Thumbnail imagePolyphosphate is a linear chain of phosphate residues linked by phosphoanhydride bonds

epipolypThis table shows the content of short chain (less than 50 units) and long chain poly Ps in the three stages of Trypanosoma cruzi.

rxnReactions catalyzed by the exopolyphosphatase, the enzyme that hydrolyzes poly Ps and the poly P kinase, the enzyme that synthesizes poly Ps in bacteria and dictyostelium discoideum.





Polyphosphate (Poly P) functions, synthesis and degradation

Poly P is a linear chain of a few to many hundreds of phosphate (Pi) residues linked by high-energy phosphoanhydride bonds and is ubiquitous from bacteria to mammals. Poly P has several functions in bacteria: as a phosphate store; an energy source to replace ATP; in cation sequestration and storage; in cell membrane formation and function; in gene transcription control; in regulation of enzyme activities; response to stress and stationary-phase; and in the structure of channels and pumps. Since the metabolic turnover of ATP is considerably higher than that of poly P, it has been suggested that poly P is not an efficient supply of energy and that it has a regulatory role. Arthur Kornberg’s group has described the function of poly P in the physiological adjustments of bacteria to growth, development, stress, and deprivation, its role in biofilm development, quorum sensing, and virulence, as well in long-term survival and expression of virulence factors. A function of poly P in adaptation to stress has been assigned in eukaryotic cells such as yeast, fungi, and algae. Poly P is also involved in eukaryotic cell proliferation, and induction of apoptosis in plasma and myeloma cells. We have found that poly P is stored in the dense granules (acidocalcisomes) of human platelets and is released upon their activation (Ruiz et al., 2004), being a potent modulator of blood clotting and fibrinolysis (Smith et al., 2006).
In many organisms the mobilization of poly P is performed primarily by the action of enzymes that catalyze the synthesis and degradation of this polymer—namely, the poly P kinase and the endo and exopolyphosphatases, respectively. Until recently, the only genes encoding an exopolyphosphatase and an endopolyphosphatase in eukaryotes were from Saccharomyces cerevisiae. We recently characterized the L. major (Rodrigues et al., 2002) and T. cruzi (Fang et al., 2007a)exopolyphosphatases that in contrast to the yeast exopolyphosphatase prefer short chain poly P as substrate. We have also identified a poly P kinase activity in acidocalcisomes of T. cruzi (Ruiz et al., 2001) and demonstrated the role of a Vacuolar Transporter Chaperone 1 (VTC1) in the synthesis of poly P in T. brucei (Fang et al., 2007b).
Poly P accumulates in very large amounts in acidocalcisomes (Ruiz et al., 2001). The storage of phosphate as poly P reduces the osmotic effect of large pools of this crucial nutrient element. Trypanosomatids and Apicomplexan parasites are especially rich in short-chain poly P such as poly P3, poly P4, and poly P5. 31P NMR spectra of purified acidocalcisomes of T. cruzi, T. brucei and L. major indicated that poly Ps have an average chain length of 3.11-3.39 phosphates (Moreno et al., 2000). Based on the total concentration of poly Ps in different stages of T. cruzi (Ruiz et al., 2001), the relative volume of the acidocalcisomes in these cells (0.86%, 2.3%, and 0.26% of the total cell volume of epimastigotes, amastigotes and trypomastigotes, respectively, Miranda et al., 2000), and assuming that these compounds are essentially concentrated in acidocalcisomes, the calculated concentration in the organelles is in the molar range (3-8 M). This is consistent with the detection of solid-state condensed phosphates by magic-angle spinning NMR techniques, and with the very high electron density of acidocalcisomes in situ (Moreno et al. 2002).
A rapid increase (within 2-4 h) in the levels of short- and long-chain poly P was detected during T. cruzi trypomastigote to amastigote differentiation and during the lag phase of growth of epimastigotes (within 12-24 h) (Ruiz et al., 2001). Levels rapidly decreased after epimastigotes resumed growth. The changes observed in the content of poly P in T. cruzi epimastigotes while Pi is present in the growth medium at high concentrations could imply some requirement of these compounds as energy source for resuming growth, while the changes observed during differentiation would suggest an adaptation to the intracellular life of amastigotes (Ruiz et al., 2001). Short- and long-chain poly P levels also rapidly decreased upon exposure of epimastigotes to hiposmotic stress while levels increased after hiperosmotic stress (Ruiz et al., 2001). This would suggest a role for Pi in the adaptation of the parasites to environmental stress.

  • Fang, J., Ruiz, F.A., Docampo, M., Luo, S., Rodrigues, J.C., Motta, L.S., Rohloff, P., and Docampo, R. (2007a) Overexpression of a Zn2+-sensitive soluble exopolyphosphatase from Trypanosoma cruzi depletes polyphosphate and affects osmoregulation. J. Biol. Chem. 282, 32501-32510.
  • Fang, J., Rohloff, P., Miranda, K., and Docampo, R. (2007b) Ablation of a small transmembrane protein of Trypanosoma brucei (TbVTC1) involved in the synthesis of polyphosphate alters acidocalcisome biogenesis and function, and leads to a cytokinesis defect. Biochem. J. 407, 161-170.
  • Miranda, K., Benchimol, M., Docampo, R., and de Souza, W. (2000) The fine structure of acidocalcisomes in Trypanosoma cruzi. Parasitol. Res. 86, 373-384.
  • Moreno, B., Urbina, J.A., Oldfield, E., Bailey, B.N., Rodrigues, C.O., and Docampo, R. (2000) 31P NMR spectroscopy of Trypanosoma brucei, Trypanosoma cruzi and Leishmania major: Evidence for high levels of condensed inorganic phosphates. J. Biol. Chem. 275, 28356-28362.
  • Moreno, B., Rodrigues, C.O., Bailey, B.N., Urbina, J.A., Moreno, S.N.J., Docampo, R., and Oldfield, E. (2002) Magic-angle spinning 31P NMR spectroscopy of condensed phosphates in parasitic protozoa: visualizing the invisible. FEBS Lett. 523, 207-212.
  • Rodrigues, C.O., Ruiz, F.A., Vieira, M., Hill, J.E., and Docampo, R. (2002) An acidocalcisomal exopolyphosphatase from Leishmania major with higher affinity for short-term polyphosphate. J. Biol. Chem. 277, 50899-50906.
  • Ruiz, F.A., Rodrigues, C.O., and Docampo, R. (2001) Rapid changes in polyphosphate content within acidocalcisomes in response to cell growth, differentiation, and environmental stress in Trypanosoma cruzi. J. Biol. Chem., 276, 26114-26121.
  • Ruiz, F. A., Lea, C. R., Oldfield, E., and Docampo, R. (2004) Human platelet dense granules contain polyphosphate and are similar to acidocalcisomes of bacteria and unicellular eukaryotes. J. Biol. Chem. 279, 44250-44257.


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