Skip to main content
NCBI home page
Journal of Experimental Botany logoLink to Journal of Experimental Botany
. 2016 May 13;67(10):2915–2918. doi: 10.1093/jxb/erw178

Photorespiration: origins and metabolic integration in interacting compartments

Martin Hagemann 1,2,3, Andreas PM Weber 1,2,3, Marion Eisenhut 1,2,3
PMCID: PMC4867902

This special issue on photorespiration focuses on recent advances in this topic. The majority of the papers summarizes and extends contributions given at the 2nd workshop, ‘Photorespiration–key to better crops’, held in Warnemuende, Germany in June 2015. This was organized by the DFG (German Research Foundation)-supported research network, ‘Photorespiration: origins and metabolic integration in interacting compartments’ (FOR 1186–Promics).

The term photorespiration (PR) describes a light-induced biochemical process that converts 2-phosphoglycolate (2PG) into 3-phosphoglycerate (3PGA) and is accompanied by O2 uptake and CO2 release. It is closely associated with photosynthetic CO2 assimilation and represents one of the major highways of carbon metabolism in most plants. By mass flow, surpassed only by photosynthesis, PR actually constitutes the second most important process in the land-based biosphere. Plants using the most widespread C3 type of photosynthesis for CO2 assimilation display particularly massive photorespiratory CO2 production. PR is initiated by competition of O2 with CO2 at the active site of the universal carboxylating enzyme Ribulose 1,5-bisphosphate Carboxylase/Oxygenase (Rubisco) (Smith, 1976), which produces large amounts of 2PG during the day. Hence, PR essentially acts as a salvage or metabolic repair process that converts the toxic by-product 2PG into the useful Calvin–Benson cycle intermediate 3PGA. It is supposedly the most important ancient ancillary metabolic process that enables plants to thrive in an O2-containing atmosphere (Osmond, 1981). To convert 2PG into 3PGA, the concerted action of many plastidial, peroxisomal, mitochondrial, and also cytosolic enzymes is necessary, which makes this pathway the most prominent example of subcellular metabolic integration in higher plants.

However, PR also leads to the loss of a considerable fraction of freshly assimilated C and N as photorespiratory CO2 and NH3. Quantitatively, PR can decrease photosynthesis by up to 30% under current atmospheric concentrations of CO2 and O2 and even more at elevated temperature (e.g. Sharkey, 1988; Zhu et al., 2004). This substantial decrease of net photosynthesis led to the somewhat misleading view of PR as a ‘wasteful’ process limiting photosynthetic productivity in C3 plants (e.g. Garrett, 1978; Siedow and Day, 2001). However, genetic analysis showed that PR is essential for all organisms performing oxygenic photosynthesis, since mutations of genes encoding for key photorespiratory enzymes always resulted in the photorespiratory phenotype and frequently in lethality (Somerville, 2001), i.e. corresponding mutants of cyanobacteria, red algae (Rademacher et al., this issue), chlorophytes, C3 and C4 plants were not viable in ambient air and could only be rescued under artificially enhanced CO2/O2 ratios (reviewed in Bauwe et al., 2010). Nevertheless, due to the large CO2 and energy losses, PR is seen as a promising target in breeding more productive crops (Ort et al., 2015). For example, attempts have been initiated to introduce photorespiratory bypasses to make the process less energy demanding or to reduce the CO2 release (reviewed in Peterhänsel et al., 2013). Interestingly, it has recently been reported that, instead of decreasing PR an increased PR flux capacity resulted in enhanced growth of Arabidopsis thaliana in ambient air. The independent over-expression of two different proteins of the mitochondrial glycine cleavage system increased photorespiratory carbon flow and also improved Calvin–Benson cycle activity, leading to higher photosynthetic activity and higher biomass production (Timm et al., 2012a, 2015).

