JXB Advance Access originally published online on April 23, 2008
Journal of Experimental Botany 2008 59(7):1569-1580; doi:10.1093/jxb/ern084
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SPECIAL ISSUE REVIEW PAPER |
Rubisco regulation: a role for inhibitors
1Centre for Crop Genetics, Department of Plant Science, Rothamsted Research, Harpenden, Herts AL5 2JQ, UK
2Centro de Engenharia Biológica and Departamento de Biologia Vegetal, Faculdade de Ciências, Universidade de Lisboa, Campo Grande, 1749–016 Lisboa, Portugal
* To whom correspondence should be addressed. E-mail: martin.parry{at}bbsrc.ac.uk
Received 25 January 2008; Revised 22 February 2008 Accepted 22 February 2008
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Abstract |
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 Top Abstract IntroductionRubisco inhibitorsRubisco activaseAbiotic stressConclusionReferences |
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In photosynthesis Rubisco catalyses the assimilation of CO2 by the carboxylation of ribulose-1,5-bisphosphate. However, the catalytic properties of Rubisco are not optimal for current or projected environments and limit the efficiency of photosynthesis. Rubisco activity is highly regulated in response to short-term fluctuations in the environment, although such regulation may not be optimally poised for crop productivity. The regulation of Rubisco activity in higher plants is reviewed here, including the role of Rubisco activase, tight binding inhibitors, and the impact of abiotic stress upon them.
Key words: Abiotic stress, CA1P, inhibitors, Rubisco, Rubisco activase
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Introduction |
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TopAbstractIntroductionRubisco inhibitorsRubisco activaseAbiotic stressConclusionReferences |
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The most abundant protein, Rubisco [ribulose-1,5-bisphosphate (RuBP) carboxylase/oxygenase; EC 4.1.1.3 [EC] 9] catalyses the assimilation of CO2, by the carboxylation of ribulose-1,5-bisphosphate (RuBP) in photosynthetic carbon assimilation (Ellis, 1979). However, the catalytic limitations of Rubisco compromise the efficiency of photosynthesis (Parry et al., 2007). Compared to other enzymes of the Calvin cycle, Rubisco has a low turnover number, meaning that relatively large amounts must be present to sustain sufficient rates of photosynthesis. Furthermore, Rubisco also catalyses a competing and wasteful reaction with oxygen, initiating the process of photorespiration, which leads to a loss of fixed carbon and consumes energy. Although Rubisco and the photorespiratory enzymes are a major N store, and can account for more than 25% of leaf nitrogen, Rubisco activity can still be limiting. Furthermore, growth studies with transgenic plants with decreased amounts of Rubisco have confirmed that, under field conditions with intense or variable irradiance, photosynthetic rate is highly correlated with the amount of Rubisco (Hudson et al., 1992). This relationship cannot be ignored in attempts to improve resource use, particularly of nitrogen and water (Lea and Azevedo, 2006, 2007; Parry et al., 2005, 2007; Parry and Reynolds, 2007; Tambussi et al., 2007; Tuberosa et al., 2007).
In higher plants, Rubisco has a hexadecameric structure, being composed of eight large, chloroplast-encoded subunits arranged as four dimers and eight small, nuclear-encoded subunits. This is also known as Form I Rubisco. Each large subunit has two major structural domains, an N-terminal domain and a larger C-terminal domain which is an alpha/beta barrel. Most of the active site residues (that interact with substrate and/or substrate analogues) are contributed by loops at the mouth of the alpha/beta barrel with the remaining residues being supplied by two loop regions in the N-terminal domain of the second large subunit within a dimer. The availability of high resolution 3-D structures has provided detailed insight into the catalytic mechanisms of the enzyme and enabled properties to be related to sequences (Parry et al., 1987; see comprehensive reviews by Andersson, 1996, 2008; Cleland et al., 1998; Spreitzer and Salvucci, 2002; Portis and Parry, 2007).
