Chloroplast thioredoxin systems: prospects for improving photosynthesis.

Thioredoxins (TRXs) are protein oxidoreductases that control the structure and function of cellular proteins by cleavage of a disulphide bond between the side chains of two cysteine residues. Oxidized thioredoxins are reactivated by thioredoxin reductases (TR) and a TR-dependent reduction of TRXs is called a thioredoxin system. Thiol-based redox regulation is an especially important mechanism to control chloroplast proteins involved in biogenesis, in regulation of light harvesting and distribution of light energy between photosystems, in photosynthetic carbon fixation and other biosynthetic pathways, and in stress responses of plants. Of the two plant plastid thioredoxin systems, the ferredoxin-dependent system relays reducing equivalents from photosystem I via ferredoxin and ferredoxin-thioredoxin reductase (FTR) to chloroplast proteins, while NADPH-dependent thioredoxin reductase (NTRC) forms a complete thioredoxin system including both reductase and thioredoxin domains in a single polypeptide. Chloroplast thioredoxins transmit environmental light signals to biochemical reactions, which allows fine tuning of photosynthetic processes in response to changing environmental conditions. In this paper we focus on the recent reports on specificity and networking of chloroplast thioredoxin systems and evaluate the prospect of improving photosynthetic performance by modifying the activity of thiol regulators in plants.This article is part of the themed issue 'Enhancing photosynthesis in crop plants: targets for improvement'.

Introduction

Photosynthesis comprises light-driven reactions in thylakoid membranes producing NADPH and ATP, and a CO2 fixation pathway storing the energy captured by light reactions into sugar phosphates. Photosynthesis end products are used to energize cell metabolism and to promote plant growth. In Nature, light intensity is constantly changing in plant growth habitats, including both seasonal alteration of daily light period and daily fluctuation of light intensity due to cloudiness and other environmental factors. Optimization of photosynthetic production under fluctuating light conditions needs strict balancing of the absorption of light energy by the photosynthetic machinery with the energy-consuming reactions of chloroplast metabolism. Photosynthetic reactions are also linked with the protective machinery that eliminates or prevents the generation of harmful reactive oxygen species (ROS). The regulatory mechanisms to balance light capture, consumption of light energy and inductive protective machinery include non-photochemical quenching (NPQ), photosynthetic control of electron flow between photosystem II (PSII) and photosystem I (PSI), state transitions, cyclic electron flow, light activation of photosynthetic enzymes both in light reactions and carbon fixation, and induction of antioxidant systems. Recently, the regulatory proteins called thioredoxins (TRXs) have been suggested to control a number of the mechanisms balancing photosynthetic reactions in chloroplasts.

TRXs are protein oxidoreductases with a redox active dithiol/disulphide motif in the active site. In the reduced state they alter the thiol-redox status of cellular proteins by reducing a disulphide bond in target proteins via a bimolecular nucleophilic substitution reaction. TRXs that become oxidized in the reaction are reactivated by thioredoxin reductases (TR). TR together with TRX form a thioredoxin system. Thioredoxin systems in plants are versatile including two TRs, one dependent on ferredoxin (FTR) and the other on NADPH (NTR) as reducing power, respectively, and multiple types of TRXs (h, o, f, m, x, y, z, and several thioredoxin-like proteins) (reviewed in [1-5]). A high number of TRXs are localized to plant chloroplasts; this underlines the impact of redox-regulation of chloroplast proteins. The ferredoxin-TRX system has been directly linked with plant production since it was originally shown to activate the enzymes of the Calvin–Benson cycle in algal and plant plastids upon illumination (see [5]). The discovery of the chloroplast NADPH-dependent thioredoxin system (NTRC) [6] and novel TRX types [7] has indicated that in addition to light, chloroplast TRX systems also control chloroplast development, respond to fluctuations in light intensity, transfer signals between chloroplast compartments and are involved in antioxidant networks (reviewed in [2-4,8-10]). Another intriguing issue is that some chloroplast proteins are targets of several TRXs. For example, NTRC, TRXf, and TRXm interact with the same biosynthetic enzymes, and the antioxidative system based on peroxiredoxins is maintained by TRXx, y, and NTRC [11-17]. The diversity and partial redundancy of chloroplast TRX systems may enable a rapid response of chloroplast metabolism to ever changing environmental conditions, raising plant fitness under natural growth conditions.

