Abstract
Plants may live and grow under suboptimal environmental conditions having certain biochemical and metabolic adaptations that facilitate their survival. Plant “metabolic flexibility” consists of the accomplishment of the same step in a metabolic pathway in a variety of different ways. Pyrophosphate which works as an energy donor when cellular ATP pools become diminished during stresses, alternative glycolytic reactions that bypass ATP-requiring steps, additional pathways for electron transport in plant mithocondria and the salvage pathways are some of the aspects related to “energetic flexibility”. This key feature that plays an important role in plant acclimation to stress can be an important target for engineering enhanced stress tolerance in crop plants.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Brodo I, Sharnoff Duran S, Sharnoff S (2001) Lichens of North America. Yale University Press, New Haven
Chivasaa S, Bongani K, Ndimbab W, Simonc J, Lindseyc K, Slabasc A (2005) Extracellular ATP functions as an endogenous external metabolite regulating plant cell viability. Plant Cell 17:3019–3034
Cohn M (2001) Adenosine triphosphate. In: Encyclopedia of life science. Nature Publishing Group
Davies JM, Poole RJ, Sanders D (1993) The computed free energy changes of hydrolysis of inorganic pyrophosphate and ATP: apparent significance of inorganic-pyrophosphate-driven reactions of intermediary metabolism. Biochim Biophys Acta 1141:29–36
DeBlock M, Verduyn C, De Brouwer D, Cornelissen M (2005) Poly(ADP-ribose) polymerase in plants affects energy homeostasis, cell death and stress tolerance. Plant J 41:95–106
Demidchik V, Nichols C, Oliynyk M, Dark A, Glover BJ, Davies JM (2003) Is ATP a signaling agent in plants? Plant Physiol 133:456–461
Dobrotă C (2004) The biology of phosphorus. In: Valsamy-Jones E, Gray R (eds) Phosphorus in environmental technology: principles and applications. IWA Publishers, London, pp 51–77
Duff SMG, Moorhead GBG, Lefebvre DD, Plaxton WC (1989) Phosphate starvation inducible ‘bypasses’ of adenylate and phosphate dependent glycolytic enzymes in Brassica nigra suspension cells. Plant Physiol 90:1275–1278
Ensminger I, Busch F, Huner NPA (2006) Photostasis and cold acclimation: sensing low temperature through photosynthesis. Physiol Plantarum 126(1):28–44
Greene R (2002) Oxidative stress and acclimation mechanisms in plants. The Arabidopsis Book: Vol. 49, No. 1 pp. 1–20, BioOne Publishers, Washington
Gurley WB (2000) HSP101: a key component for the acquisition of thermotolerance in plants. Plant Cell 12:457–460
Hamilton SG, Warburton J, Bhattacharjee A, Ward J, McMahon S (2000) ATP in human skin elicits a dose-related pain response which is potentiated under conditions of hyperalgesia. Brain 123(6):1238–1246
Huang S, Greenway H, Colmerm TD, Millar AH (2005) Protein synthesis by rice coleoptiles during prolonged anoxia: Implications for glycolysis, growth and energy utilization. Ann Bot 96:703–715
Kacperska A (2004) Sensor types in signal transduction pathways in plant cells responding to abiotic stressors: do they depend on stress intensity? Physiol Plant 122:159–168
Kwon SJ, Choi EY, Choi YJ, Ahn JH, Park O (2006) Proteomics studies of post-translational modifications in plants. J Exp Bot 57(7):1547–1551
Lin SJ, Ford E, Haigis M, Liszt G, Guarente G (2004) Calorie restriction extends yeast life span by lowering the level of NADH. Genes Dev 18:12–16
Maxwell DP, Wang Y, McIntosh L (1999) The alternative oxidase lowers mitochondrial reactive oxygen production in plant cells. Proc Natl Acad Sci USA 96:8271–8276
Messerli MA, Amaral-Zettler LA, Zettler E, Jung SK, Smith PJS, Sogin ML (2005) Life at acidic pH impose an increase energetic cost for eukaryotic acidophile. J Exp Biol 208:2569–2579
