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Part of the book series: Springer Handbook Series of Plant Ecophysiology ((KLEC,volume 1))

Abstract

The evolution of oxygenic photosynthesis altered the Earth’s atmosphere and enabled the development and sustenance of aerobic life. Thus, molecular oxygen is essential for life on Earth. However, the incomplete reduction of dioxygen (02) to water (H20) during normal aerobic metabolism generates reactive oxygen species (ROS) that pose a serious threat to all aerobic organisms (Fridovich, 1975). At the same time, it has become increasingly clear that ROS, in addition to their role as toxic agents, are also used as second messengers in various signal transduction pathways, and in many types of biological defense mechanisms (Scandalios, 1997). Thus, in addition to the historic perception of ROS as toxic and lethal agents, recent evidence indicates that they play beneficial roles as well.

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References

  • Angel, P. and Karin, M. 1991. The role of Jun, Fosand the AP-1 complex in cell-proliferation and transformation. Biochim. Biophys. Acta1072, 129–157.

    PubMed  CAS  Google Scholar 

  • Armstrong, G. A., Weisshaar, B. and Hahlbrock, K. 1992. Homodimeric and heterodimeric leucine zipper proteins and nuclear factors from parsley recognize diverse promoter elements with ACGT cores. Plant Cell4, 525–537.

    PubMed  CAS  Google Scholar 

  • Asada, K. 1992. “Production and scavenging of active oxygen in chloroplasts”. In: Molecular Biology of Free Radical Scavenging Systems, ed. J. G. Scandalios, pp. 173–192. Cold Spring Harbor Laboratory Press, Cold Spring harbor.

    Google Scholar 

  • Barrett, M. 1995. Metabolism of herbicides by cytochrome P450 in corn. Drug Metab. Drug Interact12, 299–315.

    Article  CAS  Google Scholar 

  • Becana, M., Dalton, D.A., Moran, J.F., Ormaetxe, I.I., Matamoros, M.A. and Rubio, M.C. 2000. Reactive oxygen species and antioxidants in legume nodules. Physiol. Plant109, 372–381.

    Article  CAS  Google Scholar 

  • Beeler, T. 1990. Oxidation of sulthydryl groups and inhibition of the (Ca’ and Mr)- ATPase by arsenoazolIl. Biochim. Biophys. Acta1027, 264–267.

    Article  PubMed  CAS  Google Scholar 

  • Boldt, R. and Scandalios, J.G. 1995. Circadian regulation of the Cat3catalase gene in maize (Zea maysL.): Entrainment of the circadian rhythm of Cat3by different light treatments. Plant J. 7, 989–999.

    Google Scholar 

  • Bowler, C., Van Montague, M. and Inze, D. 1992. Superoxide dismutase and stress tolerance. Ann. Rev. Plant Physiol. Plant Mol. Biol43, 83–116.

    Article  CAS  Google Scholar 

  • Boveris, A. and Cadenas, E. 1982. “Production of superoxide radicals and hydrogen peroxide in mitochondria”. In: Superoxide DismutaseVol II, ed. L.W. Oberley, pp. 15–30. CRC Press, Boca Raton.

    Google Scholar 

  • Crawford, N.M. 1995. Nitrate: Nutrient and signal for plant growth. Plant Cell7, 859–868.

    PubMed  CAS  Google Scholar 

  • Dolphin, D. 1987. “The generation of radicals during the normal and abnormal functioning of cytochromes P450”. In: Oxygen Radical in Biology and Medicine, eds. M.G. Simic, K.A. Taylor, J.F. Ward and C. von Sonntag, pp. 491–500. Plenum Press, New York.

    Google Scholar 

  • Forman, H.S., Liu, R.M. and Shi, M.M. 1995. “Glutathione synthesis in oxidative stress”. In: Biothiols in Health and Disease, eds. L. Packer and E. Cadenas, pp. 189–212. Marcel Dekker, New York.

    Google Scholar 

  • Frear, D.S. 1995. Wheat microsomal cytochrome P450 monooxygenases: characterization and importance in the metabolic detoxification and selectivity of wheat herbicides. Drug Metab. Drug Interact12, 329–357.

    Article  CAS  Google Scholar 

  • Fridovich, I. 1975. Oxygen: boon and bane. Am. Sci63, 54–59.

