Skip to main content
Browse Subject Areas

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

High-to-Low CO2 Acclimation Reveals Plasticity of the Photorespiratory Pathway and Indicates Regulatory Links to Cellular Metabolism of Arabidopsis

  • Stefan Timm ,

    Contributed equally to this work with: Stefan Timm, Michael Mielewczik, Alexandra Florian

    Affiliation University of Rostock, Department of Plant Physiology, Rostock, Germany

  • Michael Mielewczik ,

    Contributed equally to this work with: Stefan Timm, Michael Mielewczik, Alexandra Florian

    Affiliations Institute of Agricultural Sciences, ETH Zürich, Zürich, Switzerland, Institute of Bio- and Geosciences IBG-2, Forschungszentrum Jülich GmbH, Jülich, Germany

  • Alexandra Florian ,

    Contributed equally to this work with: Stefan Timm, Michael Mielewczik, Alexandra Florian

    Affiliation Max Planck Institute of Molecular Plant Physiology, Potsdam-Golm, Germany

  • Silja Frankenbach,

    Current address: Departamento de Biologia and CESAM - Centro de Estudos do Ambiente e do Mar, Universidade de Aveiro Campus de Santiago, Aveiro, Portugal

    Affiliation University of Rostock, Department of Plant Physiology, Rostock, Germany

  • Anne Dreissen,

    Affiliation Institute of Bio- and Geosciences IBG-2, Forschungszentrum Jülich GmbH, Jülich, Germany

  • Nadine Hocken,

    Current address: Institute of Plant Biochemistry, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany

    Affiliation Institute of Bio- and Geosciences IBG-2, Forschungszentrum Jülich GmbH, Jülich, Germany

  • Alisdair R. Fernie,

    Affiliation Max Planck Institute of Molecular Plant Physiology, Potsdam-Golm, Germany

  • Achim Walter,

    Affiliations Institute of Agricultural Sciences, ETH Zürich, Zürich, Switzerland, Institute of Bio- and Geosciences IBG-2, Forschungszentrum Jülich GmbH, Jülich, Germany

  • Hermann Bauwe

    Affiliation University of Rostock, Department of Plant Physiology, Rostock, Germany



Photorespiratory carbon metabolism was long considered as an essentially closed and nonregulated pathway with little interaction to other metabolic routes except nitrogen metabolism and respiration. Most mutants of this pathway cannot survive in ambient air and require CO2-enriched air for normal growth. Several studies indicate that this CO2 requirement is very different for individual mutants, suggesting a higher plasticity and more interaction of photorespiratory metabolism as generally thought. To understand this better, we examined a variety of high- and low-level parameters at 1% CO2 and their alteration during acclimation of wild-type plants and selected photorespiratory mutants to ambient air.

Methodology and Principal Findings

The wild type and four photorespiratory mutants of Arabidopsis thaliana (Arabidopsis) were grown to a defined stadium at 1% CO2 and then transferred to normal air (0.038% CO2). All other conditions remained unchanged. This approach allowed unbiased side-by-side monitoring of acclimation processes on several levels. For all lines, diel (24 h) leaf growth, photosynthetic gas exchange, and PSII fluorescence were monitored. Metabolite profiling was performed for the wild type and two mutants. During acclimation, considerable variation between the individual genotypes was detected in many of the examined parameters, which correlated with the position of the impaired reaction in the photorespiratory pathway.


Photorespiratory carbon metabolism does not operate as a fully closed pathway. Acclimation from high to low CO2 was typically steady and consistent for a number of features over several days, but we also found unexpected short-term events, such as an intermittent very massive rise of glycine levels after transition of one particular mutant to ambient air. We conclude that photorespiration is possibly exposed to redox regulation beyond known substrate-level effects. Additionally, our data support the view that 2-phosphoglycolate could be a key regulator of photosynthetic-photorespiratory metabolism as a whole.


Oxygenic photosynthesis requires operation of the photorespiratory pathway to recycle 2-phosphoglycolate (2PG), the major by-product of Rubisco, to 3-phosphoglycerate (3PGA; recently reviewed in [1], [2]). One of the enzymatic reactions of this pathway releases NH3 and CO2, which re-enter metabolism more (NH3) or less (CO2) completely. Whilst 2PG production can be reduced via CO2-concentrating mechanisms such as those occurring in green algae and C4 plants, photorespiration cannot be fully avoided and occurs with high rates in most land plants. As a result, net-CO2 assimilation is reduced in comparison with artificial low-O2 environments. The rates of photorespiration do not only depend on the concentrations of O2 and CO2 but also on other environmental parameters. Well-studied effects are, for example, the promotion of photorespiration by high temperatures [3][5] and high light intensities [6], which is thought to help in the thermal and high-light protection of plants [7]. Photorespiration is also the major source of H2O2 in plants, a compound that is involved in stress response signalling [2], [8] and pathogen defence [9]. In light of this complexity and since environmental factors interact and fluctuate on small timescales, such as hours to days, highly differentiated responses of photorespiratory metabolism to such changes are likely.

Photorespiration is thus a multifaceted process. It allows oxygenic photosynthesis by recycling 2PG, which is the indispensable function of this pathway, but it also interacts with several other cellular processes and responds to changes in the environment. The important role of photorespiration is most directly apparent from mutant studies in diverse organisms, ranging from cyanobacteria [10] to a variety of land plants [11][13]. Among these, Arabidopsis thaliana (Arabidopsis) is the only plant for which a comprehensive set of genetically well characterized photorespiratory knockout mutants exists. Several of these mutants were produced in the 1970s by chemical mutagenesis [14] and many more became available from the advent of T-DNA insertional mutagenesis [15]. With the possible exception of glycolate oxidase, where the existence of five isoforms hampered studies, this set covers all known reactions of the photorespiratory core cycle and also includes a range of associated reactions.

Traditionally, photorespiratory mutants are referred to as displaying a ‘photorespiratory phenotype’. That is, they do not survive in normal air but can be recovered in air enriched to 1% CO2 [16]. The examination of available growth data shows, however, that only some but not all photorespiratory mutants require such high CO2 levels. A high level of CO2, for example, is required for normal growth of mutants devoid of 2PG phosphatase (PGLP) [17], [18], [19], whereas null mutants of glycerate 3-kinase (GLYK) grow well with about 0.15% CO2 [20]. Mutants without peroxisomal hydroxypyruvate reductase (HPR1) can even grow and reproduce in normal air [21], [22]. Since all three mutants are defective in single-gene-encoded enzymes of the core photorespiratory cycle in Arabidopsis, their differential CO2 response indicates a much higher complexity of photorespiratory metabolism than presently assumed.

In this article, we examine this complexity by investigating the acclimation of plants grown in low-photorespiratory (1% CO2, HC for high CO2) conditions to the high-photorespiratory conditions of (0.038% CO2, LC for low CO2). We found considerable variability in the acclimation of the individual photorespiratory mutants and in the wild type. Most of these differences depend on the position of the impaired enzymatic step in the pathway and are imprinted in the diel (24 h) growth dynamics. Acclimation was typically steady and consistent for a number of features, but we also found some unexpected transition events, such as an intermittent very massive rise of glycine levels after transition of the HPR1-deficient mutant to ambient air. We will discuss these data with focus on possible regulatory interactions between photorespiration and other major metabolic pathways.


For our study, we selected four T-DNA insertional mutants of Arabidopsis: (1) pglp1, a null mutant of the chloroplastidial enzyme phosphoglycolate phosphatase (PGLP) [17], which is the first enzyme of the photorespiratory pathway; (2) shm1, a null mutant of the mitochondrial enzyme serine hydroxymethyltransferase 1 (SHM1) [23]; (3) hpr1, a null mutant of the peroxisomal enzyme hydroxypyruvate reductase 1 (HPR1) [21], [24]; and (4) glyk1, a null mutant of the chloroplastidial enzyme glycerate 3-kinase (GLYK) [20], which is the final enzyme of the photorespiratory pathway. To ensure the best comparability possible, all plants were grown to developmental stage 5.1 [25] in conditions that are normally classified as ‘non-photorespiratory’ (HC, 1% CO2; initial growth conditions). Then, keeping all other growth parameters unchanged, we reduced the CO2 level to ambient concentration and monitored transitional effects that occurred during acclimation to ambient-air conditions (LC, 0.038% CO2) for a variety of parameters. Since distinct day-length effects exist with respect to the growth of some photorespiratory mutants, for example catalase (CAT2) [26] and HPR1 [21], [24], all experiments were performed in strictly controlled short-day conditions. This approach triggered the very weak effects typically observed in long-day-grown hpr1 and moderated the very strong effects in the other three mutants typically observed in long days (as illustrated in Figure S1and Figure S2) to allow analysis of growth and photosynthesis in leaves that are not damaged to an extent that precludes an exact analysis.

