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Respiration in Photosynthetic Cells: Gas Exchange Components, Interactions with Photorespiration and the Operation of Mitochondria in the Light

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Plant Respiration

Summary

According to gas exchange measurements, mitochondrial oxygen consumption in the light is always fast, while respiratory CO2 evolution is markedly decreased (compared with rates in darkness). We analyze the metabolic events that lead to such contrasting responses. In the light, the generation of NADH in mitochondria, both in the glycine decarboxylase reaction and in the tricarboxylic acid cycle, leads to increased NAD(P)H levels, which may increase the activity of the rotenone-insensitive NAD(P)H dehydrogenases. The resulting increase of the reduction level of ubiquinone activates the alternative oxidase. Stabilization of (photo)respiratory flux during the transition from darkness to light takes place at higher NADH/NAD+ and ATP/ADP ratios. Maintenance of fast rates of mitochondrial electron transport in the light is facilitated by the import of oxaloacetate (OAA) from the cytosol to remove NADH, and by the export of citrate to the cytosol. This reduces the flow of metabolites in the tricarboxylic acid cycle, decreasing decarboxylation rates, while the rate of oxygen consumption reactions remain fast.

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References

  • Amthor JS (2000) Direct effect of elevated CO2 on nocturnal in situ leaf respiration in nine temperate deciduous tree species is small. Tree Physiol 20: 139–144

    PubMed  Google Scholar 

  • Atkin OK, Westbeek MHM, Cambridge ML, Lambers H and Pons TL (1997) Leaf respiration in light and darkness: A comparison of slow-and fast-growing Poa species. Plant Physiol 113: 961–965

    PubMed  CAS  Google Scholar 

  • Atkin OK, Evans JR and Siebke K (1998a) Relationship between the inhibition of leaf respiration by light and enhancement of leaf dark respiration following light treatment. Aust J Plant Physiol 25: 437–443

    Google Scholar 

  • Atkin OK, Schortemeyer M, McFarlane N and Evans JR (1998b) Variation in the components of relative growth rate in ten Acacia species from contrasting environments. Plant Cell Environ 21: 1007–1017

    Article  Google Scholar 

  • Atkin OK, Evans JR, Ball MC, Lambers H and Pons TL (2000a) Leaf respiration of snow gum in the light and dark. Interactions between temperature and irradiance. Plant Physiol 122: 915–923

    Article  PubMed  CAS  Google Scholar 

  • Atkin OK, Millar AH, Garderström P and Day DA (2000b) Photosynthesis, carbohydrate metabolism and respiration in leaves of higher plants. In: RC Leegood, TD Sharkey, S von Caemmerer (eds) Photosynthesis: Physiology and Metabolism, pp 153–175. Kluwer Academic Publishers, Dordrecht

    Google Scholar 

  • Avelange MH, Thiery JM, Sarrey F, Gans P and Rebeille F (1991) Mass-spectrometric determination of O2 and CO2 gas exchange in illuminated higher plant cells—evidence for light inhibition of substrate decarboxylations. Planta 183: 150–157

    CAS  Google Scholar 

  • Bauwe H, Keerberg O, Bassuner R, Pärnik T and Bassuner B (1987) Reassimilation of carbon dioxide by Flaveria (Asteraceae) species representing different types of photosynthesis. Planta 172: 214–218

    Article  CAS  Google Scholar 

  • Bergmann A, Garderström P and Ericson I (1981) Release and refixation of ammonia during photorespiration. Physiol Plant 53: 528–532

    Google Scholar 

  • Brooks A and Farquhar GD (1985) Effect of temperature on the CO2-O2 specificity of ribulose-1,5-bisphosphate carboxylase/oxygenase and the rate of respiration in the light. Estimates from gas exchange measurements on spinach. Planta 165: 397–406

    Article  CAS  Google Scholar 

  • Bruhn D, Mikkelsen TN and Atkin OK (2002) Does the direct effect of atmospheric CO2 concentration on leaf respiration vary with temperature? Responses in two species of Plantago that differ in relative growth rate. Physiol Plant 114: 57–64

    Article  PubMed  CAS  Google Scholar 

  • Budde RJA and Randall DD (1990) Pea leaf mitochondrial pyruvate dehydrogenase complex is inactivated in vivo in a light-dependent manner. Proc Natl Acad Sci USA 87: 673–676