    PubMed  CAS  Google Scholar 

  • Gadea, J., Conejero, V. and Vera, P. 1999. Developmental regulation of a cytosolic ascorbate peroxidase gene from tomato plants. Mol. Gen. Genet262, 212–219.

    Article  PubMed  CAS  Google Scholar 

  • Gronwald, J.W. 1994. “Resistance to photosystem II inhibiting herbicides”. In: Herbicide Resistance in Plants, eds. S.B. Powels and J.A.M. Holtum, pp. 27–60. CRC Press, Boca Raton.

    Google Scholar 

  • Guan, L. and Scandalios, J.G. 1995. Developmentally related responses of the maize catalase genes to salycilic acid. Proc. Natl. Acad. Sci. USA92, 5930–5934.

    Article  PubMed  CAS  Google Scholar 

  • Guan, L. and Scandalios, J.G. 1996. Molecular evolution of maize catalases and their relationship to other eukaryotic and prokaryotic catalases. J. Mol. Evol42, 570–579.

    Article  PubMed  CAS  Google Scholar 

  • Guan, L. and Scandalios, J.G. 1998. Effects of the plant growth regulator abscisic acid and high osmoticum on the developmental expression of the maize catalase genes. Physiol. Plant104, 413–422.

    Article  CAS  Google Scholar 

  • Guan, L.M., Zhao, J. and Scandalios, J.G. 2000. Characterization of cis-acting elements and trans-acting factors that regulate expression of the maize Cat1gene in response to ABA and osmotic stress. Plant J. 22, 87–95.

    Article  PubMed  CAS  Google Scholar 

  • Guan, L.M. and Scandalios, J.G. 2000. Hydrogen peroxide mediated catalase gene expression in response to wounding. Free Rad. Biol. & Med28, 1182–1190.

    CAS  Google Scholar 

  • Guiltinan, M.J., Marcotte, W.R. Jr. and Quatrano, R.S. 1990. A plant leucine zipper protein that recognizes an abscisic acid response element. Science250, 267–271.

    Article  PubMed  CAS  Google Scholar 

  • Halliwell, B. 1995. “The biological significance of oxygen-derived species”. In: Active Oxygen in Biochemistry, eds. V.J. Selverstone, C.S. Foote, A. Greenberg and J.F. Liebman, pp. 313–335. Blackie Academic and Professional, New York.

    Chapter  Google Scholar 

  • Halliwell, B. 1996. “Free radicals in biology and medicine”. In: The Encyclopedia of Molecular Biology and Molecular Medicine, Vol. 2, ed. R.A. Meyers, pp. 330–337. VCH Publishers, New York.

    Google Scholar 

  • Hatzios, K, ed. 1997. “Regulation of enzyme systems detoxifying xenobiotics in plants”. NATO-asi series, vol. 37. Kluwer Acad. Publ., Dordrecht.

    Google Scholar 

  • Havir, A.E. and McHale, N.A. 1987. Biochemical and developmental characterization of multiple forms of catalase in tobacco leaves. Plant Physiol. 84, 450–455.

    Article  PubMed  CAS  Google Scholar 

  • Higo, K. and Higo, H. 1995. Cloning and characterization of three catalase genes from rice. Plant Physiol. (suppl.)108, 74.

    Google Scholar 

  • Jamieson, D.J. and Storz, G. 1997. “Transcriptional regulators of oxidative stress responses”. In: Oxidative Stress and the Molecular Biology of Antioxidant Defenses, ed. J.G. Scandalios, pp. 91–115. Cold Spring Harbor Laboratory Press, Plainview.

    Google Scholar 

  • Joshi, S. and Hughes, J.B. 1981. Inhibiting of coupling factor B activity by cadmium ion and arsenite-2,3-dimercaptopropanol and phenylarsine oxide and preferential reactivation by dithiols. J. Biol. Chem256, 11112–11116.

    CAS  Google Scholar 

  • Kahl, R. 1997. “Phenolic antioxidants: Physiological and toxicological aspects”. In: Handbook of Synthetic Antioxidants, eds. L. Packer and E. Cadenas, pp 177–224. Marcel Dekker, New York.

    Google Scholar 

  • Kernodle, S.P. and Scandalios, J.G. 1996. A comparison of the structure and function of the highly homologous maize antioxidant Cu/Zn superoxide dismutase genes, Sod4and Sod4A. Genetics144: 317–328.

