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Photorespiratory Carbon and Nitrogen Cycling: Evidence from Studies of Mutant and Transgenic Plants

  • Chapter
Photosynthetic Nitrogen Assimilation and Associated Carbon and Respiratory Metabolism

Part of the book series: Advances in Photosynthesis and Respiration ((AIPH,volume 12))

Summary

Photorespiratory mutants represent the most complete set of mutants for any metabolic pathway in plants. The photorespiratory pathway is also a prime example of the integration and co-ordination of carbon and nitrogen (N) metabolism. Studies of mutant and transgenic plants with lesions in photorespiratory metabolism have confirmed its cyclic nature, its origin in the reductive pentose phosphate pathway, and the associated N cycling. They have led to new insights into the nature of these processes and aspects of their regulation and control. Unlike most pathways in plants, the specific isozymes in chloroplasts, mitochondria and peroxisomes involved in photorespiratory metabolism have been unequivocally identified. In the case of some mutations, isozymes not specifically involved in photorespiratory metabolism provide an alternative route and so by-pass the lesion. We discuss how, in mutant plants in which the recycling of N is defective, the normal photorespiratory pathway involving glycine decarboxylation may be partially by-passed by a modified form of photorespiration involving glyoxylate decarboxylation. Apart from metabolic feedback, we also discuss how mutants have been used to study the regulation of gene expression and the role of photorespiration during light and drought stress.

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References

  • Andersen BR, Jin G, Chen R, Ertl JR and Chen C-M (1996) Transcriptional regulation of hydroxypyruvate reductase gene expression by cytokinin in etiolated pumpkin cotyledons. Planta 198: 1–5

    Article  CAS  PubMed  Google Scholar 

  • Anderson LE (1981) Chloroplast and cytoplasmic enzymes. II. Pea leaf triose phosphate isomerase. Biochim Biophys Acta 235: 237–244

    Google Scholar 

  • Artus NN, Naito S and Somerville CR (1994) A mutant of Arabidopsis thaliana that defines a new locus for glycine decarboxylation. Plant Cell Physiol 35: 879–885

    CAS  Google Scholar 

  • Bainbridge G, Madgwick P, Parmar S, Mitchell R, Paul M, Pitts J, Keys AJ and Parry MAJ (1995) Engineering Rubisco to change its catalytic properties. J Exp Bot 46: 1269–1276

    CAS  Google Scholar 

  • Bassham JA (1964) Kinetic studies of the photosynthetic carbon reduction cycle. Annu Rev Plant Physiol 15: 101–120

    Article  CAS  Google Scholar 

  • Beckmann K, Dzuibany C, Biehler K, Fock H, Hell R, Migge A and Becker TW (1997) Photosynthesis and fluorescence quenching, and mRNA levels of GS2 or of mitochondrial Ser hydroxymethyl transferase (SHMT) in the leaves of the wild-type and of the SHMT-deficient stm mutant of Arabidopsis thaliana in relation to the rate of photorespiration. Planta 202: 379–386

    Article  CAS  PubMed  Google Scholar 

  • Bertoni GP and Becker WM (1993) Effects of light fluence and wavelength on expression of the gene encoding cucumber hydroxypyruvate reductase. Plant Physiol 103: 933–941

    Article  CAS  PubMed  Google Scholar 

  • Bertoni GP and Becker WM (1996) Expression of the cucumber hydroxypyruvate reductase gene is down-regulated by elevated CO2 Plant Physiol 112: 599–605

    CAS  PubMed  Google Scholar 

  • Besson V, Rébeillé F, Neuburger M, Douce R and Cossins EA (1993) Effects of tetrahydrofolate polyglutamates on the kinetic parameters of serine hydroxymethyltransferase and glycine decarboxylase from pea leaf mitochondria. Biochem J 292: 425–430

    CAS  PubMed  Google Scholar 

  • Blackwell RD, Murray AJS and Lea PJ (1987) Inhibition of photosynthesis in barley with decreased levels of chloroplastic glutamine synthetase activity. J Exp Bot 38: 1799–1809

    CAS  Google Scholar 

  • Blackwell RD, Murray AJS, Lea PJ, Kendall AC, Hall NP, Turner JC and Wallsgrove RM (1988a) The value of mutants unable to carry out photorespiration. Photosynth Res 16: 155–176

    Article  Google Scholar 

  • Blackwell RD, Murray AJS, Lea PJ and Joy KW (1988b) Photorespiratory amino donors, sucrose synthesis and the induction of CO2 fixation in barley deficient in glutamine synthetase and glutamate synthase. J Exp Bot 39: 845–858

