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Chapter 13 - Resistance to stress

Published online by Cambridge University Press:  05 June 2012

Helgi Öpik  and
Stephen A. Rolfe
Edited in consultation with
Arthur J. Willis
Helgi Öpik
Affiliation:
University of Wales, Swansea
Stephen A. Rolfe
Affiliation:
University of Sheffield
Arthur J. Willis
Affiliation:
University of Sheffield
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Summary

Introduction

Any factor that acts on an organism so as to impair its functions can be termed a stress. Plants growing in the field are habitually exposed to a number of environmental stresses, e.g. drought and frost. Being sessile organisms, plants cannot move away from a stressful situation. The ability to withstand environmental stresses therefore frequently becomes the limiting factor for plant growth, survival and geographical distribution. Plants in fact may possess remarkable powers of endurance. The vegetation of arctic regions can experience winter temperatures of − 70 ℃, whilst in hot deserts over 50 ℃ may be encountered, and even greater temperature extremes have been survived in the laboratory. On the other hand, some plants are killed by chilling at 10 ℃: species vary tremendously in their resistance towards a particular stress. Studies of the reactions of plants under stress, and mechanisms of stress resistance, are of great practical importance, since agricultural yield is only too often drastically reduced by stressful external factors. The demands of an expanding human population have stimulated research into improving the stress resistance of crop species in order to extend the geographical range of a crop, or with a view to utilizing land areas previously regarded as too ‘extreme’ for cultivation, such as semi-deserts.

Terminology and concepts

Stress is a very wide concept, and while the general idea is easily conveyed it is not so easy to decide where the limits should be drawn. Stress was briefly defined above as ‘impairing function’.

Type
Chapter
Information
The Physiology of Flowering Plants , pp. 344 - 372
Publisher: Cambridge University Press
Print publication year: 2005

