SEARCH

SEARCH BY CITATION

References

  • Allen RD, 1995. Dissection of oxidative stress tolerance using transgenic tobacco plants. Plant Physiology 107, 104954.
  • Amirsadeghi S, Robson CA, Vanlerberghe GC, 2007. The role of mitochondrion in plant response to biotic stress. Physiologia Plantarum 129, 25366.
  • Aono M, Kubo A, Sakamoto A, Kundo N, Tanaka K, 1995. Paraquat tolerance of transgenic Nicotiana tabacum with enhanced activities of glutathione reductase and superoxide dismutase. Plant Cell Physiology 36, 168791.
  • Asada K, 1999. The water-water cycle in chloroplasts: scavenging of active oxygen and dissipation of excess photons. Annual Review of Plant Molecular Biology 50, 60139.
  • Barba-Espin G, Diaz-Vivancos P, Clemente-Moreno MJ et al. , 2010. Interaction between hydrogen peroxide and plant hormones during germination and the early growth of pea seedlings. Plant, Cell and Environment 33, 98194.
  • Bolwell GP, Wojtaszek P, 1997. Mechanisms for the generation of reactive oxygen species in defence – a broad perspective. Physiological and Molecular Plant Pathology 51, 34766.
  • Buchanan BB, Gruissem W, Jones RL, 2000. Biochemistry and Molecular Biology of Plants. Rockville, MD, USA: American Society of Plant Physiologists.
  • Cervera M, Ortega C, Navarro A, Navarra L, Pena L, 1998. Agrobacterium-mediated transformation of citrage: factors affecting transformation and regeneration. Plant Cell Reports 18, 2718.
  • De Gara L, De Pinto MC, Tommasi F, 2003. The antioxidant systems vis-à-vis reactive oxygen species during plant–pathogen interaction. Plant Physiology and Biochemistry 41, 86370.
  • Degrave A, Fagard M, Perino C et al. , 2008. Erwinia amylovora type three-secreted proteins trigger cell death and defense responses in Arabidopsis thaliana. Molecular Plant–Microbe Interactions 21, 107686.
  • Del Rio LA, Pastori GM, Palma JM et al. , 1998. The activated oxygen role of peroxisomes in senescence. Plant Physiology 116, 1195200.
  • Díaz-Vivancos P, Rubio M, Mesonero V et al. , 2006. The apoplastic antioxidant system in Prunus: response to plum pox virus. Journal of Experimental Botany 57, 381324.
  • Díaz-Vivancos P, Clemente-Moreno MJ, Rubio M et al. , 2008. Alteration in the chloroplastic metabolism leads to ROS accumulation in pea plants in response to Plum pox virus. Journal of Experimental Botany 59, 214760.
  • Faize M, Burgos L, Faize L et al. , 2011. Involvement of cytosolic ascorbate peroxidase and Cu/Zn-superoxide dismutase for improved tolerance against drought stress. Journal of Experimental Botany 62, 2599613.
  • Halliwell B, Gutteridge JMC, 2000. Free Radicals in Biology and Medicine. London, UK: Oxford University Press.
  • Hernández JA, Ferrer MA, Jiménez A, Ros-Barceló A, Sevilla F, 2001. Antioxidant systems and O2.-/H2O2 production in the apoplast of Pisum sativum L. leaves: its relation with NaCl-induced necrotic lesions in minor veins. Plant Physiology 127, 81731.
  • King ED, Ward MK, Raney DE, 1954. Two simple media for demonstration of pyocyanin and fluorescin. Journal of Laboratory and Clinical Medicine 44, 3017.
  • Király L, Cole AB, Bourque JE, Schoelz JE, 1999. Systemic cell death is elicited by the interaction of a single gene in Nicotiana and gene VI from cauliflower mosaic virus. Molecular Plant–Microbe Interactions 12, 91925.
  • Király Z, Barna B, Kecskés A, Fodor J, 2002. Down-regulation of antioxidative capacity in a transgenic tobacco which fails to develop acquired resistance to necrotization caused by TMV. Free Radical Research 36, 98191.
  • Király L, Barna B, Király Z, 2007. Plant resistance to pathogen infection: forms and mechanisms of innate and acquired resistance. Journal of Phytopathology 155, 38596.
  • Király L, Hafez YM, Fodor J, Király Z, 2008. Suppression of tobacco mosaic virus-induced hypersensitive-type necrotization in tobacco at high temperature is associated with downregulation of NADPH oxidase and superoxide and stimulation of dehydroascorbate reductase. Journal of General Virology 89, 799808.