Rubisco is highly regulated to control flux through the photosynthetic carbon reduction cycle in response to short-term fluctuations in the environment (Geiger and Servaites, 1994). The potential Rubisco activity is determined by the amount of Rubisco protein which, in turn, is determined by the relative rate of biosynthesis and degradation. These processes are regulated by gene expression (Sheen, 1990; Krapp et al., 1993), mRNA stability, polypeptide synthesis, post-translational modification, assembly of subunits into an active holoenzyme, and various factors which impact upon protein degradation (Mehta et al., 1992; Eckardt and Pell, 1995; Desimone et al., 1996). In the short term, regulating Rubisco activity is essential to match the capacity for RuBP regeneration with the prevailing rate of RuBP utilization. This is not achieved solely by the availability of substrate (Badger et al., 1984; Mott et al., 1984) since Rubisco in excess of that needed to sustain photosynthesis in the prevailing environment is deactivated (Sage et al., 1990). From an agronomic standpoint, Rubisco regulation may not be optimallly poised for crop productivity (Parry et al., 2007). Whilst Rubisco regulation has been previously reviewed (Portis, 1992, 2003; Parry et al., 1999b; Spreitzer and Salvucci, 2002) this review focuses on the regulation of Rubisco activity in higher plants including the role of Rubisco activase, tight binding inhibitors, and the corresponding impact of abiotic stress upon them.
The mechanisms involved in Rubisco regulation are summarized in Fig. 1. Rubisco (E) activity in vivo is modulated either by the carbamylation of an essential lysine residue at the catalytic site and subsequent stabilization of the resulting carbamate by a Mg2+ ion, forming a catalytically active ternary complex (E.CO2.Mg2+); or through the tight binding of low molecular weight inhibitors (I). Note that the CO2 involved in active site carbamylation is distinct from CO2 reacting with the acceptor molecule, RuBP, during catalysis. Inhibitors bind either before (E.I) or after carbamylation (E.CO2.Mg2+.I) and block the active site of the enzyme, preventing carbamylation and/or substrate binding. The removal of tightly bound inhibitors from the catalytic site of the carbamylated and decarbamylated forms of Rubisco requires Rubisco activase and the hydrolysis of ATP. In this way Rubisco activase ensures that the Rubisco active site is not blocked by inhibitors and so free either to become carbamylated or to participate directly in catalysis.
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Rubisco inhibitors |
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TopAbstractIntroductionRubisco inhibitorsRubisco activaseAbiotic stressConclusionReferences |
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The analysis of various 3-D structures has revealed that, after substrate binding, major structural changes occur in loop 6, at the mouth of a large subunit alpha/beta barrel, in which this loop folds or slides over the active site and loses its mobility. This closed conformation is maintained by residues of the C-terminal tail and of loops in the N-terminal domain of the partnering large subunit. In the reaction between bound (enediol) RuBP and either CO2 or O2, cleavage of the C2–C3 bond triggers site opening. By analogy to the high resolution structures for the Rubisco–carboxyarabinitol-1,5-bisphosphate (E.CO2.Mg2+.CABP) complex, a number of naturally occurring sugar phosphates that are tight binding inhibitors cause the active site of carbamylated or decarbamylated Rubisco to adopt a closed conformation and impact on Rubisco regulation (Fig. 2). Tight binding inhibitors resemble transition state intermediates of catalysis and prolonged dialysis or gel filtration are insufficient to release them from the catalytic site of purified Rubisco. Other sugar phosphates and some inorganic anions also interact with the catalytic site in vitro and affect carbamylation. These have been regarded as effectors and are usually competitive inhibitors with respect to RuBP at higher concentrations, but either increase (positive effectors, e.g. 6-phosphogluconate, NADPH and inorganic orthophosphate), or decrease (negative effectors, e.g. ribose-5-phosphate and fructose 6-phosphate), the extent of carbamylation at sub-saturating concentrations of CO2 and Mg2+ (Hatch and Jensen, 1980; Badger and Lorimer, 1981; Jordan et al.,1983). Parry et al. (1985) showed that inorganic orthophosphate (Pi) increased the activity of wheat Rubisco without increasing the extent of carbamylation and thus revitalized the idea that allosteric effects might be involved in the response of Rubisco activity to effectors. Allosteric effects have been reported with Rubiscos from spinach (Yokota et al., 1992) and from cyanobacteria (Marcus and Gurevitz, 2000). A phosphate binding site on cyanobacterial Rubisco has been found that is distinct from sites binding the phosphate groups of substrate RuBP and is involved in regulation of activity (Marcus et al., 2005). The effectors, 6-phosphogluconate, NADPH, and Pi are of particular interest for the regulation of Rubisco in vivo as they are present in the chloroplasts. The extent of their involvement in Rubisco regulation still needs to be fully determined. In vitro, sulphate ions remove such effectors, as well as tight binding inhibitors, from their respective sites of interaction (Parry et al., 1997) but the inclusion of modest concentrations (25–50 mM) of sulphate ions to Rubisco extraction buffers has been shown to prevent the binding of the naturally occurring inhibitor, 2-carboxy-D-arabinitol 1-phosphate (CA1P) by Rubisco, but not to cause the release of CA1P already bound to Rubisco (Moore and Seemann, 1994).