Photorespiratory Mutants Display Different Phenotypes

We first wanted to obtain an overview over the phenotypic differences between the individual mutants and in comparison with the wild type (Figure 1A). At HC, there were no visible differences between the wild type, hpr1, glyk1, and shm1, whereas the pglp1 mutant already displayed yellowish leaves and growth retardation. After several days at LC, clear alterations were visible in the cases of glyk1 and shm1 and even stronger in the case of pglp1. By PSII fluorescence imaging (as shown in Figure S3), alterations were detectable in all four mutants already after three days at LC. As earlier reported for corresponding barley [22] and Arabidopsis mutants [21], the hpr1 mutant reacted much more mildly compared to the other three mutants. This very moderate response has been explained by extraperoxisomal bypasses [21], [22]. Interestingly, source leaves of glyk1 and shm1 were more strongly impaired by the induction of photorespiration than sink leaves. This heterogeneous phenotype was not observed before and most distinctive in the shm1 mutant, whose younger leaves stayed green and photosynthetically active while the older leaves became increasingly necrotic. Interestingly, though to a much lesser extent, even the highly impaired PGLP null-mutant displayed some long-term acclimation: following initial growth at HC, this mutant survived for up to three weeks in ambient air.

Figure 1. Phenotypes and growth performances at high CO2 and after transition to ambient air.

(A) Plants were first grown in 1% CO2 (HC) for eight weeks to stadium 5.1 [25], then transferred to ambient air (LC; 0.038% CO2) and monitored for another 2 weeks. For more detailed time courses see Figure S1 and Figure S2. (B) Absolute rosette growth rates of photorespiratory mutants before and after transfer to LC. Shown is the projected rosette area (APT) as calculated from automated image acquisition and analysis using the phenotyping platform GROWSCREEN FLUORO. Plants were transferred to LC before reaching stadium 5.1 to allow comparability with the DISP-based growth analysis (shown in Figure 5) of young developing leaves before and after transfer. Monitoring started 11 days after picking for a period of 10 days in HC conditions (stadium 1.04). Next, plants were transferred to LC and monitored for another 7 days. Data points represent mean values ± SD from 8 individual plants.

In addition to this visual inspection, absolute growth performances were calculated by automated image acquisition and analysis using the phenotyping platform GROWSCREEN FLUORO [27] (Figure 1B). Underpinning the visible effects, rosettes of pglp1 showed a reduced absolute growth rate already under HC conditions, whereas hpr1, shm1 and glyk1 displayed comparable growth rates at HC if compared to the wild type. By contrast, after plants were exposed to ambient air, clear differences in absolute growth rates became visible in the order wild type >hpr1>shm1glyk>pglp1.

Different Mutations Have Different Impact on PSII Photochemical Efficiency

Photorespiration consumes ATP and reducing equivalents, both directly within the photorespiratory carbon and nitrogen cycles and indirectly via effects on the Calvin-Benson cycle. Consequently, due to the high fluxes, perturbation of photorespiration accelerates photoinhibition [28], and it was also reported that repair of the PSII D1 protein becomes less efficient [29]. We assessed PSII maximum efficiency (Fv/Fm) of fully expanded individual leaves of dark-adapted plants (from the same set as shown in Figure 1) prior to and following HC-to-LC transition (Figure 2). In close correspondence to the visual appearance of the HC-grown plants, the Fv/Fm ratios of individual leaves were similar in wild type, hpr1, glyk1 and shm1 but significantly reduced in pglp1. However, slight but distinct impairments were also visible at the edges of younger rosette leaves of hpr1, glyk1 and shm1 (Figure S3). Transition to ambient CO2 had little effect on Fv/Fm of the hpr1 mutant, whereas Fv/Fm became rapidly, strongly and increasingly reduced in the other three mutants. Generally described, the effects of the knockouts on Fv/Fm followed the order hpr1<glyk1<shm1<pglp1.

Figure 2. Changes in PSII photochemical efficiency Fv/Fm in response to ambient air.

Plants were grown at HC and transferred to ambient air as described in the legend to Figure 1A. Fv/Fm ratios were measured before (HC control) and after transfer to normal air (LC; 1, 3, 5 and 7 days). At the indicated times after transfer, plants were dark-adapted for 10 min and Fv/Fm values determined from fully expanded individual source leaves. Mean values ± SD (n = 5) are shown. Asterisks show significant alterations according to the two-tailed Student's t-test (p<0.05, * to wild-type, ** to hpr1, *** to glyk1, **** to shm1).

In light of the clear differences between sink and source leaves of shm1, we extended the examination of this particular mutant beyond two weeks after transition to ambient air. Within the first week after HC-to-LC transition, Fv/Fm decreased strongly in the source leaves but remained nearly unaltered in the sink leaves and close to wild-type levels (Figure 3A and B). Thereafter, the shm1 mutant unexpectedly continued to produce new sink leaves and eventually even flowered and produced fertile seeds (Figure 3C).

Figure 3. The shm1 mutant shows long-term acclimation and survives if initially grown in high CO2.

(A) PSII efficiency (Fv/Fm) rapidly decreases after transfer to ambient air in source leaves but not in sink leaves. Mean values ± SD (n = 5) are shown. Asterisks mark the significance of alterations according to the two-tailed Student's t-test (p<0.05, * to wild type, ** to shm1 outer area of source leaves, and + to the day before). (B) PSII fluorescence imaging of a shm1 rosette illustrating acclimation of sink leaves with a clear gradient toward better performance of the youngest leaves (i) but not of source leaves (o) after two weeks in ambient air. A wild-type rosette is shown for comparison. (C) After transfer to LC, shm1 produces new sink-leaves, flowers, siliques, and fertile seeds. The right photo shows a germination test on ½ MS media, compared to wild-type and shm1 seeds collected from plants grown produced under elevated CO2. shm1* labels germinated seeds from shm1 plants grown under HC conditions throughout their entire life cycle.

Photorespiratory Mutants Display Differing Alterations in Leaf Gas Exchange

Perturbations of photorespiratory metabolism alter leaf gas exchange, which is a useful proxy for photosynthetic performance. We therefore examined the acclimation of net CO2 uptake rates and CO2 compensation points of fully expanded leaves, both prior to the HC-to-LC transition and at days 1, 3 and 5 thereafter (Figure 4). After transition to ambient air, the wild type slowly but progressively acclimated as visible in lowered CO2 compensation points (Γ21) and increasingly improved net-CO2 uptake rates (A). Such acclimation was not observed with hpr1, and minor changes in both parameters indicated that photorespiratory metabolism is already slightly disturbed in this mutant. Much clearer incremental changes were observed with leaves of glyk1 and shm1. These very similarly responding mutants displayed marked negative effects on gas exchange already one day after transfer to ambient CO2, followed by more gradual alterations during the subsequent four days. The pglp1 mutant behaved differently: while both the CO2 uptake and compensation point differed very strongly from the respective wild-type values already at HC, they deteriorated much less in the subsequent low-CO2 environment and even re-improved slightly though significantly between days 1 and 5.

Figure 4. Alteration of gas exchange after transfer from high CO2 to ambient air.

Plants were grown in HC and transferred to LC exactly as described in the legend to Figure 1 (short day conditions). Net CO2 uptake (A, at 380 µl L−1 CO2) and CO2 compensation points (Γ21) were measured before (HC control) and after (LC; 1, 3 and 5 days) transfer to normal air. Mean values ± SD (n = 5) are shown. Asterisks show significant alterations according to the two-tailed Student's t-test (p<0.05, * to wild-type, ** to hpr1, + to glyk1 and shm1 at the corresponding time points).

Since photosynthesis interacts closely with carbohydrate metabolism, it is not surprising that changes in the biosynthesis and contents of major carbohydrates have been observed in photorespiratory mutants, for example [30]. Moreover, sugars contribute to the regulation of many diurnally expressed controlled genes and control diel changes of leaf growth [31]. Preliminary studies (not shown) indicated that neither of the examined mutants showed any clear alterations in leaf starch content or the typical diurnal rhythm of starch synthesis and starch degradation at HC [31][33]. We hence quantified leaf starch contents two days after HC-to-LC transition to allow some metabolic re-adjustment. Under this condition in ambient air, hpr1 and pglp1 accumulated less starch than the wild type within the first 5 h of illumination (Table 1, mid of day). This trend continued over the day to include all mutant lines over the next 5 h in light (Table 1, end of day). The effect on starch accumulation was most pronounced in pglp1, in which starch accumulated only to an extremely low level. This feature was accompanied by more than five-fold reduced nocturnal levels of maltose (Table S3), the major disaccharide generated during starch degradation and subsequently exported to the cytosol [34].

