Dissecting Long-Term Adjustments of Photoprotective and Photo-Oxidative Stress Acclimation Occurring in Dynamic Light Environments
- 1IBG-2: Plant Sciences, Institute of Bio- and Geosciences, Forschungszentrum Jülich, Jülich, Germany
- 2iGRAD-Plant, Heinrich-Heine-Universität, Düsseldorf, Germany
- 3Institute of Developmental and Molecular Biology of Plants, Plant Molecular Physiology and Biotechnology Group, Heinrich-Heine-Universität and Cluster of Excellence on Plant Sciences, Düsseldorf, Germany
Changes in light intensity directly affect the performance of the photosynthetic apparatus. Light energy absorbed in excess of cells’ needs leads to production of reactive oxygen species and photo-oxidative damage. Excess light in both constant and dynamic environments induces photoprotective acclimation in plants. Distinct sets of signals and regulatory mechanisms are involved in acclimatory adjustment of photoprotection and photosynthesis under constant and dynamic (fluctuating) light conditions. We are still far away from drawing a comprehensive picture of acclimatory signal transduction pathways, particularly in dynamic environments. In this perspective article, we propose the use of Arabidopsis plants that produce H2O2 in chloroplasts (GO plants) under atmospheric CO2 levels as a tool to study the mechanisms of long-term acclimation to photo-oxidative stress. In our opinion there are new avenues to future investigations on acclimatory adjustments and signal transduction occurring in plants under dynamic light environments.
Acclimation to Photo-Oxidative Stress is Induced By Fluctuating Light
Rapid climate changes and transformation of landscapes by extensive agricultural practices impose environmental perturbations. Plants in the affected areas respond to the perturbations through acclimation (within generation) or adaptation (over generations). Light intensity can vary rapidly by a few orders of magnitude as clouds travel in the sky or wind moves outer canopy leaves and taller plants. Especially, wind can briefly expose inner canopy leaves and understory plants to intense sunlight. Upon large and abrupt increase in light intensity, photosynthetic light energy utilization is limited biochemically. This is attributed to low availability of the Calvin-Benson cycle intermediates, low activation state of Ribulose-1,5-bisphosphate carboxylase/oxygenase (RubisCO), and also low stomatal conductance measured in leaves under low light (LL) conditions (Kirschbaum and Pearcy, 1988; Pearcy, 1990).
When light energy is absorbed by photosynthetic pigments in excess of cells’ needs for reducing equivalents and chemical energy (excess light, EL), it can lead to production of reactive oxygen species (ROS) and photo-oxidative damage in oxygenic photosynthetic organisms. A range of mechanisms have evolved to reduce uncontrolled production of ROS and to protect the photosynthetic apparatus against their detrimental effects (Foyer and Noctor, 2000; Endo and Asada, 2008; Li et al., 2009). These include thermal energy dissipation which is rapidly induced in light-harvesting antenna complexes by a proton concentration gradient (ΔpH) across the thylakoid membrane (termed qE), alternative sinks for excess electrons (e.g., water-water cycle and cyclic electron flows around photosystem I, CEF) which contribute to ΔpH formation especially when liner electron transport rate (ETR) is low, and enzymatic and non-enzymatic antioxidative systems which detoxify ROS (Figure 1A).
FIGURE 1. General mechanisms of photoprotection (highlighted in red) occurring in chloroplasts of wild type (WT) (A) and the GO plants (B). Three mechanisms represented are (i) qE, the thermal energy dissipation of excess absorbed light at the light harvesting complex (LHC) of Photosystem II (PSII); (ii) CEF, the cyclic electron flow around Photosystem I (PSI), and (iii) enzymatic and non-enzymatic ROS scavenging through production of O2, H2O2 and H2O. These mechanisms operate both in FL and CL; the only difference demonstrated so far is a more dramatic effect of CEF in FL than in CL. Shown in or around the thylakoid membrane are the components of photosynthetic electron transport chain: plastoquinone (PQ), cytochrome b6f complex (Cytb6f), plastocyanin (PC), and ferredoxin (Fd). In addition, the activities of RubisCO as carboxylase and oxygenase in light and under ambient CO2 and O2 conditions are shown. In the WT, the 2-phosphoglycolate (2-PG) produced initiates the photorespiratory cycle (PR; not shown in detail in the figure; for details see (Maurino and Peterhansel, 2010)). In the GO plants, 2-PG is delivered to the PR and the glycolate produced in the chloroplasts is also used by glycolate oxidase (GO) generating H2O2. 3-PGA, 3-phosphoglycerate; PGLP: 2-phosphoglycolate phosphatase; RubP, ribulose 1-5,bisphosphate.