    CAS  Google Scholar 

  • Blackwell RD, Murray AJS and Lea PJ (1990) Photorespiratory mutants of the mitochondrial conversion of glycine to serine. Plant Physiol 94: 1316–1322

    CAS  Google Scholar 

  • Brestic M, Cornic G, Fryer MJ and Baker NR (1995) Does photorespiration protect the photosynthetic apparatus in French bean leaves from photoinhibition during drought stress? Planta 196: 450–457

    Article  CAS  Google Scholar 

  • Campbell WJ and Ogren WL (1990) Glyoxylate inhibition of ribulose bisphosphate carboxylase/oxygenase activation in intact, lysed and reconstituted chloroplasts. Photosynth Res 23: 257–268

    Article  CAS  Google Scholar 

  • Chang C-C and Huang AHC (1981) Metabolism of glycolate in isolated spinach leaf peroxisomes. Kinetics of glyoxylate, oxalate, carbon dioxide, and glycine formation. Plant Physiol 67: 1003–1006

    CAS  Google Scholar 

  • Chastain CJ and Ogren WL (1985) Photorespiration-induced reduction of ribulose bisphosphate carboxylase activation level. Plant Physiol 77: 851–856

    CAS  Google Scholar 

  • Chastain CJ and Ogren WL (1989) Glyoxylate inhibition of ribulose bisphosphate carboxylase/oxygenase activation state in vivo. Plant Cell Physiol 30: 937–944

    CAS  Google Scholar 

  • Chen C-M and Leisner SM (1985) Cytokinin-modulated gene expression in excised pumpkin cotyledons. Plant Physiol 77: 99–103

    CAS  Google Scholar 

  • Chollet R and Ogren WL (1975) Regulation of photorespiration in C3 and C4 species. Bot Rev 41: 137–179

    CAS  Google Scholar 

  • Cleland WW, Andrews TJ, Gutteridge S, Hartman FC and Lorimer GH (1998) The mechanism of Rubisco: The carbamate as general base. Chem Rev 98: 549–561

    Article  CAS  PubMed  Google Scholar 

  • Cock JM, Brock IW, Watson AT, Swarup R, Morby AP and Cullimore JV (1991) Regulation of glutamine synthetase genes in leaves of Phaseolus vulgaris. Plant Mol Biol 17: 761–771

    CAS  PubMed  Google Scholar 

  • Cook CM, Mulligan RM and Tolbert NE (1985) Inhibition and stimulation of ribulose-1,5-bisphosphate carboxylase by glyoxylate. Arch Biochem Biophys 240: 392–401

    CAS  PubMed  Google Scholar 

  • Cornic G (2000) Drought stress inhibits photosynthesis by decreasing stomatal aperture—not by affecting ATP synthesis. Trends Plant Sci 5: 187–188

    Article  Google Scholar 

  • Coschigano KT, Melo-Oliveira R, Lim J and Coruzzi GM (1998) Arabidopsis gls mutants and distinct Fd-GOGAT genes: Implications for photorespiration and primary nitrogen assimilation. Plant Cell 10: 741–752

    Article  CAS  PubMed  Google Scholar 

  • Cossins EA and Chen L (1997) Folates and one-carbon metabolism in plants and fungi. Phytochemistry 45: 437–452

    Article  CAS  PubMed  Google Scholar 

  • Créach E and Stewart CR (1982) Effects of aminoacetonitrile on net photosynthesis, ribulose-1,5-bisphosphate levels, and glycolate pathway intermediates. Plant Physiol 70: 1444–1448

    Google Scholar 

  • Day DA and Wiskich JT (1980) Glycine transport by pea leaf mitochondria. FEBS Lett 112: 191–194

    Article  CAS  Google Scholar 

  • Delgado E, Parry MAJ, Lawlor DW, Keys AJ and Medrano H (1993) Photosynthesis, ribulose-1,5-bisphosphate carboxylase and leaf characteristics of Nicotiana tabacum L. genotypes selected by survival at low CO2-concentrations. J Exp Bot 44: 1–7

    CAS  Google Scholar 

  • Demmig-Adams B, Winter K, Krüger A and Czygan F-C (1988) Zeaxanthin and the heat dissipation of excess light energy in Nerium oleander exposed to a combination of high light and water stress. Plant Physiol 87: 17–24

    Google Scholar 

  • Dever LV, Blackwell RD, Fullwood NJ, Lacuesta M, Leegood RC, Onek LA, Pearson M and Lea PJ (1995) The isolation and characterization of mutants of the C4 photosynthetic pathway. J Exp Bot 46: 1363–1376

