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Photosynthetic characteristics of marine Synechococcus spp. with special reference to light environments near the bottom of the euphotic zone of the open ocean

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Abstract

The present study aimed to resolve the question why marine Synechococcus spp. abundantly occur even at the bottom of the euphotic zone in the Kuroshio are. Photosynthesis under such conditions was examined using simulated blue-green model light (BGL). Results indicated that photosynthesis of marine Synechococcus spp. under BGL is as active enough to support growth of these organisms. Examination of light-harvesting under BGL indicated that active photosynthesis is permitted by an unusually high abundance of phycoerythrin (PE), which is the main light-harvesting pigment for photosystem II (PSII), due to a phycobilisome (PBS) structure which is different from ordinary hemidiscoidals. Although the absorption maximum of PE is located at longer wavelengths than the energy maximum of BGL, PE was found to absorb BGL significantly. Thus, BGL cannot be a typical photosystem I (PSI) light. PSII is also significantly excited by BGL. Carotenoids, which largely absorb BGL, were found to be effective in light-harvesting for PSI. Based on the results obtained, possible reasons why marine Synechococcus spp. commonly occur in warm waters were discussed. Two strains of Synechococcus spp. isolated from the Gulf Stream in 1981 and from Kuroshio, Japan in 1983 were used in the present study.

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References

  • Alberte, R. S., Wood, A. M., Kursar, T. A., Guillard, R. R. L. (1984). Novel phycoerythrins in marine Synechococcus spp.: characterization and evolutionary and ecological implications. Pl. Physiol. 75: 732–739

    Google Scholar 

  • Emerson, R., Rabinowitch, E. (1959). Red drop and role of auxiliary pigments in photosynthesis. Pl. Physiol. 35: 477–485

    Google Scholar 

  • Fujita, Y., Murakami, A. (1987). Regulation of electron transport composition in cyanobacterial photosynthetic system: stoichiometry among photosystem I and II complexes and their light-harvesting antennae and cytochrome b 6/f complex. Pl. Cell Physiol. 28: 1547–1553

    Google Scholar 

  • Fujita, Y., Ohki, K., Murakami, A. (1985). Chromatic regulation of photosystem composition in the photosynthetic system of red and blue-green algae. Pl. Cell Physiol 26: 1541–1548

    Google Scholar 

  • Fujita, Y., Ohki, K., Murakami, A. (1987a). Chromatic regulation of photosystem composition in the cyanobacterial photosynthetic system: kinetic relationship between change of photosystem composition and cell proliferation. Pl. Cell Physiol. 28: 227–234

    Google Scholar 

  • Fujita, Y., Murakami, A., Ohki, A. (1987b). Regulation of photosystem composition in the cyanobacterial photosynthetic system: the regulation occurs in response to the redox state of the electron pool located between the two photosystems. Pl. Cell Physiol. 28: 283–292

    Google Scholar 

  • Fujita, Y., Murakami, A., Ohki, K., Hagiwara, N. (1988). Regulation of photosystem composition in cyanobacterial photosynthetic system: evidence indicating that photosystem I formation is controlled in response to the electron transport state. Pl. Cell Physiol. 29: 557–564

    Google Scholar 

  • Furuya, K. (1990). Subsurface chlorophyll maximum in the tropical and subtropical western Pacific Ocean: vertical profiles of phytoplankton biomass and its relationship with chlorophyll a and particulate organic carbon. Mar. Biol. 107: 529–539

    Google Scholar 

  • Gantt, E., Lipschultz, C. A., Grabowski, J., Zimmerman, B. K. (1979). Phycobilisomes from the blue-green and red algae. Pl. Physiol. 63: 615–620

    Google Scholar 

  • Glazer, A. N., Hixon, C. S. (1975). Characterization of R-Phycocyanin. J. biol. Chem. 250: 5487–5495

    Google Scholar 

  • Glover, H. E., Keller, M. D., Guillard, R. R. L. (1986). Light quality and oceanic ultraphytoplankters. Nature, Lond. 319: 142–143

    Google Scholar 

  • Glover, H. E., Prézelin, B. B., Campbell, L., Wyman, M. (1988). Pico- and ultraplankton Sargasso Sea communities: variability and comparative distributions of Synechococcus spp. and algae. Mar. Ecol. Prog. Ser. 49: 127–139

    Google Scholar 

  • Guillard, R. R. L., Ryther, J. H. (1962). Studies of marine planktonic diatoms: I. Cyclotella nana Hastedt, and Detonula confervacea (Cleve) Gran. Can. J. Microbiol. 8: 229–239

    Google Scholar 

  • Hattori, A., Fujita, Y. (1959). Crystalline phycobilin chromopeptides obtained from a blue-green algae, Tolypothrix tenuis. J. Biochem. 46: 633–644

    Google Scholar 

  • Hiyama, T., Ke, B. (1972). Difference spectra and extinction coefficients of P700. Biochim. biophys. Acta 267: 160–171

    Google Scholar 

  • Ikeya, T., Ohki, K., Takahashi, M., Fujita, Y. (1991). Photosynthetic pigment system of picophytoplankton of cyanophytes isolated from subsurface water in the Kuroshio area. J. oceanogr. Soc. Japan 47: 1–6

    Google Scholar 

  • Jerlov, N. G. (1976). Marine optics. Elsevier Scientific Publishing Company, Amsterdam

    Google Scholar 

  • Kana, T. M., Glibert, P. M. (1987). Effect of irradiances up to 2000 μEm-2 s-1 on marine Synechococcus WH7803-I. Growth, pigmentation, and cell composition. Deep-Sea Res. 34: 479–495