Following the discovery between 1960 and 1980 of many essentials of the photorespiratory cycle (Tolbert, 1971; Ogren, 2003), research interest in this topic declined. However, the recognition of PR as a main crop-breeding target and the development of new tools for plant research resulted in a revitalization of PR research over the last 15 years. Meanwhile most contributing enzymes and genes have been identified at a molecular level and a set of corresponding mutants was generated to investigate the metabolic interaction of PR with the metabolism of the entire plant (e.g. Boldt et al., 2005; Schwarte and Bauwe, 2007; Timm et al., 2008, 2012b). For example, these results showed the close interaction of PR with plant C1-metabolism and with other metabolic pathways (Engel et al., 2007; Ewald et al., 2007). Advanced metabolomic and transcriptomic approaches allowed a system-wide characterization of PR in the wild type and mutants of Arabidopsis (e.g. Fernie et al., 2013). The first candidates for photorespiratory transporters connecting the different interacting compartments such as the chloroplastidial glycerate/glycolate exchanger were identified by bioinformatics tools and then biochemically verified (Bordych et al., 2013; Pick et al., 2013). Research on C4 plants not only showed that PR is essential for these plants (Zelitch et al., 2009), but also provided increasing evidence for the important role of PR in the evolution of C4 photosynthesis (Sage, 2004). The different location of photorespiratory enzymes in so-called C3–C4 intermediate plants generated/established an ancient CO2 pump based on the transport of glycine and serine, which is also called C2 photosynthesis, as the precursor for the final dicarboxyacid-based C4 cycle (e.g. Mallmann et al., 2014). Last but not least, the identification of functional photorespiratory processes in cyanobacteria resulted in the view that photorespiration is an ancient process which coevolved with oxygenic photosynthesis (Eisenhut et al., 2006, 2008; Kern et al., 2011, 2013; Bauwe et al., 2012; Hagemann et al., 2013).

The present special issue reports on different aspects of actual PR research. It comprises one insight paper, eight review papers, three opinion papers, and nine original research papers.

The insight paper and three reviews discuss the current view on PR and its evolution. Sage (this issue) summarized the stepwise development of C4 photosynthesis from C3 photosynthesis, whereby the localization of photorespiratory enzymes and metabolic fluxes between bundle sheath and mesophyll played a crucial role. Bräutigam and Gowik (this issue) highlight the important role of PR in the evolution of C4 photosynthesis via intermediary stages, in which the capacity for PR is lost from leaf mesophyll cells and relocated to the bundle sheath cells. As shown by Döring et al. (this issue), in fully evolved C4 plants such as sorghum, the majority of genes encoding components of PR are also expressed preferentially in bundle sheath cells. Khoshravesh et al. (this issue) highlight the importance of organelle positioning in bundle sheath cells and the relocation of photorespiratory activity to this tissue during the evolution of C4 photosynthesis in grasses. Hagemann et al. (this issue) review the current position on the continuous coevolution of photosynthesis and PR. The evolution of all photorespiratory enzymes was elucidated and it was revealed that the present-day plant photorespiratory enzymes originated from archaeal, bacterial, and cyanobacterial sources, which served as eukaryotic host cell (Archaea), and mitochondrial (proteobacteria) or plastdial (cyanobacteria) endosymbionts, respectively. Moreover, calculating in terms of the geological era, ancient CO2/O2 ratios indicated that photorespiratory metabolism existed from the invention of oxygenic photosynthesis and remained necessary in cells evolving different types of carbon-concentrating mechanisms (CCM).

Another set of contributions deals with the intertwining of the photorespiratory pathway with the central metabolism and its significance for engineering plant productivity. For example, Fromm et al. (this issue), by using mutants that lack the activity of mitochondrial NADH dehydrogenase, analysed the role of the mitochondrial electron transport chain in photosynthesis. Using transcriptomic analysis of Lotus japonicus wild type and GS2 mutant plants on a range of different nitrogen concentrations and at ambient and elevated CO2, Pérez-Delgado et al. (this issue) show that primary nitrogen assimilation and PR are transcriptionally co-regulated. They also identify candidate transcription factors mediating this co-ordinated response. Betti et al. (this issue) summarize recent advances obtained in photorespiratory engineering and discuss the potential of realizing gains in crop productivity through manipulation of the photorespiratory pathway. Nunes-Nesi et al. (this issue) explore natural genetic variation in yield and photosynthetic capacity and point to the fact that photorespiratory capacity, in part, is genetically determined. Obata et al. (this issue) review the tight integration of PR with other metabolic pathways which reach beyond the recycling of carbon from the Calvin–Benson cycle, a topic that is further extended by Hodges et al. (this issue). Timm et al. (this issue) focus on the still limited understanding of regulatory interactions between plant PR and photosynthesis and discuss its critical impact for successfully engineering photosynthesis. Montgomery et al. (this issue) also explore the regulatory effect of light reactions on PR in their opinion paper. They employ the framework of modularity in the cyanobacterium Fremyella diplosiphon and suggest a highly controlled interplay among light reactions, PR, and CCM. The opinion paper by Orf et al. (this issue) also centres on cyanobacteria. According to their comparative meta-analysis of cyanobacterial and plant metabolite profiles, the authors propose that cyanobacteria can serve as a much simpler surrogate to study the complex, highly compartmentalized, plant PR metabolism.