    CAS  Google Scholar 

  • Douce R and Heldt HW (2000) Photorespiration. In: Leegood RC, Sharkey TD and von Caemmerer S (eds) Photosynthesis: Physiology and Metabolism, pp 115–136. Kluwer Academic Publishers, Dordrecht

    Google Scholar 

  • Douce R and Neuburger M (1999) Biochemical dissection of photorespiration. Curr Opin Plant Biol 2: 214–222

    Article  CAS  PubMed  Google Scholar 

  • Dzuibany C, Haupt S, Fock H, Biehler K, Migge A and Becker TW (1998) Regulation of nitrate reductase transcript levels by glutamine accumulating in the leaves of a ferredoxin-dependent glutamate synthase-deficient gluS mutant in Arabidopsis thaliana, and by glutamine provided via the roots. Planta 206: 515–522

    Article  CAS  PubMed  Google Scholar 

  • Ebbighausen H, Chen J and Heldt HW (1985) Oxaloacetate translocator in plant mitochondria. Biochim Biophys Acta 810: 184–199

    CAS  Google Scholar 

  • Edwards JW and Coruzzi GM (1989) Photorespiration and light act in concert to regulate the expression of the nuclear gene for chloroplast glutamine synthetase. Plant Cell 1: 241–248

    Article  CAS  PubMed  Google Scholar 

  • Edwards JW, Walker EL and Coruzzi GM (1990) Cell-specific expression in transgenic plants reveals non-overlapping roles for chloroplast and cytosolic glutamine synthetase. Proc Natl Acad Sci USA 87: 3459–3463

    CAS  PubMed  Google Scholar 

  • Farquhar GD, Firth PM, Wetselaar R and Weir B (1980) On the gaseous exchange of ammonia between leaves and the environment: Determination of the ammonia compensation point. Plant Physiol 66: 710–714

    CAS  Google Scholar 

  • Ferrario-Méry S, Suzuki A, Kunz C, Valadier MH, Roux Y, Hirel B and Foyer CH (2000) Modulation of amino acid metabolism in transformed tobacco plants deficient in Fd-GOGAT. Plant Soil 221: 67–79

    Google Scholar 

  • Finnemann J and Schjoerring JK (2000) Post-translational regulation of cytosolic glutamine synthetase by reversible phosphorylation and 14-3-3 protein interaction. Plant J 24: 171–181

    Article  CAS  PubMed  Google Scholar 

  • Flügge UI, Woo KC and Heldt HW (1988) Characteristics of 2-OG and glutamate transport in spinach chloroplasts. Studies with a double-silicone-layer centrifugation technique and in liposomes. Planta 174: 534–541

    Google Scholar 

  • Genty B, Briantais JM and Baker NR (1989) The relationship between the quantum yield of photosynthetic transport and quenching of chlorophyll fluorescence. Biochim Biophys Acta 990: 87–92

    CAS  Google Scholar 

  • Gifford DJ and Cossins EA (1982a) The nature of formate metabolism in greening barley leaves. Phytochemistry 21: 1479–1484

    CAS  Google Scholar 

  • Gifford DJ and Cossins EA (1982b) Relationships between glycollate and formate metabolism in greening barley leaves. Phytochemistry 21: 1485–1490

    CAS  Google Scholar 

  • Givan CV and Kleczkowski LA (1992) The enzymic reduction of glyoxylate and hydroxypyruvate in leaves of higher plants. Plant Physiol 100: 552–556

    CAS  Google Scholar 

  • Givan CV, Tsutakawa S, Hodgson JM, David N and Randall DD (1988) Glyoxylate reductase activity in pea leaf protoplasts. Nucleotide specificity and subcellular location. J Plant Physiol 132: 593–599

    CAS  Google Scholar 

  • Grodzinski B and Butt VS (1976) Hydrogen peroxide production and release of carbon dioxide during glycolate oxidation in leaf peroxisomes. Planta 128: 225–231

    Article  CAS  Google Scholar 

  • Hall NP, Kendall AC, Lea PJ, Turner JC and Wallsgrove RM (1987) Characteristics of a photorespiratory mutant of barley (Hordeum vulgare L.) deficient in phosphoglycollate phosphatase. Photosynth Res 11: 89–96

    Article  CAS  Google Scholar 

  • Halliwell B (1973) The role of formate in photorespiration. Biochem Soc Trans 1: 1147–1150

    CAS  Google Scholar 

  • Halliwell B (1974) Oxidation of formate by peroxisomes and mitochondria from spinach leaves. Biochem J 138: 77–85

    CAS  PubMed  Google Scholar 

  • Harley PC and Sharkey TD (1991) An improved model of C3 photosynthesis at high CO2. Reversed O2 sensitivity explained by lack of glycerate reentry into chloroplasts. Photosynth Res 27: 169–178