Here, we review the prospect of improving photosynthetic performance by modifying the activity of chloroplast TRX systems based on the recent reports on the interaction, networking and overlapping functions of TRXs.

Chloroplast thioredoxin systems

Comprehensive reviews on chloroplast TRX systems have been recently published [1-5,10]; hence only an overview is presented here. Chloroplast TRXs are activated by two TRs, FTR and NTRC. The former uses photoreduced ferredoxin and the latter NADPH to activate the TRXs. FTR is a heterodimeric iron-sulphur protein consisting of a catalytic and a variable subunit encoded by a single copy and two genes in Arabidopsis, respectively [18-20]. FTR has a binding site both for ferredoxin and TRX. A single nuclear gene of Arabidopsis encodes the NTRC enzyme that has an atypical structure consisting of a NADPH-dependent TR domain (NTR) fused to a TRX domain [12]. Thus the NTRC polypeptide forms a complete NADPH-dependent TRX system in the chloroplast. In photosynthetic cells the FTR-dependent system is active in light when PSI reduces ferredoxin, whereas the NTRC-dependent TRX system is active both in light and dark conditions because of the production of NADPH by the oxidative pentose phosphate pathway in darkness.

Five types of low-molecular weight TRXs (f, m, y, x, z) are localized to the chloroplast, of which TRXf, TRXm and TRXy are present as two, four and two isoforms, respectively [7,21]. CDSP32, six ACHT-type and two WCRKC-type proteins belong to the chloroplast TRX-like proteins having an atypical redox-active motif in the active site of the regulatory protein [7,21]. In addition to the soluble TRXs, chloroplasts contain thylakoid-bound TRX-like proteins, which control the redox status of thylakoid and lumenal proteins. Internal thylakoid protein CcdA mediates redox equivalents from stromal TRXs to the TRX-like transmembrane protein HCF164 that has a redox-active site in the lumenal side of the thylakoid membrane [8]. HCF164 has been suggested to regulate the redox status of lumenal proteins [8,10]. Suppressor of quenching (SOQ1) and lumen thiol oxidoreductase 1 (LTO1) are other thylakoid TRX-like proteins with a redox-active motif in the lumenal side of thylakoids [22,23]. Additionally several uncharacterized TRX-like proteins with unknown function are predicted to be localized to thylakoid membranes.

The amount of TRXs, like the regulatory proteins in general, is low in chloroplasts. The amount of the substrates of TRXs (e.g. the redox-activated enzymes in the Calvin–Benson cycle, 2-Cys peroxiredoxins) has been estimated to be 10–100 times higher than the amount of TRXs in chloroplast [24,25]. Belin et al. [21] have analysed the relative expression level of the genes encoding TRXs and TRs in different Arabidopsis organs. Among the chloroplast TRX genes the expression of TRXm1, 2, 4 isoforms, CDSP32 and TRXf1 isoform was highest in photosynthetic tissues, followed by TRXx and TRXy2. The expression of the other chloroplast TRX genes was modest or low in photosynthetic tissues, or occurred at a specific developmental stage like ACHT4 in senescing leaves [21]. The expression level of the genes encoding the TR was 2–4 times lower than the level of highly-expressed chloroplast TRXs, FTR being more expressed than NTRC [21]. The transcript levels of TRXs correlates with the content of proteins in leaf tissues, TRXm1, 2, 4 isoforms being the most abundant followed by CDSP32 [24,25]. The amount of TRXf1 protein has been reported to be slightly lower [24,25] or higher [16] than TRXm isoforms. NTRC protein almost equals the content of abundant chloroplast TRXs in photosynthetic cells [25], whereas to our knowledge the abundance of FTR protein has not been reported.