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Identifying the role of tight binding inhibitors in Rubisco regulation followed the observation of a diurnal variation in the total extractable Rubisco activity (McDermitt et al., 1983; Vu et al., 1983) and of the inhibition of carbamylation by the prior (tight) binding of RuBP (Jordan and Chollet, 1983). Servaites (1985) and Seemann et al. (1985) demonstrated that the diurnal variation in Rubisco activity was caused by the production of a phosphorylated inhibitor in the dark that was subsequently identified as CA1P (Gutteridge et al., 1986; Berry et al., 1987).
CA1P is the best characterized of the Rubisco inhibitors. CA1P is only found in the chloroplast (Moore et al., 1995; Parry et al., 1999a) and is formed by phosphorylation of 2-carboxy-D-arabinitol (CA) during periods of low irradiance or darkness (Moore and Seemann, 1992). Once formed CA1P binds tightly to the active site of carbamylated Rubisco. The route for the de novo biosynthesis of CA1P was unambiguously established by pulse-chase experiments that sequentially followed the flow of 14C from newly assimilated 14CO2 into fructose 1,6-bisphosphate followed by hamamelose bisphosphate, hamamelose monophosphate, hamamelose, and CA (Andralojc et al., 1994, 1996, 2002) (Fig. 3). At low irradiances or in darkness, CA is converted into CA1P (Moore and Seemann, 1992; Andralojc et al., 1996; Martindale et al., 1997). Measurements using a variety of species show that the abundance of leaf CA is greater (and in some cases by at least an order of magnitude) than the corresponding CA1P concentration (Moore et al., 1991, 1992; Andralojc et al., 1994, 2002). Whilst this may simply reflect the distribution of CA across several intracellular compartments, compared to the exclusive occurrence of CA1P in the chloroplast (Moore et al., 1992, 1995; Parry et al., 1999a) it is possible that these intermediates serve other purposes. (Andralojc et al., 2002).
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The extent of carbamylation of Rubisco in vivo may be determined by comparing the initial activity (determined immediately following extraction) with the total activity (determined after incubation with saturating concentrations of CO2 and Mg2+ to carbamylate vacant catalytic sites fully). Diurnal variation in total Rubisco activity can occur as a result of RuBP binding to decarbamylated Rubisco forming E.RuBP (Jordan and Chollet, 1983; Brooks and Portis, 1988). Diurnal variation can also occur as a result of CA1P binding to carbamylated Rubisco forming E.CO2.Mg2+.CA1P (Servaites et al., 1986).
In the light, CA1P is removed from the active site of Rubisco by Rubisco activase and then dephosphorylated by a specific CA1P phosphatase. The CA thus liberated is then available for re-phosphorylation, when the light intensity falls (Fig. 1b). The overall process of CA1P removal is light-dependent and is inhibited by DCMU or methyl viologen, which block photosynthetic electron transport (Seemann et al., 1985; Salvucci and Anderson, 1987). CA1P phosphatase is redox regulated, activated by NADPH (Holbrook et al., 1989; Kingston-Smith et al., 1992), DTT or glutathione (Holbrook et al., 1991) and reduced thioredoxin (Heo and Holbrook, 1999). The redox response is mediated by redox sensitive thiol/disuphide residues (Heo and Holbrook, 1999).
