Production of Reactive Oxygen Intermediates (O2˙−, H2O2, and ˙OH) by Maize Roots and Their Role in Wall Loosening and Elongation Growth

Cell extension in the growing zone of plant roots typically takes place with a maximum local growth rate of 50% length increase per hour. The biochemical mechanism of this dramatic growth process is still poorly understood. Here we test the hypothesis that the wall-loosening reaction controlling root elongation is effected by the production of reactive oxygen intermediates, initiated by a NAD(P)H oxidase-catalyzed formation of superoxide radicals (O2˙−) at the plasma membrane and culminating in the generation of polysaccharide-cleaving hydroxyl radicals (˙OH) by cell wall peroxidase. The following results were obtained using primary roots of maize (Zea mays) seedlings as experimental material. (1) Production of O2˙−, H2O2, and ˙OH can be demonstrated in the growing zone using specific histochemical assays and electron paramagnetic resonance spectroscopy. (2) Auxin-induced inhibition of growth is accompanied by a reduction of O2˙− production. (3) Experimental generation of ˙OH in the cell walls with the Fenton reaction causes wall loosening (cell wall creep), specifically in the growing zone. Alternatively, wall loosening can be induced by ˙OH produced by endogenous cell wall peroxidase in the presence of NADH and H2O2. (4) Inhibition of endogenous ˙OH formation by O2˙− or ˙OH scavengers, or inhibitors of NAD(P)H oxidase or peroxidase activity, suppress elongation growth. These results show that juvenile root cells transiently express the ability to generate ˙OH, and to respond to ˙OH by wall loosening, in passing through the growing zone. Moreover, inhibitor studies indicate that ˙OH formation is essential for normal root growth.

[1]  A. Cross,et al.  The effect of the inhibitor diphenylene iodonium on the superoxide-generating system of neutrophils. Specific labelling of a component polypeptide of the oxidase. , 1986, The Biochemical journal.

[2]  M. Evans,et al.  Promotion of growth and hydrogen ion efflux by auxin in roots of maize pretreated with ethylene biosynthesis inhibitors. , 1982, Plant physiology.

[3]  S. McQueen-Mason,et al.  The relationship between xyloglucan endotransglycosylase and in-vitro cell wall extension in cucumber hypocotyls , 2004, Planta.

[4]  P. Schopfer,et al.  Evidence for the involvement of cell wall peroxidase in the generation of hydroxyl radicals mediating extension growth , 2003, Planta.

[5]  Jeremy Pritchard,et al.  The control of cell expansion in roots. , 1994, The New phytologist.

[6]  C. Obinger,et al.  Transient and Steady-state Kinetics of the Oxidation of Substituted Benzoic Acid Hydrazides by Myeloperoxidase* , 1999, The Journal of Biological Chemistry.

[7]  M. Böttger,et al.  Auxin-induced changes in cell wall extensibility of maize roots , 1998, Planta.

[8]  T Kawano,et al.  Mechanism of peroxidase actions for salicylic acid-induced generation of active oxygen species and an increase in cytosolic calcium in tobacco cell suspension culture. , 2000, Journal of experimental botany.

[9]  A. Ferroni,et al.  Transmembrane potential increase induced by auxin, benzyladenine and fusicoccin. Correlation with proton extrusion and cell enlargement , 1974 .

[10]  M. Evans,et al.  Geotropism in corn roots: evidence for its mediation by differential Acid efflux. , 1981, Science.

[11]  J. Crapo,et al.  Manganic porphyrins possess catalase activity and protect endothelial cells against hydrogen peroxide-mediated injury. , 1997, Archives of biochemistry and biophysics.

[12]  A. Barceló Use and misuse of peroxidase inhibitors , 1998 .

[13]  M. Evans,et al.  Auxin inhibition of acid-and fusicoccin-induced elongation in lentil roots , 2004, Planta.

