Biology of Photosystem I: Structural aspects

  • Petra Fromme

Summary

The primary step in oxygenic photosynthesis, the light induced charge separation, is driven in plants and cyanobacteria by two large membrane intrinsic protein complexes, the Photosystems I and II. Photosystem I catalyzes the light driven electron transfer from plastocyanin/cytochrome c6 at the lumenal side to ferredoxin at the stromal side of the thylakoid membrane by a chain of—at least six—electron carriers. Photosystem I of cyanobacteria consists of 11 protein subunits, about 100 chlorophyll a molecules, 20–25 carotenoids, 3 [4Fe4S] clusters and 2 phylloquinones. It exists as a trimer in the native membrane with a molecular weight of 1000 kDa for the whole complex. Information concerning the structure of Photosystem I is available from the use of several different techniques. Biochemical data, biophysical investigations as well as results from electron microscopy and X-ray structure analysis are summarized in this chapter in order to provide the readers with an overview of the structure of this large membrane protein. Its structural organization is discussed here with respect to the structure/function relationship.

Keywords

Reaction Center Photo System Transmembrane Helix Purple Bacterium Green Sulfur Bacterium 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Adman, E.T., Sieker, L.C. and Jenson, L.H. 1973. The structure of a bacterial ferredoxin J. Biol. Chem. 248: 3987–3996.PubMedGoogle Scholar
  2. Anandan, S., Vainstein, A. and Thornber, P. 1989. Correlation of some published amino acid sequences for Photosystem I polypeptides to a 17 kDa LHCI pigment-protein and to subunits III and IV of the core complex. FEBS Lett. 256: 150–154.PubMedCrossRefGoogle Scholar
  3. Andersen, B. and Scheller, H.V. 1993. Structure, function and assembly of photosystem I. In: Pigment protein complexes in plastids: synthesis and assembly. Cell Biology: A series of monographs, C Sundquist, (ed) pp. 383–418. Academic press, San Diego, CA.Google Scholar
  4. Andersen, B., Scheller, H.V. and Møller, B.L. 1992. The PSI-E subunit of photosystem I binds ferredoxin: NADPH+ oxidoreductase. FEBS Lett. 311: 169–173.PubMedCrossRefGoogle Scholar
  5. Armbrust, T.S., Chitnis, P.R. and Guikema, J.A. 1996. Organization of photosystem I polypetides examined by chemical crosslinking. Plant Physiol. 111: 1307–1312.PubMedGoogle Scholar
  6. Arnoux, B., Gaucher, J.-F., Ducruix, A. and Reiss-Husson, F. 1995. Structure of the photochemical center of a spheroidene containing purple bacterium, Rhodobacter sphaeroides, at 3Å Resolution. Acta Cryst. D51: 368–379.Google Scholar
  7. Barkoff, A., Brunkan, N., Snyder, S.W., Ostafin, A., Werst, M., Biggins, J. and Thurnauer, M. 1995. Quinone exchange at the A1 site in Photosystem I (PS I). In: Photosynthesis: from light to Biosphere, P. Mathis, (ed.) Vol II pp. 115-118. Kluver Academic Publishers.Google Scholar
  8. Bengis, C. and Nelson, N. 1977. Subunit structure of chloroplast Photosystem I reaction center. J. Biol. Chem. 252: 4564–4569.PubMedGoogle Scholar
  9. Biggins, J. and Mathis, P. 1988. Functional role of vitamine K1 in Photosystem I of the cyanobacterium Synechocystis 6803. Biochemistry 27: 1494–1500.PubMedCrossRefGoogle Scholar
  10. Bittl, R. and Zech, S.G. 1997. Pulsed EPR study of spin coupled radical pairs in photosynthetic reaction centers: Measurement of the distance between P700+• and A1-• in Photosystem I and between P865+•. and QA -• in bacterial reaction centers. J. Phys. Chem. B101: 1429–1436.Google Scholar
  11. Blankenship, R.E. 1992. Origin and early evolution of photosynthesis. Photosynth. Res. 33: 91–111.PubMedCrossRefGoogle Scholar
  12. Boekema, E.J., Dekker, J.P., van Heel, M.G., Rögner, M., Saenger, W., Witt, I. and Witt, H.T. 1987. Evidence for a trimeric organization of the Photosystem I complex from the thermophilic cyanobacterium Synechococcus sp. FEBS Lett. 217: 283–286.CrossRefGoogle Scholar