Table 1. Leaf starch contents after transition from high CO2 to ambient air.

Photorespiratory Mutants Show Differentially Altered Diel Growth Patterns

While growth data similar to those shown in Figure 1B have occasionally been reported for individual mutants in the photorespiratory pathway, the quantitative diel (24 h) growth patterns and the dynamics of leaf-growth rates of such mutants are not known. We performed such analyses by digital image sequence-processing (DISP) [31] for both high- and low-CO2 conditions at a high temporal resolution. Figure 5A shows diel growth patterns (relative growth rates, RGR) of individual leaves of wild-type plants before and after HC-to-LC transition. In HC (white circles), leaf growth was highest during the early morning hours and lowest in the first hours of the night. After transfer to ambient CO2 (black circles), the observed pattern remained essentially unchanged. The mean wild-type RGR (RGR averaged over the day or night) of about 1% h−1 remained unaffected in comparison of day and night rates but was distinctly lower in LC than in HC during the night. These control data are almost identical to some earlier results for Arabidopsis [31], [35] and hence validate the experimental setup. The hpr1 mutant (Figure 5B) showed a very similar diel growth pattern, with the exception of a significantly about 50% reduced RGR in the afternoon at LC. Much more pronounced alterations in the LC diel-growth patterns were observed in shm1 and glyk1 (Figure 5C and D). Similar to hpr1, shm1 and glyk1 displayed a considerably depressed growth in the afternoon but, in addition, nocturnal leaf growth was also distinctly lower than in hpr1. This effect was most pronounced in glyk1, where the differences between the average growth rates at day vs. night were distinctly higher than in the wild type. PGLP-knockout plants also showed a wild-type-like diel growth pattern in HC (Figure 5E) although overall leaf growth was slower than in the wild type and the other three mutants. Immediately after transition to LC, both the early-morning peak RGR and the mean RGR declined very strongly.

Figure 5. Diel (24 h) leaf growth patterns in high CO2 and thereafter in ambient air.

Grey (night) and white (day) areas mark the 10/14 h photoperiodic phases. Relative growth rates (RGR, left scale) of the Arabidopsis wild type (A) and photorespiratory mutants hpr1 (B), shm1 (C), glyk1 (D), and pglp1 (E) in HC conditions (1% CO2, open circles) and after HC-to-LC transition in ambient CO2 (closed circles). Each data point represents the mean RGR ± SE of one-hour average RGR values of the preceding hour individually measured with five leaves, each from another plant. Mean RGR values (RGR averaged over the preceding hour) over the day and night period are shown as horizontal lines (right scale; HC, dashed lines; LC, solid lines).

Metabolite Responses in the Wild Type

The gradual alteration of leaf gas exchange parameters demonstrates that acclimation to low CO2 is not a fast process but requires several days. To start understanding what exactly happens after high-to-low CO2 transition at the metabolite level, we examined the metabolic re-adjustment of the wild type and the two ‘extreme’ mutants, hpr1 and pglp1, using a metabolite profiling approach. The sampling intervals were the same as for the PSII and gas exchange measurements (developmental stage 5.1 at HC, after 1, 3 and 5 days at LC) with daily sampling times 2 h before and 4 h after switching off illumination. Relative steady-state levels of selected metabolites were analysed using gas-chromatography/mass-spectrometry (GC/MS) using wild-type values at HC as reference (individually set to 1 for both day and night values).

In the wild type, on the background of a wide range of unchanged metabolites after HC-to-LC transition shown in Table S1, some distinct short- and long-term responses became obvious (Figure 6). Most of the changes expectedly concerned photorespiratory intermediates and metabolites of pathways already known or presumed to closely interact with photorespiration, namely nitrogen metabolism [36] and the tricarboxylic acid (TCA) cycle [37]. Not all metabolites with altered contents in the leaves though displayed the same accumulation pattern. For example, day glycolate levels displayed an unexpected sharp drop on day one after transition from low- to high-photorespiratory conditions and only slowly increased thereafter. It was also unexpected that glycolate levels were only decreased in light but not in the dark, where they became increasingly higher relative to HC over five days in ambient air. Similar to glycolate, but without the initial drop during the day and the steady increase during the night, the steady-state content of glycine in the light was distinctly increased one day after transfer to low CO2 and continued to increase during the following days. The corresponding day contents of serine and glycerate were also considerably elevated on day one in LC, but these massive initial rises of serine and glycerate successively deteriorated again. Interestingly, hydroxypyruvate levels changed in a different manner: day levels did not immediately respond to the LC environment but gradually decreased to about 30% of the HC reference level, that is, at low-photorespiratory conditions.

Figure 6. Metabolite responses of the wild type after transition to ambient air.

Plants were grown in HC and transferred to LC with a continuous short-day photoperiod of 10/14 h throughout the experiment. Leaves of three individual plants were harvested 2 h before and 4 h after light was switched off in high-CO2 conditions (HC) and 1, 3 and 5 days after HC-to-LC transition. Relative metabolite contents ± SD are shown with the corresponding wild-type content at HC arbitrarily set to 1, separately for day and night values (white bars, day values; black bars, night values). Asterisks show significant changes to the corresponding wild-type HC control according to the two-tailed Student's t-test (p<0.05). The full data set is shown in Table S1.

Not only the photorespiratory metabolites but also the TCA cycle intermediates respond to the HC-to-LC transition. In the light, contents of succinate, α-ketoglutarate and citrate become distinctly elevated one day after transition, whereas fumarate and malate day levels remained unaffected. During the following days, these metabolites adjusted to LC steady-state levels, which were unchanged (succinate, α-ketoglutarate) or lower (citrate, fumarate, malate) relative to HC conditions. Nitrogen and amino acid metabolism, as evidenced by changes in glutamate and asparagine, was also affected by the massive drop of CO2 concentration. Whilst most of the changes described above are not very great in a quantitative sense, very large initial increases with a subsequent slow decrease were observed for dehydroascorbate. These changes only occurred in illuminated leaves and were not observed in the dark period.

Transient Accumulation of Glycine in hpr1 Indicates Regulation of Glycine-into-Serine Conversion

As already mentioned, hpr1 is an example for a relatively mildly perturbed photorespiratory cycle. The metabolite dynamics shown in Figure 7 (detailed list in Table S2) demonstrates that the knockout of HPR1, despite its only small effect on growth in ambient air, requires considerable more readjustment of metabolism after HC-to-LC transition than the wild type. Glycolate levels were somewhat lower in high CO2 than in the wild type at HC, but the initial drop under illumination in low CO2 was even more distinct than in the wild type, followed by a continuous slight rise. In the dark, glycolate levels were somewhat lower than in the wild type but still much higher than in the light. Glycine displayed a massive initial rise on day one after transition to low CO2 in the light (about eighty-fold) and also in the dark (about twenty-fold). This was followed by a sharp decrease on day three and another rise on day five in LC. Night levels of glycine decreased steadily but were still more than ten-fold higher than in the wild type after five days. Serine and glycerate levels also considerably increased in ambient air. This effect was strongest on day one but persistent throughout the experiment and also through the nights. In comparison with these strong effects, the initial transitional effect on hydroxypyruvate was surprisingly small with a mild increase over time in low CO2, which is opposite to the decrease observed in the wild type and can be explained by the absence of HPR1.

Figure 7. Metabolite responses of hpr1 after transition to ambient air.

Relative metabolite contents ± SD are shown with the corresponding wild-type content at HC arbitrarily set to 1 (white bars, day values; black bars, night values). See the legend to Figure 6 for more experimental details and Table S2 for the full data set.

In the TCA cycle, distinct differences relative to the wild type were observed only with respect to higher levels of α-ketoglutarate in low CO2, both during the day and night, whereas other intermediates remained unchanged. Similarly, this mutant did not behave significantly different to the wild type with respect to key metabolites of nitrogen metabolism. That said, the three-fold elevated levels of dehydroascorbate at HC compared with a lower daily increase at LC could indicate that HPR1 contributes to peroxisomal redox homeostasis beyond photorespiration. A recently reported example is NADH-reoxidation during fatty acid β-oxidation [38].