    PubMed  CAS  Google Scholar 

  • Bykova NV and Møller IM (2001) Involvement of matrix NADP turnover in the oxidation of NAD+-linked substrates by pea leaf mitochondria. Physiol Plant 111: 448–456

    Article  PubMed  CAS  Google Scholar 

  • Bykova NV, Igamberdiev AU and Møller IM (1998) Contribution of respiratory NAD(P)H dehydrogenases to glycine and glycine plus malate oxidation by pea leaf mitochondria. In: IM Møller, P Garderström, K Glimelius and E Glaser (eds) Plant Mitochondria: From Gene to Function. Backhuys Publishers, Leiden, pp 347–351

    Google Scholar 

  • Bykova NV, Egsgaard H and Møller IM (2003) Identification of 14 new phosphoproteins involved in important plant mitochondrial processes. FEBS Lett 540: 141–146

    Article  PubMed  CAS  Google Scholar 

  • Byrd GT, Sage RF and Brown RH (1992) A comparison of dark respiration between C3 and C4 plants. Plant Physiol 100: 191–198

    CAS  Google Scholar 

  • Chapman EA and Graham D (1974) The effect of light on the tricarboxylic acid cycle in green leaves. I. Relative rates of the cycle in the dark and in the light. Plant Physiol 53: 879–885

    CAS  Google Scholar 

  • Chen RD and Gadal P (1990) Structure, functions and regulation of NAD-and NADP-dependent isocitrate dehydrogenases in higher plants and in other organisms. Plant Physiol Biochem 28: 411–427

    CAS  Google Scholar 

  • Day D and Wiskich JT (1977) Factors limiting respiration by isolated cauliflower mitochondria. Phytochemistry 16: 1499–1502

    Article  CAS  Google Scholar 

  • Day D, Neuburger M and Douce R (1985) Interactions between glycine decarboxylase, the tricarboxylic acid cycle and the respiratory chain in pea leaf mitochondria. Aust J Plant Physiol 12: 119–130

    CAS  Google Scholar 

  • De Palma A, Scalera V, Bisaccia F and Prezioso G (2003) Citrate uniport by the mitochondrial tricarboxylate carrier: A basis for a new hypothesis for the transport mechanism. J Bioenerg Biomembr 35: 133–140

    PubMed  Google Scholar 

  • Di Marco G, Manes F, Tricoli D and Vitale E (1990) Fluorescence parameters measured concurrently with net photosynthesis to investigate chloroplastic CO2 concentration in leaves of Quercus ilex L. J Plant Physiol 136: 538–543

    Google Scholar 

  • Doman NG (1959) On the interaction between photosynthesis and respiration in plants. Biochemistry (Moscow) 24: 19–24

    CAS  Google Scholar 

  • Drake BG, Azcon-Bieto J, Berry J, Bunce J, Dijkstra P, Farrar J, Gifford RM, Gonzalez-Meler MA, Koch G, Lambers H, Siedow J and Wullschleger S (1999) Does elevated atmospheric CO2 concentration inhibit mitochondrial respiration in green plants? Plant Cell Environ 22: 649–657

    Article  CAS  Google Scholar 

  • Edwards GE and Walker D (1983) C3, C4: Mechanisms, and Cellular and Environmental Regulation of Photosynthesis. Blackwell, Oxford

    Google Scholar 

  • Fondy BR, Geiger DR and Servaites JC (1989) Photosynthesis, carbohydrate-metabolism and export in Beta vulgaris L and Phaseolus vulgaris L during square and sinusoidal light regimes. Plant Physiol 89: 396–402

    CAS  Google Scholar 

  • Fox TC and Geiger DR (1984) Effects of decreased net carbon exchange on carbohydrate metabolism in sugar beet source leaves. Plant Physiol 76: 762–768

    Google Scholar 

  • Gardeström P and Lernmark U (1995) The contribution of mitochondria to energetic metabolism in photosynthetic cells. J Bioenerg Biomembr 27: 415–421