When EL conditions persist, plants are able to augment their photoprotective capacities via long-term acclimation. In general, multiple mechanisms of photoprotective acclimation (Figure 1A) operate in plants under constant as well as dynamic EL environments. In particular, fluctuating light (FL) with short periods of EL (i.e., dynamic EL) induces, primarily or initially, long-term acclimatory changes that are characterized by improved protection against photo-oxidative stress and reduced carbon gain (Alter et al., 2012). For instance, LL-grown Arabidopsis plants upregulate photoprotection in highly dynamic EL conditions without developing symptoms of severe photo-oxidative injuries, such as strong photoinhibition or bleaching (Alter et al., 2012). Similar photoprotective responses are also seen during acclimation to high light (HL, i.e., constant EL), although in HL they are often accompanied by enhancement of photosynthesis and thus increased carbon gain (Leakey et al., 2002; Alter et al., 2012). There seems to be an inverse relationship between the maximum photosynthetic capacity, which is developed through photosynthetic acclimation, and the frequency of LL-HL transitions (Retkute et al., 2015). Selective upregulation of photoprotection, but not photosynthesis, in highly dynamic FL suggests that distinct sets of signals and regulatory mechanisms are involved in acclimatory adjustment of photoprotection and photosynthesis, and that signal molecules, which trigger photo-oxidative stress acclimation, are produced in leaves under the FL conditions. In this article we use the term “FL” to refer to highly dynamic EL conditions, while we are aware that FL may not always cause EL and photo-oxidative stress, depending on the amplitude and frequency of light fluctuations (Yin and Johnson, 2000; Alter et al., 2012; Retkute et al., 2015).
Chloroplast Retrograde Signaling is Involved in Photo-Oxidative Stress Acclimation
Today it is widely recognized that ROS not only can damage cellular components but also act as signals to induce abiotic and biotic stress responses (Foyer and Noctor, 2000; Apel and Hirt, 2004; Mittler et al., 2011; Karpinski et al., 2013; Dietz et al., 2016). Multiple ROS can be generated in chloroplasts under photo-oxidative stress, such as singlet oxygen (1O2), superoxide anion radical (), hydroxyl radical (OH), and hydrogen peroxide (H2O2) (Asada, 1999; Foyer and Noctor, 2000). Among these, H2O2 alone would be able to diffuse into the cytosol because high reactivity and charge of the other species prevent them from diffusing a long distance across chloroplast envelopes. Intracellular H2O2 signaling engages both compartment-specific and non-specific pathways. In the case of retrograde signaling, chloroplastic H2O2 produced by ectopic overexpression of glycolate oxidase (GO) in chloroplasts (Fahnenstich et al., 2008) (Figure 1B) induces transcriptional changes in the nucleus, which partly, but not fully, overlap with the responses to peroxisomal H2O2 (Balazadeh et al., 2012; Sewelam et al., 2014).
Though 1O2 may not move far, it can give rise to secondary messengers by reacting with nearby molecules such as β-carotene (Ramel et al., 2013). Oxidation of β-carotene produces β-cyclocitral, a reactive electrophile species that can modify transcription of 1O2-responsive genes in the nucleus (Havaux, 2014). Whilst some β-carotenes are continuously oxidized and degraded in thylakoids during illumination with or without EL (Beisel et al., 2010), elevated production of 1O2 and thus β-cyclocitral under photo-oxidative stress may trigger acclimatory responses that are distinct from 1O2-induced cell death (op den Camp et al., 2003).
The number as well as the variety of agents implicated in chloroplast retrograde signaling have been increasing in the last years. For example, the redox state of the plastoquinone pool, different metabolites (e.g., tetrapyrroles, phosphoadenosine phosphate, and methylerythritol cyclodiphosphate) and hormones (abscisic acid, salicylic acid, and jasmonic acid) are regarded as such signaling agents to trigger long-term acclimatory adjustments (Dietz and Pfannschmidt, 2011; Sun et al., 2011; Estavillo et al., 2012; Xiao et al., 2012; Barajas-Lopez Jde et al., 2013; Karpinski et al., 2013; Dietz, 2015; Laloi and Havaux, 2015). To reconstruct signaling networks from individual components and pathways is a major challenge in understanding time-dependent regulation and interaction of stress response networks in plants (Dietz, 2015). Acclimation to photo-oxidative stress has been studied extensively in the context of HL or constant EL acclimation, in which plants manifest parallel enhancement of photoprotection and photosynthesis alongside other responses related to temperature and/or water stress. Highly dynamic FL, which predominantly elicits photoprotective responses (Alter et al., 2012), offers a complementary approach to investigate signals and pathways that are primarily engaged in photo-oxidative stress acclimation.