Thioredoxin networks in chloroplast

Purified and recombinant TRX and TR proteins, TRX-affinity chromatography, the yeast-2-hybrid test (Y2H), bimolecular fluorescence complementation (BiFC) assays together with knockout mutants and overexpression lines have been used to investigate which TR mediates the reducing power of chloroplast TRXs. Originally Buchanan et al. reported the reduction of TRXf and -m isoforms by the light-activated FTR system (see the history of the chloroplast TRX system in [5]) and this discovery has been confirmed by several in vitro and in vivo tests [17,26,27]. FTR can also reduce TRXy and x isoforms in vitro [26], whereas contradictory observations have been published about the reductant for TRXz. Bohrer et al. [26] reported the inability of FTR and NTRC to reduce TRXz but that the reduced TRXf, m, x and y isoforms were able to activate TRXz. In contrast, Yoshida & Hisabori [27] reported that NTRC is a primary reductant of TRXz in vitro, while BiFC tests failed to show interactions between NTRC and TRXz [17].

Upon the discovery of NTRC [6] it was presumed that NTRC forms an independent TRX system functionally separated from the FTR system. Recently, however, we reported that transgenic Arabidopsis lines overexpressing a mutated NTRC with either an inactivated NTR or TRX domain in ntrc mutant background, showed partial recovery of the ntrc phenotype, suggesting interaction between the NTRC and FTR systems [28]. Subsequent BiFC assays indeed showed that NTRC can interact with several soluble TRXs (f1, m1 and m3, y1 and x) in vivo in the chloroplast [17]. Furthermore, the content of reduced TRXf form was significantly higher under all studied light intensities in transgenic lines overexpressing wild-type NTRC (OE-NTRC) and under low light in transgenic lines with an inactive TRX domain of NTRC [17], indicating that NTRC is capable of transferring reducing equivalents to TRXf in vivo. Our observation contradicts in vitro assays of electron donation between NTRC and TRXs [26,27]. The midpoint redox potential (Em,7.0) of NTRC was reported to be too high (−274 mV) [27] for it to reduce TRXf, m, x and y isoforms (Em,7.0 between −290 and −320 mV in [13]). Nevertheless, it has been undeniably shown that NTRC is a primary reductant for chloroplast 2-Cys peroxiredoxins (2-Cys-PRX) [12,29], although a low midpoint redox potential of −315 mV has been measured for 2-Cys-PRXs [30,31].

All the techniques used to investigate the interactions between the components of TRX systems are prone to false interpretation. In vitro conditions do not always correspond to in vivo circumstances. Purified TRXs and NTRC have a tendency to form oligomeric aggregates [32-34] that may affect the content of functional protein in in vitro assays. In BiFC assays, the tested proteins are overexpressed, which may facilitate the interactions and result in false positives. Nevertheless, the recently reported double mutants of the TRX systems support the idea that FTR and NTRC systems form a functional overlapping redox network that allows the chloroplast metabolism to flexibly respond to environmental changes in the growth habitat. The TRXf isoforms have been regarded as primary activators of redox-regulated enzymes in the Calvin–Benson cycle, but knockout of both genes encoding the two isoforms did not compromise the growth of Arabidopsis, and activation of the enzymes of the Calvin–Benson cycle in the light was only slightly impaired [16,35]. Knockout of NTRC, however, significantly compromised the development, photosynthetic activity and growth of Arabidopsis leaves [12,36], but the phenotype of the ntrc trxf1 double mutant was even more drastically affected [15], suggesting that NTRC and TRXf are involved in the regulation of the same chloroplast reactions. They either function independently in parallel or sequentially by reduction of TRXf by both FTR and NTRC [17] (figure 1).

Figure 1.