    PubMed  Google Scholar 

  • Gardeström P and Wigge B (1988) Influence of photorespiration on ATP/ADP ratios in the chloroplasts, mitochondria, and cytosol, studied by rapid fractionation of barley (Hordeum vulgare) protoplasts. Plant Physiol 88: 69–76

    Google Scholar 

  • Gardeström P, Igamberdiev AU and Raghavendra AS (2002) Mitochondrial functions in the light and significance to carbon-nitrogen interactions. In: Foyer CH and Noctor G (eds) Photosynthetic Nitrogen Assimilation and Associated Carbon and Respiratory Metabolism, pp 151–172. Kluwer Academic Publishers, Dordrecht

    Google Scholar 

  • Gemel J and Randall DD (1992) Light regulation of leaf mitochondrial pyruvate dehydrogenase complex. Plant Physiol 100: 908–914

    CAS  Google Scholar 

  • Gerbaud A and Andre M (1987) An evaluation of the recycling in measurements of photorespiration. Plant Physiol 83: 933–937

    CAS  Google Scholar 

  • Gfeller RP and Gibbs M (1984) Fermentative metabolism in Chlamydomonas reinhardtii. 1. Analysis of fermentative products from starch in dark and light. Plant Physiol 75: 212–218

    CAS  Google Scholar 

  • Goldsworthy A (1966) Experiments on the origin of CO2 released by tobacco leaf segments in the light. Phytochemistry 5: 1013–1019

    Article  CAS  Google Scholar 

  • Goldsworthy A (1970) Photorespiration. Bot Rev 36: 321–340

    CAS  Google Scholar 

  • Hanning I and Heldt HW (1993) On the function of mitochondrial metabolism during photosynthesis in spinach (Spinacia oleracea L.) leaves. Plant Physiol 103: 1147–1154

    PubMed  CAS  Google Scholar 

  • Hausler RE, Schlieben NH, Schulz B and Flugge UI (1998) Compensation of decreased triose phosphate translocator activity by accelerated starch turnover and glucose transport in transgenic tobacco. Planta 204: 366–376

    PubMed  CAS  Google Scholar 

  • Heineke D, Bykova N, Gardeström P and Bauwe H (2001) Metabolic response of potato plants to an antisense reduction of the P-protein of glycine decarboxylase. Planta 212: 880–887

    Article  PubMed  CAS  Google Scholar 

  • Hoefnagel MHN, Atkin OK and Wiskich JT (1998) Interdependence between chloroplasts and mitochondria in the light and the dark. Biochim Biophys Acta 1366: 235–255

    CAS  Google Scholar 

  • Hurry V, Keerberg O, Pärnik T, Öquist G and Gardeström P (1996) Effect of cold hardening on the components of respiratory decarboxylation in the light and in the dark in leaves of winter rye. Plant Physiol 111: 713–719

    PubMed  CAS  Google Scholar 

  • Igamberdiev AU (1999) Foundations of metabolic organization: Coherence as a basis of computational properties in metabolic networks. BioSystems 50: 1–16

    Article  PubMed  CAS  Google Scholar 

  • Igamberdiev AU and Gardeström P (2003) Regulation of NAD-and NADP-dependent isocitrate dehydrogenases by reduction levels of pyridine nucleotides in mitochondria and cytosol of pea leaves. Biochim Biophys Acta 1606: 117–125

    PubMed  CAS  Google Scholar 

  • Igamberdiev AU and Kleczkowski LA (2001) Implications of adenylate kinase-governed equilibrium of adenylates on contents of free magnesium in plant cells and compartments. Biochem J 360: 225–231

    Article  PubMed  CAS  Google Scholar 

  • Igamberdiev AU and Kleczkowski LA (2003) Membrane potential, adenylate levels and Mg2+ are interconnected via adenylate kinase equilibrium in plant cells. Biochim Biophys Acta 1607: 111–119

    PubMed  CAS  Google Scholar 

  • Igamberdiev AU and Lea PJ (2002) The role of peroxisomes in the integration of metabolism and evolution of land plants. Phytochemistry 60: 651–674

    Article  PubMed  CAS  Google Scholar 

  • Igamberdiev AU, Bykova NV and Gardeström P (1997) Involvement of cyanide-resistant and rotenone-insensitive pathways of mitochondrial electron transport during oxidation of glycine in higher plants. FEBS Lett 412: 265–269