A deeper understanding of PR requires technology to determine rates of PR and photosynthesis accurately and this is reviewed by Hanson et al. (this issue). Alonso-Cantabrana and von Caemmerer (this issue) report on using carbon isotope discrimination as a tool to quantify C4-like photosynthesis in C3–C4 intermediate species. Labelling with the stable carbon isotope 13C also revealed a strong effect of reduced mitochondrial malate dehydrogenase activity on PR (Lindén et al., this issue). Sharwood et al. (this issue) emphasize the importance of standardized and validated protocols for quantifying carbon fixation capacity in plants with differing carbon assimilation strategies, with particular emphasis on quantifying Rubisco activity.

Four papers deal with the specific role of the central enzyme, glycolate oxidase. The biochemistry of this peroxisomal enzyme converting glycolate into glyoxylate is reviewed by Hodges et al. (this issue). Dellero et al. report on the impact of reduced photorespiratory glycolate oxidase activity on leaf metabolism in Arabidopsis (Dellero et al., a, this issue) and review recent advances in the understanding of glyoxylate metabolism in different plant organs (Dellero et al., b, this issue). Knocking out glycolate oxidase of Cyanidioschyzon merolae resulted in the first mutant with a photorespiratory phenotype among red algae (Rademacher et al., this issue). This finding revealed that the plant-type photorespiratory cycle using a peroxisomal glycolate oxidase evolved before the split of red and green algae, and it represents a further example that organisms, though carrying a CCM, also depend on functional PR.

Concluding remarks

The past decades of research on the process of PR have revealed that this pathway is an indispensable companion to oxygenic photosynthesis and includes photosynthetic organisms that feature highly efficient CCMs such as cyanobacteria, many algae, and C4 plants. Not only is it essential to support photosynthetic carbon assimilation, it is also heavily intertwined with other metabolic pathways and is the driving force for the evolution of C4 photosynthesis (Heckmann et al., 2013), the most efficient mode of photosynthetic carbon assimilation in the angiosperms. In extant oxygenic photosynthetic organisms, the only means to reduce the rate of PR and hence enhance photosynthetic efficiency is to increase the concentration of CO2 at the site of Rubisco. Therefore, future research aimed at increasing the efficiency of photosynthesis in crop plants might want to focus on this aspect. In the short term, perhaps the most promising path towards increased crop efficiency might be founded on a deeper understanding of natural variation in photosynthetic capacity to unravel those genes that determine source strength. Here, a better understanding of PR regulation and its integration into the cellular metabolism via yet unidentified transporters (e.g. exchanging glycine and serine between mitochondria and peroxisomes) would be an important future aim. However, in the long-term, it is also envisaged that synthetic pathways for carbon assimilation (i.e. pathways not existing in nature), that are not affected by oxygen, might become a reality (Bar-Even et al., 2010; Ort et al., 2015), thereby enabling hitherto unimaginable gains in productivity.

