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2012 | 34 | 2 |

Tytuł artykułu

Plasma membrane-generated ROS and their possible contribution to leaf cell growth of cucumber (Cucumis sativus) MSC16 mitochondrial mutant

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Reactive oxygen species (ROS) generally regarded as harmful products of oxygenic metabolism causing oxidative stress and cell damage are also important for control and regulation of biological processes. ROS can be generated by various enzymatic activities and removed by an array of ROS-scavenging molecules in the cell. In plants, the generation of ROS initiated by the plasma membrane NADPH oxidase can be used for controlled polymer breakdown leading to cell wall loosening during extension growth. The mosaic (MSC16) mitochondrial mutant of cucumber (Cucumis sativus L.) has marked phenotypic changes, including a slower growth rate which partially may result from disturbed leaf carbon and energy metabolism and ROS/antioxidants equilibrium. Cytochemical localization of H₂O₂ in leaf cells showed lower total level of H₂O₂ particularly in the apoplast of MSC16 leaf cells as compared to WT. The activity of plasma membrane NADPH oxidase (EC 1.6.3.1) was about 30% lower in plasmalemma vesicles isolated from MSC16 leaf tissue as compared to WT. The total foliar ascorbate pool (reduced and oxidized) was about 35% higher in MSC16 compared to WT leaves due to an increased content of the oxidized form. About 3% of the whole-leaf ascorbate was localized in the apoplast but in MSC16 it was considerably more reduced. We conclude that the lower apoplastic ROS content caused by decreased activity of plasma membrane NADPH oxidase and lower amounts of H₂O₂ in the apoplast may also contribute to altered growth of the MSC16 cucumber mutant.

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-

Rocznik

Tom

34

Numer

2

Opis fizyczny

p.721-730,fig.,ref.

Twórcy

  • Institute of Experimental Plant Biology and Biotechnology, Faculty of Biology, University of Warsaw, Miecznikowa 1, 02-096 Warsaw, Poland
autor
  • Institute of Experimental Plant Biology and Biotechnology, Faculty of Biology, University of Warsaw, Miecznikowa 1, 02-096 Warsaw, Poland
  • Institute of Experimental Plant Biology and Biotechnology, Faculty of Biology, University of Warsaw, Miecznikowa 1, 02-096 Warsaw, Poland