  13. Boettcher, B., Gräber, P. and Boekema, J. 1992. The Structure of Photosystem I from the thermophilic Cyanobacterium Synechococcus sp. determined by electron microscopy of two dimensional crystals. Biochim. Biophys. Acta 1100: 125–136.CrossRefGoogle Scholar
  14. Brettel, K. 1997. Electron transfer and arrangement of the redox cofactors in Photosystem I. Biochim. Biophys. Acta 1318: 322–373.CrossRefGoogle Scholar
  15. Chitnis, V.P. and Chitnis, P.R. 1993. PsaL subunit is required for the formation of Photosystem I trimers in the cyanobacterium Synechocystis sp. PCC 6803. FEBS Lett. 336: 330–334.PubMedCrossRefGoogle Scholar
  16. Chitnis, PR., Xu Q., Chitnis, V.P. and Nechustai, R. 1995. Function and organization of Photosystem I polypeptides. Photosynth. Res. 44: 23–40.CrossRefGoogle Scholar
  17. Deisenhofer, J., Epp, O., Sinning, I. and Michel, H. 1995. Crystallographic refinement at 2.3 Å resolution and refined model of the photosynthetic reaction center from Rhodopseudomonas viridis. J. Mol. Biol. 246: 429–457.PubMedCrossRefGoogle Scholar
  18. Díaz-Quintana, A., Leibl, W., Bottin, H. and Schif, P. 1998. Electron transfer in photosystem I reaction centers follows a linear pathway in which iron sulfur cluster FB is the immediate electron donor to soluble ferrodoxin. Biochemistry 37: 2429–2439.CrossRefGoogle Scholar
  19. DiMagno, L., Chan, C.-K., Jia, Y., Lang, M.J., Newman, J.R., Mets, L., Fleming, G.R. and Haselkorn, R. 1995. Energy transfer and trapping in Photosystem I reaction centers from cyanobacteria. Proc Natl Acad Sci USA 92: 2715–2719.PubMedCrossRefGoogle Scholar
  20. Döring, G., Bailey, J.L., Weikara, J. and Witt, H.T. 1968. Some new results in Photosynthesis. The Action of two chlorophyll aI molecules in Light Reaction I of Photosynthesis. Die Naturwissenschaften 5: 219–224.CrossRefGoogle Scholar
  21. Drepper, F., Hippler, M., Nitschke, W. and Haehnel, W. 1996. Binding Dynamics and Electron Transfer between Plastocyanin and Photosystem I. Biochemistry 35: 1282–1295.PubMedCrossRefGoogle Scholar
  22. Dunn, P. and Gray, J. 1988. Localization and nucleotide sequence of the gene for the 8 kDa subunit of Photosystem I in pea and wheat chloroplast DNA. Plant Mol. Biol. 11: 311–319.CrossRefGoogle Scholar
  23. Dzuba, S. A., Gast, P. and Hoff, A.J. 1997. Electron spin echo of spin polarized radical pairs in the intact and quinone-reconstituted plant Photosystem I reaction center. Chem. Phys. Lett. 236: 595–602.CrossRefGoogle Scholar
  24. Ermler, U., Fritsch, G., Buchanan, S.K. and Michel, H. 1994. Structure of the photosynthetic reaction center from Rhodobacter sphaeroides at 2.65 Å resolution: cofactors and protein-cofactor interactions. Structure 2: 925–936.PubMedCrossRefGoogle Scholar
  25. Falzone, C.J., Kao, Y.-H., Zao, J., Bryant, D.A. and Lecomte, T.T.J. 1994. The three dimensional solution structure of PsaE from the cyanobacterium Synechococcus sp. strain PCC 7002: A Photosystem I protein that shows structural homology with SH3 domain. Biochemistry 33: 6052–6062.PubMedCrossRefGoogle Scholar
  26. Farah, J., Rappaport, F., Choquet, Y., Joliot, P. and Rochaix, J.-D. 1995. Isolation of a psaF-deficient mutant of Chlamydomonas reinhardtii: efficient interaction of plastocyanin with the Photosystem I reaction center is mediated by the PsaF subunit. EMBO J. 14: 4976–84.PubMedGoogle Scholar
  27. Feiler, U. and Hauska, G. 1995. The Reaction Center from Green sulfur Bacteria. In: Anoxygenic Bacteria, Blankenship, R.E., Madigan, M.T. and Bauer, C.E. (eds) Kluwer Academic Publishers, pp. 665-685.Google Scholar
  28. Frank, H. and Cogdell, R.J. 1996. Carotenoids in photosynthesis. Photochem. Photobiol. 63: 257–264.PubMedCrossRefGoogle Scholar
  29. Franke, J.E., Ciesla, J. and Warden, J.T. 1995. Kinetics of PsaC Reduction in Photosystem I. In: Photosynthesis: from light to Biosphere Vol II, P. Mathis (ed.) pp. 75–78. Kluwer Academic Publishers, Netherlands.Google Scholar