    CAS  Google Scholar 

  • Harpel MR and Hartman FC (1994) Structure, function, regulation and assembly of ribulose-1,5-bisphosphate carboxylase/oxygenase. Annu Rev Biochem 63: 197–234

    PubMed  Google Scholar 

  • Häusler RE, Blackwell RD, Lea PJ and Leegood RC (1994a) Control of photosynthesis in barley leaves with reduced activities of glutamine synthetase or glutamate synthase. I. Plant characteristics and changes in nitrate, ammonium and amino acids. Planta 194: 406–417

    Google Scholar 

  • Häusler RE, Lea PJ and Leegood RC (1994b) Control of photosynthesis in barley leaves with reduced activities of glutamine synthetase or glutamate synthase. II. Control of electron transport and CO2 assimilation. Planta 194: 418–435

    Google Scholar 

  • Häusler RE, Bailey KJ, Lea PJ and Leegood RC (1996) Control of photosynthesis in barley leaves with reduced activities of glutamine synthetase or glutamate synthase. III. Aspects of glyoxylate metabolism and the effects of glyoxylate on the activation state of ribulose-1,5-bisphosphate carboxylase-oxygenase. Planta 200: 388–396

    Google Scholar 

  • Havir EA and McHale NA (1988) A mutant of Nicotiana sylvestris lacking serine glyoxylate aminotransferase: Substrate specificity of the enzyme and fate of [2-14C] glycolate in plants with genetically altered enzyme levels. Plant Physiol 87: 806–808

    CAS  Google Scholar 

  • Hecht U, Oelmüller R and Mohr H (1988) Action of light, nitrate and ammonium on the levels of NADH-and ferredoxin-dependent glutamate synthases in the cotyledons of mustard seedlings. Planta 195: 130–138

    Google Scholar 

  • Heupel R and Heldt HW (1994) Protein organisation in the matrix of leaf peroxisomes. Eur J Biochem 220: 165–172

    Article  CAS  PubMed  Google Scholar 

  • Hoshida H, Tanaka Y, Hibino T, Hayashi Y, Tanaka A, Takabe T and Takabe T (2000) Enhanced tolerance to salt stress in transgenic rice that overexpresses chloroplast glutamine synthetase. Plant Mol Biol 43: 103–111

    Article  CAS  PubMed  Google Scholar 

  • Joy KW, Blackwell RD and Lea PJ (1992) Assimilation of nitrogen in mutants lacking enzymes of the glutamate synthase cycle. J Exp Bot 43: 139–146

    CAS  Google Scholar 

  • Kacser H (1987) Control of metabolism. In: Davies DD (ed) The Biochemistry of Plants: Biochemistry of Metabolism. Vol 11, pp 39–67. Academic Press, London

    Google Scholar 

  • Kaiser WM (1987) Effects of water deficit on photosynthetic capacity. Physiol Plant 71: 142–149

    CAS  Google Scholar 

  • Kendall AC, Keys AJ, Turner JC, Lea PJ and Miflin BJ (1983) The isolation of a catalase deficient mutant of barley (Hordeum vulgare). Planta 159: 505–511

    Article  CAS  Google Scholar 

  • Kendall AC, Wallsgrove RM, Hall NP, Turner JC and Lea PJ (1986) Carbon and nitrogen assimilation in barley (Hordeum vulgare L.) mutants lacking ferredoxin-dependent glutamate synthase. Planta 168: 316–323

    Article  CAS  Google Scholar 

  • Keys AJ, Bird IF, Cornelius MJ, Lea PJ, Wallsgrove RM and Miflin BJ (1978) Photorespiratory nitrogen cycle. Nature 275: 741–743

    Article  Google Scholar 

  • Kirk CD, Chen L, Imeson H and Cossins EA (1995) A 5, 10-methylenetetrahydrofolate dehydrogenase: 5,10-methenyltetrahydrofolate cyclohydrolase protein from Pisum sativum. Phytochemistry 39: 1309–1317

    Article  CAS  Google Scholar 

  • Kleczkowski LA, Givan CV, Hodgson JM and Randall DD (1988) Subcellular location of NADPH-dependent hydroxypyruvate reductase activity in leaf protoplasts of Pisum sativum L. and its role in photorespiratory metabolism. Plant Physiol 88: 1182–1185

    CAS  Google Scholar 

  • Kleczkowski LA, Edwards GE, Blackwell RD, Lea PJ and Givan CV (1990) Enzymology of the reduction of hydroxypyruvate and glyoxylate in a mutant of barley lacking peroxisomal hydroxypyruvate reductase. Plant Physiol 94: 819–825

