Photorespiration in the context of Rubisco biochemistry,CO2 diffusion and metabolism

Photorespiratory metabolism is essential for plants to maintain functional photosynthesis in an oxygen‐containing environment. Because the oxygenation reaction of Rubisco is followed by the loss of previously fixed carbon, photorespiration is often considered a wasteful process and considerable efforts are aimed at minimizing the negative impact of photorespiration on the plant’s carbon uptake. However, the photorespiratory pathway has also many positive aspects, as it is well integrated within other metabolic processes, such as nitrogen assimilation and C₁ metabolism, and it is important for maintaining the redox balance of the plant. The overall effect of photorespiratory carbon loss on the net CO₂ fixation of the plant is also strongly influenced by the physiology of the leaf related to CO₂ diffusion. This review outlines the distinction between Rubisco oxygenation and photorespiratory CO₂ release as a basis to evaluate the costs and benefits of photorespiration.     

Leaf senescence in response to elevated atmospheric CO<Subscript>2</Subscript> concentration and low nitrogen supply

This review reports the physiological and metabolic changes in plants during development under elevated atmospheric carbon dioxide concentration and/or limited-nitrogen supply in order to establish their effects on leaf senescence induction. Elevated CO₂ concentration and nitrogen supply modify gene expression, protein content and composition, various aspects of photosynthesis, sugar metabolism, nitrogen metabolism, and redox state in plants. Elevated CO₂ usually causes sugar accumulation and decreased nitrogen content in plant leaves, leading to imbalanced C/N ratio in mature leaves, which is one of the main factors behind premature senescence in leaves. Elevated CO₂ and low nitrogen decrease activities of some antioxidant enzymes and thus increase H₂O₂ production. These changes lead to oxidative stress that results in the degradation of photosynthetic pigments and eventually induce senescence. However, this accelerated leaf senescence under conditions of elevated CO₂ and limited nitrogen can mobilize nutrients to growing organs and thus ensure their functionality.     

Plant responses to elevated CO<Subscript>2</Subscript> concentration at different scales: leaf,whole plant,canopy, and population

Elevated CO₂ enhances photosynthesis and growth of plants, but the enhancement is strongly influenced by the availability of nitrogen. In this article, we summarise our studies on plant responses to elevated CO₂. The photosynthetic capacity of leaves depends not only on leaf nitrogen content but also on nitrogen partitioning within a leaf. In Polygonum cuspidatum, nitrogen partitioning among the photosynthetic components was not influenced by elevated CO₂ but changed between seasons. Since the alteration in nitrogen partitioning resulted in different CO₂-dependence of photosynthetic rates, enhancement of photosynthesis by elevated CO₂ was greater in autumn than in summer. Leaf mass per unit area (LMA) increases in plants grown at elevated CO₂. This increase was considered to have resulted from the accumulation of carbohydrates not used for plant growth. With a sensitive analysis of a growth model, however, we suggested that the increase in LMA is advantageous for growth at elevated CO₂ by compensating for the reduction in leaf nitrogen concentration per unit mass. Enhancement of reproductive yield by elevated CO₂ is often smaller than that expected from vegetative growth. In Xanthium canadense, elevated CO₂ did not increase seed production, though the vegetative growth increased by 53%. As nitrogen concentration of seeds remained constant at different CO₂ levels, we suggest that the availability of nitrogen limited seed production at elevated CO₂ levels. We found that leaf area development of plant canopy was strongly constrained by the availability of nitrogen rather than by CO₂. In a rice field cultivated at free-air CO₂ enrichment, the leaf area index (LAI) increased with an increase in nitrogen availability but did not change with CO₂ elevation. We determined optimal LAI to maximise canopy photosynthesis and demonstrated that enhancement of canopy photosynthesis by elevated CO₂ was larger at high than at low nitrogen availability. We also studied competitive asymmetry among individuals in an even-aged, monospecific stand at elevated CO₂. Light acquisition (acquired light per unit aboveground mass) and utilisation (photosynthesis per unit acquired light) were calculated for each individual in the stand. Elevated CO₂ enhanced photosynthesis and growth of tall dominants, which reduced the light availability for shorter subordinates and consequently increased size inequality in the stand.     