    Article  PubMed  CAS  Google Scholar 

  • Igamberdiev AU, Bykova NV, Lea PJ and Gardeström P (2001) The role of photorespiration in redox and energy balance of photosynthetic plant cells: A study with a barley mutant deficient in glycine decarboxylase. Physiol Plant 111: 427–438

    Article  PubMed  CAS  Google Scholar 

  • Ivanova H, Keerberg O and Pärnik T (1993) Influence of oxygen concentration on the rates of carbon fluxes in the biochemical system of CO2 assimilation. Proc Estonian Acad Sci Chem 42: 185–197

    CAS  Google Scholar 

  • Jahnke S (2001) Atmospheric CO2 concentration does not directly affect leaf respiration in bean or poplar. Plant Cell Environ 24: 1139–1151

    Article  CAS  Google Scholar 

  • Keerberg O, Drozdova IS, Pärnik TR, Keerberg HI and Voskresenskaya NP (1989) Components of photosynthetic and respiratory CO2 exchange and photosynthetic carbon metabolism in barley seedlings grown under red and blue light. Russ J Plant Physiol 36: 642–652

    CAS  Google Scholar 

  • Keerberg O, Ivanova H, Keerberg H and Pärnik T (1999) CO2 exchange of potato transformants with reduced activities of glycine decarboxylase. In: GE de Vries, K Metzlaff (eds) Phytosfere’ 99—Highlights in European Plant Biotechnology, pp 215–219. Elsevier, Amsterdam

    Google Scholar 

  • Keerberg O and Viil J (1988) Quantitative characteristics of photosynthetic carbon metabolism. In: AA Nichiporovich (ed) Photosynthesis and Production Processes, pp 40–53. Nauka, Moscow

    Google Scholar 

  • Keerberg O, Ivanova H, Keerberg H and Pärnik T (2001) Contribution of primary and stored photosynthates to photorespiration. In: PS2001 Proceedings: 12th International Congress on Photosynthesis, S15-002. CSIRO, Melbourne (CD/ROM)

    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 

  • Kirschbaum MUF and Farquhar GD (1987) Investigation of the CO2 dependence of quantum yield and respiration in Eucalyptus pauciflora. Plant Physiol 83: 1032–1036

    CAS  Google Scholar 

  • Kok B (1948) A critical consideration of the quantum yield of Chlorella photosynthesis. Enzymologia 13: 1–56

    CAS  Google Scholar 

  • Krömer S (1995) Respiration during photosynthesis. Annu Rev Plant Physiol Plant Mol Biol 46: 47–70

    Google Scholar 

  • Krömer S and Heldt HW (1991) Respiration of pea leaf mitochondria and redox transfer between the mitochondrial and extramitochondrial compartment. Biochim Biophys Acta 1057: 42–50

    Google Scholar 

  • Krömer S and Scheibe R (1996) Function of the chloroplastic malate valve for respiration during photosynthesis. Biochem Soc Trans 24: 761–766

    PubMed  Google Scholar 

  • Krömer S, Malmberg G and Gardeström P (1993) Mitochondrial contribution to photosynthetic metabolism—a study with barley (Hordeum vulgare L) leaf protoplasts at different light intensities and CO2 concentrations. Plant Physiol 102: 947–955

    PubMed  Google Scholar 

  • Krömer S, Gardeström P and Samuelsson G (1996) Regulation of the supply of oxaloacetate for mitochondrial metabolism via phosphoenolpyruvate carboxylase in barley leaf protoplasts. II. Effects of metabolites on PEPC activity at different activation states of the protein. Biochim Biophys Acta 1289: 351–361

    PubMed  Google Scholar 

  • Kruger NJ, Bulpin PV and ap Rees T (1983) The extent of starch degradation in the light is pea leaves. Planta 157: 271–273

    Article  Google Scholar 

  • Kumarasinghe KS, Keys AJ and Whittingham CP (1977) The flux of carbon through the glycolate pathway during photosynthesis in leaves. J Exp Bot 28: 1247–1257

    CAS  Google Scholar 

  • Laisk A and Oja V (1998) Dynamics of Leaf Photosynthesis. CSIRO Publishing, Collingwood