    CAS  Google Scholar 

  • Kliebenstein, D.J., Monde, R.A. and Last, R.L. 1998. Superoxide dismutase in Arabidopsis: an eclectic enzyme family with disparate regulation and protein localization. Plant Physiol. 118, 637–650.

    Article  PubMed  CAS  Google Scholar 

  • Knox, J.P. and Dodge, A.D. 1985. Singlet oxygen and plants. Phytochem. 24, 889–896.

    Article  CAS  Google Scholar 

  • Kreuz, K., Tommasini, R. and Martinoia, E. 1996. Old enzymes for a new job. Herbicide detoxification in plants. Plant Physiol. 111, 349–353.

    PubMed  CAS  Google Scholar 

  • Lewinsohn, E. and Gressel, J. 1984. Benzyl viologen-mediated counteraction of diquat and paraquat phytotoxicities. Plant Physiol. 76, 125–130.

    Article  PubMed  CAS  Google Scholar 

  • Mans, K.A. 1996. The functions and regulation of glutathione S-transferases in plants. Ann. Rev. Plant Physiol. Plant Mol. Biol47, 127–158.

    Article  Google Scholar 

  • Meyer, M., Schreck, R. and Baeuerle, P.A. 1993. Hydrogen peroxide and antioxidants have opposite effects on activation of NF-KB and AP-1 in intact cells: AP-1 as secondary antioxidant-responsive factor. EMBO J. 12, 2005–2015.

    PubMed  CAS  Google Scholar 

  • Millar, H.A. and Day, D.A. 1996. Nitric oxide inhibits cytochrome oxidase but not alternative oxidase of plant mitochondria. FEBS Lett. 398, 155–158.

    Article  PubMed  CAS  Google Scholar 

  • Minagawa, N., Koga, S., Nakano, M., Sakajo, S., and Yoshimoto, A. 1992. Possible involvement of superoxide anion in the induction of cyanide resistant respiration in Hansenula anomala. FEBS Lett. 302, 217–219.

    Article  CAS  Google Scholar 

  • Moore, R. and Smith, J.D. 1984. Growth graviresponsiveness and abscisic acid content of Zea maysseedlings treated with fluoridone. Planta162, 342–844.

    Article  PubMed  CAS  Google Scholar 

  • McClung, C.R. 1997. The regulation of catalase in Arabidopsis. Free Rad. Biol. Med. 23, 489–496.

    Article  CAS  Google Scholar 

  • Neill, Si.,. Horgan, R. and Parry, A.D. 1986. The carotenoid and abscisic acid content of viviparouskernels and seedlings of Zea maysL. Planta169, 87–96.

    Google Scholar 

  • Nguyen, T. and Pickett, B. 1990. Transcriptional regulation of the rat glutathione transferase Ya subunit. J. Biol. Chem265, 14648–14653.

    Google Scholar 

  • Pabo, C.O. and Sauer, R.T. 1992. Transcription factors: structural families and principles of DNA recognition. Ann. Rev. Biochem61, 1053–1095.

    Article  PubMed  CAS  Google Scholar 

  • Polidoros, A.N. and Scandalios, J.G. 1999. Role of hydrogen peroxide and different classes of antioxidants in the regulation of catalase and glutathione S-transferase gene expression in maize (Zea maysL.). Physiol. Plant106, 112–120.

    Article  CAS  Google Scholar 

  • Preston, C. 1994. “Resistance to photosystem I disrupting herbicides”. In: Herbicide Resistance in Plants, eds. S.B. Powels and J.A.M. Holtum, pp: 61–82. CRC Press, Boca Raton.

    Google Scholar 

  • Purvis, A.C. and Shewfelt, R.L. 1993. Does the alternative pathway ameliorate chilling injury in sensitive plant tissues? Physiol. Plant88, 712–718.

    Article  CAS  Google Scholar 

  • Rich, P.R., and Bonner, W.D. Jr. 1978. The sites of superoxide anion generation in higher plant mitochondria. Arch. Biochem. Biophys188, 206–213.

    Article  PubMed  CAS  Google Scholar 

  • Ruis, H. and Koller, F. 1997. “Biochemistry, molecular biology, and cell biology of yeast and fungal catalases”. In: Oxidative Stress and the Molecular Biology of Antioxidant Defenses. ed. J.G. Scandalios, pp. 309–342. Cold Spring Harbor Laboratory Press, Plainview.