Mittler R, Vanderauwera S, Gollery M, Van Breusegem F (2005) Reactive oxygen gene network of plants. Trends Plant Sci 9(10):490–498
Mustroph A, Albrecht G, Hajirezaei M, Grimm B, Biemelt S (2005) Low levels of pyrophosphate in transgenic potato plants expressing E.coli pyrophosphatase lead to decreased vitality under oxygen deficiency. Ann Bot 96:717–726
Öquist G, Huner NPA (1993) Photosynthesis of overwintering evergreen plants. Annu Rev Plant Biol 54:329–355
Palma DA, Blumwald E, Plaxton WC (2000) Upregulation of vacuolar H+-translocating pyrophosphatase by phosphate starvation of Brassica napus (rapeseed) suspension cell cultures. FEBS Lett 486:155–158
Pfannschmidt T (2003) Chloroplast redox signals: how photosynthesis controls its own genes. Trends Plant Sci 8:33–41
Plaxton WC (2004) Plant response to stress: Biochemical adaptations to phosphate deficiency. In: Goodman R (ed) Encyclopedia of plant and crop science. Marcel Dekker, Inc., NY
Plaxton WC (2002) Metabolic flexibility helps plants to survive stress. Web-essay (www.plantphys.net) supplement the 3rd edition of Plant Physiology (textbook by Taiz & Zeiger)
Plaxton WC (1999) Metabolic aspects of phosphate starvation in plants. In: Deikman J, Lynch J (eds) Phosphorus in plant biology: regulatory roles in molecular, cellular, organismic, and ecosystem processes. American Society of Plant Physiologists, Rockville, pp 164–176
Plaxton WC, Carswell MC (1999). Metabolic aspects of the phosphate starvation response in plants. In: Lerner HR (ed) Plant responses to environmental stress: from phytohormones to genome reorganization. Marcel-Dekker, New York, NY, USA, pp 350–372
Plaxton WC (1996) The organization and regulation of plant glycolysis. Annu Rev Plant Physiol Plant Mol Biol 47:185–214
Purvis W (2000) Lichens natural history museum. Natural World Series, London
Renaut J, Hausman J-F, Wisniewski ME (2006) Proteomics and low-temperature studies: bridging the gap between gene expression and metabolism. Physiol Plantarum 126(1):97–109
Roth GS, Ingram DK, Lane MA (2001) Caloric restriction in primates and relevance to humans. Ann NY Acad Sci 928:305–315
Sperlágh B, Vizi ES (1996) Neuronal synthesis, storage and release of ATP. Semin Neurosci 8:175–186
Stitt M (1998) Pyrophosphate as an energy donor in the cytosol of plant cells: an enigmatic alternative to ATP. Bot Acta 111:167–175
Stupnikova I, Benamar A, Tolleter D, Grelet J, Borovskii G, Dorne A, Macherel D (2006) Pea seed mitochondria are endowed with a remarkable tolerance to extreme physiological temperatures. Plant Physiol 140:326–335
Theodorou ME, Plaxton WC (1996). Purification and characterization of pyrophosphate-dependent phosphofructokinase from phosphate-starved Brassica nigra suspension cells. Plant Physiol 112:343–351
Theodorou ME, Cornel FA, Duff SM, Plaxton WC (1992) Phosphate starvation-inducible synthesis of the alpha-subunit of the pyrophosphate-dependent phosphofructokinase in black mustard suspension cells. J Biol Chem 267:21901–21905
Vance CP, Uhde-Stone C, Allan DL (2003) Phosphorus acquisition and use: critical adaptations by plants for securing a nonrenewable resource. New Phytol 157(3):423–424
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2006 Springer Science+Business Media B.V.
About this chapter
Cite this chapter
Dobrota, C. (2006). Energy dependant plant stress acclimation. In: Amils, R., Ellis-Evans, C., Hinghofer-Szalkay, H. (eds) Life in Extreme Environments. Springer, Dordrecht. https://doi.org/10.1007/978-1-4020-6285-8_17
Download citation
DOI: https://doi.org/10.1007/978-1-4020-6285-8_17
Received:
Accepted:
Published:
Publisher Name: Springer, Dordrecht
Print ISBN: 978-1-4020-6284-1
Online ISBN: 978-1-4020-6285-8
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)