    Google Scholar 

  • Laisk AH (1977) Equipment and methods for the measurement of PCW curves. In: AA Nichiporovich, ed, Kinetika Fotosinteza i Fotodykhaniya u C3 Rastenij (Kinetics of photosynthesis and Photorespiration of C3 Plants). Nauka, Moscow, pp 48–71

    Google Scholar 

  • Ligeza A, Tikhonov AN and Subczynski WK (1997) In situ measurements of oxygen production and consumption using paramagnetic fusinite particles injected into a bean leaf. Biochim Biophys Acta 1319: 133–137

    CAS  Google Scholar 

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

    Google Scholar 

  • Loreto F, Velikova V and Di Marco G (2001) Respiration in the light measured by (CO2)-C12 emission in (CO2)-C13 atmosphere in maize leaves. Aust J Plant Physiol 28: 1103–1108

    Google Scholar 

  • Luethy MH, Gemel J, Johnston ML, Mooney BP, Miernyk JA and Randall DD (2001) Developmental expression of the mitochondrial pyruvate dehydrogenase complex in pea (Pisum sativum) seedlings. Physiol Plant 112: 559–566

    Article  PubMed  CAS  Google Scholar 

  • Mahon JD, Fock H and Canvin DT (1974) Changes in specific radioactivities of sunflower leaf metabolites during photosynthesis in 14CO2 and 12CO2 at normal and low oxygen. Planta 120: 123–134

    Google Scholar 

  • Marsh HVJ, Galmiche JM and Gibbs M (1965) Effect of light on the tricarboxylic acid cycle in Scenedesmus. Plant Physiol 40: 1913–1922

    Google Scholar 

  • Maxwell DP, Wang Y and McIntosh L (1999) The alternative oxidase lowers mitochondrial reactive oxygen production in plant cells. P Natl Acad Sci USA 96: 8271–8276

    Article  CAS  Google Scholar 

  • McCashin BG, Cossins EA and Canvin DT (1988) Dark respiration during photosynthesis in wheat leaf slices. Plant Physiol 87: 155–161

    CAS  Google Scholar 

  • Melo AMP, Roberts TH and Møller IM (1996) Evidence for the presence of two rotenone-insensitive NAD(P)H dehydrogenases on the inner surface of the inner membrane of potato tuber mitochondria. Biochim Biophys Acta 1276: 133–139

    Google Scholar 

  • Melzer E and O’Leary MH (1987) Anapleurotic CO2 fixation by phosphoenolpyruvate carboxylase in C3 plants. Plant Physiol 84: 58–60

    CAS  Google Scholar 

  • Michalecka AM, Svensson AS, Johansson FI, Agius SC, Johanson U, Brennicke A, Binder S and Rasmusson AG (2003) Arabidopsis genes encoding mitochondrial type II NAD(P)H dehydrogenases have different evolutionary origin and show distinct responses to light. Plant Physiol 133: 642–652

    Article  PubMed  CAS  Google Scholar 

  • Møller IM (2001) Plant mitochondria and oxidative stress: electron transport, NADPH turnover, and metabolism of reactive oxygen species. Annu Rev Plant Physiol Plant Mol Biol 52: 561–591

    PubMed  Google Scholar 

  • Møller IM (2002) A new dawn for plant mitochondrial NAD(P)H dehydrogenases. Trends Plant Sci 7: 235–237

    PubMed  Google Scholar 

  • Møller IM and Lin W (1986) Membrane-bound NAD(P)H dehydrogenases in higher plant cells. Annu Rev Plant Physiol 37: 309–334

    Google Scholar 

  • Nakamura Y and Miyachi S (1982) Effect of temperature on starch degradation in Chlorella vulgaris 11h cells. Plant Cell Physiol 23: 333–341

    CAS  Google Scholar 

  • Ogren WL (1984) Photorespiration: Pathways, regulation, and modification. Annu Rev Plant Physiol 35: 415–442

    Article  CAS  Google Scholar 

  • Oliver DJ (1994) The glycine decarboxylase complex from plant mitochondria. Annu Rev Plant Physiol Plant Mol Biol 45: 323–337