[14]  M. Nicole,et al.  Apoplastic Peroxidase Generates Superoxide Anions in Cells of Cotton Cotyledons Undergoing the Hypersensitive Reaction to Xanthomonas campestris pv. malvacearum Race 18 , 1998 .

[15]  D. Cosgrove,et al.  A Comparison of Oligogalacturonide- and Auxin-Induced Extracellular Alkalinization and Growth Responses in Roots of Intact Cucumber Seedlings1 , 2002, Plant Physiology.

[16]  P. Schopfer,et al.  Inhibition of O2-reducing activity of horseradish peroxidase by diphenyleneiodonium. , 1998, Phytochemistry.

[17]  M. Takahashi,et al.  Assay and Inhibitors of Spinach Superoxide Dismutase , 1974 .

[18]  David B. Collinge,et al.  Subcellular localization of H2O2 in plants. H2O2 accumulation in papillae and hypersensitive response during the barley—powdery mildew interaction , 1997 .

[19]  L. Dolan,et al.  Cell expansion in roots. , 2004, Current opinion in plant biology.

[20]  M. Evans,et al.  Auxin action on proton influx in corn roots and its correlation with growth , 1980, Planta.

[21]  E. Taleisnik,et al.  Reactive Oxygen Species in the Elongation Zone of Maize Leaves Are Necessary for Leaf Extension1 , 2002, Plant Physiology.

[22]  L. Oberley,et al.  Myeloperoxidase Is Involved in H2O2-induced Apoptosis of HL-60 Human Leukemia Cells* , 2000, The Journal of Biological Chemistry.

[23]  Jonathan D. G. Jones,et al.  Reactive oxygen species produced by NADPH oxidase regulate plant cell growth , 2003, Nature.

[24]  R. Mittler Oxidative stress, antioxidants and stress tolerance. , 2002, Trends in plant science.

[25]  P. Schopfer,et al.  Hydroxyl-radical production in physiological reactions. A novel function of peroxidase. , 1999, European journal of biochemistry.

[26]  B. Britigan,et al.  Spin trapping evidence for myeloperoxidase-dependent hydroxyl radical formation by human neutrophils and monocytes. , 1992, The Journal of biological chemistry.

[27]  J. Verbelen,et al.  Xyloglucan endotransglucosylase action is high in the root elongation zone and in the trichoblasts of all vascular plants from Selaginella to Zea mays. , 2003, Journal of experimental botany.

[28]  B. Halliwell,et al.  Free radicals in biology and medicine , 1985 .

[29]  B. Babior NADPH oxidase: an update. , 1999, Blood.

[30]  M. Gidley,et al.  Probing expansin action using cellulose/hemicellulose composites. , 2000, The Plant journal : for cell and molecular biology.

[31]  M. Evans A New Sensitive Root Auxanometer: Preliminary Studies of the Interaction of Auxin and Acid pH in the Regulation of Intact Root Elongation. , 1976, Plant physiology.

[32]  A. Tiedemann Evidence for a primary role of active oxygen species in induction of host cell death during infection of bean leaves withBotrytis cinerea , 1997 .

[33]  M. Sutherland,et al.  The tetrazolium dyes MTS and XTT provide new quantitative assays for superoxide and superoxide dismutase. , 1997, Free radical research.

[34]  Jeremy Pritchard,et al.  Xyloglucan Endotransglycosylase Activity, Microfibril Orientation and the Profiles of Cell Wall Properties Along Growing Regions of Maize Roots , 1993 .

[35]  K. L. Edwards,et al.  Rapid growth responses of corn root segments: Effect of pH on elongation , 1974, Planta.

[36]  P. Schopfer,et al.  Release of reactive oxygen intermediates (superoxide radicals, hydrogen peroxide, and hydroxyl radicals) and peroxidase in germinating radish seeds controlled by light, gibberellin, and abscisic acid. , 2001, Plant physiology.

