Skip to main content
Log in

The membranes of slowly drought-stressed wheat seedlings: a freeze-fracture study

  • Published:
Planta Aims and scope Submit manuscript

Abstract

Seedlings of Triticum aestivum L. cv. Neepawa were slowly drought-stressed by witholding water after sowing in pots. Leaf extension stopped during development of the third leaf. Damage was assessed by rewatering the pots and measuring regrowth; 1–5 d after growth stopped, rewatering induced significant regrowth within several hours; 6–13 d after growth stopped, regrowth was delayed; from 14 d after growth stopped, no regrowth occurred after rewatering. Leaf bases were excised from the drought-stressed seedlings during this period of increasing damage, and were freeze-etched.

Intramembranous particles (IMP) were evenly scattered in the plasma membrane in those plants which regrew immediately after rewatering. In the plants which regrew after a delay or which did not regrow on rewatering, there were patches without IMP in plasma membrane, nuclear envelope, and other membranes. Plasma membrane, nuclear envelope and possibly other membranes were sometimes partly replaced by vesicles, possibly formed from the original membrane. Such vesiculation occurred in a few cells in plants which survived the stress with a delayed regrowth, and was commoner in the plants which did not recover. The results support the idea that slow drought induces IMP-free patches in membranes including the plasma membrane, this induces membrane reorganisation including vesiculation of membranes and coagulation of protoplasm, and that these are expressed as delayed or failed regrowth. Some IMP-free patches in the plasma membrane had a faint ordered sub-structure, possibly a hexagonal lipid phase. Such patches were infrequent and IMP sometimes occurred in areas of plasma membrane having an apparently similar sub-structure. Thus the IMP-free patches could not be explained by a lamellar-hexagonal phase transition. As the stress became damaging, vesicles and endoplasmic reticulum accumulated immediately next to the plasma membrane. Mainly during the early period of damaging stress (6–10 d after growth stopped), depressions, invaginations, and rarer “lesions” occurred in the plasma membrane, sometimes associated with some of the IMP-free patches. In the same period, many nuclear envelopes had exceptionally large nuclear pores.

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

E:

exoplasmic

IMP:

intramembranous particles

P:

protoplasmic

References

  • Branton, D., Bullivant, S., Gilula, N.B., Karnovsky, M.J., Moore, H., Mühlethaler, K., Northeote, D.H., Packer, L., Satir, B., Satir, P., Speth, V., Staehelin, L.A., Steere, R.L., Weinstein, R.S. (1975) Freeze-etching nomenclature. Science 190, 54–56

    Google Scholar 

  • Crèvecoeur, M., Deltour, R., Bronchart, R. (1976) Cytological study on water stress during germination of Zea mays. Planta 132, 21–41

    Google Scholar 

  • Deamer, D.W., Leonard, R., Tardieu, A., Branton, D. (1970) Lamellar and hexagonal lipid phases visualized by freeze-etching. Biochim. Biophys. Acta 219, 47–60

    Google Scholar 

  • Fellows, R.J., Boyer, J.S. (1976) Structure and activity of chloroplasts of sunflower leaves having various water potentials. Planta 132, 229–239

    Google Scholar 

  • Gordon-Kamm, W.J., Steponkus, P.L. (1984) Lamellar-to-hexagonalII phase transitions in the plasma membrane of isolated protoplasts after freeze-induced dehydration. Proc. Natl. Acad. Sci. USA 81, 6373–6377

    Google Scholar 

  • Hallam, N.D., Gaff, D.F. (1978) Reorganisation of fine structure during rehydration of desiccated leaves of Xerophyta villosa. New Phytol. 81, 349–355

    Google Scholar 

  • Hallam, N.D., Luff, S.E. (1980a) Fine structural changes in the mesophyll tissue of the leaves of Xerophyta villosa during desiccation. Bot. Gaz. 141, 173–179

    Google Scholar 

  • Hallam, N.D., Luff, S.E. (1980b) Fine structural changes in the leaves of the desiccation-tolerant plant Talbotia elegans during extreme water stress. Bot. Gaz. 141, 180–187

    Google Scholar 

  • Levitt, J. (1980) Responses of plants to environmental stress. 2nd edn. Academic Press, New York London

    Google Scholar 

  • Nir, I., Klein, S., Poljakoff-Mayber, A. (1969) Effect of moisture stress on submicroscopic structure of maize roots. Aust. J. Biol. Sci. 22, 17–33

    Google Scholar 

  • Nir, I., Klein, S., Poljakoff-Mayber, A. (1970) Changes in fine structure of root cells from maize seedlings exposed to water stress. Aust. J. Biol. Sci. 23, 489–491

    Google Scholar 

  • Pearce, R.S. (1985) A freeze-fracture study of membranes of rapidly drought-stressed leaf bases of wheat. J. Exp. Bot. 36

  • Pearce, R.S., Willison, J.H.M. (1983) Cell membranes of wheat laminae and leaf bases freeze-etched during exposure to extra-cellular freezing: The plasma membrane is specifically affected by damaging treatments. (Abstr.) Cryobiology 20, 706

    Google Scholar 

  • Pearce, R.S., Willison, J.H.M. (1984) Tests of a proposed mechanism of freezing damage in wheat seedlings: Drought stress induces the same ultrastructural features as extrecellular freezing. (Abstr.) Cryobiology 21, 685

    Google Scholar 

  • Pearce, R.S., Willison, J.H.M. (1985a) Cereal tissues freeze-etched during exposure to extracellular freezing: distribution of ice. Planta 163, 295–303

    Google Scholar 

  • Pearce, R.S., Willison, J.H.M. (1985b) A freeze-etch study of the effects of extracellular freezing on cellular membranes of wheat. Planta 163, 304–316

    Google Scholar 

  • Poljakoff-Mayber, A. (1981) Ultrastructural consequences of drought. In: The physiology and biochemistry of drought resistance in plants. pp. 389–403, Paleg, LG., Aspinall, D., eds. Academic Press, New York London

    Google Scholar 

  • Simon, E.W. (1974) Phospholipids and plant membrane permeability. New Phytol. 73, 377–420

    Google Scholar 

  • Sleytr, U.B., Robards, A.W., (1981) Understanding the artefact problem in freeze-fracture replication: a review. J. Microsc. 126, 101–122

    Google Scholar 

  • Steponkus, P.L. (1984) Role of the plasma membrane in freezing injury and cold acclimation. Annu. Rev. Plant Physiol. 35, 543–584

    Google Scholar 

  • Verkleij, A.J. (1984) Lipidic intramembranous particles. Biochim. Biophys. Acta 779, 43–63

    Google Scholar 

  • Virzo De Santo, A., Lingrone, R., Alfani, A., Fioretto, A., Russo, G. (1984) CAM activity and day/night changes in the ultrastructure of stem chlorenchyma of Cissus guadrangularis L. as influenced by drought. Plant Cell Environ. 7, 105–112

    Google Scholar 

  • Willison, J.H.M., Cragg, F.J. (1980) Nuclear pore structure in quiescent buds of Tilia europaea. Can. J. Bot. 58, 1814–1819

    Google Scholar 

  • Willison, J.H.M., Johnston, G.C. (1978) Altered nuclear pore diameters in Cl-arrested cells of the yeast Saccharomyces cerevisiae. J. Bacteriol. 136, 318–323

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Pearce, R.S. The membranes of slowly drought-stressed wheat seedlings: a freeze-fracture study. Planta 166, 1–14 (1985). https://doi.org/10.1007/BF00397380

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00397380

Key words

Navigation