  30. Fromme, P., Schubert, W.-D. and Krauß, N. 1994. Structure of Photosystem I: Suggestions on docking sites for plastocyanin and ferredoxin, and the coordination of P700. Biochim. Biophys. Acta 1187: 99–105.CrossRefGoogle Scholar
  31. Fromme, P., Witt, H.T., Schubert, W.-D., Klukas, O., Saenger, W. and Krauß, N. 1996. Structure of Photosystem I at 4.5 Å resolution: a short review including evolutionary aspects. Biochim. Biophys. Acta 1275: 76–83.CrossRefGoogle Scholar
  32. Gavel, Y., Steppuhn, J., Herrmann, R. and von Heijne, G. 1991. The “positive inside rule” applies to thylakoid membrane proteins. FEBS Lett. 282: 41–46.PubMedCrossRefGoogle Scholar
  33. Golbeck, J.H. 1992. Structure and function of Photosystem I. Ann. Rev. Plant. Physiol. Plant Mol. Biol. 43: 293–324.CrossRefGoogle Scholar
  34. Golbeck, J.H. 1993. The structure of Photosystem I. Curr. Opin. Struc. Biol, 3: 508–514.CrossRefGoogle Scholar
  35. Golbeck, J.H. 1994. Photosystem I in cyanobacteria. In. Adv. Photosynth. I Molecular Biology of Cyanobacteria, D. Bryant (ed.), pp. 319-360.Google Scholar
  36. Hladik, J. and Sofrova, D. 1991. Does the trimeric form of Photosystem I reaction center of cyanobacteria in vivo exist? Photosynth. Res. 29: 171–175.Google Scholar
  37. Haehnel, W., Jansen, T., Gause, K., Kloesgen, R.B., Stahl, B., Michl, D., Huvermann, B., Karas, M. and Herrmann, R.G. 1994. Electron transfer from plastocyanin to Photosystem I. EMBO J. 13: 1028–38.PubMedGoogle Scholar
  38. Hallahan, B., Purton, S., Ivison, A., Wright, D. and Evans, M.C.W. 1995. Analysis of the proposed FeSx binding region of Photosystem I by side directed mutation of PsaA in Chlamydomonas reinhardtii. Photosyn. Res. 46: 257–264.CrossRefGoogle Scholar
  39. Hamacher, E., Kruip, J., Rögner, M. and Mäntele, W. 1995. Characterization of the primary electron donor of Photosystem I, P700, by electrochemistry and Fourier transform infrared (FTIR) difference spectroscopy. In: Photosynthesis: from light to Biosphere Vol II P. Mathis (ed.) pp. 95–98. Klu wer Academic Publishers, Netherlands.Google Scholar
  40. Hastings, G., Hoshina, S., Webber, A.N. and Blankenship, R.E. 1995a. Universality of Energy and Electron Transfer Processes in Photosystem I. Biochemistry 34: 15512–15522.PubMedCrossRefGoogle Scholar
  41. Hastings, G., Reed, L.J., Lin, S. and Blankenship, R.E. 1995b. Excited state dynamics in Photosystem I: effects of detergent and excitation wavelength. Biophys. J. 69: 2044–2055.PubMedCrossRefGoogle Scholar
  42. He, W.Z. and Malkin, R. 1992. Specific release of a 9 kDa extrinsic polypeptide from spinach chloroplasts by salt washing. FEBS Lett. 308: 298–300.PubMedCrossRefGoogle Scholar
  43. He, W.Z., Mannan, R.M., Metzger, S., Whitmarsh, J., Pakrasi, H.B. and Malkin, R. 1995. EPR studies of site-directed mutants of the PsaC protein of photosystem I in Anabena variabilis ATCC 29413. In: Photosynthesis: from light to Biosphere Vol II (P. Mathis ed.) pp. 91–94. Kluwer Academic Publishers, Netherlands.Google Scholar
  44. Heathcote, P., Rigby, S.E.J. and Evans, M.C. 1995. Electron nuclear double resonance (ENDOR) studies of the phylloquinone electron acceptor (A1) in the Photosystem I reaction center. In: Photosynthesis: from light to Biosphere Vol II (P. Mathis ed.) pp. 163–166. Kluwer Academic Publishers, Netherlands.Google Scholar
  45. Hecks, B., ulf, K., Breton, J., Leibl, W. and Trissl, H.-W. 1994. Primary Charge Separation in Photosystem I: A Two-Step Electrogenic Charge Separation Connected with P700+•.Google Scholar
  46. A0-• and P700+•A1-• Formation. Biochemistry 33: 8619-8624.Google Scholar
  47. Hippler, M., Ratajczak, R., and Haehnel, W. 1989. Identification of the plastocyanin binding subunit of Photosystem I. FEBS Lett. 250: 280–284.CrossRefGoogle Scholar
  48. Hippler, M., Reichert, J., Sutter, M., Zak, E., Altschmied, L., Schröder, U., Schütz, E., Herrmann, R.G. and Haehnel, W. 1997. The plastocyanin binding domain of Photosystem I. EMBO J. 23: 6374–6384.Google Scholar