Bibliografia

  • Bartoszewski G, Malepszy S, Havey MJ (2004) Mosaic (MSC) cucumber regenerated from independent cell cultures possess different mitochondrial rearrangements. Curr Genet 45:45–53
  • Baxter-Burrell A, Yang Z, Springer PS, Bailey-Serres J (2002) RopGAP4-dependent Rop GTPase Rheostat control of Arabidopsis oxygen deprivation tolerance. Science 269:2025–2028
  • Bestwick CS, Brown IR, Bennett MHR, Mansfield JM (1997) Localization of hydrogen peroxide accumulation during the hypersensitive reaction of lettuce cells to Pseudomonas syringae pv. phaseolicola. Plant Cell 9:209–221
  • Bolwell GP, Butt VS, Davies DR, Zimmerlin A (1995) The origin of the oxidative burst in plants. Free Radic Res. 23:517–532
  • Bradford MM (1976) A rapid and sensitive method for quantification of microgram quantities of protein utilizing the principle of protein–dye binding. Anal Biochem 72:248–254
  • Chen Y, Gill PS, Welch WJ (2005) Oxygen availability limits renal NADPH dependent superoxide production. Am J Physiol Renal Physiol 289:F749–F573
  • Desican R, Burnett E, Hancock JT, Neill SJ (1998) Harpin and hydrogen peroxide induce the expression of a homologue of gp91-phox in Arabidopsis thaliana suspension cultures. J Exp Bot 49:1767–1771
  • Fato R, Bergamini CH, Bortolus M, Maniero AL, Leoni S, Ohnishi T, Lenaz G (2009) Differential effects of mitochondrial Complex I inhibitors on production of reactive oxygen species. Biochim Biophys Acta 1787:384–392
  • Foreman J, Demidchik V, Bothwell JHF, Mylona P, Miedema H, Torres MA, Linstead P, Costa S, Brownlee C, Jones JDG, Davies JM, Dolan J (2003) Reactive oxygen species produced by NADPH oxidase regulate plant cell growth. Nature 422:442–446
  • Foyer CH, Noctor G (2005) Oxidant and antioxidant signalling in plants: a re-evaluation of the concept of oxidative stress in a physiological context. Plant Cell Environ 28:1056–1071
  • Foyer CH, Noctor G (2009) Redox regulation in photosynthetic organisms: signalling, acclimation, and practical implications. Antioxid Redox Signal 11:861–905
  • Horemans N, Foyer CH, Asard H (2000) Transport and action of ascorbate at the plant plasma membrane. Trends Plant Sci 5:263–267
  • Juszczuk IM, Rychter AM (2009) BN-PAGE analysis of the respiratory chain complexes in mitochondria of cucumber MSC16 mutant. Plant Physiol Biochem 47:397–406
  • Juszczuk IM, Flexas J, Szal B, Dąbrowska Z, Ribas-Carbo M, Rychter AM (2007) Effect of mitochondrial genome rearrangement on respiratory activity, photosynthesis, photorespiration and energy status of MSC16 cucumber (Cucumis sativus) mutant. Physiol Plant 131:527–541
  • Kampfenkel K, Van Montagu M, Inzé D (1995) Extraction and determination of ascorbate and dehydroascorbate from plant tissue. Anal Biochem 225:165–167
  • Kato N, Esaka M (1999) Changes in ascorbate oxidase gene expression and ascorbate levels in cell division and cell elongation in tobacco cells. Physiol Plant 105:321–329
  • Kerk NM, Feldman LJ (1995) A biochemical model for the initiation and maintenance of the quiescent center: implications for organization of root meristems. Development 121:2825–2833
  • Laloi C, Apel K, Danon A (2004) Reactive oxygen signaling: latest news. Curr Opin Plant Biol 7:323–328
  • Lamb C, Dixon RA (1997) The oxidative burst in plant disease resistance. Annu Rev Plant Physiol Plant Mol Biol 48:251–275
  • Lin LS, Varner JE (1991) Expression of ascorbate oxidase in zucchini squash (Cucurbita pepo). Plant Physiol 96:159–165
  • Liszkay A, van der Zalm E, Schopfer P (2004) Production of reactive oxygen intermediates (O₂⁻, H₂O₂, and OH) by maize roots and their role in wall loosening and elongation growth. Plant Physiol 136:3114–3123
  • Low PS, Merida JR (1996) The oxidative burst in plant defence: function and signal transduction. Physiol Plant 96:533–542
  • Malepszy S, Burza W, Śmiech M (1996) Characterization of a cucumber (Cucumis sativus L.) somaclonal variation with paternal inheritance. J Appl Genet 37:65–78
  • Nanasato Y, Akashi K, Yokota A (2005) Co-expression of cytochrome b₅₆₁ and ascorbate oxidase in leaves of wild watermelon under drought and high light conditions. Plant Cell Physiol 46:1515–1524
  • Neill SJ, Desikan R, Hancock JT (2002) Hydrogen peroxide signaling. Curr Opin Plant Biol 5:388–395
  • Orozco-Cárdenas M, Ryan CA (1999) Hydrogen peroxide is generated systemically in plant leaves by wounding and systemin via the octadecanoid pathway. Proc Natl Acad Sci USA 96:6553–6557