Proposed model for regulation of photosynthesis and stress reactions by the chloroplast thioredoxin network. Light activates the FTR-dependent TRX system, while NTRC can be activated both by light and by NADPH produced in the oxidative pentose phosphate pathway (OPPP). NTRC, TRXf and to a lesser extent TRXm are involved in the activation of enzymes in biosynthetic pathways that promote photosynthetic productivity and growth in plants. TRXy and x and probably also TRXm control the proteins involved in stress reactions. Hydrogen peroxide, 2-Cys PRXs and ACHT form an oxidation loop to the TRX network that controls the redox homeostasis of chloroplast metabolism under fluctuating light conditions and light–dark transitions. Enhancement of NTRC activity promotes growth by increasing biosynthetic activity of the chloroplast and decreasing the accumulation of oxidized 2-Cys PRXs. Reducing signals are depicted by blue arrows and oxidizing signals by red arrows. For details, see §3.

Much less is known about the reduction of chloroplast TRX-like proteins. ACHT1 protein was shown to be reduced in the light but the electron donor was not identified [37]. TRXm has been demonstrated to donate electrons to thylakoid HCF164 protein via reduction of CcdA [8].

Reduction of ferredoxin and NADP+ in light reactions links the TRX systems to the regulation of chloroplast processes in the dark–light transition. However, what is less well-characterized is how the reduced state of TRXs and their target proteins is maintained under continuous and fluctuating light. Molecular oxygen has been shown to oxidize the redox-regulated enzymes [13], and because of the evolution of oxygen by light reactions, a continuous supply of reducing equivalents from the TRX systems is needed to maintain the activation state of enzymes in illuminated chloroplasts. However, in addition to the reducing step of redox regulation, also the oxidation cycle of TRX systems may be strictly controlled under fluctuating light [2]. Danon and his colleagues [37,38] have described an oxidizing loop for a TRX system employing chloroplast 2-Cys-PRXs that controls starch synthesis under fluctuating light and in light–dark transition. 2-Cys-PRXs are abundant chloroplast proteins that are oxidized by a reaction with hydrogen peroxide [30]. Oxidized 2-Cys-PRXs are primarily reactivated by NTRC [12,17], but they can also take electrons from TRX-like proteins, ACHT1 and ACHT4 [37,38]. Oxidized ACHT4, in turn inactivated ADP-glucose pyrophosphorylase (AGPase), a redox-regulated enzyme in starch synthesis, thus slowing down starch synthesis in the light–dark transition and under fluctuating light [38]. We have shown that the high accumulation of oxidized 2-Cys-PRXs in Arabidopsis leaves lacking functional NTRC correlates with the oxidation of redox-regulated Calvin–Benson enzymes [17], suggesting that oxidized 2-Cys-PRXs may act as a general oxidizing loop for redox-regulated enzymes in the chloroplast [39] (figure 1).

Thioredoxin-dependent regulation of photosynthesis

Potential target proteins regulated by TRXs cover all the essential processes in chloroplasts, including biogenesis of plastids, gene expression, translation, photosynthesis, antioxidant and stress reactions and biosynthetic metabolism [2-4,13,40], underlining a vital role of TRXs in plant chloroplasts. In this review we shall focus on the TRX-dependent regulation of photosynthetic light reactions and carbon fixation, and evaluate the prospects for improving photosynthetic productivity by modification of chloroplast TRX systems.

TRXs regulate a number of proteins directly or indirectly linked to photosynthetic reactions, including the biogenesis of chloroplasts through activation of the redox-controlled enzymes in the tetrapyrrole pathway that synthethizes chlorophyll and haem [41]. Additionally, the redox-active Cys residues in the γ-subunit of ATP synthase are rapidly reduced in the light and oxidized in darkness, so forming an on/off regulatory loop for ATP production in chloroplasts [42]. Previously the FTR system had been regarded as the primary reductant of the γ-subunit upon illumination [13], but recent results have provided both biochemical and biophysical evidence that also identifies NTRC as a key regulator of the ATP synthase, with a non-redundant role in reducing the γ-subunit under low irradiance [17,43,44]. Thiol regulation of the other primary components in light reactions has not been reported but the mechanisms controlling light harvesting and distribution of light energy in thylakoid photosystems are prone to redox regulation by TRXs. STN7 kinase is inactivated by TRX that switches off state transition in plants transferred to high light conditions [45,46] and NPQ is stimulated in the soq1 knockout mutant that lacks a thylakoid-bound TRX-like protein [23]. The latter finding is supported by the observation that dithiothreitol treatment decreased NPQ yield in Arabidopsis leaves [44]. Thioredoxins have also been reported to regulate PGR5/PGRL1-dependent cyclic electron flow [47,48].