    CAS  Google Scholar 

  • Kozaki A and Takeba G (1996) Photorespiration protects C3 plants from photooxidation. Nature 384: 557–560

    Article  CAS  Google Scholar 

  • Lal A, Ku MSB and Edwards GE (1996) Analysis of inhibition of photosynthesis due to water stress in the C3 species Hordeum vulgare and Vicia faba: Electron transport, CO2 fixation and carboxylation capacity. Photosynth Res 49: 57–69

    Article  CAS  Google Scholar 

  • Lawyer AL, Cornwell KL, Gee SL and Bassham JA (1983) Glyoxylate and glutamate effects on photosynthetic carbon metabolism in isolated chloroplasts and mesophyll cells of spinach. Plant Physiol 72: 420–425

    CAS  Google Scholar 

  • Lea PJ and Forde BG (1994) The use of mutants and transgenic plants to study amino acid metabolism. Plant Cell Environ 17: 541–556

    CAS  Google Scholar 

  • Leek AE, Halliwell B and Butt VS (1972) Oxidation of formate and oxalate in peroxisomal preparations from leaves of spinach beet (Beta vulgaris L.). Biochim Biophys Acta 286: 299–311

    CAS  PubMed  Google Scholar 

  • Lopez-Siles FJ, Cardenas J and Franco AR (1999) Biochemical and genetic analysis of a Chlamydomonas reinhardtii mutant devoid of chloroplastic glutamine synthetase activity. Planta 207: 436–441

    CAS  Google Scholar 

  • Loreto F, Delphine S and di Marco G (1999) Estimation of photorespiratory carbon dioxide recycling during photosynthesis. Aust J Plant Physiol 26: 733–736

    Google Scholar 

  • Lorimer GH and Andrews TJ (1981) The C3 chemo-and photorespiratory carbon oxidative cycle. In: Stumpf PK. and Conn EE (eds) The Biochemistry of Plants, Vol 8, pp 329–374. Academic Press, London

    Google Scholar 

  • Madore M and Grodzinski B (1984) Effect of oxygen concentration on 14C-photoassimilate transport from leaves of Salvia splendens L. Plant Physiol 76: 782–786

    CAS  Google Scholar 

  • Mattsson M, Häusler RE, Leegood RC, Lea PJ and Schjoerring JK (1997) Leaf-atmosphere ammonia exchange in barley mutants with reduced activities of glutamine synthetase. Plant Physiol 114: 1307–1312

    CAS  PubMed  Google Scholar 

  • McClung CR, Hsu M, Painter JE, Gagne JM, Karlsberg SD and Salomé PA (2000) Integrated temporal regulation of the photorespiratory pathway. Circadian regulation of two Arabidopsis genes encoding serine hydroxymethyltransferase. Plant Physiol 123: 381–391

    Article  CAS  PubMed  Google Scholar 

  • McHale NA, Havir EA and Zelitch I (1989) Photorespiratory toxicity in autotrophic cell cultures of a mutant of Nicotiana sylvestris lacking serine-glyoxylate aminotransferase activity. Planta 179: 67–72

    Article  CAS  Google Scholar 

  • Migge A and Becker TW (1996) In tobacco leaves, the genes encoding the nitrate reducing or the ammonium-assimilating enzymes are regulated differently by external nitrogen-sources. Plant Physiol Biochem 34: 665–671

    CAS  Google Scholar 

  • Migge A, Meya G, Carrayol E, Hirel B and Becker TW (1996) Regulation of the subunit composition of tomato plastidic glutamine synthetase by light and the nitrogen source. Planta 200: 213–220

    Article  CAS  Google Scholar 

  • Migge A, Carrayol E, Kunz C, Hirel B, Fock H and Becker T (1997) The expression of the tobacco genes encoding plastidic glutamine synthetase or ferredoxin-dependent glutamate synthase does not depend on the rate of nitrate reduction, and is unaffected by suppression of photorespiration. J Exp Bot 48: 1175–1184

    CAS  Google Scholar 

  • Migge A, Carrayol E, Hirel B and Becker B (2000) Leaf-specific overexpression of plastidic glutamine synthetase stimulates the growth of transgenic tobacco seedlings. Planta 210: 252–260

    CAS  PubMed  Google Scholar 

  • Mouillon J-M, Aubert S, Bourguignon J, Gout E, Douce R and Rébeillé F (1999) Glycine and serine catabolism in non-photosynthetic higher plant cells: Their role in Cl metabolism. Plant J 20: 197–205