References

  1. Alonso-Cantabrana H, von Caemmerer S. 2016. Carbon isotope discrimination as a diagnostic tool for C4 photosynthesis in C3–C4 intermediate species. Journal of Experimental Botany 67, 3109–3121. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bar-Even A, Noor E, Lewis NE, Milo R. 2010. Design and analysis of synthetic carbon fixation pathways. Proceedings of the National Academy of Sciences, USA 107, 8889–8894. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bauwe H, Hagemann M, Fernie AR. 2010. Photorespiration: players, partners and origin. Trends in Plant Science 15, 330–336. [DOI] [PubMed] [Google Scholar]
  4. Bauwe H, Hagemann M, Kern R, Timm S. 2012. Photorespiration has a dual origin and manifold links to central metabolism. Current Opinion in Plant Biology 15, 269–275. [DOI] [PubMed] [Google Scholar]
  5. Betti M, Bauwe H, Busch FA, et al. 2016. Manipulating photorespiration to increase plant productivity: recent advances and perspectives for crop improvement. Journal of Experimental Botany 67, 2977–2988. [DOI] [PubMed] [Google Scholar]
  6. Boldt R, Edner C, Kolukisaoglu Ü, Hagemann M, Weckwerth W, Wienkoop S, Morgenthal K, Bauwe H. 2005. d-Glycerate 3-kinase, the last unknown enzyme in the photorespiratory cycle in Arabidopsis, belongs to a novel kinase family. The Plant Cell 17, 2413–2420. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Bordych C, Eisenhut M, Pick TR, Kuelahoglu C, Weber APM. 2013. Co-expression analysis as tool for the discovery of transport proteins in photorespiration. Plant Biology (Stuttgart) 15, 686–693. [DOI] [PubMed] [Google Scholar]
  8. Bräutigam A, Gowik U. 2016. Photorespiration connects C3 and C4 photosynthesis. Journal of Experimental Botany 67, 2953–2962. [DOI] [PubMed] [Google Scholar]
  9. Dellero Y, Jossier M, Glab N, Oury C, Tcherkez G, Hodges M. 2016. a. Decreased glycolate oxidase activity leads to altered carbon allocation and leaf senescence after a transfer from high CO2 to ambient air in Arabidopsis thaliana . Journal of Experimental Botany 67, 3149–3163. [DOI] [PubMed] [Google Scholar]
  10. Dellero Y, Jossier M, Schmitz J, Maurino VG, Hodges M. 2016. b. Photorespiratory glycolate-glyoxylate metabolism. Journal of Experimental Botany 67, 3041–3052. [DOI] [PubMed] [Google Scholar]
  11. Döring F, Streubel M, Bräutigam A, Gowik U. 2016. Most photorespiratory genes are preferentially expressed in the bundle sheath cells of the C4 grass Sorghum bicolor . Journal of Experimental Botany 67, 3053–3064. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Eisenhut M, Kahlon S, Hasse D, Ewald R, Lieman-Hurwitz J, Ogawa T, Ruth W, Bauwe H, Kaplan A, Hagemann M. 2006. The plant-like C2 glycolate cycle and the bacterial-like glycerate pathway cooperate in phosphoglycolate metabolism in cyanobacteria. Plant Physiology 142, 333–342. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Eisenhut M, Ruth W, Haimovich M, Bauwe H, Kaplan A, Hagemann M. 2008. The photorespiratory glycolate metabolism is essential for cyanobacteria and might have been conveyed endosymbiontically to plants. Proceedings of the National Academy of Sciences, USA 105, 17199–17204. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Engel N, van den Daele K, Kolukisaoglu Ü, Morgenthal K, Weckwerth W, Pärnik T, Keerberg O, Bauwe H. 2007. Deletion of glycine decarboxylase in Arabidopsis is lethal under non-photorespiratory conditions. Plant Physiology 144, 1328–1335. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Ewald R, Kolukisaoglu Ü, Bauwe U, Mikkat S, Bauwe H. 2007. Mitochondrial protein lipoylation does not exclusively depend on the mtKAS pathway of de-novo fatty acid synthesis in Arabidopsis. Plant Physiology 145, 41–48. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Fernie AR, Bauwe H, Eisenhut M, et al. 2013. Perspectives on plant photorespiratory metabolism. Plant Biology (Stuttgart) 15, 748–753. [DOI] [PubMed] [Google Scholar]
  17. Fromm S, Senkler S, Eubel H, Peterhänsel C, Braun HP. 2016. Life without complex I: proteome analyses of an Arabidopsis mutant lacking the mitochondrial NADH dehydrogenase complex. Journal of Experimental Botany 67, 3079–3093. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Garrett MK. 1978. Control of photorespiration at RuBP carboxylase/oxygenase level in ryegrass cultivars. Nature 274, 913–915. [Google Scholar]
  19. Hagemann M, Fernie AR, Espie GS, Kern R, Eisenhut M, Reumann S, Bauwe H, Weber APM. 2013. Evolution of the biochemistry of the photorespiratory C2 cycle. Plant Biology (Stuttgart) 15, 639–647. [DOI] [PubMed] [Google Scholar]