    Article  CAS  Google Scholar 

  • Osmond CB and Grace SC (1995) Perspectives on photoinhibition and photorespiration in the field—quintessential inefficiencies of the light and dark reactions of photosynthesis. J Exp Bot 46: 1351–1362

    CAS  Google Scholar 

  • Pärnik T and Keerberg O (1995) Decarboxylation of primary and end-products of photosynthesis at different oxygen concentrations. J Exp Bot 46: 1439–1447

    Google Scholar 

  • Pärnik T, Keerberg O and Viil J (1976) Estimation of photorespiration in bean and maize leaves. Newslett Appl Nucl Meth Biol Agr 6: 5–7

    Google Scholar 

  • Pärnik TR, Voronin PY, Ivanova HN and Keerberg OF (2002) Respiratory CO2 fluxes in photosynthesizing leaves of C3 species varying in rates of starch synthesis. Russ J Plant Physiol 49: 821–827

    Google Scholar 

  • Pascal N, Dumas R and Douce R (1990) Comparison of the kinetic behavior toward pyridine nucleotides of NAD+-linked dehydrogenases from plant mitochondria. Plant Physiol 94: 189–193

    CAS  Google Scholar 

  • Picault N, Palmieri L, Pisano I, Hodges M and Palmieri F (2002) Identification of a novel transporter for dicarboxylates and tricarboxylates in plant mitochondria—bacterial expression, reconstitution, functional characterization, and tissue distribution. J Biol Chem 277: 24204–24211

    Article  PubMed  CAS  Google Scholar 

  • Pinelli P and Loreto F (2003) (CO2)-C12 emission from different metabolic pathways measured in illuminated and darkened C3 and C4 leaves at low, atmospheric and elevated CO2 concentration. J Exp Bot 54: 1761–1769

    Article  PubMed  CAS  Google Scholar 

  • Pons TL and Welschen RAM (2002) Overestimation of respiration rates in commercially available clamp-on leaf chambers. Complications with measurement of net photosynthesis. Plant Cell Environ 25: 1367–1372

    Article  Google Scholar 

  • Purvis AC (1997) Role of the alternative oxidase in limiting superoxide production by plant mitochondria. Physiol Plant 100: 165–170

    Article  CAS  Google Scholar 

  • Raghavendra AS, Padmasree K and Saradadevi K (1994) Interdependence of photosynthesis and respiration in plant cells—interactions between chloroplasts and mitochondria. Plant Sci 97: 1–14

    Article  CAS  Google Scholar 

  • Rasulov BH (1986) Photosynthetic parameters of cotton leaves at various source-sink relations within the whole plant system. Russ J Plant Physiol 33: 922–929

    CAS  Google Scholar 

  • Rasulov BH and Oja V (1982) Estimation of components of respiration in the light considering the presence of residual oxygen. Russ J Plant Physiol 30: 616–622

    Google Scholar 

  • Rasulov BH, Laisk AH and Asrorov KA (1983) Photosynthesis and photorespiration in some cotton species during ontogeny. Russ J Plant Physiol 30: 616–645

    Google Scholar 

  • Raven JA and Farquhar GD (1990) The influence of N-metabolism and organic acid synthesis on the natural abundance of isotopes of carbon in plants. New Phytol 116: 505–529

    CAS  Google Scholar 

  • Ribas-Carbo M, Lennon AM, Robinson SA, Giles L, Berry JA and Siedow JN (1997) The regulation of electron partitioning between the cytochrome and alternative pathways in soybean cotyledon and root mitochondria. Plant Physiol 113: 903–911

    PubMed  CAS  Google Scholar 

  • Ribas-Carbo M, Robinson SA, Gonzalez-Meler MA, Lennon AM, Giles L, Siedow JN and Berry JA (2000) Effects of light on respiration and oxygen isotope fractionation in soybean cotyledons. Plant Cell Environ 23: 983–989

    Article  CAS  Google Scholar 

  • Robinson JM (1988) Does O2 photoreduction occur within chloroplasts in vivo? Physiol Plant 72: 666–680

    CAS  Google Scholar 

  • Sharkey TD (1988) Estimating the rate of photosynthesis in leaves. Physiol Plant 73: 147–152