    Google Scholar 

  • Kawamura, M., Mimuro, M., Fujita, Y. (1979). Quantitative relationship between two reaction centers in the photosynthetic systems of blue-green algae. Pl. Cell Physiol. 20: 697–705

    Google Scholar 

  • Kishino, M., Okami, N., Takahashi, M., Ichimura, S. (1986). Light utilization efficiency and quantum yield of phytoplankton in a thermally stratified sea. Limnol. Oceanogr. 31: 557–566

    Google Scholar 

  • Klotz, A., Glazer, A. N. (1985). Characterization of the bilin attachment site in R-Phycoerythrin. J. biol. Chem. 260: 4856–4863

    Google Scholar 

  • Ley, A. C., Butler, W. L. (1980). Effects of chromatic adaptation on the photochemical apparatus of photosynthesis in Porphyridium cruentum. Pl. Physiol. 65: 714–722

    Google Scholar 

  • Li, W. K. W., Wood, A. M. (1988). Vertical distribution of North Atlantic ultraphytoplankton: analysis by flow cytometry and epifluorescence microscopy. Deep-Sea Res. 35: 1615–1638

    Google Scholar 

  • Mackinney, G. (1941). Absorption of light by chlorophyll solutions. J. biol. Chem. 140: 315–322

    Google Scholar 

  • Murakami, A., Fujita, Y. (1988). Steady state of photosynthesis in cyanobacterial photosynthetic systems before and after regulation of electron transport composition: overall rate of photosynthesis and PSI/PSII composition. Pl. Cell Physiol. 29: 305–311

    Google Scholar 

  • Myers, J., Graham, J. (1963). Enhancement in Chlorella. Pl. Physiol. 38: 105–116

    Google Scholar 

  • Ohki, K., Fujita, Y. (1987). Non-hemidiscoidal phycobilisome in cyanophytes. In: Biggins, J. (ed.) Progress in photosynthesis research. Martinus Nijhoff Publishers, Dordrecht, p. 157–160

    Google Scholar 

  • Ohki, K., Okabe, Y., Fujita, Y. (1987). Comparative study of quantitative relationship between phycobiliproteins and photosystem II in cyanobacteria and red algae. Pl. Cell Physiol. 28: 1219–1226

    Google Scholar 

  • Olson, R. J., Chisholm, S. W., Zettler, E. R., Armbrust, E. V. (1990). Pigments, size, and distribution of Synechococcus in the North Atlantic and Pacific Oceans. Limnol. Oceanogr. 35: 45–48

    Google Scholar 

  • Ong, L. J., Glazer, A. N. (1987). R-phycocyanin II, a new phycocyanin occurring in marine Synechococcus species. Identification of the terminal energy acceptor bilin in phycocyanins. J. biol. Chem. 262: 6323–6327

    Google Scholar 

  • Ong, L. J., Glazer, A. N., Waterbury, J. B. (1984). An usual phycoerythrin from a marine cyanobacterium. Science, N.Y. 224: 80–83

    Google Scholar 

  • Prézelin, B. B., Glover, H. E., Hoven, B. V., Steinberg, D., Matlik, H. A., Schofield, O., Nelson, N., Wyman, M., Campbell, L. (1989). Blue-green light effects on light-limited rates of photosynthesis: relationship to pigmentation and productivity estimates for Synechococcus populations from the Sargasso Sea. Mar. Ecol. Prog. Ser. 54: 121–136

    Google Scholar 

  • Savitzky, A., Golay, M. J. E. (1964). Smoothing and differentiation of data by simplified least squares procedures. Analyt. Chem. 36: 1627–1639

    Google Scholar 

  • Takahashi, M., Hori, T. (1984). Abundance of picophytoplankton in the subsurface chlorophyll maximum layer in subtropical and tropical waters. Mar. Biol. 79: 177–186

    Google Scholar 

  • Takahashi, M., Kikuchi, K., Hara, Y. (1985). Importance of picocyanobacteria biomass (unicellular, blue-green algae) in the phytoplankton population of the coastal waters off Japan. Mar. Biol. 89: 63–69

    Google Scholar 

  • Tsuji, T., Ohki, K. (1989). Analysis of photosynthetic pigments of individual phytoplankton cells in seas and lakes by microscope fluorometry. In: Hattori, T., Uchida, A. (eds.) Recent advances in microbial ecology. Japan Sci. Soc. Press, Tokyo, p. 702–706

    Google Scholar 

  • Tsuji, T., Ohki, K., Fujita, Y. (1986). Determination of photosynthetic pigment composition in an individual phytoplankton cell in seas and lakes using fluorescence microscopy: properties of the fluorescence emitted from picoplankton cells. Mar. Biol. 93: 343–349

    Google Scholar 

  • Waterbury, J. B., Watson, S. W., Valois, F. W., Franks, D. G. (1986). Biological and ecological characterization of the marine unicellular cyanobacterium Synechococcus. In: Platt, T., Li, W. K. W. (eds.) Photosynthetic picoplankton. Can. Bull. Fish. aquat. Sciences 214: 71–120

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Communicated by T. Ikeda, Nagasaki

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Ikeya, T., Ohki, K., Takahashi, M. et al. Photosynthetic characteristics of marine Synechococcus spp. with special reference to light environments near the bottom of the euphotic zone of the open ocean. Marine Biology 118, 215–221 (1994). https://doi.org/10.1007/BF00349787

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  • DOI: https://doi.org/10.1007/BF00349787

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