  49. Iwaki, M., Kumazaki, S., Yoshihara, K., Erabi, T. and Itoh, S. 1996. ΔG dependence of the electron transfer rate in the photosynthetic reaction center of plant Photosystem I: natural optimization of reaction between chlorophyll a (A0) and quinone. J. Phys. Chem. 100: 10802–10809.CrossRefGoogle Scholar
  50. Jansson, S. Andersen, B. and Scheller, H.V. 1996. Crosslinking studies of PS I: Nearest neighbour analysis of higher plant Photosystem I holocomplex. Plant Physiol. 112: 409–420.PubMedCrossRefGoogle Scholar
  51. Jekow, P., Fromme, P., Witt, H.T. and Saenger, W. 1995. Photosystem I from Synechococcus elongates:Preparation and crystallisation of monomers with varying subunit composition. Biochim. Biophys. Acta 1229: 115–120.CrossRefGoogle Scholar
  52. Jung, Y.-S., Yu, L.Y. and Golbeck, J.H. 1995. Reconstitution of the iron-sulfur center FB results in complete restoration of NADP+ photoreduction in Hg-treated Photosystem I complexes from Synechococcus sp. PCC 6301. Photosynth. Res. 46: 249–255.CrossRefGoogle Scholar
  53. Käß, H. 1995. Die Struktur des primären Donators P700 in Photosystem I: Untersuchungen mit Methoden der stationären und gepulsten Elektronenspinresonanz. Dissertation TU Berlin, Germany.Google Scholar
  54. Käß, H., Bittersmann-Weidlich, E., Andreasson, L.-E., Boenigk, B. and Lubitz, W. 1995. ENDOR and ESEEM of the 15N labeled radical cations of chlorophyll a and the primary donor P700 in Photosystem I. Chem. Phys. 194: 419–32.CrossRefGoogle Scholar
  55. Kamlowski, A., van der Est, A., Fromme, P. and Stehlik, D. 1997a. Low temperature EPR on Photosystem I single crystals: orientation of the iron-sulfur centers FA and FB. Biochim. Biophys. Acta 1319: 185–198.CrossRefGoogle Scholar
  56. Kamlowski, A., van der Est, A., Fromme, P., Krauß. N., Schubert, W.-D., Klukas, O. and Stehlik, D. 1997b. The structural organization of the PsaC protein in Photosystem I from single crystal EPR and X-ray crystallographic studies. Biochim. Biophys. Acta 1319: 199–213.PubMedCrossRefGoogle Scholar
  57. Karrasch, S., Boullough, P.A. and Ghosh, R. 1995. The 8.5 Å projection map of the light harvesting complex I from Rhodospirillum rubrum reveals a ring composed of 16 subunits. EMBO J. 14: 631–638.PubMedGoogle Scholar
  58. Krauß, N., Hinrichs, W., Witt, I., Fromme, P., Pritzkow, W., Dauter, Z., Betzel, C., Wilson, K.S., Witt, H.T. and Saenger, W. 1993. Three-dimensional structure of system I of photosynthesis at 6 Å resolution. Nature 361: 326–331.CrossRefGoogle Scholar
  59. Krauß, N., Schubert, W.-D., Klukas, O., Fromme, P., Witt, H.T. and Saenger, W. 1996. Photosystem I at 4 A resolution: A joint photosynthetic reaction center and core antenna system. Nature Struct. Biol. 3: 365–370.CrossRefGoogle Scholar
  60. Kruip, J., Bald, D., Hankamer, B., Nield, J., Boonstra, A.F., Barber, J., Boekema, E.J. and Roegner, M. 1995. Localization of subunits in PS1, PS2 and in a PS2/Light harvesting supercomplex. In: Photosynthesis: from light to Biosphere Vol II P. Mathis (ed.) pp. 405–408. Kluwer Academic Publishers, Netherlands.Google Scholar
  61. Kruip, J., Chitnis, P., Lagoutte, B., Rögner, M. and Bockema, E.J. 1997. Structural organization of the major subunits in cyanobacterial photosystem I. J. Biol. Chem. 272: 7068–7069.CrossRefGoogle Scholar
  62. Kühlbrandt, W. Wang, D.N. and Fujiyoshi, Y 1994. Atomic model of plant light harvesting complex by electron crystallography. Nature 367: 614–621.PubMedCrossRefGoogle Scholar
  63. Kumazaki, S., Kandori, H., Petek, H., Yoshihara, K. and Ikegami, I. 1994. Primary photochemical processes in P700 enriched photosystem I particles: Trap limited excitation decay and primary charge separation. J. Phys. Chem. 98: 10335–10342.CrossRefGoogle Scholar
  64. Lagoutte, B., Barth, P. and Setif, P. 1995. Photosystem I/ferredoxin interaction: site directed mutagenesis of PSI-E. In: Photosynthesis: from light to Biosphere Vol II. P. Mathis (ed.) pp. 71–74. Kluwer Academic Publishers, Netherlands.Google Scholar