Decrease of mesophyll conductance to CO<Subscript>2</Subscript> is a possible mechanism of abscisic acid influence on photosynthesis in seedlings of pea and wheat

Treatment of plants by phytohormones is a perspective method of regulation of the plant stress resistance and productivity. However, the mechanisms of phytohormone effects on physiological processes require investigations. The aim of this work was the analysis of the influence of exogenous abscisic acid (ABA) on photosynthesis in seedlings of pea and wheat, and in particular, an estimation of the involvement of the mesophyll conductance to CO₂ in the realization of the ABA effects. A standard system for recording of photosynthetic parameters and a system for intracellular measurements of electrical activity were used in the experiments. It was shown that the effect of exogenous ABA on photosynthesis was most prominent 1 day after spraying of a plant. A detailed analysis of photosynthetic processes showed that ABA decreased photosynthetic assimilation of CO₂ and increased cyclic electron flow in plants under study; these processes were interconnected. A decrease of the mesophyll conductance to CO₂ was probably a mechanism of the decrease in the photosynthetic assimilation of CO₂, because ABA did not significantly influence water conductance of a leaf and parameters of the CO₂ fixation in Calvin–Benson cycle. It is likely that the decrease of the mesophyll conductance to CO₂ was related with a decrease of the plasma membrane conductance to carbon dioxide. Inactivation of H⁺-ATP-ase and changes in extracellular pH can be a mechanism of this decrease. A decrease of the metabolic component of the electrical resting potential after the ABA treatment testifies in favor of this possibility.     

Innate and evolutionarily increased advantages of invasive <Emphasis Type="Italic">Eupatorium adenophorum</Emphasis> over native <Emphasis Type="Italic">E. japonicum</Emphasis> under ambient and doubled atmospheric CO<Subscript>2</Subscript> concentrations

Both innate and evolutionarily increased ecophysiological advantages can contribute to vigorous growth, and eventually to invasiveness of alien plants. Little effort has been made to explore the roles of innate factors of alien plants in invasiveness and the effects of CO₂ enrichment on alien plant invasions. To address these problems, we compared invasive Eupatorium adenophorum, its native conspecific, and a native congener (E. japonicum) under ambient and doubled atmospheric CO₂ concentrations. Native E. adenophorum from Mexico grew slower than invasive E. adenophorum but faster than native E. japonicum under both CO₂ concentrations. The faster growth rate of invasive E. adenophorum was associated with higher photosynthetic capacity and leaf area ratio. For invasive E. adenophorum, the higher photosynthetic capacity was associated with higher nitrogen (N) allocation to photosynthesis, which was related to lower leaf mass per area; the higher leaf area ratio was due to lower leaf mass per area and higher leaf mass fraction. Tradeoff between N allocations to photosynthesis versus defenses was found. CO₂ enrichment significantly increased relative growth rate and biomass accumulation by increasing actual photosynthetic rate for all studied materials. However, the relative increase in growth was not significantly different among them. CO₂ enrichment did not influence N allocation to photosynthesis, but increased N allocation to cell walls. The reduced leaf N content decreased N content in photosynthesis, explaining the down-regulation of photosynthetic capacity under prolonged elevated CO₂ concentration. Our results indicate that both innate and evolutionary advantages in growth and related ecophysiological traits contribute to invasiveness of invasive E. adenophorum, and CO₂ enrichment may not aggravate E. adenophroum’s invasion in the future.     

