Monitoring the in vivo redox state of plant mitochondria: Effect of respiratory inhibitors, abiotic stress and assessment of recovery from oxidative challenge

Biochimica et Biophysica Acta - Bioenergetics

Volumn 1787, Issue 5, 2009, Pages 468-475

  Schwarzländer, Markus ^a   Fricker, Mark D ^a   Sweetlove, Lee J ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

Glutathione; Mitochondria; Oxidative stress; Redox; roGFP

Indexed keywords

ANTIMYCIN A1; CYTOCHROME C OXIDASE; GREEN FLUORESCENT PROTEIN; HEAVY METAL; MENADIONE; REACTIVE OXYGEN METABOLITE; ROTENONE; SALICYLHYDROXAMIC ACID; SODIUM CHLORIDE;

ABIOTIC STRESS; ARABIDOPSIS; ARTICLE; CHLOROPLAST; ELECTRON TRANSPORT; HEAT; HYPEROSMOTIC STRESS; MITOCHONDRION; NONHUMAN; OXIDATION REDUCTION REACTION; OXIDATIVE STRESS; PEROXISOME; PHOTOSYNTHESIS; PRIORITY JOURNAL;

ANTIMYCIN A; ARABIDOPSIS; CYTOSOL; GENES, REPORTER; GREEN FLUORESCENT PROTEINS; MITOCHONDRIA; OXIDATION-REDUCTION; OXIDATIVE PHOSPHORYLATION; OXYGEN CONSUMPTION; PLANT LEAVES; REACTIVE OXYGEN SPECIES; ROTENONE; SALICYLAMIDES;

ANIMALIA; ARABIDOPSIS; EMBRYOPHYTA;

EID: 65449157678     PISSN: 00052728     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbabio.2009.01.020     Document Type: Article

References (38)