    Article  CAS  PubMed  Google Scholar 

  • Murray AJS, Blackwell RD, Joy KW and Lea PJ (1987) Photorespiratory N donors, aminotransferase specificity and photosynthesis in a mutant barley deficient in serine: glyoxylate aminotransferase activity. Planta 172: 106–113

    Article  CAS  Google Scholar 

  • Murray AJS, Blackwell RD and Lea PJ (1989) Metabolism in a mutant of barley lacking NADH-dependent hydroxypyruvate reductase, an important photorespiratory enzyme. Plant Physiol 91: 395–400

    CAS  Google Scholar 

  • Ninnemann O, Jauniaux J-C and Frommer WB (1994) Identification of a high affinity NH +4 transporter from plants. EMBO J 13: 3464–3471

    CAS  PubMed  Google Scholar 

  • Noctor G, Arisi AC-M, Jouanin L, Kunert KJ, Rennenberg H and Foyer CH (1998) Glutathione: Biosynthesis, metabolism and relationship to stress tolerance explored in transformed plants. J Exp Bot 49: 623–647

    CAS  Google Scholar 

  • Nour JM and Rabinowitz JC (1991) Isolation, characterization, and structural organization of 10-formyltetrahydrofolate synthetase from spinach leaves. J Biol Chem 266: 18363–18369

    CAS  PubMed  Google Scholar 

  • Nour JM and Rabinowitz JC (1992) Isolation and sequencing of the cDNA for spinach 10-formyltetrahydrofolate synthetase. Comparisons with the yeast, mammalian, and bacterial proteins. J Biol Chem 23: 16292–16296

    Google Scholar 

  • Oliver DJ (1987) Glycine uptake by pea leaf mitochondria: A proposed model for the mechanism of glycine-serine exchange. In: Moore AL, Beechey RB eds. Plant Mitochondria. Structural, Functional and Physiological Aspects. New York: Plenum Press, 219–222

    Google Scholar 

  • Oliver DJ (1994) The glycine decarboxylase complex from plant mitochondria. Annu Rev Plant Physiol Plant Mol Biol 45: 323–327

    Article  CAS  Google Scholar 

  • Oliver DJ and Zelitch I (1977) Increasing photosynthesis by inhibiting photorespiration with glyoxylate. Science 196: 1450–1451

    CAS  PubMed  Google Scholar 

  • Ongun A and Stocking CR (1965) Effects of light on the incorporation of serine into the carbohydrates of chloroplast and non-chloroplast fractions of tobacco leaves. Plant Physiol 40: 819–824

    CAS  Google Scholar 

  • Osmond CB (1981) Photorespiration and photoinhibition. Some implications for the energetics of photosynthesis. Biochim Biophys Acta 639: 77–98

    CAS  Google Scholar 

  • Prabhu V, Chatson KB, Abrams GD and King J (1996) 13C nuclear magnetic resonance detection of interactions of serine hydroxymethyltransferase with Cl-tetrahydrofolate synthase and glycine decarboxylase complex activities in Arabidopsis. Plant Physiol 112: 207–216

    Article  CAS  PubMed  Google Scholar 

  • Raman R and Oliver DJ (1997) Light-dependent control of photorespiratory gene expression. In: Pessarakli M (ed) Handbook of Photosynthesis, pp 381–389. Marcel Dekker, New York

    Google Scholar 

  • Sánchez-Rodríguez J, Pérez P and Martínez-Carrasco R (1999) Photosynthesis, carbohydrate levels and chlorophyllfluorescence estimated intercellular CO2 in water-stressed Casuarina equisetifolia Forst. & Forst. Plant Cell Environ 22: 867–873

    Google Scholar 

  • Schimkat D, Heineke D and Heldt HW (1990) Regulation of sedoheptulose-1,7-bisphosphatase by sedoheptulose-7-phosphate and glycerate, and of fructose-1,6-bisphosphatase by glycerate in spinach chloroplasts. Planta 181: 97–103

    Article  CAS  Google Scholar 

  • Schjoerring JK, Kyllingsbaek A, Mortensen JV and Byskov-Nielsen S (1993) Field investigations of ammonia exchange between barley plants and the atmosphere. I. Concentration profiles and flux densities of ammonia. Plant Cell Environ 16: 161–167

    CAS  Google Scholar 

  • Sharkey TD and Seemann JR (1989) Mild water stress effects on carbon-reduction-cycle intermediates, ribulose bisphosphate carboxylase activity, and spatial homogeneity of photosynthesis in intact leaves. Plant Physiol 89: 1060–1065

    CAS  Google Scholar 

  • Shingles R, Woodrow L and Grodzinski B (1984) Effects of glycolate pathway intermediates on glycine decarboxylation and serine synthesis in pea (Pisum sativum L.). Plant Physiol 74: 705–710