  • Palmgren MG (1990) An H⁺ ATPase assay: proton pumping and ATPase activity determined simultaneously in the same sample. Plant Physiol 94:882–886
  • Palmgren MG, Sommarin M (1989) Lysophosphatidylcholine stimulates ATP dependent proton accumulation in isolated oat root plasma membrane vesicles. Plant Physiol 90:1009–1014
  • Pastori GM, Kiddle G, Antoniw J, Bernard S, Veljovic-Jovanovic S, Verrier PJ, Noctor G, Foyer CH (2003) Leaf vitamin C content modulate plant defense transcripts and regulate genes that control development through hormone signaling. Plant Cell 15:939–951
  • Pei ZM, Murata Y, Benning G, Thomine S, Klusener B, Allen GJ, Grill E, Schroeder JI (2000) Calcium channels activated by hydrogen peroxide mediate abscisic signalling in guard cells. Nature 406:731–734
  • Pignocchi C, Foyer CH (2003) Apoplastic ascorbate metabolism and its role in the regulation of cell signalling. Curr Opin Plant Biol 6:379–389
  • Pignocchi C, Fletcher JM, Wilkinson JE, Barnes JD, Foyer CH (2003) The function of ascorbate oxidase in tobacco. Plant Physiol 132:1631–1641
  • Piotrovskii MS, Shevyreva TA, Zhestkova IM, Trofimova MS (2011) Activation of plasmalemmal NADPH oxidase in etiolated maize seedlings exposed to chilling temperatures. Russ J Plant Physiol 58:234–242
  • Polle A, Chakrabarti K, Schürmann W, Rennenberg H (1990) Composition and properties of hydrogen peroxide decomposing systems in extracellular and total extracts from needles of Norway spruce (Picea abies L. Karst.). Plant Physiol 94:312–319
  • Rodriguez AA, Grunberg KA, Taleisnik EL (2002) Reactive oxygen species in the elongation zone of maize leaves are necessary for leaf extension. Plant Physiol 129:1627–1632
  • Ros-Barceló A (1998) The generation of H₂O₂ in the xylem of Zinnia elegans is mediated by an NADPH-oxidase-like enzyme. Planta 207:207–216
  • Ros-Barceló A, Pomar F, Lopez-Serrano M, Martinez P, Pedreno MA (2002) Developmental regulation of the H₂O₂-producing system and of a basic peroxidase isoenzyme in the Zinnia elegans lignifying xylem. Plant Physiol Biochem 40:325–332
  • Rychter AM, Mikulska M (1990) The relationship between phosphate status and cyanide-resistant respiration in bean roots. Physiol Plant 79:663–667
  • Sagi M, Fluhr R (2006) Production of reactive oxygen species by plant NADPH oxidases. Plant Physiol 141:336–340
  • Schopfer P, Liszkay A (2006) Plasma membrane-generated reactive oxygen intermediates and their role in cell growth of plants. Bio Factors 28:73–81
  • Smirnoff N (2000) Ascorbate biosynthesis and function in photoprotection. Phil Trans R Soc Lond Ser B Biol Sci 355:1455–1464
  • Smirnoff N, Wheeler GL (2000) Ascorbic acid in plants: biosynthesis and function. Crit Rev Plant Sci 19:267–290
  • Solecka D, Żebrowski J, Kacperska A (2008) Are pectins involved in cold acclimation and de-acclimation of winter oil-seed rape plants? Ann Bot 101:521–530
  • Szal B, Dąbrowska Z, Malmberg G, Gardeström P, Rychter AM (2008) Changes in energy status of leaf cells as the consequence of mitochondrial genome rearrangement. Planta 227: 697–706
  • Szal B, Łukawska K, Zdolińska I, Rychter AM (2009) Chilling stress and mitochondrial genome rearrangement in the MSC16 cucumber mutant affect the alternative oxidase and antioxidant defense system to a similar extent. Physiol Plant 137:435–445
  • Szal B, Jastrzębska A, Kulka M, Leśniak K, Podgórska A, Pärnik T, Ivanova H, Keerberg O, Gardeström P, Rychter AM (2010) Influence of mitochondrial genome rearrangement on cucumber leaf carbon and nitrogen metabolism. Planta 232:1371–1382
  • Van den Berg BM, Van Huystee RB (1984) Rapid isolation of plant peroxidase. Purification of peroxidase a from Petunia. Physiol Plant 60:299–304
  • Vanacker H, Carver TLW, Foyer CH (1998) Pathogen-induced changes in the antioxidant status of the apoplast in barley leaves. Plant Physiol 117:1103–1114
  • Wigge B, Gardeström P (1987) The effect of different ionic conditions on the activity of cytochrome c oxidase in purified plant mitochondria. In: Moore AL, Beechey RB (eds) Plant mitochondria. Structural, functional, and physiological aspects. Plenum Press, New York, pp 127–130
  • Wojtaszek P (1997) The oxidative burst: a plant’s early response against infection. Biochem J 322:681–692
  • Wu Y, Sharp RE, Durachko DM, Cosgrove DJ (1998) Growth maintenance of the maize primary root at low water potentials involves increases in cell-wall extension properties, expansin activity, and wall susceptibility to expansions. Plant Physiol 111:765–772

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