Strategies to maintain redox homeostasis during photosynthesis under changing conditions.
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S. Holtgrefe | R. Scheibe | J. Backhausen | Renate Scheibe | Jan E Backhausen | Vera Emmerlich | Simone Holtgrefe | V. Emmerlich
[1] John F. Allen,et al. Plastoquinone redox control of chloroplast thylakoid protein phosphorylation and distribution of excitation energy between photosystems: discovery, background, implications , 2004, Photosynthesis Research.
[2] U. Heber. Irrungen, Wirrungen? The Mehler reaction in relation to cyclic electron transport in C3 plants , 2004, Photosynthesis Research.
[3] R. Scheibe,et al. Adaptation of tobacco plants to elevated CO2: influence of leaf age on changes in physiology, redox states and NADP-malate dehydrogenase activity , 1999 .
[4] V. Hurry,et al. Cold acclimation of Arabidopsis thaliana results in incomplete recovery of photosynthetic capacity, associated with an increased reduction of the chloroplast stroma , 2001, Planta.
[5] H. Hirt,et al. Reactive oxygen species: metabolism, oxidative stress, and signal transduction. , 2004, Annual review of plant biology.
[6] J. Jobst,et al. Senescence-related gene expression profiles of rosette leaves of Arabidopsis thaliana: leaf age versus plant age. , 2004, Plant biology.
[7] S. Kiyota,et al. Degradation of Endogenous Organic Acids Induced by Pi Uptake in Catharanthus roseus Cells: Involvement of the Biochemical pH-Stat , 1998 .
[8] N. Huner,et al. Acclimation to low temperature or high light mitigates sensitivity to photoinhibition: roles of the Calvin cycle and the Mehler reaction , 2000 .
[9] R. Scheibe,et al. Redox-modulation of chloroplast enzymes : a common principle for individual control. , 1991, Plant physiology.
[10] J. Lallemand,et al. Cytoplasmic pH Regulation in Acer pseudoplatanus Cells: I. A P NMR Description of Acid-Load Effects. , 1986, Plant physiology.
[11] D. Davies. The fine control of cytosolic pH , 1986 .
[12] P. Rey,et al. The mitochondrial type II peroxiredoxin from poplar , 2007 .
[13] K. Dietz. Redox control, redox signaling, and redox homeostasis in plant cells. , 2003, International review of cytology.
[14] M. Stitt,et al. Comparison of Nadp-Malate Dehydrogenase Activation, Qa Reduction and O-2 Evolution in Spinach Leaves , 1988 .
[15] K. Sakano. Revision of Biochemical pH-Stat: Involvement of Alternative Pathway Metabolisms , 1998 .
[16] R. Scheibe. Malate valves to balance cellular energy supply. , 2004, Physiologia plantarum.
[17] H. Hirt,et al. REACTIVE OXYGEN SPECIES: Metabolism, , 2004 .
[18] L. Mcintosh,et al. Transgenic tobacco (Nicotiana tabacum L.) plants with increased expression levels of mitochondrial NADP+-dependent isocitrate dehydrogenase: evidence implicating this enzyme in the redox activation of the alternative oxidase. , 2004, Plant & cell physiology.
[19] C. Laloi,et al. Reactive oxygen signalling: the latest news. , 2004, Current opinion in plant biology.
[20] R. Mittler. Oxidative stress, antioxidants and stress tolerance. , 2002, Trends in plant science.
[21] C. Foyer,et al. Redox sensing and signalling associated with reactive oxygen in chloroplasts, peroxisomes and mitochondria , 2003 .
[22] Kun An,et al. Loss‐of‐function mutations in DET2 gene lead to an enhanced resistance to oxidative stress in Arabidopsis , 2005 .
[23] I. Cotgreave,et al. Recent trends in glutathione biochemistry--glutathione-protein interactions: a molecular link between oxidative stress and cell proliferation? , 1998, Biochemical and biophysical research communications.
[24] K. Takizawa,et al. Integrating the proton circuit into photosynthesis: progress and challenges , 2005 .
[25] P. Horton,et al. Transgenic potato plants with altered expression levels of chloroplast NADP-malate dehydrogenase: interactions between photosynthetic electron transport and malate metabolism in leaves and in isolated intact chloroplasts , 1998, Planta.
[26] L. Sweetlove,et al. The Mitochondrial Type II Peroxiredoxin F Is Essential for Redox Homeostasis and Root Growth of Arabidopsis thaliana under Stress* , 2005, Journal of Biological Chemistry.
[27] R. G. Walters,et al. Towards an understanding of photosynthetic acclimation. , 2004, Journal of experimental botany.
[28] B. Winkel,et al. Metabolic channeling in plants. , 2004, Annual review of plant biology.
[29] E. Issakidis‐Bourguet,et al. Oxidation-reduction properties of the regulatory disulfides of sorghum chloroplast nicotinamide adenine dinucleotide phosphate-malate dehydrogenase. , 2000, Biochemistry.