  65. Leibl, W., Toupance, B. and Breton, J. 1995. Photoelectric characterization of forward electron transfer to iron-sulfur centers in photosystem I. Biochemistry 34: 10237–10244.PubMedCrossRefGoogle Scholar
  66. Lelong, C., Setif, P., Lagoutte, B. and Bottin, H. 1994. Identification of the amino acids involved in the functional interaction between Photosystem I and ferredoxin from Synechocystis sp. PCC 6803 by chemical cross-linking. J. Biol. Chem. 269: 10034–10039.PubMedGoogle Scholar
  67. Lelong, C., Boekema, E., Kruip, J., Bottin, H., Rogner, M. and Setif, P. 1996. Characterization of a redox active cross-linked complex between cyanobacterial photosystem I and soluble ferredoxin. EMBO J. 15: 101–109.Google Scholar
  68. Li, N., Zhao, J., Warren, P.V., Warden, J.T., Bryant, D.A. and Golbeck, J.H. 1991. PsaD is required for the stable binding of PsaC to the photosystem I core protein of Synechococcus sp. PCC 6301. Biochemistry 30: 7863–72.CrossRefGoogle Scholar
  69. Lüneberg, J., Fromme, P., Jekow, P. and Schlodder, E. 1994. Spectroscopic characterization of PS I core complexes from the thermophilic Synechococcus sp.: Identical reoxidation kinetics of A1-before and after removal of the iron-sulfur-clusters FA and FB. FEBS Lett. 338: 197–202.PubMedCrossRefGoogle Scholar
  70. Malkin, R. 1986. On the function of two vitamin K1 molecules in the PS I electron acceptor complex. FEBS Lett. 208: 343–346.CrossRefGoogle Scholar
  71. Margulies, M.M. 1991. Sequence similarity between Photosystem I and II. Identification of a Photosystem I reaction center transmembrane helix that is similar to transmembrane helix IV of the D2 subunit of Photosystem II and the M subunit of the non-sulfur purple and flexible green bacteria. Photosynth. Res. 29: 133–147.Google Scholar
  72. Mc Dermott, G., Prince, S.M., Freer, A.A., Hawthormthwaite-Lawless, A.M., Papiz, M.Z., Cogdell, R.J. and Isaacs, N.W. 1995. Crystal structure of an integral membrane light harvesting complex from photosynthetic bacteria. Nature 374: 517–521.CrossRefGoogle Scholar
  73. Mehari, T., Qiao, F., Scott, M., Nellis, D.F., Zhao, J., Bryant, D.A. and Golbeck, J.H. 1995. Modified Ligands to FA and FB in Photosystem I: Structural constraints for the Formation of Iron sulfur clusters in free and rebound PsaC. J. Biol. Chem. 270: 28108–28117.PubMedCrossRefGoogle Scholar
  74. Moser, C.C. and Dutton, P.L. 1992. Engineering protein structure for electron transfer function in photosynthetic reaction centers. Biochim. Biopys. Acta 1101: 171–176.Google Scholar
  75. Mühlenhoff, U. and Chauvat, F. 1996. Gene Transfer and Manipulation in the Thermophilic Cyanobacterium Synechococcus elongatus. Mol. Gen. Genet. 252: 93–100.PubMedCrossRefGoogle Scholar
  76. Mühlenhoff, U., Kruip, J., Bryant, D.A., Rögner, M., Setif, P. and Boekema, E. 1996. Characterization of a redox-active cross-linked complex between cyanobacterial Photosystem I and its physiological flavodoxin. EMBO J. 15: 488–497.PubMedGoogle Scholar
  77. Naver, H., Scott, M.P., Golbeck, J.H., Moller, B.L. and Scheller, H.V.J. 1996. Reconstitution of barley Photosystem I with modified PS I-C allows identification of domains interacting with PS I D and PS I-A/B. J. Biol. Chem. 271: 8996–9001.PubMedCrossRefGoogle Scholar
  78. Nitschke, W., Feiler, U. and Rutherford, W. 1990. Photosynthetic Reaction Center of Green Sulfur Bacteria studied by EPR. Biochemistry 29: 3834–3842.PubMedCrossRefGoogle Scholar
  79. Norris, J.R., Uphaus, R.A., Crespi, H.L. and Katz, J.J. 1971. Electron spin resonance of chlorophyll and the origin of signal I in photosynthesis. Proc. Natl. Acad. Sci. USA 68: 625–628.PubMedCrossRefGoogle Scholar
  80. Ohyama, K., Fukuzawa, H., Kohchi, T., Shirai, H., Tohru, S., Sano, S., Umesono, K., Shiki, Y., Takeuchi, M., Chang, Z., Aota, S.I., Inokuchi, H. and Ozeki, H. 1986. Chloroplast gene organization deduced from complete sequence of liverwort Marchandapolymorpha Chloroplast D.N.A. Nature 322: 572–574.CrossRefGoogle Scholar