Knockout of PGLP1 Displays Links to TCA cycle and Metabolism of Branched-Chain Amino Acids

pglp1 represents the other extreme of photorespiratory phenotypes and responds very strongly to low-CO2 conditions. In light of the severely impaired photosynthetic parameters of this mutant, correspondingly massive changes were expectedly observed at the metabolite level (Figure 8, full data set in Table S3). First, leaf glycolate content was four-fold (day) or even nine-fold (night) elevated in 1% CO2 in comparison with the wild type and even more so in comparison with hpr1. The high day-levels decreased in ambient air and resembled wild-type levels at day five in LC. Glycine levels were also much higher than in the wild type, both during the day and night. They were not very different at HC and LC and remained at a relatively constant high level throughout the experiment, with the exception of an intermittent strong increase on day one. These high levels of glycolate and glycine in leaves of the HC-grown pglp1 mutant are not to be anticipated from the direction of carbon flow through the photorespiratory cycle and therefore indicate extensive metabolic reprogramming. Glycerate, which is a more downstream intermediate of the photorespiratory pathway, also accumulates at HC but to lower levels than glycine and without the initial intermittent increase observed with glycine on day one in LC. Hydroxypyruvate levels, on the other hand, were relatively low in pglp1 at HC and LC but increased rather than decreased (as in the wild type) during five days in ambient air.

Figure 8. Metabolite responses of pglp1 after transition to ambient air.

Relative metabolite contents ± SD are shown with the corresponding wild-type content at HC arbitrarily set to 1 (white bars, day values; black bars, night values). See the legend of Figure 6 for more experimental details and Table S3 for the full data set.

Among the metabolites of the TCA cycle, both day and night levels of succinate were distinctly elevated at HC relative to the wild type control under otherwise identical conditions and remained high at LC. By contrast to succinate, citrate levels were similar to the wild type but intermittently accumulated to three-fold higher level on days one and three but remained about unchanged during the nights in low CO2. The opposite trend prevails for α-ketoglutarate, which decreased below the wild-type level on day one followed by a gradual but moderate increase during the following days. A similar increase occurred over the following nights, but α-ketoglutarate levels of the mutant were always below the corresponding wild-type levels. Quantitatively similar, day-levels of fumarate and malate were also lower than in the wild type, both under high or low CO2 and in light or dark conditions, respectively. Taken together, these effects suggest reduced TCA cycle flow at the complex II (succinate dehydrogenase) step, which links the pathway to mitochondrial electron transport. Notably, γ-aminobutyric acid (GABA) was also elevated, up to ten-fold, under all these conditions and over the entire period analysed. Since glutamate is strongly reduced, this could possibly indicate backflow from the elevated succinate content [39].

Concerning key metabolites of nitrogen and amino acid metabolism, in addition to α-ketoglutarate and apart from the less significant changes observed in the levels of glutamate, relative day aspartate contents were reduced already in high CO2 and went down to even lower levels on day one of low CO2 before they eventually recovered on day five. This is a clear day effect since the aspartate content was relatively stable during the night. While effects on these metabolites were all relatively small, they were much higher for asparagine, arginine, and ornithine. All three compounds rapidly increased in pglp1 under low-CO2 conditions, both during the day and the night but with a much stronger night effect at least for ornithine. A similar trend was observed with isoleucine, lysine, valine, and tyrosine, which also showed a very strong accumulation under low-CO2 conditions. With the exception of lysine, the highest accumulation occurred during the night. Alanine showed a less strong accumulation with prolonged growth in low CO2; however, this amino acid showed the highest accumulation in high CO2. Finally, dehydroascorbate levels were much lower than in the wild type (Table S3).


Traditionally, photorespiration is described as a pathway that is attached to the Calvin-Benson cycle to convert 2PG back to 3PGA but without much interaction to other areas of cellular metabolism except ammonia assimilation. This view has changed in recent years when, for example, links to energy metabolism [40], glutathione biosynthesis [41] and folate interconversion pathways [42] were discovered. Much of the knowledge on photorespiration gained after its initial biochemical dissection [43], [44] was based on the analysis of knockout mutants, which are now available for nearly all known constituent enzymes in Arabidopsis. Most of these mutants were only individually characterized in different laboratories and parallel investigations on several mutants were a rare exception. It is natural that the applied experimental conditions were often not fully comparable during this decades-spanning research.

In this study, we attempted a direct comparison of the wild type of Arabidopsis with four photorespiratory mutants to examine the plasticity of the photorespiratory pathway and possibly identify unknown interactions with other areas of cellular metabolism. These five genotypes were grown, side by side, in carefully controlled ‘non-photorespiratory’ HC conditions (1% CO2 in air) to a defined developmental stage [25]. Then, individual plants were analysed with respect to a variety of parameters first in HC conditions and then for several days after transition to ambient-air CO2 levels.

From a birds-eye perspective, the wild type and hpr1 did not reveal any clear visible phenotypic alterations after HC-to-LC transition, whereas leaves of the other three mutants became increasingly necrotic (Figure 1, Figure S1, Figure S2) as it was reported before for these and many other photorespiratory mutants, for example [11], [16]. As mentioned above, HPR1 can be efficiently substituted by a cytosolic bypass [21], [24], [45], which well explains the only very moderate low-CO2 effects in the hpr1 mutant. The phenotype of the PGLP-deficient mutant, which is located at the other end of the scale of photorespiratory phenotypes, is clearly different from wild type already at HC. This observation is in some contrast to earlier reports that the phenotypes of another Arabidopsis mutant, pcoA-1 [18] and a corresponding barley mutant, RPr 84/90 [19] are indistinguishable from the wild type at 0.8–1% CO2. However, it is fully supported by PSII photochemical efficiencies. The HC data in Figure 2, which were collected from individual source leaves, clearly confirm impairment of photosynthetic electron transport in pglp1. For methodical reasons, we did not determine levels of 2PG, but it appears that the cellular level of this compound is a critical factor and an only slight increase above wild-type concentration impairs normal metabolism. This interpretation is in-line with observations on a glycolate dehydrogenase null-mutant of the cyanobacterium Synechocystis PCC 6803 [10]. Despite the operation of a carbon-concentrating mechanism, which strongly inhibits the oxygenase reaction of Rubisco and hence 2PG production, this mutant grows distinctly slower than wild-type cells even in 5% CO2 (5%) conditions. Interestingly, in addition to the very strong effects seen in pglp1, slight but distinct impairments at HC were also visible in the younger rosette leaves of the other three mutants examined in this study, including hpr1 (Figure S3). This observation indicates a tissue-dependent pattern of metabolic disturbances in leaves of photorespiratory mutants. Additionally, the data consistently suggest that photorespiration cannot be fully inhibited even by 1% CO2, which causes an approximately thirty-fold higher carboxylation/oxygenation ratio of Rubisco relative to air conditions.

Expectedly [46], leaf growth activity of the wild type and somewhat more of hpr1 was only slightly decreased in LC relative to HC (Figure 5). This indicates that our studies are not biased by a reduction of maximum stomatal conductance as it was observed after long-term adaptation of a number of species to HC [47], [48], but this phenomenon is not yet very well understood and most of the relevant studies concern LC-to-HC transitions on a more moderate scale. Growth of the other three mutants, in particular pglp1, responds distinctly stronger to the HC-to-LC transition. Their diel leaf growth patterns were more variable in comparison to wild-type plants at HC. The minor alterations visible in Figure 5 to a higher or lesser degree for the individual mutants may indicate disturbed temporal synchronization of metabolic or source-to-sink transport processes on a diel timescale similar as it was shown with circadian-clock mutants [49]. Taken together, while the diel growth patterns of the mutants did not show very clear alterations, the impairment of mean diurnal and nocturnal leaf growth in LC is evident and results in smaller rosettes some days after transition from HC to LC (Figure 1B). This effect is strongest in pglp1, where leaf growth activity ceases immediately after transition from HC to LC (Figure 1B) and does not recover, neither at day or night. The most likely explanation for this extreme feature is the massive negative effect on starch metabolism in pglp1 (Table 1). Moderate impairments of starch metabolism in photorespiratory mutants have been previously reported [50], [51] and were observed in all mutants examined during this study. This includes hpr1, indicating that a fully operational photorespiratory carbon recycling is required for chloroplasts to maintain normal levels of starch synthesis. The effects on starch metabolism in pglp1, however, were unexpectedly strong. In a sense, they remind to observations with the starch-less phosphoglucomutase mutant, in which low nocturnal sugar levels rather than high levels in the light trigger responses of diurnal gene regulation [52], [53].