For reasons which are unclear, the amount of CA1P that accumulates during the night varies from species to species. Whilst many species (e.g. rice, soya, potato, tobacco, French bean, and tomato) contain sufficient CA1P to have a significant effect on Rubisco activity others (e.g. maize and wheat) do not (Servaites et al., 1986). Curiously, members of the latter group may still contain the CA1P-specific phophatase (Charlet et al., 1997) whilst a wide ranging survey suggests that all vascular plants contain CA (Moore et al., 1992, 1993). Such observations imply functions unrelated to the regulation of Rubisco or the metabolism of CA1P.
As well as the nocturnal decline, a depression in the total Rubisco activity (Keys et al., 1995; Hrstka et al., 2007) has been reported during the day and also in response to stress (Parry et al., 1993, 1997, 2002; Medrano et al., 1997) (Fig. 4). In wheat and French bean this depression in total activity was caused by a phosphorylated inhibitor, but not by CA1P or xylulose-1,5- bisphosphate (XuBP) (Keys et al., 1995). This phosphorylated daytime inhibitor was subsequently identified as pentadiulose-1,5-bisphosphate (PDBP) (Kane et al., 1998) whose formation from RuBP had previously been reported in Form II Rubisco from an autotrophic bacterium (Chen and Hartman, 1995). Products of catalytic ‘misfire’ arise at various points in the catalytic pathway of both carboxylation and oxygenation and are themselves potent and tight binding inhibitors. XuBP is formed by misprotonation of the initial enediol intermediate (Edmondson et al., 1990). Although XuBP is released from the catalytic site (Zhu et al., 1998) and has been shown to act as a (poor) substrate, being slowly carboxylated to form 3-phosphoglycerate by carbamylated Rubisco (Yokota, 1991) it can (like RuBP) also bind tightly to uncarbamylated Rubisco (Edmondson et al., 1990; Zhu and Jensen, 1991; Pearce and Andrews, 2003). 3-Ketoarabinitol-1,5-bisphosphate (KABP) has been proposed to be derived from the breakdown of an unstable peroxy intermediate of the oxygenase reaction (Zhu and Jensen, 1991; Zhu et al., 1998). However, it has been reported that identification of KABP as an inhibitor may be incorrect, on account of the stereoselective reduction of the true inhibitor in the presence of borate ions at low ionic strength. Similar analyses at high ionic strength are regarded to be unbiased and show a distribution of reduction products consistent with PDBP as the inhibitor, not KABP (Chen and Hartman, 1995, and reiterated by Pearce and Andrews, 2003; Kim and Portis, 2004). For this reason, other identifications of KABP as a physiologically relevant inhibitor, based on the products of borohydride reduction (Zhu and Jensen, 1991; Zhu et al., 1998) are open to question.
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The ‘daytime’ inhibitor, pentadiulose 1,5-bisphosphate (PDBP) is formed by the elimination of H2O2 from a peroxyketone intermediate of the oxygenation reaction and, on average, occurs once in every 260 turnovers (Kane et al., 1998; Pearce and Andrews, 2003; Kim and Portis, 2004). PDBP is thought to accumulate progressively at the catalytic site causing progressive inhibition, known as ‘fallover’ (Robinson and Portis, 1989a; Edmondson et al., 1990; Zhu et al., 1998; Kim and Portis, 2004). Therefore, any conditions that favour the oxygenase reaction and photorespiration, such as stomatal closure (increasing O2/CO2) and high temperature (because of the increased relative solubility of O2 compared to CO2 and the decreased specificity of Rubisco) will lead to increased PDBP production and will promote fallover. Likewise, Rubiscos with lower specificity factors have been shown to generate more PDBP (Kim and Portis, 2004). These properties are consistent with a depression in the total Rubisco activity reported for drought-stressed wheat and tobacco (Parry et al., 1993, 2002). Although the production of all misfire products (including PDBP) increases with temperature, the corresponding fallover has been shown to become less severe, because at the higher temperatures the structure of Rubisco becomes more mobile so that the same inhibitors do not bind so tightly (Schrader et al., 2006). Whilst the enzymes from all species produce misfire products under RuBP-saturated conditions these products do not cause fallover in Form I Rubisco from cyanobacteria and red algae, or the Form II Rubisco (composed of a single large subunit dimer) from autotrophic bacteria (Pearce and Andrews, 2003; Pearce, 2006).