    Google Scholar 

  • Rushmore, T.H., Morton, M.R. and Pickett, C.B. 1991. The antioxidant responsive element. J. Biol. Chem266, 11632–11639.

    PubMed  CAS  Google Scholar 

  • Scandalios, J.G. 1965. Subunit dissociation and recombination of catalase isozymes. Proc. Natl. Acad. Sci. USA53, 1035–1040.

    Article  PubMed  CAS  Google Scholar 

  • Scandalios, J.G. 1993. Oxygen stress and superoxide dismutases. Plant Physiol. 101, 7–12.

    PubMed  CAS  Google Scholar 

  • Scandalios, J.G. 1996. “Genomic responses to environmental stress IP”. In: The Encyclopedia of Molecular Biology and Molecular Medicine, vol. 2, ed. R. A. Meyers, pp. 216–222. VCH Publishers, New York.

    Google Scholar 

  • Scandalios, J.G. 1997a. “Molecular genetics of superoxide dismutases in plants”. In: Oxidative Stress and the Molecular Biology of Antioxidant Defenses, ed. J.G. Scandalios, pp. 527–568. Cold Spring Harbor Laboratory Press, Cold Spring Harbor.

    Google Scholar 

  • Scandalios, J.G. ed. 1997b. Oxidative Stress and the Molecular Biology of Antioxidant Defenses. Cold Spring Harbor Laboratory Press, Plainview.

    Google Scholar 

  • Scandalios, J.G., Guan, L. and Polidoros, A.N. 1997. “Catalases in plants: gene structure, properties, regulation, and expression”. In: Oxidative Stress and the Molecular Biology of Antioxidant Defenses, ed. J.G. Scandalios pp. 343–406. Cold Spring Harbor Laboratory Press. Plainview.

    Google Scholar 

  • Siebenlist, U., Brown, K. and Franzoso, G. 1995. “NF-KB: a mediator of pathogen and stress responses”. In: Progress in Gene Expression: Inducible Gene Expression. Vol.1 Environmental Stresses and Nutrients, ed. P.A. Baeuerle, pp. 93–141. Birkhaeuser Boston, New York.

    Chapter  Google Scholar 

  • Storz, G. and Imlay, J A 1999. Oxidative stress. Curr. Opin. Microbiol. 2, 188–194. Valentine, J.S., Wertz, D.L., Lyons, T.J., Liou, L.L. and Gralla, E.B. 1998. The dark side of dioxygen biochemistry. Curr. Opin. Chem. Biol2, 253–262.

    Google Scholar 

  • Vaz, A.D.N., Roberts, E.S. and Coon, M.J. 1987. “Radical intermediates in the catalytic cycles of cytochrome P450”. In: Oxygen Radical in Biology and Medicine, eds. M.G. Simic, K.A. Taylor, J.F. Ward and C. von Sonntag, pp. 501–507. Plenum Press, New York.

    Google Scholar 

  • Wagner, A.M. and Krab, K. 1995. The alternative respiratory pathway in plants: role and regulation. Physiol. Plant95, 318–325.

    Article  CAS  Google Scholar 

  • Williamson, J.D. and Scandalios, J.G. 1992a. Differential response of maize catalases and superoxide dismutases to the photoactivated fungal toxin cercosporin. Plant J. 2, 351–358.

    PubMed  CAS  Google Scholar 

  • Williamson, J.D. and Scandalios, J.G. 1992b. Differential response of maize catalases to abscisic acid: Vpl transcriptional activator is not required for abscisic acid-regulated Catlexpression. Proc. Natl. Acad. Sci. USA89, 8842–8846.

    Google Scholar 

  • Williamson, J.D. and Scandalios, J.G. 1993. Plant antioxidant gene responses to fungal pathogens. Trends Microbiol. 1, 239–245.

    Article  PubMed  CAS  Google Scholar 

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Scandalios, J.G. (2001). Molecular Responses to Oxidative Stress. In: Hawkesford, M.J., Buchner, P. (eds) Molecular Analysis of Plant Adaptation to the Environment. Springer Handbook Series of Plant Ecophysiology, vol 1. Springer, Dordrecht. https://doi.org/10.1007/978-94-015-9783-8_9

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  • DOI: https://doi.org/10.1007/978-94-015-9783-8_9

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