In principle, it is known for decades that the perturbation of photorespiratory carbon flow dramatically restricts photosynthesis. It is an unresolved question though whether this inhibition of photosynthesis is simply caused by drainage of carbon from the Calvin-Bassham cycle [54] or due to the downregulation of specific enzymes, for example by higher levels of intermediates of the photorespiratory pathway. Since starch metabolism was less impaired in glyk1 and also impaired in hpr1, it is not very likely that the strong inhibition in pglp1 is simply due to drainage of Calvin-Benson cycle metabolites. Instead, the intra-chloroplastidial level of 2PG could be one of the factors controlling photosynthetic carbon-metabolism as a whole, and PGLP activity could be of key regulatory importance in the coordination of photorespiration and photosynthesis. Mechanistically, such control could be exerted via the reported 2PG inhibition of triose-phosphate isomerase [55], [56] and phosphofructokinase [57], which are both central enzymes of photosynthetic carbohydrate metabolism. Alternatively, the very low starch contents of pglp1 leaves could also indicate elevated diurnal breakdown of transitory starch, but such an explanation would be unsound in light of the very low maltose levels during day and night (Table S3). Hence, our data suggest that the virtually starch-free phenotype of pglp1 is mainly due to inhibited starch synthesis rather than accelerated degradation.

A very interesting long-term adaptation effect was observed with shm1 (Figure 3). Following transfer to LC, only the fully developed leaves (source leaves) but not the young leaves (sink leaves) of this mutant displayed a strong visible response. Following initial growth for some weeks in HC, shm1 was not only able to survive in ambient air but even flowered and produced viable seeds. This is both unexpected and remarkable since shm1 represents one of the classical photorespiratory mutants [51]. Moreover, overexpression of the second mitochondrial SHM, SHM2, cannot complement the shm1 allele [23]. We found that this feature very likely results from specific features of the SHM2's mitochondrial targeting peptide, which seemingly does not allow import into mesophyll mitochondria of Arabidopsis leaves, restricting SHM2 to the vasculature [58]. This phenomenon is not yet fully understood but, since there is no other mitochondrial SHM in the shm1 mutant, the import restrictions for SHM2 could be relaxed after acclimation of shm1 to HC conditions.

On a smaller time-scale, slow acclimation to low CO2 was also visible in photosynthetic gas exchange, in which net CO2 uptake increased and CO2 compensation points decreased over five days after transition of the wild type to LC (Figure 4). Even higher alterations though in the opposite direction were observed with glyk1 and shm1, whereas the differences in these two parameters between HC and LC conditions were much smaller with hpr1 and pglp1. Particularly the small changes in hpr1 suggest, but do not fully exclude, that a superimposition by stomata effects is relatively small and that the observed changes are due to metabolic adaptation.

After transition to LC - unsurprisingly - the strongest metabolic changes were observed within the group of photorespiratory metabolites (Figure 6, Figure 7, Figure 8). It is worth noting that the relatively slow speed with which metabolic adjustment to LC proceeds in all lines approximately corresponds to the slow acclimation of photosynthetic gas exchange. In particular, we consider three of the observed effects as most stimulating.

First, the PGLP-deficient mutant accumulates glycolate to four-fold (day) and nearly ten-fold (night) higher levels at 1% CO2. These data confirm the above conclusion that photorespiration is not fully inhibited at 1% CO2. In quantitative terms, it shall be stressed that these and all other metabolite data represent relative changes and do not allow any conclusion on absolute levels.

Second, day glycolate levels consistently showed a clear decrease on day one in LC with a small but steady increase during the following days, with the exception of further decreasing values in pglp1. The initial drop was most pronounced in the wild type and hpr1 but significant also in pglp1. This is an intriguing observation since it cannot be easily explained with the assumption that photorespiration is an essentially unregulated pathway. It is reasonable to assume that transfer from HC to ambient air will immediately trigger 2PG production and subsequently glycolate synthesis. One possible explanation for the observed decline in glycolate levels could be that glycolate oxidation becomes down-regulated in HC (and possibly in the dark) and light-dependently activated in ambient air [59]. This hypothesis would correspond to the observed massive rise of dehydroascorbate in the wild type on day one at LC and the high levels of dehydroascorbate in hpr1. Since this compound is generated, amongst other processes, during capture of reactive oxygen species (ROS) in the ascorbate-glutathione cycle [60], [61], the observed changes indicate a massive alteration in the cellular redox balance during HC-to-LC transition including the induction of ROS. Such induction could occur due to several reasons including an intermittent massive increase in H2O2 production by glycolate oxidase. Interestingly, it was recently shown that that all five members of the Arabidopsis glycolate oxidase family are important for non-host disease resistance [9], which includes regulation of biosynthesis and probably activity.

Third, hpr1 shows very high leaf glycine levels with a massive about 80-fold intermittent rise on day one after HC-to-LC transition. Over the following days, this peak drops sharply to then increase again. A similar but distinctly less pronounced dynamics of glycine levels is visible in pglp1. Increases in daily leaf glycine levels following transition from high to low CO2, as shown in Figure 6 for the Arabidopsis wild type, are to be expected and were often observed before. Barley leaves, for example, accumulate about 40% more glycine in air than in 0.7% CO2 [12], and the steady-state glycine content of potato and wheat leaves varies strongly depending on environmental conditions [62]. By contrast to these predictable changes, the remarkable massive intermittent rise immediately after HC-to-LC transition of hpr1 though has not been observed before and cannot be explained with present knowledge of the biochemistry of photorespiratory metabolism. Since this peak was not observed with the wild type, it cannot simply be related to a ‘photorespiratory shock’ but is related to the function(s) of HPR1. We speculate that at least one of the two glycine-to-serine conversion reactions could be down-regulated at very low photorespiratory flux (1% CO2). Up-regulation could then require high photorespiratory flux (at LC) in combination with fully functional peroxisomal recycling of NADH to NAD+ (by HPR1). Since the peroxisomal membrane forms a permeability barrier for NAD(P)+ and NAD(P)H, it is thought that HPR1 and malate dehydrogenase are important enzymes for the redox equilibration within the peroxisomes [38], [63], [64]. HPR1 hence has an extraordinary position relative to other enzymes of the photorespiratory core cycle not only because it can be efficiently circumvented by the cytosolic enzyme HPR2 but also in light of its role for peroxisomal and possibly cellular redox homeostasis. Therefore, it is tempting to speculate that glycine decarboxylase (GDC), beyond the established substrate-level regulation via NAD+ [65], [66], could be under direct redox-control. This would correspond to the opposite trends observed with dehydroascorbate in the wild type and hpr1 discussed above, which also indicate that the deletion of HPR1 disturbs cellular redox homeostasis.

The coordination of photorespiration with the TCA cycle has been presumed for some time, but our understanding of how this is precisely achieved is currently fragmentary [37]. Since the activity of several enzymes of this pathway is affected by metabolites produced or consumed during photorespiration, for example [67], it is not too surprising that there were also moderate effects of the HC-to-LC transition on the TCA cycle in the wild type and in hpr1. On the other hand, a massive reprogramming takes place in pglp1 at HC and even more so at LC: the TCA cycle becomes disrupted and a massive accumulation of branched-chain and aromatic amino acids occurs. All these changes indicate up-regulation of alternative pathways of respiration relying on protein, fatty acid and maybe also chlorophyll degradation [68]. It is also remarkable that several amino acids accumulate to very high levels in pglp1. These values indicate an additional block in the degradation of branched-chain and aromatic amino acids and therefore a possible link of photorespiration to this part of metabolism. Given the close relationship between photorespiration and respiration, these pathways could be invoked to maintain electron supply to the mitochondria. In addition, fumarate and malate are strongly decreased and a function as alternative respiratory metabolites under carbon starvation has been described [68], [69], supporting this notion. Moreover, succinate and GABA are consequently elevated in pglp1, indicating an activation of the GABA shunt to replenish the TCA cycle [70]. These data from metabolic profiling of the transition from high to low CO2 further support our assumption of a key position of PGLP1 in the concerted regulation of photosynthetic-photorespiratory metabolism and possibly beyond. Currently, the observed high levels of glycolate and glycine in pglp1 are very difficult to explain; this even more so in light of the low levels of serine, hydroxypyruvate and glycerate at high-CO2, which confirm an expectedly low photorespiratory flux under this condition. Possibly, these low levels could be related to alternative routes of serine biosynthesis [71], [72], which would at least explain the nearly unaltered serine levels.

Particularly in light of the observed very massive metabolic impact of the PGLP1 knockout, the interesting question arises whether the photorespiratory pathway or some of its parts are essential for other metabolic processes in addition to its importance for the Calvin-Benson cycle. Our data do not provoke a substantiated new answer to this old question but demonstrate that an undisturbed photorespiratory carbon flow is essential for the ‘normal’ operation of several other metabolic pathways.