Arabidopsis Plants that Produce H2O2 in Chloroplasts are a Model to Study Photo-Oxidative Stress Acclimation and Signaling
Arabidopsis plants, in which GO is targeted to chloroplasts, generate H2O2 in chloroplasts under ambient CO2 concentrations (photorespiratory conditions) (Fahnenstich et al., 2008; Strand et al., 2015). Because the GO reaction depends on the substrate provided by the oxygenase activity of RubisCO in the light (Figure 1B), the level of GO-dependent H2O2 production can be controlled by changing the growth conditions. When growing in LL (75 μmol photons m-2 s-1) and ambient CO2 concentration (380 ppm), the GO plants are smaller than the wild-type (WT) plants and present patchy pale-green leaf lamina (Figure 2A; constant light, CL) as a result of H2O2 production in chloroplasts and overload of the antioxidant machinery (Fahnenstich et al., 2008). Under HL the GO plants develop severe oxidative lesions and ultimately bleach, whereas combinations of very LL (30 μmol photons m-2 s-1) and ambient CO2 or LL and high CO2 (4,000 ppm) allow them to grow like WT (Fahnenstich et al., 2008; Balazadeh et al., 2012; Sewelam et al., 2014). Also, they become as big and green as WT and recover the WT level of photosynthetic ETR in LL when transferred from ambient to high CO2 conditions (Fahnenstich et al., 2008). These features make the GO plants a unique, well-established model to study the action of H2O2 in chloroplast retrograde signaling (Balazadeh et al., 2012; Sewelam et al., 2014).
FIGURE 2. Phenotypes of wild-type (WT) and GO plants grown under fluctuating light (FL) and constant light (CL) conditions in ambient CO2. (A) Under FL (switching between ∼50 μmol photons m-2 s-1 for 280 s and ∼1000 μmol photons m-2 s-1 for 20 s) the GO plants have normal green leaves, while under CL (∼75 μmol photons m-2 s-1) they develop pale-green patches due to the chloroplastic production of H2O2. The pictures were taken after 8-days exposure to FL or CL. (B) The FL condition reduces leaf growth of the WT plants (left y-axis). The GO plants (right y-axis) are much smaller than the WT and the exposure to FL does not impair growth in the GO plants compared to the CL condition. Projected leaf area is the leaf area that is visible in a 2D top-view image. Solid and broken lines show exponential regression for the CL and FL data sets, respectively. The R2 values of the fitting are: 0.996 (WT CL), 0.991 (WT FL), 0.997 (GO CL), and 0.999 (GO FL). Relative growth rates (% d-1) obtained by the regression are: 22.1 ± 0.6 (WT CL), 18.7 ± 0.8 (WT FL), 25.7 ± 0.7 (GO CL), and 25.4 ± 0.3 (GO FL). The difference in relative growth rate between CL and FL is significant for the WT (P = 0.002). n = 16 (WT) and 9 (GO).
Interestingly, FL conditions applied to the GO plants growing in ambient CO2 —in spite of (or maybe because of) the effect of FL to impose photo-oxidative stress— provoke disappearance of the characteristic patchy pale-green phenotype of these plants (Figure 2A). This reversion to normal green leaf lamina under FL allows the GO plants to maintain similar relative growth rates in CL and FL, whereas WT exhibits growth reduction in FL (Figure 2B). The FL-induced recovery of leaf color in the GO plants is most probably due to upregulation of H2O2 scavenging in the chloroplast, as the patchy pale-green phenotype is a consequence of H2O2 accumulation (Fahnenstich et al., 2008). This assumption, i.e., FL-induced acclimatory enhancement of ROS (H2O2) scavenging systems in the GO plants, is supported by the observations made in carotenogenic mutants of Arabidopsis; despite having reduced capacities for qE and carotenoid-dependent ROS (mainly 1O2) scavenging, these mutants do not suffer from chronic photo-oxidative damage under FL conditions because they can upregulate other photoprotective and ROS scavenging mechanisms by long-term acclimation (Caliandro et al., 2013). The increased activity of superoxide dismutase (SOD) found in leaves of WT following FL acclimation (Alter et al., 2012) also points to an increased detoxification capacity for H2O2 which arises from disproportionation of catalyzed by SOD.
