Dissecting the superoxide dismutase-ascorbate-glutathione-pathway in chloroplasts by metabolic modeling. Computer simulations as a step towards flux analysis.

The present study introduces metabolic modeling as a new tool to analyze the network of redox reactions composing the superoxide dismutase-ascorbate (Asc)-glutathione (GSH) cycle. Based on previously determined concentrations of antioxidants and defense enzymes in chloroplasts, kinetic properties of antioxidative enzymes, and nonenzymatic rate constants of antioxidants with reactive oxygen, models were constructed to simulate oxidative stress and calculate changes in concentrations and fluxes of oxidants and antioxidants. Simulated oxidative stress in chloroplasts did not result in a significant accumulation of O2*- and H2O2 when the supply with reductant was sufficient. Model results suggest that the coupling between Asc- and GSH-related redox systems was weak because monodehydroascorbate radical reductase prevented dehydroascorbate (DHA) formation efficiently. DHA reductase activity was dispensable. Glutathione reductase was mainly required for the recycling of GSH oxidized in nonenzymatic reactions. In the absence of monodehydroascorbate radical reductase and DHA reductase, glutathione reductase and GSH were capable to maintain the Asc pool more than 99% reduced. This suggests that measured DHA/Asc ratios do not reflect a redox balance related to the Asc-GSH-cycle. Decreases in Asc peroxidase resulted in marked H2O2 accumulation without significant effects on the redox balance of Asc/DHA or GSH/GSSG. Simulated loss of SOD resulted in higher H2O2 production rates, thereby affecting all subsequent steps of the Asc-GSH-cycle. In conclusion, modeling approaches contribute to the theoretical understanding of the functioning of antioxidant systems by pointing out questions that need to be validated and provide additional information that is useful to develop breeding strategies for higher stress resistance in plants.

[1]  O. Arrigoni,et al.  Purification and properties of ascorbate free-radical reductase from potato tubers , 1986, Planta.

[2]  K. Asada,et al.  Purification of ascorbate peroxidase in spinach chloroplasts; its inactivation in ascorbate-depleted medium and reactivation by monodehydroascorbate radical , 1987 .

[3]  A. Polle,et al.  Differential stress responses of antioxidative systems to drought in pendunculate oak (Quercus robur) and maritime pine (Pinus pinaster) grown under high CO(2) concentrations. , 2001, Journal of experimental botany.

[4]  J. M. Robinson Does O2 photoreduction occur within chloroplasts in vivo , 1988 .

[5]  O. Arrigoni Ascorbate system in plant development , 1994, Journal of bioenergetics and biomembranes.

[6]  K. Asada,et al.  Production and scavenging of active oxygen in photosynthesis , 1987 .

[7]  R. Scheibe,et al.  Regulation of Steady-State Photosynthesis in Isolated Intact Chloroplasts under Constant Light: Responses of Carbon Fluxes, Metabolite Pools and Enzyme-Activation States to Changes of Electron Pressure , 1997 .

[8]  K. Asada,et al.  Monodehydroascorbate reductase from cucumber is a flavin adenine dinucleotide enzyme. , 1985, The Journal of biological chemistry.

[9]  B. Halliwell,et al.  PURIFICATION AND PROPERTIES OF DEHYDROASCORBATE REDUCTASE FROM SPINACH LEAVES , 1977 .

[10]  D. Heineke,et al.  Subcellular Volumes and Metabolite Concentrations in Potato (Solanum tuberosum cv. Désirée) Leaves1 , 1995 .

[11]  K. Asada The Role of Ascorbate Peroxidase and Monodehydroascorbate Reductase in H 2 O 2 Scavenging in Plants , 1997 .

[12]  C. Sgherri,et al.  Activated oxygen production and detoxification in wheat plants subjected to a water deficit programme , 1995 .

[13]  P. Mullineaux,et al.  The presence of dehydroascorbate and dehydroascorbate reductase in plant tissues , 1998, FEBS letters.

[14]  A. Polle,et al.  Growth under elevated CO(2) ameliorates defenses against photo-oxidative stress in poplar (Populus alba x tremula). , 2001, Environmental and experimental botany.

[15]  A. Polle,et al.  Preliminary studies of ascorbate metabolism in green and albino regions of variegated leaves of Coleus blumei, Benth. , 1999, Free radical research.

[16]  C. Winterbourn,et al.  Reactivity of biologically important thiol compounds with superoxide and hydrogen peroxide. , 1999, Free radical biology & medicine.

[17]  C. Foyer,et al.  ASCORBATE AND GLUTATHIONE: Keeping Active Oxygen Under Control. , 1998, Annual review of plant physiology and plant molecular biology.

[18]  L. A. Río,et al.  Evidence for the Presence of the Ascorbate-Glutathione Cycle in Mitochondria and Peroxisomes of Pea Leaves , 1997, Plant physiology.

[19]  L. Jouanin,et al.  Glutathione: biosynthesis, metabolism and relationship to stress tolerance explored in transformed plants , 1998 .

[20]  L. Jouanin,et al.  Overexpression of Glutathione Reductase but Not Glutathione Synthetase Leads to Increases in Antioxidant Capacity and Resistance to Photoinhibition in Poplar Trees , 1995, Plant physiology.

[21]  S. Idso,et al.  Antioxidants in sun and shade leaves of sour orange trees (Citrus aurantium) after long-term acclimation to elevated CO2 , 1996 .

[22]  M. Van Montagu,et al.  Ascorbate biosynthesis in Arabidopsis cell suspension culture. , 1999, Plant physiology.