  81. Ort, D.R. and Yocum, C.F. (eds.) 1996. Oxygenic Photosynthesis: the Light Reactions. Kluwer Academic, Publishers, Netherlands.Google Scholar
  82. Pakrasi, H.B. 1995. Genetic analysis of the form and function of Photosystem I and Photosystem II. Ann. Rev. Genet. 995, 29: 755–756.CrossRefGoogle Scholar
  83. Roegner, M., Mühlenhoff, U., Boekema, E.J. and Witt, H.T. 1990. Mono-, di-and trimeric PS I reaction center complexes isolated from the thermophilic cyanobacterium Synechococcus sp.: Size, shape and activity. Biochim. Biophys. Acta 1015: 415–424.CrossRefGoogle Scholar
  84. Rodday, S.M., Webber, A.N., Bingham, S.E. and Biggins, J. 1995. Evidence that the Fx domain in Photosystem I interacts with the subunits PsaC: side directed changes in PsaB destabilize the subunit interaction in Chlamydomonas rheinbordtii. Biochemistry 34: 6328–6334.PubMedCrossRefGoogle Scholar
  85. Roemer, S., Senger, H. and Bishop, N.I. 1995. Characterization of the carotenoid-lessstrain of Scenedesmus obliquas, mutant C-6E, a living Photosystem I model. Bot. Acta 108: 80–86.Google Scholar
  86. Rousseau, F., Serif, P. and Lagoutte, B. 1993, Evidence for the Involvement of PSI-E subunit in the reduction of ferredoxin by Photosystem I. EMBO J. 12: 1755–1765.PubMedGoogle Scholar
  87. Sakurai, H., Kusumoto, N., and Inoue, K. 1996. Function of the reaction center of Green Sulfur Bacteria. Photochem. Photobiol. 64: 5–13.CrossRefGoogle Scholar
  88. Schubert, W.D., Klukas, O., Krauß, N., Saenger, W., Fromme, P. and Witt, H.T. 1995. Present state of the crystal structure analysis of Photosystem I at 4.5 Å resolution. In: Photosynthesis: from light to Biosphere Vol II, P. Mathis (ed.) pp. 3–10. Kluwer Academic Publishers, Netherlands.Google Scholar
  89. Schubert, W.-D., Klukas, O., Klauß, N. Saenger, W., Fromme, P. and Witt, H.T. 1997. Photosystem I at 4 Å resolution: Comprehensive structure analysis. J. Mol. Biol. 272: 741–769.PubMedCrossRefGoogle Scholar
  90. Schubert, W.-D., Klukas, O., Saenger, W., Witt, H.T., Fromme, P. and Krauß, N. 1998. A common ancestor for oxygenic and anoxygenic photosynthetic systems: A comparison based on the structural model of photosystem I. J. Mol. Biol. in press.Google Scholar
  91. Schulz, R. Smart, L.B., Yu, J. and McIntosh, L. 1995. A new set of site-directed mutations in Photosystem I core reaction center from Synechocystis sp. PCC 6803. In: Photosynthesis: from light to biosphere Vol II, P. Mathis (ed.) pp. 119–122. Kluwer Academic Publishers, Netherlands.Google Scholar
  92. Schwartz, T. and Brettel, K. 1995. Search for the presence and role of a second quinone in the core of Photosystem I. In: Photosynthesis: from light to Biosphere Vol II P. Mathis (ed.) pp. 43–46. Kluwer Academic Publishers, Netherlands.Google Scholar
  93. Serif, P. 1992. Energy transfer and trapping in Photosystem I. In: The Photosysteins: Structure, Function and Molecular Biology. J. Braber (ed.) pp. 471–499, Elsevier Science Publishers B.V.Google Scholar
  94. Setif, P. and Brettel, K. 1993. Forward electron transfer from Phylloquinone A1 to iron sulfur centers in spinach photosystem I. Biochemistry 32: 7846–7854.PubMedCrossRefGoogle Scholar
  95. Setif. P. and Bottin, H. 1995. Laser flash absorption spectroscopy study of ferredoxin reduction by photosystem I: spectral and kinetic evidence for the existence of several photosystem I-ferredoxin complexes. Biochemistry 34: 9059–9070.PubMedCrossRefGoogle Scholar
  96. Setif, P., Hanley, J., Barth, P., Bottin, H., Lagoutte, B. 1995. Ferredoxin reduction by PS I with wild type, deleted and site-directed mutants from the cyanobacterium Synechocystis sp. PCC 6803. In: Photosynthesis: from light to Biosphere Vol II (P. Mathis ed.) pp. 23–28. Kluwer Academic Publishers, Netherlands.Google Scholar
