1887

Abstract

Downregulation of photosystem I (PSI) content is an essential process for cyanobacteria to grow under high-light (HL) conditions. In a (sll1968) mutant of sp. PCC 6803, the levels of PSI content, chlorophyll and transcripts of the genes encoding reaction-centre subunits of PSI could not be maintained low during HL incubation, although the causal relationship among these phenotypes remains unknown. In this study, we modulated the activity of transcription or that of chlorophyll synthesis to estimate their contribution to the regulation of PSI content under HL conditions. Analysis of the -OX strain, in which the genes were overexpressed under HL conditions, revealed that the amount of transcript could not affect PSI content by itself. Suppression of chlorophyll synthesis by an inhibitor, laevulinic acid, in the mutant revealed that chlorophyll availability could be a determinant of PSI content under HL. It was also suggested that chlorophyll content under HL conditions is mainly regulated at the level of 5-aminolaevulinic acid synthesis. We conclude that, upon the shift to HL conditions, activities of transcription and of 5-aminolaevulinic acid synthesis are strictly downregulated by regulatory mechanism(s) independent of PmgA during the first 6 h, and then a PmgA-mediated regulatory mechanism becomes active after 6 h onward of HL incubation to maintain these activities at a low level.

Loading

Article metrics loading...

/content/journal/micro/10.1099/mic.0.024018-0
2009-03-01
2024-04-26
Loading full text...

Full text loading...

/deliver/fulltext/micro/155/3/989.html?itemId=/content/journal/micro/10.1099/mic.0.024018-0&mimeType=html&fmt=ahah