[23]  P. Schuler,et al.  Ascorbic Acid as Indicator of Damage to Forest. A Correlation with Air Quality , 1991 .

[24]  J. González-Reyes,et al.  Ascorbate and plant cell growth , 1994, Journal of bioenergetics and biomembranes.

[25]  K.,et al.  Changes in Isozyme Profiles of Catalase, Peroxidase, and Glutathione Reductase during Acclimation to Chilling in Mesocotyls of Maize Seedlings , 1995, Plant physiology.

[26]  P. Mullineaux,et al.  Glutathione Reductase: Regulation and Role in Oxidative Stress , 1997 .

[27]  É. Hideg,et al.  Increased Levels of Monodehydroascorbate Radical in UV-B-Irradiated Broad Bean Leaves , 1997 .

[28]  H. Follmann,et al.  Dehydroascorbate and dehydroascorbate reductase are phantom indicators of oxidative stress in plants , 1997, FEBS letters.

[29]  W. Junkermann,et al.  Inhibition of Apoplastic and Symplastic Peroxidase Activity from Norway Spruce by the Photooxidant Hydroxymethyl Hydroperoxide , 1994, Plant physiology.

[30]  C. Neubauer,et al.  Membrane barriers and Mehler-peroxidase reaction limit the ascorbate available for violaxanthin de-epoxidase activity in intact chloroplasts , 1994, Photosynthesis Research.

[31]  Mike J. May,et al.  Glutathione homeostasis in plants: implications for environmental sensing and plant development , 1998 .

[32]  K. Asada,et al.  Attachment of CuZn-Superoxide Dismutase to Thylakoid Membranes at the Site of Superoxide Generation (PSI) in Spinach Chloroplasts: Detection by Immuno-Gold Labeling After Rapid Freezing and Substitution Method , 1995 .

[33]  P. Hedden,et al.  Isolation and Expression of Three Gibberellin 20-Oxidase cDNA Clones from Arabidopsis , 1995, Plant physiology.

[34]  P. Mullineaux,et al.  Oxygen Metabolism and the Regulation of Photosynthetic Electron Transport , 2019, Causes of Photooxidative Stress and Amelioration of Defense Systems in Plants.

[35]  A. Polle Defense against Photooxidative Damage in Plants , 1997 .

[36]  A. Mehler Studies on reactions of illuminated chloroplasts. I. Mechanism of the reduction of oxygen and other Hill reagents. , 1951, Archives of biochemistry and biophysics.

[37]  K. Biehler,et al.  Evidence for the Contribution of the Mehler-Peroxidase Reaction in Dissipating Excess Electrons in Drought-Stressed Wheat , 1996, Plant physiology.

[38]  K. Asada,et al.  THE WATER-WATER CYCLE IN CHLOROPLASTS: Scavenging of Active Oxygens and Dissipation of Excess Photons. , 1999, Annual review of plant physiology and plant molecular biology.

[39]  K. Werdan,et al.  Alkalization of the chloroplast stroma caused by light-dependent proton flux into the thylakoid space. , 1973, Biochimica et biophysica acta.

[40]  R. Allen,et al.  Dissection of Oxidative Stress Tolerance Using Transgenic Plants , 1995, Plant physiology.

[41]  K. Asayama,et al.  Effect of peroxisome proliferator on extracellular glutathione peroxidase in rat. , 1999, Free radical research.

[42]  K. Asada,et al.  Production and Action of Active Oxygen Species in Photosynthetic Tissues , 2019, Causes of Photooxidative Stress and Amelioration of Defense Systems in Plants.

[43]  P. Mullineaux,et al.  Systemic signaling and acclimation in response to excess excitation energy in Arabidopsis. , 1999, Science.

[44]  K. Asada,et al.  Purification of Dehydroascorbate Reductase from Spinach and Its Characterization as a Thiol Enzyme , 1984 .

[45]  J. Mano,et al.  Monodehydroascorbate Radical Detected by Electron Paramagnetic Resonance Spectrometry Is a Sensitive Probe of Oxidative Stress in Intact Leaves , 1996 .

[46]  W. Haehnel Photosynthetic Electron Transport in Higher Plants , 1984 .

[47]  J. Urano,et al.  Purification and Characterization of Dehydroascorbate Reductase from Rice , 1997 .

[48]  K. Asada,et al.  Ferredoxin-Dependent Photoreduction of the Monodehydroascorbate Radical in Spinach Thylakoids , 1994 .

[49]  Dirk Inzé,et al.  SUPEROXIDE DISMUTASE AND STRESS TOLERANCE , 1992 .

[50]  J. G. Scandalios Oxygen Stress and Superoxide Dismutases , 1993, Plant physiology.

[51]  A. Yokota,et al.  Purification and characterization of chloroplast dehydroascorbate reductase from spinach leaves. , 2000, Plant & cell physiology.

[52]  M. Rooney ASCORBIC ACID AS A PHOTOOXIDATION INHIBITOR , 1983 .

[53]  Alfred Hausladen,et al.  Effects of artificially enhanced levels of ascorbate and glutathione on the enzymes monodehydroascorbate reductase, dehydroascorbate reductase, and glutathione reductase in spinach (Spinacia oleracea) , 1990 .

[54]  M. May Review article. Glutathione homeostasis in plants: implications for environmental sensing and plant development , 1998 .

[55]  G. Noctor Review article. Glutathione: biosynthesis, metabolism and relationship to stress tolerance explored in transformed plants , 1998 .