While the presence of PDBP is undoubtedly associated with Rubisco inactivation, 2-carboxytetritol-1,4-bisphosphate (CTBP) derived from a benzilic acid-type rearrangement (Harpel et al., 1995) of enzyme bound PDBP (Pearce and Andrews, 2003) is likely to be a tighter binding inhibitor than PDBP itself (Pearce and Andrews, 2003). From Fig. 2 it can be seen that CTBP closely resembles both the transition state intermediate of the carboxylase reaction and CABP, rationalizing its high affinity for Rubisco and its potency as an inhibitor.
The structural changes that occur during catalytic turnover make the protein more compact and protect Rubisco from proteolytic breakdown in vitro (Houtz and Mulligan, 1991; Khan et al., 1999). Since tight binding inhibitors cause similar structural changes involving immobilization of hitherto exposed structural elements, it is not surprising that they also protect Rubisco from degradation by exogenous and endogenous proteases. Judging by the effect of CA1P (Khan et al., 1999) other tight binding inhibitors may also confer protection against inactivation by active oxygen species.
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Rubisco activase |
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TopAbstractIntroductionRubisco inhibitorsRubisco activaseAbiotic stressConclusionReferences |
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The importance of Rubisco activase for complete activation of Rubisco in vivo, was first recognized during the analysis of an Arabidopsis (rca) mutant that was unable to survive under ambient CO2 (Somerville et al., 1982). Salvucci et al. (1985) showed this to be due to the absence of a novel enzyme, Rubisco activase. It has subsequently been shown that Rubisco activase is essential for the activation and maintenance of Rubisco catalytic activity by promoting the removal of any tightly bound, inhibitory, sugar phosphates from the catalytic site of both the carbamylated and decarbamylated forms of Rubisco (Robinson and Portis, 1988a, 1989a; Edmondson et al., 1990; Wang and Portis, 1992; Mate et al., 1993). Rubisco activase has been detected in all plant species examined thus far and is a member of the AAA+ super family whose members perform chaperone like functions (Spreitzer and Salvucci, 2002).
Although no stable complexes between Rubisco and Rubisco activase have yet been isolated, Rubisco activase must interact directly with Rubisco to alter the enzyme structure, making the active site accessible for carbamylation or catalysis (Portis et al., 2008). Whilst early electron micrographs (Büchen-Osmond et al, 1992) suggested a complex between Rubisco and Rubisco activase, there is little additional direct evidence for an interaction between them (Parry et al., 1999b). However, the subunits of Rubisco activase have been cross-linked to the large subunit of Rubisco using disuccinimidyl suberate (Yokota and Tsujimoto, 1992) and the Rubisco large and small subunits were subsequently co-precipitated using Rubisco activase antisera (Zhang and Komatsu, 2000) providing evidence for direct interaction (Spreitzer and Salvucci, 2002). Interactions between Rubisco and Rubisco activase have been revealed through studies involving genetic recombination which exploited differences in compatibility between Rubisco and Rubisco activase from different species (Li et al., 2005). Studies have shown that the C-terminus of Rubisco activase is important in Rubisco recognition (Esau et al., 1998) and that, although the N-terminus is not needed for ATP hydrolysis, it is necessary for Rubisco activation. A highly conserved Rubisco activase residue Trp 16 (tobacco) or Trp 12 (spinach) is important in Rubisco recognition (van de Loo et al., 1996; Esau et al., 1996). Elucidating the mechanism by which Rubisco activase triggers inhibitor release from Rubisco remains a major challenge. However, experience with Rubisco suggests that even high resolution 3-D structures for Rubisco activase may not provide all the answers for this dynamic interaction.
In many species, including Arabidopsis, spinach, and rice (Wernke et al., 1988, 1989; Werneke et al., 1989; To et al., 1999) Rubsico activase occurs in two isoforms which result from the alternative splicing of a single gene transcript. In Arabidopsis the isoforms are of MW 43 kDa and 46 kDa. The additional amino acids of the larger isoform occur at the C-terminus. Activase activity is enhanced by illumination (Lan et al., 1992) and by electron transport through PSI which provides the basis for the light regulation of Rubisco (Campbell and Ogren, 1990). Furthermore, the ATP/ADP ratio influences the activity of Rubisco activase (Robinson and Portis, 1989b) and this effect is mediated by the C-terminal extension of the larger activase isoform (Shen et al., 1991) due to an interaction with the nucleotide-binding pocket (Wang and Portis, 2006). The report that reactivation of Rubisco in lysed spinach chloroplasts was dependent on the presence of ADP and Pi, together with illumination (Parry et al., 1988) and of the involvement of stromal ATP in intact chloroplasts (Robinson and Portis, 1988b) are both consistent with the currently held model for activase function.
