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Effect of Si-status on diel variation of intracellular free amino acids in Thalassiosira weissflogii under low-light intensity

  • Part Three: Cell Cycle and Productivity
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Abstract

Twenty-one intracellular free amino acids were analysed during a 12-12 h light-dark cycle, on duplicate axenic cultures of Thalassiosira weissflogii (clone Actin, Provasoli-Guillard CCMP) under either Si-sufficient or Si-starved conditions. Total concentrations ranged between 40 and 165 fmol/cell. Total level as well as individual levels of amino acids decreased during the dark period, and GLN/GLU ratio was lower during the dark period. All these results were correlated with the light-dark carbon metabolism of the algae and related to the protein synthesis at night. The Si-starved cultures showed a lower total level of FAA compare to the Si-sufficient cultures, especially in the light period. Silica status of the cells affected more the metabolites of the dark respiration than the photorespiratory metabolites SER and GLY. Si deprivation induced higher range of ALA and VAL, and a decrease of the TCA metabolites GLU & ASP. Additionally, the relative percentage of ASP increased under Si starvation, at the expense of GLU, and this shift was emphasized in the dark period.

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References

  • Admiraal, W., H. Peletier & R. W. P. M. Laane, 1986. Nitrogen metabolism of marine planktonic diatoms; excretion, assimilation and cellular pools of free amino acids in seven species with different cell size. J. exp. mar. Biol. Ecol. 98: 241–263.

    Google Scholar 

  • Al-Amoudi, O. A. & K. J. Flynn, 1989. Effect of nitrate-N incorporation on the composition of the intracellular amino acid pool of N-deprived Tetraselmis marina. Br. Phycol. J. 24: 53–61.

    Google Scholar 

  • Beardall, J. & I. Morris, 1976. The concept of light intensity adaptation in marine phytoplankton: some experiments with Phaeodactylum tricornutum. Mar. Biol. 37: 377–387.

    Google Scholar 

  • Blank, G. S. & C. W. Sullivan, 1979. Diatom mineralization of silicic acid. III. Si(OH)4 binding and light dependent transport in Nitzschia angularis. Arch. Microbiol. 123: 157–164.

    Google Scholar 

  • Brzezinski, M. A. & D. M. Nelson, 1988. Interactions between pulsed nutrient supplies and a photocycle affect phytoplankton competition for limiting nutrients in long-term culture. J. Phycol. 24: 346–356.

    Google Scholar 

  • Brzezinski, M. A., 1985. The Si:C:N ratio of marine diatoms: interspecific variability and the effect of some environmental variables. J. Phycol. 21: 347–357.

    Google Scholar 

  • Chisholm, S. W., F. Azam & R. W. Eppley, 1978. Silicic acid incorporation in marine diatoms on light:dark cycles: Use as an assay for phased cell division. Limnol. Oceanogr. 23: 518–529.

    Google Scholar 

  • Coombs, J., P. J. Halicki, O. Holm-Hansen & B. E. Volcani, 1967. Studies on the biochemistry and fine structure of silica shell formation in diatoms. II. Changes in concentration of nucleoside triphosphates in silicon-starvation synchrony of Navicula pelliculosa (Breb.) Hilse. Exp. Cell Res. 47:315–328.

    Google Scholar 

  • Cosper, E., 1982. Influence of light intensity on diel variations in rates of growth, respiration and organic release of a marine diatom: comparison of diurnally constant and fluctuating light. J. Plankton Res. 4: 705–724.

    Google Scholar 

  • Cuhel, R. L., P. B. Ortner & D. R. Lean, 1984. Night synthesis of protein by algae. Limnol. Oceanogr. 29: 731–744.

    Google Scholar 

  • Darley, W. M., C. W. Sullivan & B. E. Volcani, 1976. Studies on the biochemistry and fine structure of silica shell formation in diatoms. Division cycle and chemical composition of Navicula pelliculosa during light-dark synchronized growth. Planta 130: 159–167.

    Google Scholar 

  • Dawson, R., J. Kalbfleisch, G. Liebezeit, C. A. Llewellyn, R. F. C. Mantoura, F. Moreau & S. A. Poulet, 1985. HPLC analyses of dissolved free amino acids, pigments and vitamins in plankton and particles. Oceanis 11: 521–530.

    Google Scholar 

  • Descolas-Gros, C., 1983. Les voies d'incorporation photosynthétique du carbone du phytoplancton. Thèse Doct. ès sciences, Université Paris VI, 117 pp.