    CAS  Google Scholar 

  • Svensson AS and Rasmusson AG (2001) Light-dependent gene expression for proteins in the respiratory chain of potato leaves. Plant J 28: 73–82

    Article  PubMed  CAS  Google Scholar 

  • Tovar-Méndez A, Miernyk JA and Randall DD (2003) Regulation of pyruvate dehydrogenase complex activity in plant cells. Eur J Biochem 270: 1043–1049

    PubMed  Google Scholar 

  • Turpin DH, Botha FC, Smith RG, Feil R, Horsey AK and Vanlerberghe GC (1990) Regulation of carbon partitioning to respiration during dark ammonium assimilation by the green alga Selenastrum minutum. Plant Physiol 93: 166–175

    CAS  Google Scholar 

  • Vanlerberghe GC and McIntosh L (1996) Signals regulating the expression of the nuclear gene encoding alternative oxidase of plant mitochondria. Plant Physiol 111: 589–595

    PubMed  CAS  Google Scholar 

  • Vanlerberghe GC, Day DA, Wiskich JT, Vanlerberghe AE and McIntosh L (1995) Alternative oxidase activity in tobacco leaf mitochondria — dependence on tricarboxylic acid cycle-mediated redox regulation and pyruvate activation. Plant Physiol 109: 353–361

    PubMed  CAS  Google Scholar 

  • Villar R, Held AA and Merino J (1994) Comparison of methods to estimate dark respiration in the light in leaves of 2 woody species. Plant Physiol 105: 167–172

    PubMed  CAS  Google Scholar 

  • Villar R, Held AA and Merino J (1995) Dark leaf respiration in light and darkness of an evergreen and a deciduous plant species. Plant Physiol 107: 421–427

    PubMed  CAS  Google Scholar 

  • von Caemmerer S and Evans JR (1991) Determination of the average partial pressure of CO2 in chloroplasts from leaves of several C3 plants. Aust J Plant Physiol 18: 287–305

    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 

  • Weger HG, Birch DG, Elrifi IR and Turpin DH (1988) Ammonium assimilation requires mitochondrial respiration in the light—a study with the green alga Selenastrum minutum. Plant Physiol 86: 688–692

    CAS  Google Scholar 

  • Wigge B, Krömer S and Gardeström P (1993) The redox levels and subcellular distribution of pyridine nucleotides in illuminated barley leaf protoplasts studied by rapid fractionation. Physiol Plant 88: 10–18

    Article  CAS  Google Scholar 

  • Wingler A, Lea PJ and Leegood RC (1999a) 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 (1999b) The role of photorespiration during drought stress: An analysis utilizing barley mutants with reduced activities of photorespiratory enzymes. Plant Cell Environ 22: 361–373

    Article  CAS  Google Scholar 

  • Winter H, Robinson DG and Heldt HW (1993) Subcellular volumes and metabolite concentrations in barley leaves. Planta 191: 180–190

    Article  CAS  Google Scholar 

  • Winter H, Robinson DG and Heldt HW (1994) Subcellular volumes and metabolite concentrations in spinach leaves. Planta 193: 530–535

    CAS  Google Scholar 

  • Wiskich JT and Dry IB (1985) The tricarboxylic acid cycle in plant mitochondria: Its operation and regulation. In: R Douce, D Day (eds) Higher Plant Cell Respiration, Vol 18, pp 281–313. Springer-Verlag, Berlin

    Google Scholar 

  • Yamauchi M and Yamada Y (1985) Glycolate synthesis in tomato leaf disks: Involvement of storage material in photorespiration. J Fac Agr Kyushu Univ 30: 135–147

    CAS  Google Scholar 

  • Zalensky OV, Voznesensky VL, Ponomaryeva MM and Shtanko TP (1955) Effect of temperature on the metabolism of carbon fixed in the process of photosynthesis. Bot J (Russia) 40: 347–358

    Google Scholar 

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Hurry, V. et al. (2005). Respiration in Photosynthetic Cells: Gas Exchange Components, Interactions with Photorespiration and the Operation of Mitochondria in the Light. In: Lambers, H., Ribas-Carbo, M. (eds) Plant Respiration. Advances in Photosynthesis and Respiration, vol 18. Springer, Dordrecht. https://doi.org/10.1007/1-4020-3589-6_4

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