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References

Bohnert, H. J., Nelson, D. E. & Jensen, R. G.Adaptations to environmental stresses. The Plant Cell, 7 (1995), 1099–111.CrossRefGoogle ScholarPubMed
Campalans, A., Messeguer, R., Goday, A. & Pagès, M.Plant responses to drought, from ABA signal transduction events to the action of the induced proteins. Plant Physiology and Biochemistry, 37 (1999), 327–40.CrossRefGoogle Scholar
Giorni, E., Crosatti, C., Baldi, P.et al. Cold-regulated gene expression during winter in frost tolerant and frost susceptible barley cultivars grown under field conditions. Euphytica, 106 (1999), 149–57.CrossRefGoogle Scholar
Hernandez, J. A., Jiménez, A., Mullineaux, P. & Sevila, F.Tolerance of pea (Pisum sativum L.) to long-term salt stress is associated with induction of antioxidant defences. Plant, Cell and Environment, 23 (2000), 853–62.CrossRefGoogle Scholar
Hughes, M. A., & Dunn, M. A.The molecular biology of plant acclimation to low temperature. Journal of Experimental Botany, 47 (1996), 291–305.CrossRefGoogle Scholar
McNeil, S. D., Nuccio, L. & Hanson, A. D.Betaines and related osmoprotectants. Targets for metabolic engineering of stress resistance. Plant Physiology, 120 (1999), 945–9.CrossRefGoogle ScholarPubMed
Munns, R.Comparative physiology of salt and water stress. Plant, Cell and Environment, 25 (2002), 153–61.CrossRefGoogle ScholarPubMed
Murata, N. & Los, D. A.Membrane fluidity and temperature perception. Plant Physiology, 115 (1997), 875–9.CrossRefGoogle ScholarPubMed
Pastori, G. M. & Foyer, C. H.Common components, networks and pathways of cross-tolerance to stress. The central role of ‘redox’ and abscisic acid mediated controls. Plant Physiology, 129 (2002), 460–8.CrossRefGoogle ScholarPubMed
Queiroz, C. G. S., Alonso, A., Mares-Guia, M. & Magalhães, A. C.Chilling-induced changes in membrane fluidity and antioxidant enzyme activities in Coffea arabica L. roots. Biologia Plantarum, 41 (1998), 403–13.CrossRefGoogle Scholar
Queitsch, C., Hong, S. -W., Vierling, E. & Lindquist, S.Heat shock protein 101 plays a crucial role in thermotolerance in Arabidopsis. The Plant Cell, 12 (2000), 479–92.CrossRefGoogle Scholar
Ramanjulu, S. & Bartels, D.Drought- and desiccation-modulated gene expression in plants. Plant, Cell and Environment, 25 (2002), 141–51.CrossRefGoogle ScholarPubMed
Tabaeizadeh, Z.Drought-induced responses in plant cells. International Review of Cytology, 182 (1998), 193–237.CrossRefGoogle ScholarPubMed
Webb, M. S., Gilmour, S. J., Thomashow, M. F. & Steponkus, P. L.Effects of COR6.6 and COR15am polypeptides encoded by COR (cold-regulated) genes of Arabidopsis thaliana on dehydration-induced phase transitions of phospholipid membranes. Plant Physiology, 111 (1996), 301–12.CrossRefGoogle ScholarPubMed
Wolkers, W. F., Tetteroo, F. A. A., Alberda, M. & Hoekstra, F. A.Changed properties of the cytoplasmic matrix associated with desiccation tolerance of dried carrot somatic embryos: an in situ Fourier transform infrared spectroscopic study. Plant Physiology, 120 (1999), 153–63.CrossRefGoogle Scholar
Xin, Z. & Browse, J.Cold comfort farm: the acclimation of plants to freezing temperatures. Plant, Cell and Environment, 23 (2000), 893–902.CrossRefGoogle Scholar
Yu, X.-M. & Griffith, M.Antifreeze proteins in winter rye leaves form oligomeric complexes. Plant Physiology, 119 (1999), 1361–9.CrossRefGoogle ScholarPubMed
Bray, E. A. (2002). Abscisic acid regulation of gene expression during water-deficit stress in the era of the Arabidopsis genome. Plant, Cell and Environment, 25, 153–61.CrossRefGoogle ScholarPubMed
Gurley, W. B. (2000). HSP101: a key component of the acquisition of thermotolerance in plants. The Plant Cell, 12, 457–60.CrossRefGoogle ScholarPubMed
Holmström, K., Mäntyla, E., Welin, B., Mandal, A. & Palva, E. T. (1996). Drought tolerance in tobacco. Nature.CrossRefGoogle Scholar
Howarth, C. J. (1991). Molecular responses of plants to increased incidence of heat shock. Plant, Cell and Environment, 14, 831–41.CrossRefGoogle Scholar
Howarth, C. J. & Ougham, H. J. (1993). Gene expression under temperature stress. New Phytologist, 125, 1–26.CrossRefGoogle Scholar
Hsiao, T. C., Acevedo, E.Fereres, E. & Henderson, D. W. (1976). Stress metabolism, water stress, growth and osmotic adjustment. Philosophical Transactions of the Royal Society of London, B 273, 479–500.CrossRefGoogle Scholar
Kasuga, M., Liu, Q., Miura, S., Yamaguchi-Shinozaki, K. & Shinozaki, K. (1999). Improving plant drought, salt, and freezing tolerance by gene transfer of a single stress-inducible transcription factor. Nature Biotechnology, 17, 287–91.CrossRefGoogle ScholarPubMed
Kishor, P. B. K., Hong, Z., Miao, G. -H., Hu, C. A. A. & Verma, D. P. S. (1995). Overexpression of Δ1-pyrroline-5-carboxylate synthetase increases proline production and confers osmotolerance in transgenic plants. Plant Physiology, 108, 1387–94.CrossRefGoogle Scholar
McKersie, B. D., Bowley, S. B. & Jones, K. S. (1999). Winter survival of transgenic alfalfa overexpressing superoxide dismutase. Plant Physiology, 119, 839–47.CrossRefGoogle ScholarPubMed
Murata, N., Ishizaki-Nishizawa, O., Higashi, S., Hayashi, H., Tasaka, Y. & Nishida, I. (1992). Genetically engineered alteration in the chilling sensitivity of plants. Nature, 356, 710–13.CrossRefGoogle Scholar
Parker, J. (1962). Relationships among cold hardiness, water-soluble protein, anthocyanins and free sugars in Hedera helix L. Plant Physiology, 37, 809–13.CrossRefGoogle ScholarPubMed
Pilon-Smits, E. A. H., Ebskamp, M. J. M., Paul, M. J., Jeuken, M. J. W., Weisbeek, P. J. & Smeekens, S. C. M. (1995). Improved performance of transgenic fructan-accumulating tobacco under drought stress. Plant Physiology, 107, 125–30.CrossRefGoogle ScholarPubMed
Romero, C., Bellés, J. M., Vayá, J. L., Serrano, R. & Culiáñes-Maciá, F. A. (1997). Expression of the yeast trehalose-6-phosphate synthase gene in transgenic tobacco plants: pleiotropic phenotypes include drought tolerance. Planta, 201, 293–7.CrossRefGoogle ScholarPubMed
Seki, M., Narusaka, M., Abe, H.et al. (2001). Monitoring the expression pattern of 1300 Arabidopsis genes under drought and cold stresses by using a full-length cDNA microarray. The Plant Cell, 13, 61–72.CrossRefGoogle ScholarPubMed
Street, H. E. & Öpik, H. (1984). The Physiology of Flowering Plants, 3rd edn. London: Edward Arnold.Google Scholar
Strand, Å., Hurry, V., Henkes, S.et al. (1999). Acclimation ofArabidopsis leaves developing at low temperatures: increasing cytoplasmic volume accompanies increased activities of enzymes in the Calvin cycle and in the sucrose-biosynthetic pathway. Plant Physiology, 119, 1387–97.CrossRefGoogle Scholar
Breusegem, F., Slooten, L., Stassart, J. -M.et al. (1999). Overproduction of Arabidopsis thaliana FeSOD confers oxidative stress tolerance to transgenic maize. Plant and Cell Physiology, 40, 515–23.CrossRefGoogle ScholarPubMed
Vranová, E., Inzé, D. & Breusegem, F. (2002). Signal transduction during oxidative stress. Journal of Experimental Botany, 53, 1227–36.CrossRefGoogle ScholarPubMed
Xu, D., Duan, X., Wang, B., Ho, D. & Wu, R. (1996). Expression of a late embryogenesis abundant protein gene, HVA1, from barley confers tolerance to water deficit and salt stress in transgenic rice. Plant Physiology, 110, 249–57.CrossRefGoogle ScholarPubMed
Zhang, H. -X. & Blumwald, E. (2001). Transgenic salt-tolerant tomato plants accumulate salt in foliage but not in fruit. Nature Biotechnology, 19, 765–8.CrossRefGoogle ScholarPubMed

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