Skip to main content
Log in

Observations of the water expulsion vacoule ofPhytophthora palmivora

  • Published:
Protoplasma Aims and scope Submit manuscript

Summary

The water expulsion vacuole ofPhytophthora palmivora was studied with the light microscope after the motility of the spores had been slowed by using a low Ca2 + medium. For transmission electron microscopy, the zoospores were prepared using freeze substitution. The water expulsion vacuole consisted of a central vacuole that collapsed and emptied its contents to the external medium. The central vacuole was surrounded by a series of interconnected vacuoles that are called the surrounding vacuole. The surrounding vacuole and the central vacuole were always associated with coated pits. The vesicles found in the region between the central and surrounding vacuole were exclusively coated vesicles. Consistent changes in the organization of the water expulsion vacuole led us to conclude that, as the central vacuole collapses, the surrounding vacuole is transformed and becomes the new central vacuole. No evidence was obtained for contraction of the central vacuole. The processes involved in membrane recycling during the functioning of the water expulsion vacuole are discussed.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

WEV:

water expulsion vacuole

CT:

central vacuole

SU:

surrounding vacuole

MV:

multivesicular body

SS:

smooth spherical vacuole

dH2O:

distilled water

References

  • Cho CW, Fuller MS (1989) Ultrastructural organization of freeze substituted zoospores ofPhytophthora palmivora. Can J Bot (in press)

  • Crump E, Branton D (1966) Behavior of primary and secondary zoospores ofSaprolegnia sp. Can J Bot 44: 1393–1400

    Google Scholar 

  • Gilkey JC, Staehelin LA (1986) Advances in ultrarapid freezing for the preservation of cellular ultrastructure. J Electron Microsc Tech 3: 177–210

    Google Scholar 

  • Graham RC, Karnovsky MJ (1966) The early stages of absorption of injected horseradish peroxidase in the proximal tubules of mouse kidney: ultrastructural cytochemistry by a new technique. J Histochem Cytochem 14: 291–302

    Google Scholar 

  • Grove SN, Bracker C (1978) Protoplasmic changes during zoospore encystment and cyst germination inPythium aphanidermatum. Exp Mycol 2: 51–98

    Google Scholar 

  • Hardham AR, Suzaki E, Perkin JL (1986) Monoclonal antibodies to isolate-, species-, and genus-specific components on the surface of zoospore and cysts of the fungusPhytophthoria cinnamomi. Can J Bot 64: 311–321

    Google Scholar 

  • Hausmann K, Patterson DJ (1984) Contractile vacuole complexes in algae. In: Wiessner W, Robinson D, Starr RC (eds) Compartments in algal cells and their interaction. Springer, Berlin Heidelberg New York, pp 139–156

    Google Scholar 

  • Heath IB, Greenwood AD (1971) Ultrastructural observations on the kinetosomes and Golgi bodies during the asexual life cycle ofSaprolegnia. Z Zellforsch 112: 371–389

    Google Scholar 

  • —, Rethort K, Arsenault AL, Ottensmyer FP (1985) Improved preservation of the form and contents of wall vesicles and the Golgi apparatus in freeze-substituted hyphae ofSaprolegnia. Protoplasma 128: 81–93

    Google Scholar 

  • Ho HH, Zachariah K, Hickman CJ (1968) The ultrastructure of zoospores ofPhytophthora megasperma var.sojae. Can J Bot 46: 37–41

    Google Scholar 

  • Hoch HC, Howard RJ (1980) Ultrastructure of freeze-substituted hyphae of the basidiomyceteLaetisaria arvalis. Protoplasma 103: 281–297

    Google Scholar 

  • —, Mitchell JE (1972) The ultrastructure of zoospores ofAphanomyces euteiches and of their encystment and subsequent germination. Protoplasma 75: 113–138

    Google Scholar 

  • —, Staples RC (1983) Ultrastructural organization of the nondifferentiated uredospore germling ofUromyces phaseoli varietytypica. Mycologia 75: 795–824

    Google Scholar 

  • Holloway SA, Heath IB (1977) An ultrastructural analysis of the changes in organelle arrangement and structure between the various types ofSaprolegnia. Can J Bot 55: 1328–1339

    Google Scholar 

  • Howard RJ, Aist JR (1979) Hyphal tip cell ultrastructure of the fungusFusarium: improved preservation by freeze-substitution. J Ultrastruct Res 66: 224–234

    Google Scholar 

  • Kitching JA (1956) Contractile vacuoles of Protozoa. In: Heilbrunn LV, Weber F (eds) Protoplasmatologia, vol III, D, vacuome. Springer, Wien, part 3 a

    Google Scholar 

  • — (1967) Contractile vacuoles, ionic regulation and excretion. In: Chen TT (ed) Research in protozoology, vol. 1. Pergamon Press, Oxford, pp 307–336

    Google Scholar 

  • Koetzel JA (1973) A simplified method of preparing optically clear flat embedments with epoxy resin. Stain Technol 48: 349–351

    Google Scholar 

  • Leedale GF (1967) Euglenoid flagellates. Prentice Hall, Englewood Cliffs, NJ

    Google Scholar 

  • Meeuse BJD, Pringsheim EG (1965) Structure and physiology ofEuglena spirogyra. Arch Mikrobiol 50: 68–102

    Google Scholar 

  • Lunney CZ, Bland CE (1976) Ultrastructural observations of mature and encysting zoospores ofPythium proliferum de Bary. Protoplasma 90: 119–137

    Google Scholar 

  • McKanna JA (1973) Membrane recycling: vesiculation of the amoeba contracile vacuole at systole. Science 179: 88–90

    Google Scholar 

  • Pastan IH, Willingham MC (1983) Receptor-mediated endocytosis: coated pits, receptosomes and the Golgi. Trends Biochem Sci 8: 250–254

    Google Scholar 

  • Patterson DJ (1980) Contractile vacuoles and associated structures: their organization and function. Biol Rev 55: 1–46

    Google Scholar 

  • Pearse BMF (1980) Foreword. In: Ockleford CD, Whyte A (eds) Coated vesicles. Cambridge University Press, Cambridge, MA

    Google Scholar 

  • Powell MJ (1981) Zoospore structure of the mycoparasitic chytridCaulochytrium protostelioides Olive. Am J Bot 68: 1074–1089

    Google Scholar 

  • Simionescu N, Simionescu M, Palade GE (1972) Permeability of intestinal capillaries. Pathway followed by dextrans and glycogens. J Cell Biol 53: 365–392

    Google Scholar 

  • Spurr AR (1969) A low-viscosity expoxy resin embedding medium for electron microscopy. J. Ultrastruct Res 26: 31–43

    Google Scholar 

  • Taylor JW, Fuller MS (1981) The Golgi apparatus, zoosporogenesis, and developement of the zoospore discharge apparatus ofChytridium confervae. Exp Mycol 5: 35–59

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Cho, C.W., Fuller, M.S. Observations of the water expulsion vacoule ofPhytophthora palmivora . Protoplasma 149, 47–56 (1989). https://doi.org/10.1007/BF01623982

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01623982

Keywords

Navigation