  20. Hagemann M, Kern R, Maurino VG, Hanson DT, Weber AP, Sage RF, Bauwe H. 2016. Evolution of photorespiration from cyanobacteria to land plants, considering protein phylogenies and acquisition of carbon concentrating mechanisms. Journal of Experimental Botany 67, 2963–2976. [DOI] [PubMed] [Google Scholar]
  21. Hanson ST, Stutz SS, Boyer JS. 2016. Why small fluxes matter: the case and approaches for improving measurements of photosynthesis and (photo)respiration. Journal of Experimental Botany 67, 3027–3039. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Heckmann D, Schulze S, Denton A, Gowik U, Westhoff P, Weber APM, Lercher M. 2013. Predicting C4 photosynthesis evolution: modular, individually adaptive steps on a Mount Fuji Fitness Landscape. Cell 153, 1579–1588. [DOI] [PubMed] [Google Scholar]
  23. Hodges M, Dellero Y, Keech O, Betti M, Raghavendra AS, Sage R, Zhu X, Allen DK, Weber APM. 2016. Perspectives for a better understanding of the metabolic integration of photorespiration within a complex plant primary metabolism network. Journal of Experimental Botany 67, 3015–3026. [DOI] [PubMed] [Google Scholar]
  24. Kern R, Bauwe H, Hagemann M. 2011. Evolution of enzymes involved in the photorespiratory 2-phosphoglycolate cycle from cyanobacteria via algae toward plants. Photosynthesis Research 109, 103–114. [DOI] [PubMed] [Google Scholar]
  25. Kern R, Eisenhut M, Bauwe H, Weber APM, Hagemann M. 2013. Does the Cyanophora paradoxa genome revise our view on the evolution of photorespiratory enzymes? Plant Biology (Stuttgart) 15, 759–768. [DOI] [PubMed] [Google Scholar]
  26. Khoshravesh R, Stinson C, Stata M, Busch F, Sage RF, Ludwig M, Sage TL. 2016. Facilitating C2 photosynthesis in grasses: centripetal organelle enrichment and cell-specific GDC expression in bundle sheath cells. Journal of Experimental Botany 67, 3065–3078. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Lindén P, Keech O, Stenlund H, Gardeström P, Moritz T. 2016. Reduced mitochondrial malate dehydrogenase activity has a strong effect on photorespiratory metabolism as revealed by 13C-labelling. Journal of Experimental Botany 67, 3123–3135. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Mallmann J, Heckmann D, Bräutigam A, Lercher MJ, Weber AP, Westhoff P, Gowik U. 2014. The role of photorespiration during the evolution of C4 photosynthesis in the genus Flaveria . Elife 3, e02478. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Montgomery BL, Lechno-Yossef S, Kerfeld CA. 2016. Interrelated modules in cyanobacterial photosynthesis: the carbon concentrating mechanism, photorespiration and light perception. Journal of Experimental Botany 67, 2931–2940. [DOI] [PubMed] [Google Scholar]
  30. Nunes-Nesi A, Nascimento VL, Silva FMO, Zsogon A, Araújo WL, Sulpice R. 2016. Natural genetic variation for morphological and molecular determinants of plant growth and yield. Journal of Experimental Botany 67, 2989–3001. [DOI] [PubMed] [Google Scholar]
  31. Obata T, Florian A, Timm S, Bauwe H, Fernie AR. 2016. On the metabolic interaction of (photo)respiration. Journal of Experimental Botany 67, 3003–3014. [DOI] [PubMed] [Google Scholar]
  32. Ogren WL. 2003. Affixing the O to Rubisco: discovering the source of photorespiratory glycolate and its regulation. Photosynthesis Research 76, 53–63. [DOI] [PubMed] [Google Scholar]
  33. Orf I, Timm S, Bauwe H, Fernie AR, Hagemann M, Kopka J, Nikoloski Z. 2016. Can cyanobacteria serve as a model of plant photorespiration? A comparative meta-analysis of metabolite profiles. Journal of Experimental Botany 67, 2941–2952. [DOI] [PubMed] [Google Scholar]
  34. Ort DR, Merchant SS, Alric J, et al. 2015. Redesigning photosynthesis to sustainably meet global food and bioenergy demand. Proceedings of the National Academy of Sciences, USA 112, 8529–8536. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Osmond CB. 1981. Photorespiration and photoinhibition. Some implications for the energetics of photosynthesis. Biochimica et Biophysica Acta 639, 77–98. [Google Scholar]
  36. Pérez-Delgado CM, Moyano TC, García-Calderón M, Canales J, Gutiérrez RA, Márquez AJ, Betti M. 2016. Use of transcriptomics and co-expression networks to analyse the interconnections between nitrogen assimilation and photorespiratory metabolism. Journal of Experimental Botany 67, 3095–3108. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Peterhänsel C, Krause K, Braun HP, Espie GS, Fernie AR, Hanson DT, Keech O, Maurino VG, Mielewczik M, Sage RF. 2013. Engineering photorespiration: current state and future possibilities. Plant Biology (Stuttgart) 15, 754–758. [DOI] [PubMed] [Google Scholar]