In vitro, the additional residues at the C-terminus of the 46 kDa isoform of Rubisco activase render both ATPase and Rubisco activation activities responsive to a combination of the ATP/ADP ratio, and the ambient redox status. The redox response is mediated by thioredoxin-f, which, combined with dithiothreitol (DTT), make the ATP/ADP ratio much less inhibitory, causing an increase in both activities of this isoform. Conversely, a combination of thioredoxin-f and oxidized glutathione makes the ambient ATP/ADP ratio more inhibitory, suppressing activase activities (Zhang and Portis, 1999). This response invloves a redox-sensitive disulphide bond formed between two cysteine residues in the C-terminus unique to the larger isoform (Zhang and Portis, 1999). Substitution of either one of these C-terminal cysteine residues for alanine diminished the ATP/ADP sensitivity of activase (Zhang and Portis, 1999) and the light responsiveness of Rubisco activity in vivo (Zhang et al., 2002). Other manipulations using Arabidopsis rca plants have been described, with the introduction of either the 43 kDa or the 46 kDa isoform of Rubisco activase. Rubisco activity in plants expressing only the shorter isoform was not down-regulated following a light–dark transition, while the activity in plants expressing the larger isoform was strongly down-regulated (Zhang et al., 2002). In vitro, a ratio of Rubisco activase isoforms of 1:1 displayed between 4-fold and 6-fold changes in activity in response to redox status (Zhang and Portis, 1999; Zhang et al., 2002). However, assayed alone, the 43 kDa isoform was not redox sensitive. The large change in activity of a 1:1 mixture of the two isoforms in response to redox status indicates that the 46 kDa isoform allosterically regulates the activity of the 43 kDa isoform. In vivo, the expression of both isoforms in rca plants conferred a light-dependent activation of Rubisco very similar to that observed in the wild type. Wild-type Arabidopsis (wt) contains roughly equal amounts of both isoforms (Eckardt et al., 1997) and, since functional activase is believed to be multimeric, it has been proposed that the 46 kDa isoform allosterically modulates the activity of neighbouring 43 kDa isoforms in activase complexes containing both isoforms.
Manipulation of Rubisco activase expression has also provided the opportunity to examine the release of CA1P from Rubisco during light-induction of photosynthesis, since this process is slowed sufficiently in antisense Rubisco activase tobacco to be resolved from accompanying changes in the rate of CO2 assimilation attributable both to the (rapid) onset of RuBP supply and to the (slow) activation of non-carbamylated Rubisco (Hammond et al., 1998). Since the dephosphorylation of CA1P subsequent to its release from Rubisco was slower than Rubisco activation, it was concluded that Rubisco activase drives the activation of CA1P-inhibited Rubisco, rather than the dephosphorylation of CA1P by the CA1P-specific phosphatase. This suggests that attempts to manipulate Rubisco activity by altering the expression of CA1P-phosphatase alone are unlikely to be successful. By contrast, a promising role for altered Rubisco activase expression in enhancing crop performance is apparent from the correlation between greatly improved grain yield in maize grown in the field—obtained after 20 agronomic selection cycles for improvement of grain yield—and parallel increases in abundance of Rubisco activase and activity of Rubisco, both of which were increased more than 2-fold over the 40 d period following anthesis (i.e. during grain filling) relative to the initial cultivar (Martinez-Barajas et al., 1997).
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Abiotic stress |
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TopAbstractIntroductionRubisco inhibitorsRubisco activaseAbiotic stressConclusionReferences |
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The abundance and ease with which Rubisco can be purified, quantified, and assayed, make it an ideal model protein in studies of the effects of stress on photosynthetic metabolism. The extent to which the continual process of Rubisco protein turnover (a function of synthesis, maintenance, and degradation) represents a drain on cellular resources is uncertain, but on account of its abundance could be considerable, particularly in the presence of a relatively oxidising environment induced by stress (Feller et al., 2008).