  • Klutz MG, Hutcheston SW, 1992. Multiple periplasmic catalases in phytopathogenic strains of Pseudomonas syringae. Applied and Environmental Microbiology 58, 246873.
  • Kwon SY, Joeng YJ, Lee HS, Cho KY, Allen RD, Kwak SS, 2002. Enhanced tolerance of transgenic tobacco plants expressing both superoxide dismutase and ascorbate peroxidase in chloroplasts against methyl viologen mediated oxidative stress. Plant, Cell and Environment 25, 87382.
  • Lamb C, Dixon RA, 1997. The oxidative burst in plant disease resistance. Annual Review of Plant Physiology and Plant Molecular Biology 48, 25175.
  • Lindeberg M, Myers CR, Collmer A, Schneider DJ, 2008. Roadmap to new virulence determinants in Pseudomonas syringae: insights from comparative genomics and genome organization. Molecular Plant–Microbe Interactions 21, 685700.
  • Lucas G, 1975. Diseases of Tobacco. Fuquay-Varina, NC, USA: Harold E. Parker & Sons.
  • Mittler R, Herr EH, Örvar BL et al. , 1999. Transgenic tobacco plants with reduced capability to detoxify reactive oxygen intermediates are hyperresponsive to pathogen infection. Proceeding of the National Academy of Sciences, USA 96, 1416570.
  • Mittler R, Van derauwera S, Gollery M, Van Breusegem F, 2004. Reactive oxygen network of plant. Trends in Plant Science 9, 4908.
  • Oh HS, Park DH, Collmer A, 2010. Components of the Pseudomonas syringae type III secretion system can suppress and may elicit plant innate immunity. Molecular Plant–Microbe Interactions 23, 72739.
  • Örvar BL, Ellis BE, 1997. Transgenic tobacco plants expressing antisense RNA for cytosolic ascorbate peroxidase show increased susceptibility to ozone injury. The Plant Journal 11, 1297305.
  • Pageau K, Reisdorf-Cren M, Morot-Gaudry JF, Masclaux-Daubresse C, 2006. The two senescence markers, GS1 (cytosolic glutamine synthetase) and GDH (glutamate dehydrogenase), involved in nitrogen mobilization, are differentially regulated during pathogen attack and by stress hormones and reactive oxygen species in Nicotiana tabacum L. leaves. Journal of Experimental Botany 57, 54757.
  • Palma JM, Sandalio LM, Del Rio LA, 1986. Manganese superoxide dismutase and higher plant chloroplasts: a reappraisal of a controverted cellular localization. Journal of Plant Physiology 125, 42739.
  • Ros Barceló A, 1998. The generation of H2O2 in the xylem of Zinnia elegans is mediated by an NADPH-oxidase-like enzyme. Planta 207, 20716.
  • Sarowar S, Kim EN, Kim YJ et al. , 2005. Overexpression of a pepper ascorbate peroxidase-like 1 gene in tobacco plants enhances tolerance to oxidative stress and pathogens. Plant Science 169, 5563.
  • Tertivanidis K, Goudoula K, Vasilikiotis K, Hassiotou E, Perl-Treves R, 2004. Superoxide dismutase transgenes in sugarbeets confer resistance to oxidative agents and the fungus C. beticola. Transgenic Research 13, 22533.
  • Thomas MD, Langston-Unkefer PJ, Uchytil TF, Durbin RD, 1983. Inhibition of glutamine synthetase from pea by tabtoxinine-beta-lactam. Plant Physiology 71, 9125.
  • Torres MA, Jones JDG, Dangl JL, 2006. Reactive oxygen species signaling in response to pathogens. Plant Physiology 141, 3738.
  • Vacca RA, de Pinto MC, Valenti D, Passarella S, Marra E, de Gara L, 2004. Production of reactive oxygen species, alteration of cytosolic ascorbate peroxidase, and impairment of mitochondrial metabolism are early events in heat shock-induced programmed cell death in tobacco bright-yellow 2 cells. Plant Physiology 134, 110012.
  • Van Breusegem F, Dat JF, 2006. Reactive oxygen species in plant cell death. Plant Physiology 141, 38490.
  • Xu XQ, Pan SQ, 2000. An Agrobacterium catalase is a virulence factor involved in tumorigenesis. Molecular Microbiology 35, 40714.
  • Yoshimura K, Yabuta Y, Ishikawa T, Shigeoka S, 2000. Expression of spinach ascorbate peroxidase isoenzymes in response to oxidative stress. Plant Physiology 123, 22333.