In chloroplast carbon metabolism, light-induced activation of the enzymes in the Calvin–Benson cycle is the best-characterized action of chloroplast TRXs. The TRX system activates the following Calvin–Benson cycle enzymes in the dark–light transition by reduction of redox-active Cys residues (see [5]): glyceraldehyde-3-phosphate dehydrogenase (GAPDH), fructose-bisphosphatase (FBPase), sedoheptulose-bisphosphatase (SBPase) and phosphoribulokinase (PRK). Rubisco is also indirectly regulated by thioredoxin via activation of Rubisco activase. Also the key enzymes in the pathways closely linked to photosynthesis (AGPase in starch synthesis and NADP-malate dehydrogenase (NADP-MDH) in the malate oxaloacetate shuttle) are regulated by TRXs.

The specificity of TRX isoforms in the regulation of carbon fixation has recently been widely debated. The double (trxf1 trxf2) [16,35] and triple (trxm1 trxm2 trxm4) [49] knockout mutants support the original in vitro observations that TRXf and m isoforms are involved in the regulation of photosynthetic enzymes. Furthermore, NTRC is shown to interact with the PRK and FBPase in BiFC tests and the activation levels of these enzymes were higher in illuminated Arabidopsis leaves overexpressing the NTRC gene [17], whereas the light-dependent redox-activation of FBPase was more impaired in a ntrc trxf1 double mutant than in a single ntrc or trxf1 mutant [15]. These observations suggest that either NTRC directly regulates the enzymes in the Calvin–Benson cycle or that NTRC is involved in the activation of TRXf which in turn controls the activity of these enzymes. However, the conclusions drawn from the knockout mutants of TRXs should be viewed with caution, because apart from a direct effect of a missing TRX on the enzymes, the overall redox state of the chloroplast may be altered in the mutants. Especially if the mutation modifies the oxidation loop in the reversible redox-regulation cycle of TRX targets (figure 1), the amount of redox-activated enzymes may be lower in mutants than in wild-type plants. Knockout of NTRC [29] and TRXm1, 2 and 4 isoforms [50] increases production of ROS. Elevated oxidative stress induces the accumulation of oxidized components, including 2-Cys-PRXs in the chloroplast [17,29] that in turn may remodify the redox state of chloroplast enzymes in vivo as described in [38] (figure 1). In this case the lower level of activated enzymes is not directly due to the loss of a knockout TRX but to the elevated amount of oxidant(s) in chloroplast.