In the light, under conditions which might promote heat and cold stress, an increase in active oxygen species in the chloroplast is likely to cause increased oxidative damage to thylakoid-bound and stromal proteins. Stress-induced oxidative modification of specific residues on Rubisco mark the enzyme for degradation (Mehta et al., 1992; Desimone et al., 1996; Ishida et al., 1999; Moreno and Spreitzer, 1999; Marin-Navarro and Moreno, 2003; Moreno et al., 2008). For example, the importance of cysteine 172 of the large subunit was demonstrated by creating a C172S substitution in Chlamydomonas reinhardtii (Moreno and Spreitzer, 1999). While growth rates under normal conditions were unchanged, the mutated Rubisco was more resistant to proteinase K at low redox potential in vitro and also showed delayed stress-induced degradation (by hydrogen peroxide or mannitol) in vivo (Moreno and Spreitzer, 1999). The additional observation that the modified Rubisco inactivation was faster than the control at elevated temperatures (40 °C and 50 °C) may have resulted either from inherent differences in the large subunit or altered interactions with Rubisco activase. Site-directed mutagenesis was also used to investigate the role of large subunit residues Cys 449 and Cys 459 in Chlamydomonas. When both these residues were substituted by serine, Rubisco degradation and the polymerization of the enzyme during salt stress were both increased (Marin-Navarro and Moreno, 2006).
Apart from the oxidative modifications which initiate these processes, the mechanisms involved in such accelerated Rubisco degradation remain obscure, although the process may involve association of oxidation-damaged Rubisco with chloroplast membranes (Mehta et al., 1992). Oxidative stress also impacts on Rubisco abundance through reduced transcript levels for the small subunit, possibly as the result of increased ethylene levels (Glick et al., 1995). It is becoming clear, however, that Rubisco expression is regulated by elements which also influence the regulation of other chloroplast and cytosolic enzymes. For example, in Chlamydomonas, translation of Rubisco large subunit transcript has been shown to be transiently arrested by active oxygen species and/or a reduction in stromal signals, resulting from high-light stress (Irihimovitch and Shapira, 2000). In addition, the drought-induced decrease of rbcS transcript is accompanied by increased expression of cytosolic glutamine synthetase (Bauer et al., 1997). This highlights the co-ordinated changes in expression of enzymes of primary metabolism initiated by oxidative stress.
A plausible model for Rubisco turnover in cereal leaves by Irving and Robinson (2006) was shown to describe previously published experimental data accurately (Friedrich and Huffaker, 1980; Mae et al., 1983, 1989; Suzuki et al., 2001). According to this model, control of Rubisco concentration is exerted by altering biosynthesis, with degradation being regarded as a simple first-order decay process, where the amount of Rubisco at any time (t) would be given by [Rubisco]t=[Rubisco]0e–kt, where k is the first-order rate constant for degradation and [Rubisco]0 is the initial concentration of Rubisco. The protection of Rubisco against proteolysis afforded by CA1P (Khan et al., 1999) and the variation in protease sensitivity accompanying changes in redox status (Moreno and Spreitzer, 1999; Marin-Navarro and Moreno, 2003, 2006), both imply that the rate constant for degradation cannot be fixed but must assume different values according to catalytic site occupancy or redox status. Protection of Rubisco from degradation has only been demonstrated using CA1P, but it is likely that the fallover inhibitors would have a similar effect. This may explain why transformed tobacco with reduced expression of Rubisco activase contained more Rubisco with lower catalytic activity, throughout leaf development (He et al., 1997), the accumulation of inhibitors at the catalytic site would confer resistance against the normal process of degradation.
