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Alkaline inorganic pyrophosphatase and starch synthesis in amyloplasts

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Abstract

The aim of this work was to see if amyloplasts contained inorganic pyrophosphatase. Alkaline pyrophosphatase activity, largely dependant upon MgCl2 but not affected by 100 μM ammonium molybdate or 60–100 mM KCl, was demonstrated in exracts of developing and mature clubs of the spadix of Arum maculatum L. and of suspension cultures of Glycine max L., but not in extracts of the developing bulb of Allium cepa L. The maximum catalytic activity of alkaline pyrophosphatase in the above tissues showed a positive correlation with starch synthesis, and in the first two tissues was shown to exceed the activity of ADPglucose pyrophosphorylase. Of the alkaline pyrophosphatase activity in lysates of protoplasts of suspension cultures of Glycine max, 57% was latent. Density-gradient centrifugation of these lysates showed a close correlation between the distribution of alkaline pyrophosphatase and the plastid marker, nitrite reductase. It is suggested that much, if not all, of the alkaline pyrophosphatase in suspension cultures of Glycine max is located in the plastids.

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Abbreviations

PPase:

inorganic pyrophosphatase

PPi:

inorganic pyrophosphate

References

  • ap Rees, T. (1980) Integration of pathways of synthesis and degradation of hexose phosphates. In: The biochemistry of plants, pp. 1–42, Preiss, J., ed. Academic Press, New York London

    Google Scholar 

  • ap Rees, T., Bryce, J.H., Wilson, P.M., Green, J.H. (1983) Role and location of NAD malic enzyme in thermogenic tissues of Araceae. Arch. Biochem. Biophys. 227, 511–521

    Google Scholar 

  • ap Rees, T., Green, J.H., Wilson, P.M. (1985) Pyrophosphate: fructose 6-phosphate 1-phosphotransferase and glycolysis in nonphotosynthetic tissues of higher plants. Biochem. J. 227, 299–304

    Google Scholar 

  • ap Rees, T., Fuller, W.A., Wright, B.W. (1976) Pathways of carbohydrate oxidation during thermogenesis by the spadix of Arum maculatum. Biochim. Biophys. Acta 437, 22–35

    Google Scholar 

  • ap Rees, T., Leja, M., Macdonald, F.D., Green, J.H. (1984) Nucleotide sugars and starch synthesis in spadix of Arum maculatum and suspension cultures of Glycine max. Phytochemistry 23, 2463–2468

    Google Scholar 

  • Bucke, C. (1970) The distribution and properties of alkaline inorganic pyrophosphatase from higher plants. Phytochemistry 9, 1303–1309

    Google Scholar 

  • de Duve, C. (1964) Principles of tissue fractionation. J. Theor. Biol. 6, 33–59

    Google Scholar 

  • Edwards, J., ap Rees, T., Wilson, P.M., Morrell, S. (1984) Measurement of inorganic pyrophosphate in tissues of Pisum sativum L. Planta 162, 188–191

    Google Scholar 

  • Gould, J.M., Winget, G.D. (1973) A membrane-bound alkaline inorganic pyrophosphatase in isolated spinach chloroplasts. Arch. Biochem. Biophys. 154, 606–613

    Google Scholar 

  • Leigh, R.A., ap Rees, T., Fuller, W.A., Banfield, J. (1979) The location of acid invertase activity and sucrose in the vacuoles of storage roots of beetroot (Beta vulgaris). Biochem. J. 178, 539–547

    Google Scholar 

  • Leigh, R.A., Walker, R.R. (1980) ATPase and acid phosphatase activities associated with vacuoles isolated from storage roots of red beet (Beta vulgaris L.). Planta 150, 222–229

    Google Scholar 

  • Macdonald, F.D., ap Rees, T. (1983) Enzymic properties of amyloplasts from suspension cultures of soybean. Biochim. Biophys. Acta 755, 81–89

    Google Scholar 

  • Parkin, J. (1899) Contribution to our knowledge of the formation, storage, and depletion of carbohydrates in monocotyledons. Philos. Trans. R. Soc. London B 191, 35–80

    Google Scholar 

  • Simmons, S., Butler, L.G. (1969) Alkaline inorganic pyrophosphatase of maize leaves. Biochim. Biophys. Acta 172, 150–157

    Google Scholar 

  • Smythe, D.A., Black, C.C. (1984) Measurement of pyrophosphate content of plant tissues. Plant Physiol. 75, 862–864

    Google Scholar 

  • Taussky, H.H., Shorr, E. (1953) A microcolorimetric method for the determination of inorganic phosphorus. J. Biol. Chem. 202, 675–685

    Google Scholar 

  • Walker, R.R., Leigh, R.A. (1981) Mg2+-dependant, cation-stimulated inorganic pyrophosphatase associated with vacuoles isolated from storage roots of red beet (Beta vulgaris L.). Planta 153, 150–155

    Google Scholar 

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Gross, P., ap Rees, T. Alkaline inorganic pyrophosphatase and starch synthesis in amyloplasts. Planta 167, 140–145 (1986). https://doi.org/10.1007/BF00446381

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  • DOI: https://doi.org/10.1007/BF00446381

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