    CAS  Google Scholar 

  • Smith IK, Kendall AC, Keys AJ, Turner JC and Lea PJ (1984) Increased levels of glutathione in a catalase-deficient mutant of barley (Hordeum vulgare L). Plant Sci Lett 37: 29–33

    CAS  Google Scholar 

  • Somerville CR and Ogren WL (1979) A phosphoglycolate phosphatase-deficient mutant of Arabidopsis. Nature 280: 833–836

    Article  CAS  Google Scholar 

  • Somerville CR and Ogren WL (1980a) Photorespiration mutants of Arabidopsis thaliana deficient in serine-glyoxylate aminotransferase activity. Proc Natl Acad Sci USA 77: 2684–2687

    CAS  Google Scholar 

  • Somerville CR and Ogren WL (1980b) Inhibition of photosynthesis in Arabidopsis mutants lacking leaf glutamate synthase activity. Nature 286: 257–289

    Article  CAS  Google Scholar 

  • Somerville CR and Ogren WL (1981) Photorespiratory deficient mutants of Arabidopsis thaliana lacking mitochondrial serine transhydroxymethylase activity. Plant Physiol 67: 666–671

    CAS  Google Scholar 

  • Somerville CR and Ogren WL (1982a) Genetic modification of photorespiration. Trends Biochem Sci 7: 171–174

    Article  CAS  Google Scholar 

  • Somerville CR and Ogren WL (1982b) Mutants of the cruciferous plant Arabidopsis thaliana lacking glycine decarboxylase activity. Biochem J 202: 373–380

    CAS  PubMed  Google Scholar 

  • Somerville SC and Ogren WL (1983) An Arabidopsis thaliana mutant defective in chloroplast dicarboxylate transport. Proc Natl Acad Sci USA 80: 1290–1294

    CAS  Google Scholar 

  • Somerville SC and Somerville CR (1983) The effect of oxygen and carbon dioxide on photorespiratory flux determined from glycine accumulation in a mutant of Arabidopsis thaliana. J Exp Bot 34: 415–424

    CAS  Google Scholar 

  • Somerville SC and Somerville CR (1985) A mutant of Arabidopsis deficient in chloroplast dicarboxylate transport is missing an envelope protein. Plant Sci Lett 37: 217–220

    CAS  Google Scholar 

  • Somerville CR, Portis AR and Ogren WL (1982) A mutant of Arabidopsis thaliana which lacks activation of RuBP carboxylase in vivo. Plant Physiol 70: 381–387

    CAS  Google Scholar 

  • Stitt M and Schulze ED (1994) Does Rubisco control the rate of photosynthesis and plant growth? An exercise in molecular ecophysiology. Plant Cell Environ 17: 465–487

    CAS  Google Scholar 

  • Thibaud M-C, Cortez N, Rivière H and Betsche T (1995) Photorespiration and related enzymes in pea (Pisum sativum) grown in high CO2. J Plant Physiol 146: 596–603

    CAS  Google Scholar 

  • Vincentz M, Moureaux T, Leydecker M-T, Vaucheret H and Caboche M (1993) Regulation of nitrate and nitrite reductase expression in Nicotiana plumbaginifolia leaves by nitrogen and carbon metabolites. Plant J 3: 315–324

    Article  CAS  PubMed  Google Scholar 

  • von Wirén N, Lauter F-R, Ninnemann O, Gillissen B, Walch-Liu P, Engels C, Jost W and Frommer WB (2000) Differential regulation of three functional ammonium transporter genes by nitrogen in root hairs and by light in leaves of tomato. Plant J 21: 167–175

    Google Scholar 

  • Wallsgrove RM, Keys AJ, Bird IF, Cornelius MJ, Lea PJ and Miflin BJ (1980) The location of glutamine synthetase in leaf cells and its role in the reassimilation of ammonia release in photorespiration. J Exp Bot 31: 1005–1017

    CAS  Google Scholar 

  • Wallsgrove RM, Kendall AC, Hall NP, Turner JC and Lea PJ (1986) Carbon and nitrogen metabolism in a barley (Hordeum vulgare) mutant with impaired chloroplast dicarboxylate transport. Planta 168: 324–329.