Rubisco is exceptionally heat stable, since the purified, carbamylated spinach enzyme suffers no loss in activity after incubation for 1 h at 57 °C (Eckardt and Portis, 1997). In contrast, for over a decade it has been known that Rubisco activase is exceptionally heat labile: both activities of the purified enzyme (Rubisco activation and ATP hydrolysis) falling by 80% after only 5 min at 40 °C (Robinson and Portis, 1989b). Assayed separately, the smaller activase isoform has been shown to be considerably more heat-labile than the larger isoform, while the temperature sensitivity of a mixture containing equal amounts of each isoform resembled that of the larger isoform (Crafts-Brandner et al., 1997). In other words, the larger isoform confers increased thermal stability to the smaller isoform of activase. The demonstration of increased amounts of the larger isoform during heat shock in young maize leaves suggests that it may have a protective effect in vivo (Jimenéz et al., 1995) preventing large decreases in activase activity during heat stress. However, the evidence supporting an additional hypothesis that Rubisco activase is a molecular chaperone, maintaining Rubisco activity during and after heat shock (Jimenéz et al., 1995) has been questioned by Eckardt and Portis (1997) who showed that Rubisco activase is likely to be totally inactivated long before the irreversible loss of Rubisco activity and that Rubisco activase did not restore the activity of heat-denatured Rubisco. The report that elevated temperatures cause the functional association between Rubisco activase and thylakoid-bound polysomes (Rokka et al., 2001) and that the bound activase assumed the role of a molecular chaperone, omitted to demonstrate this specific function by activase. The demonstration that such an association was more rapid for the smaller than for the larger isoform of activase (Rokka et al., 2001) is reminiscent of the heat-denaturation characteristics of the two activase isoforms (Crafts-Brandner et al., 1997), suggesting that this association may be an intermediate state of activase heat inactivation.
The relationship between the effects of high temperature on Rubisco activase and Rubisco activity in vivo has been investigated using leaves of cotton and wheat (Feller et al., 1998). The very close correlation between CO2 assimilation and Rubisco activity over a range of temperatures from 28 °C to 45 °C (Law and Crafts-Brandner, 1999) provides further evidence that elevated temperatures inhibit Rubisco (and photosynthesis) primarliy as a result of the temperature sensitivity of Rubisco activase. Furthermore, in agreement with the correlation between Rubisco activase content and grain yield in maize (Martinez-Barajas et al., 1997), higher Rubisco activities, in vitro, were observed between 25 °C and 42 °C in the presence of higher concentrations of activase (Crafts-Brandner and Salvucci, 2000). In addition, post-transcriptional mechanisms are involved in modulating Rubisco activase gene expression in cotton and maize which may contribute to acclimation of photosynthesis to heat stress (Vargas-Suarez et al., 2004; DeRidder et al., 2006). Such studies provide compelling evidence that the activity of Rubisco is limiting to net photosynthesis at elevated temperatures and that this is determined by the activity of Rubisco activase. Indeed, when allowance was made for the decline in Rubisco activity at elevated temperatures, the kinetic properties of Rubisco accurately predicted the experimentally determined rate of photosynthesis over the same temperature range (Crafts-Brandner and Salvucci, 2000). The potential for improving Rubisco activity, and therefore photosynthesis, at elevated temperatures by engineering an increase in the abundance of activase is clear. Indeed, recent reports have confirmed that photosynthesis at elevated temperatures is increased by the introduction of rca variants [generated by gene shuffling (Kurek et al., 2007) or chimeric constructs (Portis et al., 2007)] with improved thermostability even at moderate temperatures. However, others (e.g. Cen and Sage, 2005; Sage and Kubien, 2007) have reported that electron transport, RuBP pool size, and the RuBP-to-PGA ratio declined with increasing temperature consistent with the hypothesis that the reduction in the activation state of Rubisco at high temperature is caused by limitation in RuBP regeneration. The reasons for the conflicting reports remain unclear, but may relate species differences and preconditioning.
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Conclusion |
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TopAbstractIntroductionRubisco inhibitorsRubisco activaseAbiotic stressConclusionReferences |
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Rubisco activity is not always poised for optimal crop productivity. The effect of naturally occurring inhibitors on catalytic activity is dependent on the prevailing activity of Rubisco activase. The production of tight binding inhibitors and the activity of activase are intricately choreographed in response to environmental changes. Manipulating Rubisco activase and the abundance of inhibitors, by targeting their synthesis or degradation, offers opportunities to modulate Rubisco activity and also to control the stability of Rubisco under stress.
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Acknowledgements |
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Rothamsted is a grant aided institute of the BBSRC.
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TopAbstractIntroductionRubisco inhibitorsRubisco activaseAbiotic stressConclusionReferences |
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