With this side-by-side comparison of mutants impaired in selected individual steps of the photorespiratory pathway, we arrived at five major conclusions:

Firstly, there is not a single photorespiratory phenotype, but rather there are many: the phenotypes of photorespiratory mutants heavily depend on the interrupted reaction and the availability of short-term (hpr1) and long-term (shm1) compensation processes. In fact, glyk1 was the only mutant in our set of four which displayed the whole set of ‘classical’ features of a photorespiratory mutant. Additionally, the perturbation of photorespiratory metabolism shows a tissue-dependent pattern.

Secondly, acclimation of the wild type and photorespiratory mutants from high to low CO2 typically is not a fast process but requires several days. In case of shm1, it can be influenced by the duration of a preceding preconditioning period in high CO2.

Thirdly, photorespiratory metabolism is not as isolated as often thought but integrated into whole-plant metabolism in a manifold and complex manner. Metabolic and regulatory links appear to go far beyond the obvious direct interactions with the Calvin-Benson cycle and N-metabolism but include at the very least starch metabolism, the TCA cycle, the metabolism of branched-chain amino acids, and redox metabolism. Therefore, an undisturbed photorespiratory carbon flow is essential for the ‘normal’ operation of these metabolic pathways.

Fourthly, our data support the role of 2PG as a likely key metabolic regulator. This compound is seemingly produced even at 1% CO2, indicating that photorespiration is not fully inhibited at this condition.

Fifthly, although photorespiration is driven by light, some important and dynamically varying phenotypic properties such as leaf growth or metabolite contents were shown to be most prominently altered at night. This fact alone demonstrates that photorespiration is a temporally highly organized process which is involved in many regulatory and maintenance processes on a short timescale in a non-intuitive manner. The fine-tuning of this dynamic control however remains to be elucidated at higher resolution in future studies.

Materials and Methods

Plant Material and Growth

Arabidopsis thaliana ecotype Columbia (Col-0) was used as wild-type reference. The isolation of the individual homozygous mutant lines from SALK lines SALK_ 130837 (pglp1-1, At5g36700), SALK_ 083735 (shm1-2, At4g37930), SALK_067724 (hpr1-1, At1g68010) and SALK_ 085479 (glyk1-1, At1g80380) has been described before [17], [20], [21], [58]. Seeds were incubated at 4°C for at least 2 days to break dormancy prior to germination. Plants were grown in ambient air (LC, 0.038% CO2) or elevated CO2 conditions (HC, 1% CO2) in controlled environment Percival chambers (10/14 h or 16/8 h day/night-cycle, 20/18°C, ∼120 µmol·m−2·s−1 irradiance) on a 4∶1 mixture of soil (Type Mini Tray; Einheitserdewerk, Uetersen) and vermiculite and regularly watered with 0.2% Wuxal liquid fertilizer (Aglukon). If other conditions were not specifically mentioned, we analysed leaves from plants at growth stadium 5.1 according to Boyes et al. [25]. For the HC-to-LC transitions, CO2 levels were reduced in a controlled manner without transfer to different growth cabinets.

PSII Photochemical Efficiency and Gas Exchange

For fluorescence-imaging and the determination of Fv/Fm ratios, we used an Imaging PAM (M-series, Walz) according to Schreiber et al. [73]. Measurements were performed before (HC control) and one, three and five days after HC-to-LC transition (LC) as described in Fahnenstich et al. [74]. Net-photosynthetic rates (A, at 380 µL L−1 CO2) and CO2 compensation points (Γ21) were measured at 21% O2 with a Licor-6400 (LICOR, Lincoln, NE, USA) using fully developed rosette leaves before and after transition to ambient air. Photosynthetic photon flux density was 200 µmol m−2 s−1 (red/blue LED light source), and the leaf temperature was 25°C. Γ21 values were calculated from A/ci curves by regression analysis in the linear range of the response curve (400, 300, 200, 100, 50, and 400 µL L−1 external CO2). Plants were adapted to the respective conditions for 10–15 minutes before measurement.

General and Diel Growth Analysis

General growth of plants grown in HC and LC conditions was analysed non-invasively by monitoring the projected area of complete rosettes of wild-type and mutant populations using the automated high-throughput phenotyping platform GROWSCREEN FLUORO as described previously [27]. Diel leaf growth patterns of plants from the same populations as used for general phenotyping and starch analysis were monitored with high spatial and temporal resolution using the DISP method as described elsewhere in more detail [31]. After one day of acclimation in HC conditions, diel leaf growth was recorded for leaf number 10 of every plant with leaves less than 50% fully grown with a length of 6–12 mm (typical sink leaves). Image acquisition was performed using a set of progressive CCD cameras (Sony XC55 or XC75, Sony, Cologne, Germany) equipped with manually focused standard lenses and an infrared interference filter. Constant day and night illumination was provided using six clusters of infrared diodes (940 nm, Conrad Electronics, Hirschau, Germany). Gray-value images were taken every 90 s and image sequences used to calculate diel growth patterns by calculation velocities from moving visible structures as described before [31]. Relative growth rates (RGR) in % h−1 were calculated as divergence from estimated velocity fields by selecting an area of interest (AOI) on the leaf surface within the first image of the acquired image sequence. Structures within this AOI were tracked over 48 h before and 48 h after HC-to-LC transition along the complete image sequence to calculate RGRs in high temporal resolution. The data points in Figure 5 the mean RGR ± SE of the one-hour average RGR values of the preceding hour measured with one leaf each from five individual plants. Grey (night) and white (day) mark the photoperiodic phases.

Starch Analysis

After two days in LC, leaf samples were harvested at the end of the night (EON), the middle (MOD) and the end of the day (EOD). Samples were weighed, immediately frozen in liquid nitrogen and stored at −80°C until analysis. They were then repeatedly extracted in 400 µl 80% ethanol (2 mM HEPES) at 78°C and the residues subjected to quantitative starch analysis (in hexose units) as described in Walter et al. [46], using a coupled enzymatic assay [75] in a micro-plate absorption spectrophotometer (HT II Plate reader; Anthos Mikrosysteme GmbH, Krefeld, Germany).


Metabolite analysis was performed using fully expanded rosette leaves from plants at developmental stage 5.1 [25]. A first set of samples was taken under 1% CO2 (HC control) and more sets after transition to ambient air at days 1, 3 and 5 after shifting (LC), 2 h before and 4 h after light was switched off. Samples were immediately frozen in liquid nitrogen and stored at −80°C until analysis. Fifty mg of each sample were extracted and analysed as described previously [76].

Accession Numbers

Sequence data related to this article can be found in the EMBL/GenBank data libraries under accession number(s) At5g36700 (PGLP1), At4g37930 (SHM1), At1g68010 (HPR1), and At1g80380 (GLYK).

Supporting Information

Figure S1.

Phenotypes before and after transition from high CO2 to ambient air (short days, 10/14 h). Plants were grown in high CO2 (1%) with a 10/14 h day/night cycle. After reaching developmental stadium 5.1 (about 8 weeks), CO2 concentration was reduced to air levels and plants monitored. Individual panels show two representative plants from each line (hpr1, glyk1, shm1, or pglp1) next to two wild-type plants (Col-0) grown under identical conditions. Photos were taken before and 3, 5, 7 and 14 days after transition to ambient air.


Figure S2.

Phenotypes before and after transition from high CO2 to ambient air (long days, 16/8 h). Plants were grown exactly as described in the legend to Figure S1 but with a 16/8 h photoperiod and only for 6 weeks since developmental stage 5.1 was reached earlier in long days. The display format also corresponds to Figure S1.


Figure S3.

PSII fluorescence imaging before and after transition to ambient air. Plants were grown exactly as described in the legend to Figure S1. At the indicated times after transition to ambient CO2, plants were dark-adapted for 10 min and fluorescence images collected. Images are normalized to the Fv/Fm color bar at the bottom at the figure. Shown is one representative image from a total of five examined individuals per line and time point.


Table S1.

Metabolic response of Arabidopsis wild type after transition to ambient air.


Table S2.

Metabolic response of hpr1 after transition to ambient air.


Table S3.

Metabolic response of pglp1 after transition to ambient air.



We are grateful to Andreas P.M. Weber and Marion Eisenhut (Düsseldorf) and to Martin Hagemann (Rostock) for helpful suggestions on the experimental setup and the manuscript. We also thank Kathrin Jahnke (Rostock) for excellent technical assistance, and Siegfried Jahnke and Anika Wiese-Klinkenberg (Jülich) for help and advice during diel growth analysis. This work was made possible by the availability of SALK lines from the Nottingham Arabidopsis Stock Centre.