[37]  S. Fry Oxidative scission of plant cell wall polysaccharides by ascorbate-induced hydroxyl radicals. , 1998, The Biochemical journal.

[38]  D J Cosgrove,et al.  Water Uptake by Growing Cells: An Assessment of the Controlling Roles of Wall Relaxation, Solute Uptake, and Hydraulic Conductance , 1993, International Journal of Plant Sciences.

[39]  P. Schopfer,et al.  NADH-stimulated, cyanide-resistant superoxide production in maize coleoptiles analyzed with a tetrazolium-based assay , 2001, Planta.

[40]  R. E. Sharp,et al.  Spatial distribution of turgor and root growth at low water potentials. , 1991, Plant physiology.

[41]  D. Cook,et al.  Nod factor induction of reactive oxygen species production is correlated with expression of the early nodulin gene rip1 in Medicago truncatula. , 2002, Molecular plant-microbe interactions : MPMI.

[42]  R. E. Sharp,et al.  Growth Maintenance of the Maize Primary Root at Low Water Potentials Involves Increases in Cell-Wall Extension Properties, Expansin Activity, and Wall Susceptibility to Expansins , 1996, Plant physiology.

[43]  J. Kangasjärvi,et al.  Reactive oxygen species and hormonal control of cell death. , 2003, Trends in plant science.

[44]  M. Böttger,et al.  The Role of Protons in the Auxin‐induced Root Growth Inhibition ‐ A Critical Reexamination , 1993 .

[45]  T. Hoson Regulation of polysaccharide breakdown during auxin-induced cell wall loosening , 1993, Journal of Plant Research.

[46]  J. Dumville,et al.  A proposed role for copper ions in cell wall loosening , 2002, Plant and Soil.

[47]  D J Cosgrove,et al.  New genes and new biological roles for expansins. , 2000, Current opinion in plant biology.

[48]  I. Fridovich,et al.  Characterization of a superoxide dismutase mimic prepared from desferrioxamine and MnO2. , 1989, Archives of biochemistry and biophysics.

[49]  P. Schopfer,et al.  Physical extensibility of maize coleoptile cell walls: apparent plastic extensibility is due to elastic hysteresis , 1992, Planta.

[50]  D. Inzé,et al.  The role of active oxygen species in plant signal transduction , 2001 .

[51]  P. Schopfer,et al.  Hydroxyl radical-induced cell-wall loosening in vitro and in vivo: implications for the control of elongation growth. , 2002, The Plant journal : for cell and molecular biology.

[52]  H. Kosaka,et al.  EPR evidence for generation of hydroxyl radical triggered byN-acetylchitooligosaccharide elicitor and a protein phosphatase inhibitor in suspension-cultured rice cells , 1995, Protoplasma.

[53]  M. I. D. Michelis,et al.  Fusicoccin-induced, K+-stimulated proton secretion and acid-induced growth of apical root segments , 1976 .

[54]  D J Cosgrove,et al.  Enzymes and other agents that enhance cell wall extensibility. , 1999, Annual review of plant physiology and plant molecular biology.

[55]  N. Carpita STRUCTURE AND BIOGENESIS OF THE CELL WALLS OF GRASSES. , 1996, Annual review of plant physiology and plant molecular biology.

[56]  H. Mohr,et al.  Die Beeinflussung der Farnsporen-Keimung [Osmunda cinnamomea (L.) undO. claytoniana (L.)] über das Phytochromsystem und die Photosynthese , 1964, Planta.

[57]  D J Cosgrove,et al.  Expansive growth of plant cell walls. , 2000, Plant physiology and biochemistry : PPB.

[58]  P. Schopfer,et al.  Evidence that hydroxyl radicals mediate auxin-induced extension growth , 2002, Planta.

[59]  Peters,et al.  The Correlation of Profiles of Surface pH and Elongation Growth in Maize Roots. , 1999, Plant physiology.