References

  1. Anderson J. M. 1986; Photoregulation of the composition, function, and structure of thylakoid membranes. Annu Rev Plant Physiol 37:93–136
    [Google Scholar]
  2. Anderson J. M., Chow W. S., Park Y.-I. 1995; The grand design of photosynthesis: acclimation of the photosynthetic apparatus to environmental cues. Photosynth Res 46:129–139
    [Google Scholar]
  3. Arnon D. I., McSwain B. D., Tsujimoto H. Y., Wada K. 1974; Photochemical activity and components of membrane preparations from blue-green algae. I. Coexistence of two photosystems in relation to chlorophyll a and removal of phycocyanin. Biochim Biophys Acta 357:231–245
    [Google Scholar]
  4. Bjorkman O. 1981; Responses to different quantum flux densities. In Encyclopedia of Plant Physiology, vol. 12A, Physiological Plant Ecology I pp 57–107 Edited by Lange O. L., Nobel P. S., Osmond C. B., Ziegler H. Berlin: Springer;
    [Google Scholar]
  5. Falciatore A., Merendino L., Barneche F., Ceol M., Meskauskiene R., Apel K., Rochaix J. D. 2005; The FLP proteins act as regulators of chlorophyll synthesis in response to light and plastid signals in Chlamydomonas . Genes Dev 19:176–187
    [Google Scholar]
  6. Fujimori T., Hihara Y., Sonoike K. 2005a; PsaK2 subunit in photosystem I is involved in state transition under high light condition in the cyanobacterium Synechocystis sp. PCC 6803. J Biol Chem 280:22191–22197
    [Google Scholar]
  7. Fujimori T., Higuchi M., Sato H., Aiba H., Muramatsu M., Hihara Y., Sonoike K. 2005b; The mutant of sll1961, which encodes a putative transcriptional regulator, has a defect in regulation of photosystem stoichiometry in the cyanobacterium Synechocystis sp. PCC 6803. Plant Physiol 139:408–416
    [Google Scholar]
  8. Goslings D., Meskauskiene R., Kim C., Lee K. P., Nater M., Apel K. 2004; Concurrent interactions of heme and FLU with Glu tRNA reductase (HEMA1), the target of metabolic feedback inhibition of tetrapyrrole biosynthesis, in dark- and light-grown Arabidopsis plants. Plant J 40:957–967
    [Google Scholar]
  9. Grace S. C., Logan B. A. 1996; Acclimation of foliar antioxidant systems to growth irradiance in three broad-leaved evergreen species. Plant Physiol 112:1631–1640
    [Google Scholar]
  10. Harel E., Klein S. 1972; Light dependent formation of 5-aminolevulinic acid in etiolated leaves of higher plants. Biochem Biophys Res Commun 49:364–370
    [Google Scholar]
  11. Hihara Y., Sonoike K. 2001; Regulation, inhibition and protection of photosystem I. In Advances in Photosynthesis XI, Regulation of Photosynthesis pp 507–531 Edited by Anderson B., Aro E. M. Dordrecht: Kluwer;
    [Google Scholar]
  12. Hihara Y., Sonoike K., Ikeuchi M. 1998; A novel gene, pmgA, specifically regulates photosystem stoichiometry in the cyanobacterium Synechocystis species PCC 6803 in response to high light. Plant Physiol 117:1205–1216
    [Google Scholar]
  13. Hihara Y., Kamei A., Kanehisa M., Kaplan A., Ikeuchi M. 2001; DNA microarray analysis of cyanobacterial gene expression during acclimation to high light. Plant Cell 13:793–806
    [Google Scholar]
  14. Kada S., Koike H., Satoh K., Hase T., Fujita Y. 2003; Arrest of chlorophyll synthesis and differential decrease of photosystems I and II in a cyanobacterial mutant lacking light-independent protochlorophyllide reductase. Plant Mol Biol 51:225–235
    [Google Scholar]
  15. Kashino Y., Enami I., Satoh K., Katoh S. 1990; Immunological cross-reactivity among corresponding proteins of Photosystems I and II from widely divergent photosynthetic organisms. Plant Cell Physiol 31:479–488
    [Google Scholar]
  16. Laemmli U. K. 1970; Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227:680–685
    [Google Scholar]
  17. Melis A. 1991; Dynamics of photosynthetic membrane composition and function. Biochim Biophys Acta 1058:87–106
    [Google Scholar]
  18. Meskauskiene R., Nater M., Goslings D., Kessler F., op den Camp R., Apel K. 2001; FLU: a negative regulator of chlorophyll biosynthesis in Arabidopsis thaliana . Proc Natl Acad Sci U S A 98:12826–12831
    [Google Scholar]
  19. Murakami A., Fujita Y. 1991; Regulation of photosystem stoichiometry in the photosynthetic system of the cyanophyte Synechocystis PCC 6714 in response to light-intensity. Plant Cell Physiol 32:223–230
    [Google Scholar]
  20. Muramatsu M., Hihara Y. 2003; Transcriptional regulation of genes encoding subunits of photosystem I during acclimation to high-light conditions in Synechocystis sp. PCC 6803. Planta 216:446–453
    [Google Scholar]
  21. Muramatsu M., Hihara Y. 2006; Characterization of high-light-responsive promoters of the psaAB genes in Synechocystis sp. PCC 6803. Plant Cell Physiol 47:878–890
    [Google Scholar]
  22. Muramatsu M., Hihara Y. 2007; The coordinated high-light response of genes encoding subunits of photosystem I is achieved by AT-rich upstream sequences in the cyanobacterium Synechocystis sp. PCC 6803. J Bacteriol 189:2750–2758
    [Google Scholar]
  23. Nakamura K., Hihara Y. 2006; Photon flux density-dependent gene expression in Synechocystis sp. PCC 6803 is regulated by a small, redox-responsive, LuxR-type regulator. J Biol Chem 281:36758–36766
    [Google Scholar]
  24. Neale P. J., Melis A. 1986; Algal photosynthetic membrane complexes and the photosynthesis-irradiance curve: a comparison of light-adaptation responses in Chlamydomonas reinhardtii ( Chlorophyta . J Phycol 22:531–538
    [Google Scholar]
  25. Niyogi K. K. 1999; Photoprotection revisited: genetic and molecular approaches. Annu Rev Plant Physiol Plant Mol Biol 50:333–359
    [Google Scholar]
  26. Ozaki H., Ikeuchi M., Ogawa T., Fukuzawa H., Sonoike K. 2007; Large scale analysis of chlorophyll fluorescence kinetics in Synechocystis sp. PCC 6803: identification of the factors involved in the modulation of photosystem stoichiometry. Plant Cell Physiol 48:451–458
    [Google Scholar]
  27. Reinbothe S., Reinbothe C. 1996; The regulation of enzymes involved in chlorophyll biosynthesis. Eur J Biochem 237:323–343
    [Google Scholar]
  28. Rieble S., Beale S. I. 1991; Purification of glutamyl-tRNA reductase from Synechocystis sp. PCC 6803. J Biol Chem 266:9740–9745
    [Google Scholar]
  29. Sambrook J., Fritsch E. F., Maniatis T. 1989 Molecular Cloning: a Laboratory Manual , 2nd edn. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory;
    [Google Scholar]
  30. Sonoike K., Hihara Y., Ikeuchi M. 2001; Physiological significance of the regulation of photosystem stoichiometry upon high light acclimation of Synechocystis sp. PCC 6803. Plant Cell Physiol 42:379–384
    [Google Scholar]
  31. Stanier R. Y., Kunisawa R., Mandel M., Cohen-Bazire G. 1971; Purification and properties of unicellular blue-green algae (order Chroococcales . Bacteriol Rev 35:171–205
    [Google Scholar]
  32. Vavilin D. V., Vermaas W. F. 2002; Regulation of the tetrapyrrole biosynthetic pathway leading to heme and chlorophyll in plants and cyanobacteria. Physiol Plant 115:9–24
    [Google Scholar]
  33. Walters R. G. 2005; Towards an understanding of photosynthetic acclimation. J Exp Bot 56:435–447
    [Google Scholar]
  34. Xu H., Vavilin D., Funk C., Vermaas W. 2002; Small Cab-like proteins regulating tetrapyrrole biosynthesis in the cyanobacterium Synechocystis sp. PCC 6803. Plant Mol Biol 49:149–160
    [Google Scholar]
  35. Xu H., Vavilin D., Funk C., Vermaas W. 2004; Multiple deletions of small Cab-like proteins in the cyanobacterium Synechocystis sp. PCC 6803: consequences for pigment biosynthesis and accumulation. J Biol Chem 279:27971–27979
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/micro/10.1099/mic.0.024018-0
Loading
/content/journal/micro/10.1099/mic.0.024018-0
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error