Author Contributions

Conceived and designed the experiments: ST MM AF SF AD NH ARF AW HB. Performed the experiments: ST MM AF SF AD NH . Analyzed the data: ST MM AF AD NH ARF AW HB. Contributed reagents/materials/analysis tools: ARF AW HB. Wrote the paper: ST MM ARF AW HB.


  1. 1. Bauwe H, Hagemann M, Fernie AR (2010) Photorespiration: players, partners and origin. Trends Plant Sci 15: 330–336.
  2. 2. Foyer CH, Bloom AJ, Queval G, Noctor G (2009) Photorespiratory metabolism: genes, mutants, energetics, and redox signaling. Annu Rev Plant Biol 60: 455.
  3. 3. Troughton JH, Slatyer RO (1969) Plant water status, leaf temperature, and calculated mesophyll resistance to carbon dioxide of cotton leaves. Aust J Biol Sci 22: 815–827.
  4. 4. Oberhuber W, Edwards GE (1993) Temperature dependence of the linkage of quantum yield of photosystem II to CO2 fixation in C4 and C3 plants. Plant Physiol 101: 507–512.
  5. 5. Hofstra G, Hesketh JD (1969) Effects of temperature on gas exchange of leaves in light and dark. Planta 85: 228–237.
  6. 6. Chollet R, Ogren WL (1975) Regulation of photorespiration in C3 and C4 species. Bot Rev 41: 137–179.
  7. 7. Sage RF (2000) C3 versus C4 photosynthesis in rice: ecophysiological perspectives. 13–38.
  8. 8. Noctor G, Veljovic-Jovanovic S, Driscoll SP, Novitskaya L, Foyer CH (2002) Drought and oxidative load in the leaves of C3 plants: a predominant role for photorespiration? Ann Bot 89: 841–850.
  9. 9. Rojas CM, Senthil-Kumar M, Wang K, Ryu CM, Kaundal A, et al. (2012) Glycolate oxidase modulates reactive oxygen species-mediated signal transduction during nonhost resistance in Nicotiana benthamiana and Arabidopsis. Plant Cell 24: 226–352.
  10. 10. Eisenhut M, Ruth W, Haimovich M, Bauwe H, Kaplan A, et al. (2008) The photorespiratory glycolate metabolism is essential for cyanobacteria and might have been conveyed endosymbiontically to plants. Proc Natl Acad Sci USA 105: 17199–17204.
  11. 11. Blackwell RD, Murray AJS, Lea PJ, Kendall A, Hall NP, et al. (1988) The value of mutants unable to carry out photorespiration. Photosynth Res 16: 155–176.
  12. 12. Wingler A, Lea PJ, Leegood RC (1999) Photorespiratory metabolism of glyoxylate and formate in glycine-accumulating mutants of barley and Amaranthus edulis. Planta 207: 518–526.
  13. 13. 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 Physiol 149: 195–204.
  14. 14. Somerville CR (2001) An early Arabidopsis demonstration resolving a few issues concerning photorespiration. Plant Physiol 125: 20–24.
  15. 15. Alonso JM, Stepanova AN, Leisse TJ, Kim CJ, Chen H, et al. (2003) Genome-wide insertional mutagenesis of Arabidopsis thaliana. Science 301: 653–657.
  16. 16. Somerville CR, Ogren WL (1982) Genetic modification of photorespiration. Trends Biochem Sci 7: 171–174.
  17. 17. Schwarte S, Bauwe H (2007) Identification of the photorespiratory 2-phosphoglycolate phosphatase, PGLP1, in Arabidopsis. Plant Physiol 144: 1580–1586.
  18. 18. Somerville CR, Ogren WL (1979) A phosphoglycolate phosphatase-deficient mutant of Arabidopsis. Nature 280: 833–836.
  19. 19. Hall NP, Kendall AC, Lea PJ, Turner JC, Wallsgrove RM (1987) Characteristics of a photorespiratory mutant of barley (Hordeum vulgare L) deficient in phosphoglycollate phosphatase. Photosynth Res 11: 89–96.
  20. 20. Boldt R, Edner C, Kolukisaoglu Ü, Hagemann M, Weckwerth W, et al. (2005) D-Glycerate 3-kinase, the last unknown enzyme in the photorespiratory cycle in Arabidopsis, belongs to a novel kinase family. Plant Cell 17: 2413–2420.
  21. 21. Timm S, Nunes-Nesi A, Pärnik T, Morgenthal K, Wienkoop S, et al. (2008) A cytosolic pathway for the conversion of hydroxypyruvate to glycerate during photorespiration in Arabidopsis. Plant Cell 20: 2848–2859.
  22. 22. Murray AJS, Blackwell RD, Lea PJ (1989) Metabolism of hydroxypyruvate in a mutant of barley lacking NADH-dependent hydroxypyruvate reductase, an important photorespiratory enzyme activity. Plant Physiol 91: 395–400.
  23. 23. Voll LM, Jamai A, Renné P, Voll H, McClung CR, et al. (2006) The photorespiratory Arabidopsis shm1 mutant is deficient in SHM1. Plant Physiol 140: 59–66.
  24. 24. Timm S, Florian A, Jahnke K, Nunes-Nesi A, Fernie AR, et al. (2011) The hydroxypyruvate-reducing system in Arabidopsis: Multiple enzymes for the same end. Plant Physiol 155: 694–705.
  25. 25. Boyes DC, Zayed AM, Ascenzi R, McCaskill AJ, Hoffman NE, et al. (2001) Growth stage-based phenotypic analysis of Arabidopsis: A model for high throughput functional genomics in plants. Plant Cell 13: 1499–1510.
  26. 26. Queval G, Issakidis-Bourguet E, Hoeberichts FA, Vandorpe M, Gakiere B, et al. (2007) Conditional oxidative stress responses in the Arabidopsis photorespiratory mutant cat2 demonstrate that redox state is a key modulator of daylength-dependent gene expression, and define photoperiod as a crucial factor in the regulation of H2O2-induced cell death. Plant J 52: 640–657.
  27. 27. Jansen M, Gilmer F, Biskup B, Nagel KA, Rascher U, et al. (2009) Simultaneous phenotyping of leaf growth and chlorophyll fluorescence via GROWSCREEN FLUORO allows detection of stress tolerance in Arabidopsis thaliana and other rosette plants. Funct Plant Biol 36: 902–914.
  28. 28. Takahashi S, Badger MR (2011) Photoprotection in plants: a new light on photosystem II damage. Trends Plant Sci 16: 53–60.
  29. 29. Takahashi S, Bauwe H, Badger M (2007) Impairment of the photorespiratory pathway accelerates photoinhibition of photosystem II by suppression of repair but not acceleration of damage processes in Arabidopsis. Plant Physiol 144: 487–494.
  30. 30. Häusler RE, Bailey KJ, Lea PJ, Leegood RC (1996) Control of photosynthesis in barley mutants with reduced activities of glutamine synthetase and glutamate synthase. 3. Aspects of glyoxylate metabolism and effects of glyoxylate on the activation state of ribulose-1,5-bisphosphate carboxylase-oxygenase. Planta 200: 388–396.
  31. 31. Wiese A, Christ MM, Virnich O, Schurr U, Walter A (2007) Spatio-temporal leaf growth patterns of Arabidopsis thaliana and evidence for sugar control of the diel leaf growth cycle. New Phytol 174: 752–761.
  32. 32. Niittyla T, Messerli G, Trevisan M, Chen J, Smith AM, et al. (2004) A previously unknown maltose transporter essential for starch degradation in leaves. Science 303: 87–89.
  33. 33. Graf A, Schlereth A, Stitt M, Smith AM (2010) Circadian control of carbohydrate availability for growth in Arabidopsis plants at night. Proc Natl Acad Sci USA 107: 9458–9463.
  34. 34. Weise SE, Weber AP, Sharkey TD (2004) Maltose is the major form of carbon exported from the chloroplast at night. Planta 218: 474–482.
  35. 35. Biskup B, Scharr H, Fischbach A, Wiese-Klinkenberg A, Schurr U, et al. (2009) Diel growth cycle of isolated leaf discs analyzed with a novel, high-throughput three-dimensional imaging method is identical to that of intact leaves. Plant Physiol 149: 1452–1461.
  36. 36. Keys AJ, Bird IF, Cornelius MJ, Lea PJ, Wallsgrove RM, et al. (1978) Photorespiratory nitrogen cycle. Nature 275: 741–743.
  37. 37. Nunes-Nesi A, Araujo WL, Fernie AR (2011) Targeting mitochondrial metabolism and machinery as a means to enhance photosynthesis. Plant Physiol 155: 101–107.