  • Dugdale, R. C., B. H. Jones Jr., J. J. MacIsaac & J. J. Goering, 1981. Adaptation of nutrient assimilation. In T. Platt (ed.), Physiological bases of phytoplankton ecology. Can. Bull. Fish. aquat. Sci. 210: 234–291.

  • Eppley, R. W., 1977. The growth and culture of diatoms. In D. Werner (ed.), The Biology of Diatoms. Botanical Monographs, Blackwell Scientific Publication, London. 13: 24–64.

    Google Scholar 

  • Falkowski, P. G. & J. La Roche, 1991. Acclimation to spectral irradiance in algae. J. Phycol. 27: 8–14.

    Google Scholar 

  • Falkowski, P. G., 1984. Physiological responses of phytoplankton to natural light regimes. J. Plankton Res. 6: 295–307.

    Google Scholar 

  • Flynn, K. J. & O. A. Al-Amoudi, 1988. Effects of N deprivation and darkness on composition of free amino acid pool in and on amino acid release from diatom Phaeodactylum tricornutum Bohlin. J. exp. mar. Biol. Ecol. 119: 131–143.

    Google Scholar 

  • Flynn, K. J., 1990. The determination of nitrogen status in microalgae. Mar. Ecol. Prog. Ser. 61: 297–307.

    Google Scholar 

  • Flynn, K. J., D. M. J. Dickson & O. A. Al-Amoudi, 1989. The ratio of glutamine: glutamate in microalgae: a biomarker for N-status suitable for use at natural cell densities. J. Plankton Res. 11: 165–170.

    Google Scholar 

  • Glover, H., J. Beardall & I. Morris, 1975. Effects of environmental factors on photosynthesis patterns in Phaeodactylum tricornutum (Bacillariophyceae). I. Effect of nitrogen deficiency and light intensity. J. Phycol. 11: 424–429.

    Google Scholar 

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

    Google Scholar 

  • Harrison, P. J., H. L. Conway & R. C. Dugdale, 1976. Marine diatoms grown in chemostats under silicate or ammonium limitation. I. Cellular chemical composition and steady state growth kinetics of Skeletonema costatum. Mar. Biol. 35: 177–186.

    Google Scholar 

  • Harrison, P. J., H. L. Conway, R. W. Holmes & C. O. Davis, 1977. Marine diatoms grown in chemostats under silicate or ammonium limitation. III. Cellular chemical composition and morphology of three marine diatoms. Mar. Biol. 43: 19–31.

    Google Scholar 

  • Hecky, R. E., K. Mopper, P. Kilham & E. T. Degens, 1973. The amino acid and sugar composition of diatom cell-walls. Mar. Biol. 19: 323–331.

    Google Scholar 

  • Holm, N. P. & D. E. Armstrong, 1981. Effects of Si:P concentration ratios and nutrient limitation on the cellular composition and morphology of Asterionella formosa (Bacillariophyceae). J. Phycol. 17: 420–424.

    Google Scholar 

  • Lewin, J. & B. E. F. Reimann, 1969. Silicon and plant growth. Ann. Rev. Pl. Physiol. 20: 289–304.

    Google Scholar 

  • Lewin, J. C., 1954. Silicon metabolism in diatoms. I. Evidence for the role of reduced sulfur compounds in silicon utilization. J. Gen. Physiol. 37: 589–599.

    Google Scholar 

  • Lewin, J. C., 1955. Silicon metabolism in diatoms. III. Respiration and silicon uptake in Navicula pelliculosa. J. Gen. Physiol. 39: 1–10.

    Google Scholar 

  • Lindroth, P. & K. Mopper, 1979. High performance liquid chromatographic determination of sub-picomole amounts of amino acids by precolumn fluorescence derivatization with O-phtaldialdehyde. Analyt. Chem. 51: 1667–1674.

    Google Scholar 

  • Martin-Jézéquel, V., S. A. Poulet, R. P. Harris, J. Moal & J. F. Samain, 1988. Interspecific and intraspecific composition and variation of free amino acids in marine phytoplankton. Mar. Ecol. Prog. Ser. 44: 303–313.

    Google Scholar 

  • McCarthy, J. J., 1981. The kinetics of nutrient assimilation. In T. Platt (ed.), Physiological bases of phytoplankton ecology. Can. Bull. Fish. aquat. Sc. 210; 211–233.

  • Morris, I., 1981. Photosynthesis products, physiological state, and phytoplankton growth. In T. Platt (ed.), Physiological bases of phytoplankton ecology. Can. Bull. Fish. aquat. Sc. 210: 83–102.