Thus, we hypothesize that long-term acclimatory upregulation of H2O2 scavenging occurs in chloroplasts under FL conditions. H2O2 reduction in chloroplasts could proceed mainly via peroxidase systems, including glutathione peroxidase (Gpx) and peroxiredoxin (Prx) in the stroma, as well as thylakoid-bound and stromal ascorbate peroxidase (tAPX, sAPX) coupled to monodehydroascorbate reductase (MDHAR) and also dehydroascorbate reductase (DHAR) (Foyer and Noctor, 2011). Gpx and Prx use thiol-based peroxide-detoxification mechanisms that are maintained by glutathione and glutathione reductase (GR) (Dietz and Pfannschmidt, 2011). Regeneration of ascorbate by DHAR is also dependent on glutathione and GR, while MDHAR uses NAD(P)H to regenerate ascorbate. In addition to the removal of H2O2, other photoprotective mechanisms such as CEF and carotenoid-dependent reactions could also contribute to the rescuing of the GO phenotype in FL by keeping the level of ROS production under control (Figure 1). Indeed, CEF is activated by chloroplastic H2O2 produced in HL (Strand et al., 2015) and carotenoid contents (especially xanthophyll-cycle pigments) increase in leaves exposed to FL (Alter et al., 2012; Caliandro et al., 2013).
So far it is not known whether, and if yes, which H2O2 scavenging pathways are upregulated in chloroplasts during FL acclimation. This could be studied by analyzing antioxidant defense systems in the GO plants during acclimation to CL and FL conditions. An important question that can then be tackled is the long-term acclimation of H2O2 scavenging systems. Signal agents, which are generated in FL conditions and lead to acclimatory enhancement of H2O2 scavenging, must be different from the signals induced by chloroplastic H2O2 produced in the GO plants under CL and ambient CO2 levels. Close inspections of the GO plants during FL acclimation at different response levels —from gene expression, protein and metabolite accumulation to physiological phenotype— could shed light on components and signal agents involved in upregulation of H2O2 scavenging under photo-oxidative stress. Once candidate molecules are identified, the unique feature of the GO plants, which visualizes acclimatory changes in H2O2 metabolism under FL, can be exploited again as the genetic background to assess the efficacy of those molecules in upregulating H2O2 detoxification. The nature of chloroplast retrograde signaling in FL (dynamic EL), as compared with that in HL (constant EL), inspires further experiments and investigations.
SM and VM contributed equally to writing the manuscript. TS performed the growth analysis shown in Figure 2.
This work was supported by the Deutsche Forschungsgemeinschaft.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Alter, P., Dreissen, A., Luo, F. L., and Matsubara, S. (2012). Acclimatory responses of Arabidopsis to fluctuating light environment: comparison of different sunfleck regimes and accessions. Photosynth. Res. 113, 221–237. doi: 10.1007/s11120-012-9757-2
Asada, K. (1999). The water-water cycle in chloroplasts: scavenging of active oxygens and dissipation of excess photons. Annu. Rev. Plant Physiol. Plant Mol. Biol. 50, 601–639. doi: 10.1146/annurev.arplant.50.1.601
Balazadeh, S., Jaspert, N., Arif, M., Mueller-Roeber, B., and Maurino, V. G. (2012). Expression of ROS-responsive genes and transcription factors after metabolic formation of H2O2 in chloroplasts. Front. Plant Sci. 3:234. doi: 10.3389/fpls.2012.00234
Barajas-Lopez Jde, D., Blanco, N. E., and Strand, A. (2013). Plastid-to-nucleus communication, signals controlling the running of the plant cell. Biochim. Biophys. Acta 1833, 425–437. doi: 10.1016/j.bbamcr.2012.06.020
Beisel, K. G., Jahnke, S., Hofmann, D., Koppchen, S., Schurr, U., and Matsubara, S. (2010). Continuous turnover of carotenes and chlorophyll a in mature leaves of Arabidopsis revealed by 14CO2 pulse-chase labeling. Plant Physiol. 152, 2188–2199. doi: 10.1104/pp.109.151647
Caliandro, R., Nagel, K. A., Kastenholz, B., Bassi, R., Li, Z., Niyogi, K. K., et al. (2013). Effects of altered alpha- and beta-branch carotenoid biosynthesis on photoprotection and whole-plant acclimation of Arabidopsis to photo-oxidative stress. Plant Cell Environ. 36, 438–453. doi: 10.1111/j.1365-3040.2012.02586.x
Dietz, K. J., Turkan, I., and Krieger-Liszkay, A. (2016). Redox- and reactive oxygen species-dependent signaling into and out of the photosynthesizing chloroplast. Plant Physiol. 171, 1541–1550. doi: 10.1104/pp.16.00375
Endo, T., and Asada, K. (2008). “Photosystem I and photoprotection: cycling electron flow and water-water cycle,” in Photoprotection, Photoinhibition, Gene Regulation, and Environment, eds B. Demmig-Adams, W. W. Adams, and A. K. Wattoo (Berlin: Springer), 205–211.