Improving photosynthesis by modification of the chloroplast thioredoxin network

Among the chloroplast TRXs, TRXf and NTRC have been specifically linked to the activation of photosynthesis and biosynthetic pathways in the chloroplast by several publications reviewed in §3 (figure 1). They control ATP synthase and the redox-activated enzymes in the tetrapyrrole pathway producing haem and chlorophylls, the shikimate pathways synthesizing aromatic amino acids, the Calvin–Benson cycle and starch synthesis (reviewed in [2,3]). NTRC also functions as an antioxidant in the chloroplast by primarily activating the hydrogen peroxide scavengers 2-Cys PRXs. TRXf and the TRX domain of NTRC have very similar electrostatic surface charges, suggesting that they can have overlapping targets in chloroplasts [28]. Thus it is presumable that boosting the activity of these TRXs may promote biosynthetic activities in chloroplasts and enhance plant growth. Indeed, the overexpression of TRXf in tobacco (OE-TRXf) [51] and NTRC in Arabidopsis (OE-NTRC) [17,28] stimulated the biomass production of plants and increased leaf size (OE-NTRC) or specific leaf mass (OE-TRXf). It is remarkable that the overexpression of TRXm did not stimulate growth of tobacco [51]. The overexpressed protein content was 10- to 20-fold (OE-NTRC) and 20- to 200-fold higher (OE-TRXf) than in wild-type leaves, which roughly equals the concentration of TRX targets in the chloroplast [24]. Overexpression of TRXf did not increase the steady-state photosynthesis of tobacco but the accumulation of starch and sugars (glucose, fructose, sucrose) in the leaves had risen significantly [51]. In contrast, overexpression of NTRC increased photosynthetic activity in Arabidopsis [17]. The quantum yield of PSI was increased under light intensities lower than growth light and NPQ decreased under high light, suggesting that OE-NTRC plants can efficiently use absorbed light energy in the chloroplast. Steady-state CO2 fixation was about 20% higher than in wild-type and the changes in the photosynthetic parameters correlated with the higher accumulation of reduced forms of redox-controlled enzymes. Accumulation of fully-oxidized 2-Cys PRXs was eliminated both in darkness and light, suggesting that also the oxidation loop of redox-regulated enzymes was modified in OE-NTRC plants. Overexpression of NTRC did not cause any visible reduction of growth under optimal growth conditions, but seed production was about 20% lower than in wild-type (Lauri Nikkanen 2016, unpublished), suggesting that high NTRC content favours vegetative growth.

OE-NTRC and OE-TRXf plants have a crucial difference that may affect the phenotype of the plants. NTRC represents a fully active TRX system including both the reductase activity and TRX activity in a single protein. Thus the activity of NTRC in overexpression plants depends only on the availability of NADPH in the chloroplasts. We have shown that overexpression of NTRC also increases the amount of reduced TRXf in vivo and this reduction depends on the reductase domain of NTRC [17]. Thus, boosting the NTRC system also stimulates the regulation of TRXf targets, which may partly explain the overall positive effect of OE-NTRC on photosynthesis. However, high NTRC content also decreased the accumulation of oxidized 2-Cys PRXs under all light conditions [17]. If, as suggested by Eliyahu et al. [38], oxidized 2-Cys PRXs are involved in the transient modification of redox-regulated proteins, the extra amount of NTRC may alter the responses of photosynthesis to fluctuating light conditions. In OE-TRXf tobacco plants, only the amount of TRXf was raised, while the leaves still had endogenous content of TRs. The amount of active TRXf in tobacco leaves overexpressing TRXf was not estimated [51] but the low endogenous amount of TR may limit the effective utilization of extra TRXf in chloroplasts. We have constructed a chimeric NTRC, in which the TRX domain of NTRC has been replaced by the TRXf sequence (Jouni Toivola 2016, unpublished). NTRC-TRXf would be reduced by NADPH in vivo, like NTRC, and thus the overexpression of this chimeric NTRC-TRXf may elevate the active TRXf content in chloroplasts over that found in OE-TRXf tobacco plants. We have transferred the NTRC-TRXf construct to Arabidopsis and the screening of transgenic lines are ongoing.

Future prospects

The present experimental data emphasize that elevated activity of specific chloroplast TRXs (NTRC, TRXf) promotes vegetative growth and sugar production in plants under optimal greenhouse conditions. The growth stimulation is linked to photosynthesis with improved capacity to use light energy (OE-NTRC) and increased production of starch and soluble sugars in leaves (OE-TRXf). These modifications of photosynthetic activity and sugar production may improve the potential of plants for production of biofuels or other sugar-based valuable compounds. Further studies are needed to evaluate whether the increased activity of NTRC and/or TRXf promotes the growth of other plant species and whether this modification does or does not compromise the growth under stress conditions, including fluctuating light. The other chloroplast TRXs, especially TRXm, TRXy, TRXx, and CDP32 have been shown to regulate chloroplast proteins under stress conditions [11,52-54]. It remains to be elucidated whether the elevated activity of these TRXs will improve plant tolerance to stresses.