 3, pp. 172–180, 1999. View at Publisher · View at Google Scholar · View at Scopus
  27. E. V. Vassilieva, V. L. Stirewalt, C. U. Jakobs et al., “Subcellular localization of chlorosome proteins in Chlorobium tepidum and characterization of three new chlorosome proteins: CsmF, CsmH, and CsmX,” Biochemistry, vol. 41, no. 13, pp. 4358–4370, 2002. View at Publisher · View at Google Scholar · View at Scopus
  28. H. Li, N-U Frigaard, and D. A. Bryant, “Molecular contacts for chlorosome envelope proteins revealed by cross-linking studies with chlorosomes from Chlorobium tepidum,” Biochemistry, vol. 45, no. 30, pp. 9095–9103, 2006. View at Publisher · View at Google Scholar · View at Scopus
  29. M. Ø. Pedersen, J. Underhaug, J. Dittmer, M. Miller, and N. C. Nielsen, “The three-dimensional structure of CsmA: a small antenna protein from the green sulfur bacterium Chlorobium tepidum,” FEBS Letters, vol. 582, no. 19, pp. 2869–2874, 2008. View at Publisher · View at Google Scholar · View at Scopus
  30. N-U Frigaard, E. V. Vassilieva, H. Li et al., “The remarkable chlorosome,” in Proceedings of the 12th International Congress on Photosynthesis (PS '01), pp. S1–S3, CSIRO, Melbourne, 2001.
  31. E. V. Vassilieva, J. G. Ormerod, and D. A. Bryant, “Biosynthesis of chlorosome proteins is not inhibited in acetylene-treated cultures of Chlorobium vibrioforme,” Photosynthesis Research, vol. 71, no. 1-2, pp. 69–81, 2002. View at Publisher · View at Google Scholar · View at Scopus
  32. N-U Frigaard, H. Li, K. J. Milks, and D. A. Bryant, “Nine mutants of Chlorobium tepidum each unable to synthesize a different chlorosome protein still assemble functional chlorosomes,” Journal of Bacteriology, vol. 186, no. 3, pp. 646–653, 2004. View at Publisher · View at Google Scholar · View at Scopus
  33. D. A. Bryant, E. V. Vassilieva, N-U Frigaard, and H. Li, “Selective protein extraction from Chlorobium tepidum chlorosomes using detergents. Evidence that CsmA forms multimers and binds bacteriochlorophyll a,” Biochemistry, vol. 41, no. 48, pp. 14403–14411, 2002. View at Publisher · View at Google Scholar · View at Scopus
  34. N-U Frigaard, H. Li, P. Martinsson et al., “Isolation and characterization of carotenosomes from a bacteriochlorophyll c-less mutant of Chlorobium tepidum,” Photosynthesis Research, vol. 86, no. 1-2, pp. 101–111, 2005. View at Publisher · View at Google Scholar · View at Scopus
  35. A. S. Taisova, O. I. Keppen, E. P. Lukashev, A. M. Arutyunyan, and Z. G. Fetisova, “Study of the chlorosomal antenna of the green mesophilic filamentous bacterium Oscillochloris trichoides,” Photosynthesis Research, vol. 74, no. 1, pp. 73–85, 2002. View at Publisher · View at Google Scholar · View at Scopus
  36. A. S. Taisova, O. I. Keppen, A. A. Novikov, M. G. Naumova, and Z. G. Fetisova, “Some factors controlling the biosynthesis of chlorosome antenna bacteriochlorophylls in green filamentous anoxygenic phototrophic bacteria of the family Oscillochloridaceae,” Microbiology, vol. 75, no. 2, pp. 129–135, 2006. View at Publisher · View at Google Scholar · View at Scopus
  37. A. S. Taisova, O. I. Keppen, and Z. G. Fetisova, “Pigment composition of the light-harvesting antenna of the green bacterium from the new family Oscillochloridaceae,” Biophysics, vol. 49, no. 6, pp. 958–962, 2004. View at Google Scholar · View at Scopus
  38. A. S. Taisova, E. P. Lukashev, O. I. Keppen, and Z. G. Fetisova, “Comparative study of the fluorescence characteristics of the chlorosomal antennae of the green bacteria from oscillochloridaceae and two other families,” Biophysics, vol. 50, no. 2, pp. 260–264, 2005. View at Google Scholar · View at Scopus
  39. A. V. Zobova, A. S. Taisova, and Z. G. Fetisova, “Search for an optimal interfacing of subantennae in superantenna of photosynthetic green bacteria from Oscillochloridaceae Family: model calculations,” Doklady Biochemistry and Biophysics, vol. 433, no. 1, pp. 148–151, 2010. View at Publisher · View at Google Scholar · View at Scopus
  40. R. G. Feick, M. Fitzpatrick, and R. C. Fuller, “Isolation and characterization of cytoplasmic membranes and chlorosomes from the green bacterium Chloroflexus aurantiacus,” Photosynthesis Research, vol. 150, no. 2, pp. 905–915, 1982. View at Google Scholar · View at Scopus
  41. C. A. van Walree, Y. Sakuragi, D. B. Steensgaard et al., “Effect of alkaline treatment on bacteriochlorophyll a, quinones and energy transfer in chlorosomes from Chlorobium tepidum and Chlorobium phaeobacteroides,” Photochemistry and Photobiology, vol. 69, no. 3, pp. 322–328, 1999. View at Google Scholar · View at Scopus
  42. H. Schägger and G. van Jagow, “Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa,” Analytical Biochemistry, vol. 166, no. 2, pp. 368–379, 1987. View at Google Scholar · View at Scopus
  43. A. M. L. van de Meene, T. L. Olson, A. M. Collins, and R. E. Blankenship, “Initial characterization of the photosynthetic apparatus of "Candidatus Chlorothrix halophila," a filamentous, anoxygenic photoautotroph,” Journal of Bacteriology, vol. 189, no. 11, pp. 4196–4203, 2007. View at Publisher · View at Google Scholar · View at Scopus