  • Mortrain-Bertrand, A., C. Descolas-Gros & H. Jupin, 1987a. Stimulating effect of light-to-dark transitions on carbon assimilation by a marine diatom. J. exp. mar. Biol. Ecol. 112: 11–26.

    Google Scholar 

  • Mortrain-Bertrand, A., C. Descolas-Gros & H. Jupin, 1987b. Short-term 14C incorporation in Skeletonema costatum (Greville) Cleve (Bacillariophyceae) as a function of light regime. Phycologia 26: 262–269.

    Google Scholar 

  • Nelson, D. M. & J. J. Goering, 1978. Assimilation of silicic acid by phytoplankton in the Baja California and northwest Africa upwelling system. Limnol. Oceanogr. 23: 508–517.

    Google Scholar 

  • Nelson, D. M. & L. E. Brand, 1979. Cell division periodicity in 13 species of marine phytoplankton on a light:dark cycle. J. Phycol. 15: 67–75.

    Google Scholar 

  • Nelson, D. M., J. J. Goering, S. Kilham & R. R. L. Guillard, 1976. Kinetics of silicic acid uptake and rates of silica dissolution in the marine diatom Thalassiosira pseudonana. J. Phycol. 12: 246–252.

    Google Scholar 

  • Putt, M. & B. B. Prézelin, 1988. Diel periodicity of photosynthesis and cell division compared in Thalassiosira weissflogii (Bacillariophyceae). J. Phycol. 24: 315–324.

    Google Scholar 

  • Richardson, K., J. Beardall & J. A. Raven, 1983. Adaptation of unicellular algae to irradiance: analysis of strategies. New. Phytol. 93: 157–191.

    Google Scholar 

  • Roessler, P. G., 1988. Effects of silicon deficiency on lipid composition and metabolism in the diatom Cyclotella cryptica. J. Phycol. 24: 394–400.

    Google Scholar 

  • Roessler, P. G., 1990. Environmental control of glycerolipid metabolism in microalgae: commercial implications and future research directions. J. Phycol. 26: 393–399.

    Google Scholar 

  • Shifrin, N. S. & S. W. Chisholm, 1981. Phytoplankton lipids: interspecific differences and effects of nitrate, silicate and light-dark cycle. J. Phycol. 17: 374–384.

    Google Scholar 

  • Sullivan, C. W., 1977. Diatom mineralization of silicic acid. II. Regulation of Si(OH)4 transport rate during the cell cycle of Navicula pelliculosa. J. Phycol. 13: 86–91.

    Google Scholar 

  • Taylor, N. J., 1985. Silica incorporation in the diatom Coscinodiscus granii as affected by light intensity. Br. Phycol. J. 20: 365–374.

    Google Scholar 

  • Terry, K. L., 1982. Nitrate uptake and assimilation in Thalassiosira weissflogii and Phaeodactylum tricornutum: interactions with photosynthesis and with the uptake of other ions. Mar. Biol. 69: 21–30.

    Google Scholar 

  • Terry, K. L., J. Hirata & R. A. Laws, 1985. Light-, nitrogen-, and phosphorus-limited growth of Phaeodactylum tricornutum Bohlin strain TFX-1: chemical composition, carbon partitioning, and the diel periodicity of physiological processes. J. exp. mar. Biol. Ecol. 86: 85–100.

    Google Scholar 

  • Werner, D., 1977. Silicate metabolism. In D. Werner (ed.), The biology of diatoms. Botanical Monographs, Blackwell Scientific Publication, London 13: 110–149.

    Google Scholar 

  • Werner, D., 1966. Die Kieselsäure im Stoffwechsel von Cyclotella cryptica. Arch. Microbiol. 55: 278–308.

    Google Scholar 

  • Werner, D., 1968. Stoffwechselregulation durch den Zellwandbaustein Kieselsäure: Poolgrößenänderungen von a-Ketoglutarsäure, Aminosäuren und Nukleosidphosphaten. Z. Naturforsch. 23: 268–272.

    Google Scholar 

  • Wheeler, P. A., R. J. Olson & S. W. Chisholm, 1983. Effects of photocycles and periodic ammonium supply on three marine phytoplankton species. II Ammonium uptake and assimilation. J. Phycol. 19: 528–533.

    Google Scholar 

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Martin-Jézéquel, V. Effect of Si-status on diel variation of intracellular free amino acids in Thalassiosira weissflogii under low-light intensity. Hydrobiologia 238, 159–167 (1992). https://doi.org/10.1007/BF00048784

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