[30] J. Anderson,et al. Adjustments of photosystem stoichiometry in chloroplasts improve the quantum efficiency of photosynthesis. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[31] J. Hancock,et al. Hydrogen peroxide signalling. , 2002, Current opinion in plant biology.
[32] C. Foyer. Oxygen processing in photosynthesis. , 1996, Biochemical Society transactions.
[33] T. Zhu,et al. Networks of transcription factors with roles in environmental stress response. , 2004, Trends in plant science.
[34] A. Igamberdiev,et al. Mitochondrial functions in the light and significance to carbon-nitrogen interactions. , 2002 .
[35] H. Felle. pH: Signal and Messenger in Plant Cells , 2001 .
[36] M. M. Lucas,et al. Legume nodule senescence: roles for redox and hormone signalling in the orchestration of the natural aging process. , 2004, The New phytologist.
[37] P. Horton,et al. Electron acceptors in isolated intact spinach chloroplasts act hierarchically to prevent over-reduction and competition for electrons , 2004, Photosynthesis Research.
[38] J. Lallemand,et al. Cytoplasmic pH Regulation in Acer pseudoplatanus Cells: II. Possible Mechanisms Involved in pH Regulation during Acid-Load. , 1986, Plant physiology.
[39] C. Foyer,et al. Use of mitochondrial electron transport mutants to evaluate the effects of redox state on photosynthesis, stress tolerance and the integration of carbon/nitrogen metabolism. , 2003, Journal of experimental botany.
[40] Yujiang Shi,et al. Metabolic enzymes and coenzymes in transcription--a direct link between metabolism and transcription? , 2004, Trends in genetics : TIG.
[41] A. von Schaewen,et al. Decreased Content of Leaf Ferredoxin Changes Electron Distribution and Limits Photosynthesis in Transgenic Potato Plants1 , 2003, Plant Physiology.
[42] Mike J. May,et al. Glutathione homeostasis in plants: implications for environmental sensing and plant development , 1998 .
[43] F. Carrari,et al. Respiratory metabolism: glycolysis, the TCA cycle and mitochondrial electron transport. , 2004, Current opinion in plant biology.
[44] Graham R Fleming,et al. Toward an understanding of the mechanism of nonphotochemical quenching in green plants. , 2004, Biochemistry.
[45] B. Buchanan. The ferredoxin/thioredoxin system: a key element in the regulatory function of light in photosynthesis. , 1984, Bioscience.
[46] W. A. Zellmer. Toward understanding. , 1988, American journal of hospital pharmacy.
[47] A. S. Raghavendra,et al. Essentiality of Mitochondrial Oxidative Metabolism for Photosynthesis: Optimization of Carbon Assimilation and Protection Against Photoinhibition , 2002, Critical reviews in biochemistry and molecular biology.
[48] Govindjee,et al. Negative feedback regulation is responsible for the non-linear modulation of photosynthetic activity in plants and cyanobacteria exposed to a dynamic light environment. , 2003, Biochimica et biophysica acta.
[49] S. Tabata,et al. Identifying and characterizing plastidic 2-oxoglutarate/malate and dicarboxylate transporters in Arabidopsis thaliana. , 2002, Plant & cell physiology.
[50] Andrea Polle,et al. Mehler Reaction: Friend or Foe in Photosynthesis? , 1996 .
[51] S. Ramaswamy,et al. Redox signaling in chloroplasts: cleavage of disulfides by an iron-sulfur cluster. , 2000, Science.
[52] G. Johnson. Thiol regulation of the thylakoid electron transport chain--a missing link in the regulation of photosynthesis? , 2003, Biochemistry.
[53] C. Lamb,et al. Glutathione causes a massive and selective induction of plant defense genes. , 1988, Plant physiology.
[54] J. Wiskich,et al. Over-reduction of cultured tobacco cells mediates changes in respiratory activities , 2003 .
[55] H. Zhang,et al. Transgenic tobacco plants containing Bt and GNA genes , 2007, Biologia Plantarum.
[56] A. von Schaewen,et al. Transgenic Tobacco Plants Expressing Pea Chloroplast Nmdh cDNA in Sense and Antisense Orientation (Effects on NADP-Malate Dehydrogenase Level, Stability of Transformants, and Plant Growth) , 1997, Plant physiology.
[57] A. Murakami,et al. Regulation of Photosystem Composition in the Cyanobacterial Photosynthetic System: the Regulation Occurs in Response to the Redox State of the Electron Pool Located between the Two Photosystems , 1987 .
[58] C. Foyer,et al. Leaf Mitochondria Modulate Whole Cell Redox Homeostasis, Set Antioxidant Capacity, and Determine Stress Resistance through Altered Signaling and Diurnal Regulation Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.009464. , 2003, The Plant Cell Online.
[59] S. Khorobrykh,et al. Participation of photosynthetic electron transport in production and scavenging of reactive oxygen species. , 2003, Antioxidants & redox signaling.
[60] K. Niyogi,et al. PHOTOPROTECTION REVISITED: Genetic and Molecular Approaches. , 1999, Annual review of plant physiology and plant molecular biology.