    Article  CAS  Google Scholar 

  • Wallsgrove RM, Turner JC, Hall NP, Kendall AC and Bright SWJ (1987) Barley mutants lacking chloroplast glutamine synthetase. Biochemical and genetic analysis. Plant Physiol 83: 155–158

    CAS  Google Scholar 

  • Walton NJ (1982) Glyoxylate decarboxylation during glycolate oxidation by pea leaf extracts: Significance of glyoxylate and extract concentrations. Planta 155: 218–224

    Article  CAS  Google Scholar 

  • Wendler C, Putzer A and Wild A (1992) Effect of glufosinate (phosphinothricin) and inhibitors of photorespiration on photosynthesis and ribulose-1,5-bisphosphate carboxylase activity. J Plant Physiol 139: 666–671

    CAS  Google Scholar 

  • Wingler A, Lea PJ and Leegood RC (1997) Control of photosynthesis in barley plants with reduced activities of glycine decarboxylase. Planta 202: 171–178

    Article  CAS  Google Scholar 

  • Wingler A, von Schaewen A, Leegood RC, Lea PJ and Quick WP (1998) Regulation of leaf senescence by cytokinin, sugars and light. Plant Physiol 116: 329–335

    Article  CAS  Google Scholar 

  • Wingler A, Ann VJ, Lea PJ and Leegood RC (1999a) Serineglyoxylate aminotransferase exerts no control on photosynthesis. J Exp Bot 50: 719–722

    Article  CAS  Google Scholar 

  • Wingler A, Lea PJ and Leegood RC (1999b) Photorespiratory metabolism of glyoxylate and formate in glycine accumulating mutants of barley and Amaranthus edulis. Planta 207: 518–526

    Article  CAS  Google Scholar 

  • Wingler A, Quick WP, Bungard RA, Bailey KJ, Lea PJ and Leegood RC (1999c) The role of photorespiration during drought stress: an analysis utilising barley mutants with reduced activities of photorespiratory enzymes. Plant Cell Environ 22: 361–373

    Article  CAS  Google Scholar 

  • Wingler A, Lea PJ, Quick WP and Leegood RC (2000) Photorespiration: Metabolic pathways and their role in stress protection. Phil Trans R Soc Lond B 355: 1517–1529

    CAS  Google Scholar 

  • Woo K.C, Flügge UI and Heldt HW (1987) A two translocator model for the transport of 2-oxoglutarate and glutamate in chloroplasts during ammonia assimilation in the light. Plant Physiol 84: 624–632

    CAS  Google Scholar 

  • Yamaguchi K and Nishimura M (2000) Reduction to below threshold levels of glycolate oxidase activities in transgenic tobacco enhances photoinhibition during irradiation. Plant Cell Physiol 41: 1397–1406

    Article  CAS  PubMed  Google Scholar 

  • Yokota A, Komura H and Kitaoka S (1985) Different metabolic fate of two carbons of glycolate in its conversion to serine in Euglena gracilis. Arch Biochem Biophys 242: 498–506

    CAS  PubMed  Google Scholar 

  • Yu J-W and Woo KC (1992) Ammonia assimilation and metabolite transport in isolated chloroplasts. I. Kinetic measurement of 2-oxoglutarate and malate uptake via the 2-oxoglutarate translocator in oat and spinach chloroplasts. Aust J Plant Physiol 19: 653–658

    CAS  Google Scholar 

  • Zelitch I (1972) The photooxidation of glyoxylate by envelope-free spinach chloroplasts and its relation to photorespiration. Arch Biochem 150: 698–707

    CAS  PubMed  Google Scholar 

  • Zelitch I (1989) Selection and characterization of tobacco plants with novel O2-resistant photosynthesis. Plant Physiol 90: 1457–1464

    CAS  Google Scholar 

  • Zelitch I (1992) Factors affecting expression of enhanced catalase activity in a tobacco mutant with O2-resistant photosynthesis. Plant Physiol 98: 1330–1335

    CAS  Google Scholar 

  • Zelitch I and Day PR (1968) Variation in photorespiration. The effect of genetic differences in photorespiration on net photosynthesis in tobacco. Plant Physiol 43: 1838–1844

    CAS  Google Scholar 

  • Zoglowek C, Krömer S and Heldt HW (1988) Oxaloacetate and malate transport of plant mitochondria. Plant Physiol 87: 109–115

    CAS  Google Scholar 

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Keys, A.J., Leegood, R.C. (2002). Photorespiratory Carbon and Nitrogen Cycling: Evidence from Studies of Mutant and Transgenic Plants. In: Foyer, C.H., Noctor, G. (eds) Photosynthetic Nitrogen Assimilation and Associated Carbon and Respiratory Metabolism. Advances in Photosynthesis and Respiration, vol 12. Springer, Dordrecht. https://doi.org/10.1007/0-306-48138-3_8

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  • DOI: https://doi.org/10.1007/0-306-48138-3_8

  • Publisher Name: Springer, Dordrecht

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