  97. Soinike, K., Hatanaka, H. and Katoh, S. 1993. Small subunits of Photosystem I reaction center complexes from Synechococcus elongatus II. The psaE gene product has a role to promote interaction between the terminal electron acceptor and ferredoxin. Biochim. Biophys. Acta 1141: 52–57.CrossRefGoogle Scholar
  98. Strotmann, H. and Weber, N. 1993. On the function of PsaE in chloroplast photosystem I. Biochim. Biophys. Acta 1143: 204–210.PubMedCrossRefGoogle Scholar
  99. Svensson, B., Vass, I., Cedergren, E. and Styring, S. 1990. Structure of donor site components in photosystem II predicted by computer modelling. EMBO J. 9: 2051–2059.PubMedGoogle Scholar
  100. Valkunas, L., Liuolia, V., Dekker, J.P. and van Grondelle, R. 1995. Description of energy migration and trapping in Photosystem I by a model with two distance scaling parameters. Photosyn. Res. 43: 149–54.CrossRefGoogle Scholar
  101. Van der Est, A., Bock, C., Golbeck, J.H., Brettel, K., Setif, P. and Stehlik, D. 1994. Electron transfer from the acceptor A1 to the iron sulfur centers in photosystem I as studied by transient EPR Spectroscopy. Biochemistry 33: 11789–11797.PubMedCrossRefGoogle Scholar
  102. Van der Est, A., Sieckmann, I., Lubitz, W. and Stehlik, D. 1995. Differences in the binding of the primary quinone acceptor in Photosystem I and reaction centers of Rhodobacter sphaeroides-R26 studied with transient EPR spectroscopy. Chem. Phys., 194: 349–59.CrossRefGoogle Scholar
  103. van Grondelle, R., Dekker, J.P., Gillbro, T. and Sundström, V. 1994. Energy transfer and trapping in photosynthesis. Biochim. Biophys. Acta 1187: 1–65.CrossRefGoogle Scholar
  104. Vassiliev, I.R., Jung, Y.S., Smart, L., Lawrence, B., Schulz, R., Mclntosh, L. and Golbeck, J.H. 1995. A mixed-ligand iron sulfur cluster (C556PsaB or C5655PsaB) in the Fx- binding Site leads to a decreased quantum efficiency of electron transfer in photosystem I. Biophys. J., 69: 1544–1553.PubMedCrossRefGoogle Scholar
  105. Vassiliev, I.R., Jung, Y.-S., Yang, F. and Golbeck, J. 1998. Psac subunit of photosystem I is oriented with iron-sulfur cluster FB as the immediate electron donor to ferredoxin and flavodoxin, Biophys. J. in press.Google Scholar
  106. Vermaas, W. 1994. Evolution of heliobactria: implications for photosynthetic reaction center complexes, Photosynth. Res. 41: 285–294.PubMedCrossRefGoogle Scholar
  107. von Heijne, G., and Gavel, Y. 1988. Topogenic signals in integral membrane proteins. Eur. J. Biochem. 174: 671–674.CrossRefGoogle Scholar
  108. Webber, A.N., Su, H., Bingham, S.E., Käß, H., Krabben, L., Kuhn, M., Jordan, R., Schlodder, E. and Lubitz, W. 1996. Site-directed mutations affecting the spectroscopic characteristics and midpoint potential of the primary donor in photosystem I. Biochemistry 35: 12857–12863.PubMedCrossRefGoogle Scholar
  109. Witt, I., Witt, H.T., DiFiore, D., Rögner, M., Hinrichs, W., Granzin, J., Betzel, C. and Dauter, Z. 1988. X-ray characterization of single crystals of the reaction center I of photosynthesis. Ber. Bunsenges. Phys. Chem. 92: 1503–1506.Google Scholar
  110. Witt, H.T., Krauß, N., Hinrichs, W., Witt, I., Fromme, P. and Saenger, W. 1992. Three dimensional crystals of Photosystem I from Synechococcus sp. and X-ray structure analysis at 6 Å resolution. In: Res. Photosynth. Res., Proc. Int., 9th Cong. Photosynth., pp. 521–528 Murata, N., (ed.) Kluwer, Dordrecht.Google Scholar
  111. Wynn, R. and Malkin, R. 1990. The Photosystem I 5.5 kDa subunit (the psaK gene product). An intrinsic subunit of the PSI reaction center complex. FEBS Lett. 262: 45–48.CrossRefGoogle Scholar
  112. Yeates, T.O., Komiya, H., Chirino, A., Rees, D.C., Allen, J. and Feher, G. 1988. Structure of the reaction center from Rhodobacter spaeroides R-26 and 2.4.1: Protein cofactor (bacteriochlorophyll, bacteriopheophytin and carotenoid) interactions. Proc. Natl. Acad. Sci. USA 85: 7993–7997.PubMedCrossRefGoogle Scholar