Estavillo, G. M., Chan, K. X., Phua, S. Y., and Pogson, B. J. (2012). Reconsidering the nature and mode of action of metabolite retrograde signals from the chloroplast. Front. Plant Sci. 3:300. doi: 10.3389/fpls.2012.00300
Fahnenstich, H., Scarpeci, T. E., Valle, E. M., Flugge, U. I., and Maurino, V. G. (2008). Generation of hydrogen peroxide in chloroplasts of Arabidopsis overexpressing glycolate oxidase as an inducible system to study oxidative stress. Plant Physiol. 148, 719–729. doi: 10.1104/pp.108.126789
Karpinski, S., Szechynska-Hebda, M., Wituszynska, W., and Burdiak, P. (2013). Light acclimation, retrograde signalling, cell death and immune defences in plants. Plant Cell Environ. 36, 736–744. doi: 10.1111/pce.12018
Kirschbaum, M. U., and Pearcy, R. W. (1988). Gas exchange analysis of the relative importance of stomatal and biochemical factors in photosynthetic induction in Alocasia macrorrhiza. Plant Physiol. 86, 782–785. doi: 10.1104/pp.86.3.782
Leakey, A. D. B., Press, M. C., Scholes, J. D., and Watling, J. R. (2002). Relative enhancement of photosynthesis and growth at elevated CO2 is greater under sunflecks than uniform irradiance in a tropical rain forest tree seedling. Plant Cell Environ. 25, 1701–1714. doi: 10.1046/j.1365-3040.2002.00944.x
op den Camp, R. G., Przybyla, D., Ochsenbein, C., Laloi, C., Kim, C., Danon, A., et al. (2003). Rapid induction of distinct stress responses after the release of singlet oxygen in Arabidopsis. Plant Cell 15, 2320–2332. doi: 10.1105/tpc.014662
Retkute, R., Smith-Unna, S. E., Smith, R. W., Burgess, A. J., Jensen, O. E., Johnson, G. N., et al. (2015). Exploiting heterogeneous environments: does photosynthetic acclimation optimize carbon gain in fluctuating light? J. Exp. Bot. 66, 2437–2447. doi: 10.1093/jxb/erv055
Sewelam, N., Jaspert, N., Van der Kelen, K., Tognetti, V. B., Schmitz, J., Frerigmann, H., et al. (2014). Spatial H2O2 signaling specificity: H2O2 from chloroplasts and peroxisomes modulates the plant transcriptome differentially. Mol. Plant 7, 1191–1210. doi: 10.1093/mp/ssu070
Strand, D. D., Livingston, A. K., Satoh-Cruz, M., Froehlich, J. E., Maurino, V. G., and Kramer, D. M. (2015). Activation of cyclic electron flow by hydrogen peroxide in vivo. Proc. Natl. Acad. Sci. U.S.A. 112, 5539–5544. doi: 10.1073/pnas.1418223112
Sun, X., Feng, P., Xu, X., Guo, H., Ma, J., Chi, W., et al. (2011). A chloroplast envelope-bound PHD transcription factor mediates chloroplast signals to the nucleus. Nat. Commun. 2:477. doi: 10.1038/ncomms1486
Xiao, Y., Savchenko, T., Baidoo, E. E., Chehab, W. E., Hayden, D. M., Tolstikov, V., et al. (2012). Retrograde signaling by the plastidial metabolite MEcPP regulates expression of nuclear stress-response genes. Cell 149, 1525–1535. doi: 10.1016/j.cell.2012.04.038
Keywords: acclimation, fluctuating light, photoprotection, reactive oxygen species, retrograde signaling
Citation: Matsubara S, Schneider T and Maurino VG (2016) Dissecting Long-Term Adjustments of Photoprotective and Photo-Oxidative Stress Acclimation Occurring in Dynamic Light Environments. Front. Plant Sci. 7:1690. doi: 10.3389/fpls.2016.01690
Received: 12 July 2016; Accepted: 26 October 2016;
Published: 09 November 2016.
Edited by:Massimiliano Tattini, National Research Council, Italy
Reviewed by:Or Sperling, Agricultural Research Organization, Volcani Center, Israel
Lucia Guidi, Università di Pisa, Italy
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*Correspondence: Veronica G. Maurino, email@example.com