  38. Pick TR, Bräutigam A, Schulz MA, Obata T, Fernie AR, Weber APM. 2013. PLGG1, a plastidic glycolate glycerate transporter, is required for photorespiration and defines a unique class of metabolite transporters. Proceedings of the National Academy of Sciences, USA 110, 3185–3190. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Rademacher N, Kern R, Fujiwara T, Mettler-Altmann T, Miyagishima SY, Hagemann M, Eisenhut M, Weber AP. 2016. Photorespiratory glycolate oxidase is essential for the survival of the red alga Cyanidioschyzon merolae under ambient CO2 conditions. Journal of Experimental Botany 67, 3165–3175. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Sage RF. 2004. The evolution of C4 photosynthesis. New Phytologist 161, 341–370. [DOI] [PubMed] [Google Scholar]
  41. Sage RF. 2016. Tracking the evolutionary rise of C4 metabolism. Journal of Experimental Botany 67, 2919-2922. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Schwarte S, Bauwe H. 2007. Identification of the photorespiratory 2-phosphoglycolate phosphatase, PGLP1, in Arabidopsis. Plant Physiology 144, 1580–1586. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Sharkey TD. 1988. Estimating the rate of photorespiration in leaves. Physiologia Plantarum 73, 147–152. [Google Scholar]
  44. Sharwood RE, Sonawane B, Ghannoum O, Whitney S. 2016. Improved analysis of C4 and C3 photosynthesis via refined in vitro assays of their carbon fixation biochemistry. Journal of Experimental Botany 67, 3137–3148. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Siedow JN, Day DA. 2001. Respiration and photorespiration. In: Buchanan BB, Gruissem W, Jones RL. (eds). Biochemistry and molecular biology of plants.American Society of Plant Physiologists: Rockville, 676–728. [Google Scholar]
  46. Smith BN. 1976. Evolution of C4 photosynthesis in response to changes in carbon and oxygen concentrations in the atmosphere through time. BioSystems 8, 24–32. [DOI] [PubMed] [Google Scholar]
  47. Somerville CR. 2001. An early Arabidopsis demonstration. Resolving a few issues concerning photorespiration. Plant Physiology 125, 20–24. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Timm S, Florian A, Arrivault S, Stitt M, Fernie AR, Bauwe H. 2012. a Glycine decarboxylase controls photosynthesis and plant growth. FEBS Letters 586, 3692–3697. [DOI] [PubMed] [Google Scholar]
  49. Timm S, Florian A, Fernie AR, Bauwe H. 2016. The regulatory interplay between photorespiration and photosynthesis. Journal of Experimental Botany 67, 2923–2929. [DOI] [PubMed] [Google Scholar]
  50. Timm S, Mielewczik M, Florian A, Frankenbach S, Dreissen A, Hocken N, Fernie AR, Walter A, Bauwe H. 2012. b High-to-low CO2 acclimation reveals plasticity of the photorespiratory pathway and indicates regulatory links to cellular metabolism of Arabidopsis. PLoS One 7, e42809. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Timm S, Nunes-Nesi A, Pärnik T, Morgenthal K, Wienkoop S, Keerberg O, Weckwerth W, Kleczkowski LA, Fernie AR, Bauwe H. 2008. A cytosolic pathway for the conversion of hydroxypyruvate to glycerate during photorespiration in Arabidopsis. The Plant Cell 20, 2848–2859. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Timm S, Wittmiß M, Gamlien S, Ewald R, Florian A, Frank M, Wirtz M, Hell R, Fernie AR, Bauwe H. 2015. Mitochondrial dihydrolipoyl dehydrogenase activity shapes photosynthesis and photorespiration of Arabidopsis thaliana . The Plant Cell 27, 1968–1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Tolbert NE. 1971. Microbodies—peroxisomes and glyoxysomes. Annual Review of Plant Physiology 22, 45–74. [Google Scholar]
  54. Zelitch I, Schultes NP, Peterson RB, Brown P, Brutnell TP. 2009. High glycolate oxidase activity is required for survival of maize in normal air. Plant Physiology 149, 195–204. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Zhu XG, Portis AR, Long SP. 2004. Would transformation of C3 crop plants with foreign Rubisco increase productivity? A computational analysis extrapolating from kinetic properties to canopy photosynthesis. Plant, Cell and Environment 27, 155–165. [Google Scholar]

Articles from Journal of Experimental Botany are provided here courtesy of Oxford University Press

RESOURCES