  113. Xiong, J., Subramaniam, S. and Govindjee 1996. Modelling of the D1/D2 proteins and cofactors of the photosystem II reaction center: Implications for herbicide and bicarbonate binding. Protein Science 5: 2054–2073.PubMedCrossRefGoogle Scholar
  114. Xu, Q. and Chitnis, P.R. 1995. Organization of Photosystem I polypeptides, identification of PsaB domains that may interact with PsaD. Plant Physiol. 108: 1067–1075.PubMedCrossRefGoogle Scholar
  115. Xu, Q., Armbrust, T.S., Guikema, J.A. and Chitnis, P.R. 1994a. Organization of Photosystem I polypeptides: A structural interactions between PsaD and PsaL subunits. Plant Physiol. 106: 1057–1063.PubMedCrossRefGoogle Scholar
  116. Xu, Q., Jung, Y.S., Chitnis, V.P., Guikema, J.A., Golbeck, J.H. and Chitnis, P.R. 1994b. Mutational analysis of Photosystem I polypeptides in Synechocystis sp. PCC 6803. Subunit requirements for reduction of NADP+ mediated by ferredoxin and flavodoxin. J. Biol. Chem. 26924: 291–302.Google Scholar
  117. Xu, Q., Odom, W.R., Guikema, J.A., Chitnis, V.P. and Chitnis, P.R. 1994c. Target deletion of psaJ from the cyanobacterium Synechocystis sp. PCC 6803 indicates structural interactions between the PsaJ and PsaF subunits of Photosystem I. Plant Mol. Biol. 2624: 291–302.CrossRefGoogle Scholar
  118. Xu, Q., Yu, L., Chitnis, V.P. and Chitnis, P.R. 1994d. Function and organization of Photosystem I in cyanobacterial mutant strain, that lacks PsaF and PsaJ subunits. J. Biol. Chem. 269: 3205–3211.PubMedGoogle Scholar
  119. Xu, Q., Hoppe, D., Chitins, V.P., Odom, W.R., Guikema, J.A. and Chitnis, P.R. 1995. Mutational Analysis of Photosystem I polypeptides in the cyanobacterium Synechocystis sp. PCC 6803: target inactivation of psaI reveals the function of PsaI in the structural organization of PsaL. J. Biol. Chem. 270: 16243–16250.PubMedCrossRefGoogle Scholar
  120. Yu, L., Zhao, J., Mühlenhoff, U., Bryant, D.A. and Golbeck, J.H. 1993. PsaE is required for cyclic electron flow around Photosystem I in the cyanobacterium Synechococcus sp. PCC 7002. Plant Physiol. 103: 171–180.PubMedGoogle Scholar
  121. Yu, L., Vassiliev, I.R., Jung, Y.-S., Bryant, D.A., and Golbeck, J.H. 1995a. Modified ligands to FA and FB in Photosystem I: II. Characterization of a mixed Ligand [4Fe-4S] cluster in the C51D mutant of PsaC upon rebinding to P700-Fx cores. J. Biol. Chem. 270: 28118–28125.PubMedCrossRefGoogle Scholar
  122. Yu, L., Bryant, D.A. and Golbeck, J.H. 1995b. Evidence for a mixed-ligand [4Fe4S] cluster in the C14D mutant of PsaC. Altered reduction Potentials and EPR Spectral properties of the FA and FB clusters on rebinding of the P700-Fx Core. Biochemistry 34: 7861–7868.PubMedCrossRefGoogle Scholar
  123. Zanetti, G. and Merati, G. 1987. Interaction between photosystem I and ferredoxin. Identification by chemical cross-linking of the polypeptide which binds ferredoxin. Eur. J. Biochem. 169: 143–146.PubMedCrossRefGoogle Scholar
  124. Zao, J., Li N., Warren, P.V., Golbeck, J.H. and Bryant, D.A. 1992. Site-directed conversion of a cystein to aspartate leads to the assembly of a [3Fe-4S] cluster in PsaC of Photosystem I. The photoreduction of FA is independent of FB. Biochemistry 31: 5093–5099.CrossRefGoogle Scholar
  125. Zilber, A.L. and Malkin, R. 1988. Ferredoxin cross-links to a 22 kD a subunit of photosystem I. Plant. Physiol. 88: 810–814.PubMedCrossRefGoogle Scholar
  126. Zilber, A.L. and Malkin, R. 1992. Organization and topology of Photosystem I subunits. Plant. Physiol. 99: 901–911.PubMedCrossRefGoogle Scholar
  127. Zinth, W., Arlt, T. and Wachveitl, J. 1996. The primary process of bacterial photosynthesis-ultrafast reaction of the optimum use of light energy. Ber. Bunsenges. Phys. Chem. 100: 1962–1966.CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media Dordrecht 1999

Authors and Affiliations

  • Petra Fromme
    • 1
  1. 1.Max-Volmer-Institut für Biophysikalische Chemie und BiochemieTechnical University BerlinBerlinGermany

Personalised recommendations