[61] A. Atteia,et al. Control of Mitochondrial Function via Photosynthetic Redox Signals , 2004, Photosynthesis Research.
[62] S. Reid,et al. Glycolysis — new concepts in an old pathway , 1987, Molecular and Cellular Biochemistry.
[63] O. Arrigoni,et al. Ascorbic acid: much more than just an antioxidant. , 2002, Biochimica et biophysica acta.
[64] P. Mullineaux,et al. Signal transduction in response to excess light: getting out of the chloroplast. , 2002, Current opinion in plant biology.
[65] F. Carrari,et al. Enhanced Photosynthetic Performance and Growth as a Consequence of Decreasing Mitochondrial Malate Dehydrogenase Activity in Transgenic Tomato Plants1 , 2005, Plant Physiology.
[66] L. Mcintosh,et al. Lower growth temperature increases alternative pathway capacity and alternative oxidase protein in tobacco. , 1992, Plant physiology.
[67] P. Schürmann,et al. PLANT THIOREDOXIN SYSTEMS REVISITED. , 2000, Annual review of plant physiology and plant molecular biology.
[68] S. Holtgrefe,et al. Redox equilibria between the regulatory thiols of light/dark-modulated chloroplast enzymes and dithiothreitol: fine-tuning by metabolites. , 1995, Biochimica et biophysica acta.
[69] E. Martinoia,et al. The plant homolog to the human sodium/dicarboxylic cotransporter is the vacuolar malate carrier , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[70] David M Kramer,et al. Dynamic flexibility in the light reactions of photosynthesis governed by both electron and proton transfer reactions. , 2004, Trends in plant science.
[71] S. Driscoll,et al. Drought and oxidative load in the leaves of C3 plants: a predominant role for photorespiration? , 2002, Annals of botany.
[72] P. Horton,et al. Acclimation of Arabidopsis thaliana to the light environment: the role of photoreceptors , 1999, Planta.
[73] G. Johnson. Cyclic electron transport in C3 plants: fact or artefact? , 2004, Journal of experimental botany.
[74] Hisashi Ito,et al. The sugar-metabolic enzymes aldolase and triose-phosphate isomerase are targets of glutathionylation in Arabidopsis thaliana: detection using biotinylated glutathione. , 2003, Plant & cell physiology.
[75] E. Aro,et al. Dithiol Oxidant and Disulfide Reductant Dynamically Regulate the Phosphorylation of Light-Harvesting Complex II Proteins in Thylakoid Membranes1 , 2003, Plant Physiology.
[76] Y. Meyer,et al. New targets of Arabidopsis thioredoxins revealed by proteomic analysis , 2004, Proteomics.
[77] P. Rustin,et al. The central role of malate in plant metabolism , 1984 .
[78] D. Klessig,et al. Nitric oxide: a new player in plant signalling and defence responses. , 2004, Current opinion in plant biology.
[79] 進 小沢,et al. ラットの成長に伴う膵外分泌と小腸の negative feedback regulation の発達 , 1991 .
[80] Tsuyoshi Endo,et al. Cyclic electron flow around photosystem I is essential for photosynthesis , 2004, Nature.
[81] P. Schürmann,et al. The plant-specific function of 2-Cys peroxiredoxin-mediated detoxification of peroxides in the redox-hierarchy of photosynthetic electron flux , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[82] A. Weber,et al. The Arabidopsis mutant dct is deficient in the plastidic glutamate/malate translocator DiT2. , 2003, The Plant journal : for cell and molecular biology.
[83] G. Öquist,et al. Energy balance and acclimation to light and cold , 1998 .
[84] K. Asada. The water-water cycle as alternative photon and electron sinks. , 2000, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[85] T. Sakurai,et al. Monitoring the expression profiles of genes induced by hyperosmotic, high salinity, and oxidative stress and abscisic acid treatment in Arabidopsis cell culture using a full-length cDNA microarray , 2004, Plant Molecular Biology.
[86] Stefan Jansson,et al. Acclimation of Arabidopsis thaliana to the light environment: the existence of separate low light and high light responses , 2001, Planta.
[87] C. Foyer,et al. Photosynthetic Nitrogen Assimilation and Associated Carbon and Respiratory Metabolism , 2002, Advances in Photosynthesis and Respiration.
[88] G. Coupland,et al. Photoperiodic flowering of Arabidopsis: integrating genetic and physiological approaches to characterization of the floral stimulus , 2005 .
[89] N. Smirnoff,et al. Vitamin C : Its Functions and Biochemistry in Animals and Plants , 2004 .
[90] G. Finazzi,et al. Reduction of the thylakoid electron transport chain by stromal reductants—evidence for activation of cyclic electron transport upon dark adaptation or under drought , 2004, Planta.
[91] Meyer,et al. Plant thioredoxins and glutaredoxins: identity and putative roles. , 1999, Trends in plant science.
[92] A. Peeters,et al. GENETIC CONTROL OF FLOWERING TIME IN ARABIDOPSIS. , 1998, Annual review of plant physiology and plant molecular biology.