1. Halliwell B. Reactive species and antioxidants. Redox biology is a fundamental theme of aerobic life. Plant Physiol. 141 (2006) 312-322
2. Mittler R., Vanderauwera S., Gollery M., and Van Breusegem F. Reactive oxygen gene network of plants. Trends Plant Sci. 9 (2004) 490-498
3. Halliwell B., and Gutteridge J.M.C. Free Radicals in Biology and Medicine. 4 ed. (2007), Oxford University Press, Oxford
4. Noctor G., and Foyer C.H. Ascorbate and glutathione: keeping active oxygen under control. Annu. Rev. Plant Physiol. Plant Mol. Biol. 49 (1998) 249-279
5. Foyer C.H., and Noctor G. Redox homeostasis and antioxidant signaling: a metabolic interface between stress perception and physiological responses. Plant Cell 17 (2005) 1866-1875
6. Meyer A.J., and Hell R. Glutathione homeostasis and redox-regulation by sulfhydryl groups. Photosynth. Res. 86 (2007) 435-457
7. Noctor G. Metabolic signalling in defence and stress: the central roles of soluble redox couples. Plant Cell Environ. 29 (2006) 409-425
8. Apel K., and Hirt H. Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu. Rev. Plant Biol. 55 (2004) 373-399
9. Davletova S., Rizhsky L., Liang H., Shengqiang Z., Oliver D.J., Coutu J., Shulaev V., Schlauch K., and Mittler R. Cytosolic ascorbate peroxidase 1 is a central component of the reactive oxygen gene network of Arabidopsis. Plant Cell 17 (2005) 268-281
10. Chew O., Whelan J., and Millar A.H. Molecular definition of the ascorbate-glutathione cycle in Arabidopsis mitochondria reveals dual targeting of antioxidant defenses in plants. J. Biol. Chem. 278 (2003) 46869-46877
11. Noctor G., De Paepe R., and Foyer C.H. Mitochondrial redox biology and homeostasis in plants. Trends Plant Sci. 12 (2007) 125-134
12. Noctor G., Dutilleul C., De Paepe R., and Foyer C.H. Use of mitochondrial electron transport mutants to evaluate the effects of redox state on photosynthesis, stress tolerance and the integration of carbon/nitrogen metabolism. J. Exp. Bot. 55 (2004) 49-57
13. Vidal G., Ribas-Carbo M., Garmier M., Dubertret G., Rasmusson A.G., Mathieu C., Foyer C.H., and De Paepe R. Lack of respiratory chain complex I impairs alternative oxidase engagement and modulates redox signaling during elicitor-induced cell death in tobacco. Plant Cell 19 (2007) 640-655
14. Finkemeier I., Goodman M., Lamkemeyer P., Kandlbinder A., Sweetlove L.J., and Dietz K.J. The mitochondrial type II peroxiredoxin F is essential for redox homeostasis and root growth of Arabidopsis thaliana under stress. J. Biol. Chem. 280 (2005) 12168-12180
15. Giraud E., Ho L.H., Clifton R., Carroll A., Estavillo G., Tan Y.F., Howell K.A., Ivanova A., Pogson B.J., Millar A.H., and Whelan J. The absence of alternative oxidase1a in Arabidopsis results in acute sensitivity to combined light and drought stress. Plant Physiol. 147 (2008) 595-610
16. Morgan M.J., Lehmann M., Schwarzlander M., Baxter C.J., Sienkiewicz-Porzucek A., Williams T.C., Schauer N., Fernie A.R., Fricker M.D., Ratcliffe R.G., Sweetlove L.J., and Finkemeier I. Decrease in manganese superoxide dismutase leads to reduced root growth and affects TCA cycle flux and mitochondrial redox homeostasis. Plant Physiol. 147 (2008) 101-114
17. Hanson G.T., Aggeler R., Oglesbee D., Cannon M., Capaldi R.A., Tsien R.Y., and Remington S.J. Investigating mitochondrial redox potential with redox-sensitive green fluorescent protein indicators. J. Biol. Chem. 279 (2004) 13044-13053
18. Schwarzlander M., Fricker M.D., Muller C., Marty L., Brach T., Novak J., Sweetlove L.J., Hell R., and Meyer A.J. Confocal imaging of glutathione redox potential in living plant cells. J. Microsc. 231 (2008) 299-316
19. Meyer A.J., Brach T., Marty L., Kreye S., Rouhier N., Jacquot J.P., and Hell R. Redox-sensitive GFP in Arabidopsis thaliana is a quantitative biosensor for the redox potential of the cellular glutathione redox buffer. Plant J. 52 (2007) 973-986
20. Jiang K., Schwarzer C., Lally E., Zhang S., Ruzin S., Machen T., Remington S.J., and Feldman L. Expression and characterization of a redox-sensing green fluorescent protein (reduction-oxidation-sensitive green fluorescent protein) in Arabidopsis. Plant Physiol. 141 (2006) 397-403
21. Thor H., Smith M.T., Hartzell P., Bellomo G., Jewell S.A., and Orrenius S. The metabolism of menadione (2-methyl-1,4-naphthoquinone) by isolated hepatocytes. A study of the implications of oxidative stress in intact cells. J. Biol. Chem. 257 (1982) 12419-12425
22. Amirsadeghi S., Robson C.A., McDonald A.E., and Vanlerberghe G.C. Changes in plant mitochondrial electron transport alter cellular levels of reactive oxygen species and susceptibility to cell death signaling molecules. Plant Cell Physiol. 47 (2006) 1509-1519
23. M. Garmier, A.J. Carroll, E. Delannoy, C. Vallet, D.A. Day, I.D. Small and A.H. Millar, Complex I dysfunction redirects cellular and mitochondrial metabolism in Arabidopsis, Plant Physiol. 148 (2008)1324-1341.
24. Scarpeci T.E., and Valle E.M. Rearrangement of carbon metabolism in Arabidopsis thaliana subjected to oxidative stress condition: an emergency survival strategy. Plant Growth Regul. 54 (2008) 133-142
25. Vanlerberghe G.C., and McIntosh L. Mitochondrial electron transport regulation of nuclear gene expression. Studies with the alternative oxidase gene of tobacco. Plant Physiol. 105 (1994) 867-874
26. Zarkovic J., Anderson S.L., and Rhoads D.M. A reporter gene system used to study developmental expression of alternative oxidase and isolate mitochondrial retrograde regulation mutants in Arabidopsis. Plant Mol. Biol. 57 (2005) 871-888
27. Fiorani F., Umbach A.L., and Siedow J.N. The alternative oxidase of plant mitochondria is involved in the acclimation of shoot growth at low temperature. A study of Arabidopsis AOX1a transgenic plants. Plant Physiol. 139 (2005) 1795-1805
28. Losch R., and Kohl K.I. In: Prasad M.N.V., and Hagemeyer J. (Eds). Heavy Metal Stress in Plants: From Molecules to Ecosystems (1999), Springer-Verlag, Berlin 139-156
29. Bartoli C.G., Gomez F., Martinez D.E., and Guiamet J.J. Mitochondria are the main target for oxidative damage in leaves of wheat (Triticum aestivum L.). J. Exp. Bot. 55 (2004) 1663-1669
30. Clifton R., Lister R., Parker K.L., Sappl P.G., Elhafez D., Millar A.H., Day D.A., and Whelan J. Stress-induced co-expression of alternative respiratory chain components in Arabidopsis thaliana. Plant Mol. Biol. 58 (2005) 193-212
31. Rasmusson A.G., Geisler D.A., and Moller I.M. The multiplicity of dehydrogenases in the electron transport chain of plant mitochondria. Mitochondrion 8 (2008) 47-60
32. Popov V.N., Ruuge E.K., and Starkov A.A. Effect of electron-transport inhibitors on the generation of reactive oxygen species by pea mitochondria during succinate oxidation. Biochemistry (Mosc.) 68 (2003) 747-751
33. Moller I.M., and Kristensen B.K. Protein oxidation in plant mitochondria detected as oxidized tryptophan. Free Radical Biol. Med. 40 (2006) 430-435
34. Maxwell D.P., Nickels R., and McIntosh L. Evidence of mitochondrial involvement in the transduction of signals required for the induction of genes associated with pathogen attack and senescence. Plant J. 29 (2002) 269-279
35. St-Pierre J., Buckingham J.A., Roebuck S.J., and Brand M.D. Topology of superoxide production from different sites in the mitochondrial electron transport chain. J. Biol. Chem. 277 (2002) 44784-44790
36. Balk J., Leaver C.J., and McCabe P.F. Translocation of cytochrome c from mitochondria to cytosol occurs during heat-induced programmed cell death in cucumber plants. FEBS Lett. 463 (1999) 151-154
37. Larkindale J., Hall J.D., Knight M.R., and Vierling E. Heat stress phenotypes of Arabidopsis mutants implicate multiple signaling pathways in the acquisition of thermotolerance. Plant Physiol. 138 (2005) 882-897
38. Beckman K.B., and Ames B.N. The free radical theory of aging matures. Physiol. Rev. 78 (1998) 547-581