  38. 38. Pracharoenwattana I, Zhou WX, Smith SM (2010) Fatty acid beta-oxidation in germinating Arabidopsis seeds is supported by peroxisomal hydroxypyruvate reductase when malate dehydrogenase is absent. Plant Mol Biol 72: 101–109.
  39. 39. Allan WL, Clark SM, Hoover GJ, Shelp BJ (2009) Role of plant glyoxylate reductases during stress: a hypothesis. Biochem J 423: 15–22.
  40. 40. Sweetlove LJ, Lytovchenko A, Morgan M, Nunes-Nesi A, Taylor NL, et al. (2006) Mitochondrial uncoupling protein is required for efficient photosynthesis. Proc Natl Acad Sci USA 103: 19587–19592.
  41. 41. Noctor G, Arisi AM, Jouanin L, Foyer CH (1999) Photorespiratory glycine enhances glutathione accumulation in both the chloroplastic and cytosolic compartments. J Exp Bot 50: 1157–1167.
  42. 42. Collakova E, Goyer A, Naponelli V, Krassovskaya I, Gregory JF, et al. (2008) Arabidopsis 10-formyl tetrahydrofolate deformylases are essential for photorespiration. Plant Cell 20: 1818–1832.
  43. 43. Tolbert NE (1963) Glycolate pathway. In: Photosynthetic Mechanisms in Green Plants. Publication 1145. Washington, DC: National Academy of Science, National Research Council. pp. 648–662.
  44. 44. Tolbert NE (1973) Glycolate biosynthesis. Curr Top Cell Regul 7: 21–50.
  45. 45. Givan CV, Kleczkowski LA (1992) The enzymatic reduction of glyoxylate and hydroxypyruvate in leaves of higher plants. Plant Physiol 100: 552–556.
  46. 46. Walter A, Christ MM, Barron-Gafford GA, Grieve KA, Murthy R, et al. (2005) The effect of elevated CO2 on diel leaf growth cycle, leaf carbohydrate content and canopy growth performance of Populus deltoides. Glob Change Biol 11: 1207–1219.
  47. 47. Hetherington AM, Woodward FI (2003) The role of stomata in sensing and driving environmental change. Nature 424: 901–908.
  48. 48. Morison JIL (1998) Stomatal response to increased CO2 concentration. J Exp Bot 49: 443–452.
  49. 49. Dodd AN, Salathia N, Hall A, Kevei E, Toth R, et al. (2005) Plant circadian clocks increase photosynthesis, growth, survival, and competitive advantage. Science 309: 630–633.
  50. 50. Somerville CR, Ogren WL (1980) Photorespiration mutants of Arabidopsis thaliana deficient in serine-glyoxylate aminotransferase activity. Proc Natl Acad Sci USA 77: 2684–2687.
  51. 51. Somerville CR, Ogren WL (1981) Photorespiration-deficient mutants of Arabidopsis thaliana lacking mitochondrial serine transhydroxymethylase activity. Plant Physiol 67: 666–671.
  52. 52. Kofler H, Häusler RE, Schulz B, Groner F, Flügge UI, et al. (2000) Molecular characterisation of a new mutant allele of the plastid phosphoglucomutase in Arabidopsis, and complementation of the mutant with the wild-type cDNA. Mol Gen Genet 263: 978–986.
  53. 53. Bläsing OE, Gibon Y, Gunther M, Hohne M, Morcuende R, et al. (2005) Sugars and circadian regulation make major contributions to the global regulation of diurnal gene expression in Arabidopsis. Plant Cell 17: 3257–3281.
  54. 54. Kleczkowski LA (1994) Inhibitors of photosynthetic enzymes/carriers and metabolism. Ann Rev Plant Physiol 45: 339–367.
  55. 55. Anderson LE (1971) Chloroplast and cytoplasmic enzymes. 2. Pea leaf triose phosphate isomerases. Biochim Biophys Acta 235: 237–244.
  56. 56. Johnson LN, Wolfenden R (1970) Changes in absorption spectrum and crystal structure of triose phosphate isomerase brought about by 2-phosphoglycollate, a potential transition state analogue. J Mol Biol 47: 93–100.
  57. 57. Kelly GJ, Latzko E (1976) Inhibition of spinach-leaf phosphofructokinase by 2-phosphoglycollate. FEBS Lett 68: 55–58.
  58. 58. Engel N, Ewald R, Gupta KJ, Zrenner R, Hagemann M, et al. (2011) The presequence of Arabidopsis serine hydroxymethyltransferase SHM2 selectively prevents import into mesophyll mitochondria. Plant Physiol 157: 1711–1720.
  59. 59. Barak S, Nejidat A, Heimer Y, Volokita M (2001) Transcriptional and posttranscriptional regulation of the glycolate oxidase gene in tobacco seedlings. Plant Mol Biol 45: 399–407.
  60. 60. Potters G, De Gara L, Asard H, Horemans N (2002) Ascorbate and glutathione: guardians of the cell cycle, partners in crime? Plant Physiol Biochem 40: 537–548.
  61. 61. Foyer CH, Noctor G (2011) Ascorbate and glutathione: The heart of the redox hub. Plant Physiol 155: 2–18.
  62. 62. Novitskaya L, Trevanion SJ, Driscoll S, Foyer CH, Noctor G (2002) How does photorespiration modulate leaf amino acid contents? A dual approach through modelling and metabolite analysis. Plant Cell Environ 25: 821–835.
  63. 63. Cousins AB, Pracharoenwattana I, Zhou W, Smith SM, Badger MR (2008) Peroxisomal malate dehydrogenase is not essential for photorespiration in Arabidopsis but its absence causes an increase in the stoichiometry of photorespiratory CO2 release. Plant Physiol 148: 786–795.
  64. 64. Reumann S, Weber AP (2006) Plant peroxisomes respire in the light: Some gaps of the photorespiratory C2 cycle have become filled - others remain. Biochim Biophys Acta 1763: 1496–1510.
  65. 65. Douce R, Neuburger M (1989) The uniqueness of plant mitochondria. Ann Rev Plant Physiol 40: 371–414.
  66. 66. Dutilleul C, Driscoll S, Cornic G, De Paepe R, Foyer CH, et al. (2003) Functional mitochondrial complex I is required by tobacco leaves for optimal photosynthetic performance in photorespiratory conditions and during transients. Plant Physiol 131: 264–275.
  67. 67. Bykova NV, Keerberg O, Pärnik T, Bauwe H, Gardeström P (2005) Interaction between photorespiration and respiration in transgenic potato plants with antisense reduction in glycine decarboxylase. Planta 222: 130–140.
  68. 68. Araujo WL, Tohge T, Ishizaki K, Leaver CJ, Fernie AR (2011) Protein degradation - an alternative respiratory substrate for stressed plants. Trends Plant Sci 16: 489–498.
  69. 69. Fernie AR, Martinoia E (2009) Malate. Jack of all trades or master of a few? Phytochemistry 70: 828–832.
  70. 70. Fait A, Fromm H, Walter D, Galili G, Fernie AR (2008) Highway or byway: the metabolic role of the GABA shunt in plants. Trends Plant Sci 13: 14–19.
  71. 71. Munoz-Bertomeu J, Cascales-Minana B, Mulet JM, Baroja-Fernandez E, Pozueta-Romero J, et al. (2009) Plastidial glyceraldehyde-3-phosphate dehydrogenase deficiency leads to altered root development and affects the sugar and amino acid balance in Arabidopsis. Plant Physiol 151: 541–558.
  72. 72. Ho CL, Saito K (2001) Molecular biology of the plastidic phosphorylated serine biosynthetic pathway in Arabidopsis thaliana. Amino Acids 20: 243–259.
  73. 73. Schreiber U, Schliwa U, Bilger W (1986) Continuous recording of photochemical and nonphotochemical chlorophyll fluorescence quenching with a new type of modulation fluorometer. Photosynth Res 10: 51–62.
  74. 74. Fahnenstich H, Scarpeci TE, Valle EM, Flügge UI, Maurino VG (2008) Generation of H2O2 in chloroplasts of Arabidopsis thaliana overexpressing glycolate oxidase as an inducible system to study oxidative stress. Plant Physiol 148: 729.
  75. 75. Jones MGK, Outlaw WH, Lowry OH (1977) Enzymic assay of 10−7 to 10−14 moles of sucrose in plant tissues. Plant Physiol 60: 379–383.
  76. 76. Lisec J, Schauer N, Kopka J, Willmitzer L, Fernie AR (2006) Gas chromatography mass spectrometry-based metabolite profiling in plants. Nat Protoc 1: 387–396.