Dissecting metabolic flux in C<Subscript>4</Subscript> plants: experimental and theoretical approaches

C₄ photosynthesis is the carbon fixation pathway in specific plant species, so called C₄ plants including maize, sorghum and sugarcane. It is characterized by the carboxylation reaction that forms four-carbon (C₄) molecules, which are then used to transport CO₂ to the proximity of RubisCO in the bundle sheath cells. Since C₄ photosynthesis confers high photosynthetic as well as water and nitrogen use efficiency on plants, worldwide efforts have been made to understand the mechanisms of C₄ photosynthesis and to properly introduce the pathway into C₃ crops. Metabolic flux analysis (MFA) is a research field trying to analyze the metabolic pathway structure and activity (i.e., flux) in vivo. Constraint-based reconstruction and analysis tools theoretically study the distribution of metabolic flux in genome-scale network-based models. Different types of MFA and model-based analyses have been contributing to the discovery of C₄ photosynthetic pathways and to analyze its operation in C₄ plant species. This article reviews the studies to dissect the operation of C₄ photosynthesis and adjacent pathways, from the pioneer studies using radioisotope-based MFA to the recent stable isotope-based MFA and the model-based approaches. These studies indicate complex interconnections among metabolic pathways and the importance of the integration of experimental and theoretical approaches. Perspectives on the integrative approach and major obstacles are also discussed.     

Mechanisms underlying leaf photosynthetic acclimation to warming and elevated CO2 as inferred from least‐cost optimality theory

The mechanisms responsible for photosynthetic acclimation are not well understood, effectively limiting predictability under future conditions. Least‐cost optimality theory can be used to predict the acclimation of photosynthetic capacity based on the assumption that plants maximize carbon uptake while minimizing the associated costs. Here, we use this theory as a null model in combination with multiple datasets of C₃ plant photosynthetic traits to elucidate the mechanisms underlying photosynthetic acclimation to elevated temperature and carbon dioxide (CO₂). The model‐data comparison showed that leaves decrease the ratio of the maximum rate of electron transport to the maximum rate of Rubisco carboxylation (J_max/V_cmax) under higher temperatures. The comparison also indicated that resources used for Rubisco and electron transport are reduced under both elevated temperature and CO₂. Finally, our analysis suggested that plants underinvest in electron transport relative to carboxylation under elevated CO₂, limiting potential leaf‐level photosynthesis under future CO₂ concentrations. Altogether, our results show that acclimation to temperature and CO₂ is primarily related to resource conservation at the leaf level. Under future, warmer, high CO₂ conditions, plants are therefore likely to use less nutrients for leaf‐level photosynthesis, which may impact whole‐plant to ecosystem functioning.     

Root restriction as a factor in photosynthetic acclimation of cotton seedlings grown in elevated carbon dioxide

Interactive effects of root restriction and atmospheric CO₂ enrichment on plant growth, photosynthetic capacity, and carbohydrate partitioning were studied in cotton seedlings (Gossypium hirsutum L.) grown for 28 days in three atmospheric CO₂ partial pressures (270, 350, and 650 microbars) and two pot sizes (0.38 and 1.75 liters). Some plants were transplanted from small pots into large pots after 20 days. Reduction of root biomass resulting from growth in small pots was accompanied by decreased shoot biomass and leaf area. When root growth was less restricted, plants exposed to higher CO₂ partial pressures produced more shoot and root biomass than plants exposed to lower levels of CO₂. In small pots, whole plant biomass and leaf area of plants grown in 270 and 350 microbars of CO₂ were not significantly different. Plants grown in small pots in 650 microbars of CO₂ produced greater total biomass than plants grown in 350 microbars, but the dry weight gain was found to be primarily an accumulation of leaf starch. Reduced photosynthetic capacity of plants grown at elevated levels of CO₂ was clearly associated with inadequate rooting volume. Reductions in net photosynthesis were not associated with decreased stomatal conductance. Reduced carboxylation efficiency in response to CO₂ enrichment occurred only when root growth was restricted suggesting that ribulose-1,5-bisphosphate carboxylase/oxygenase activity may be responsive to plant source-sink balance rather than to CO₂ concentration as a single factor. When root-restricted plants were transplanted into large pots, carboxylation efficiency and ribulose-1,5-bisphosphate regeneration capacity increased indicating that acclimation of photosynthesis was reversible. Reductions in photosynthetic capacity as root growth was progressively restricted suggest sink-limited feedback inhibition as a possible mechanism for regulating net photosynthesis of plants grown in elevated CO₂.     

Photosynthesis and fluorescence responses of C<Subscript>4</Subscript> plant <Emphasis Type="Italic">Andropogon gerardii</Emphasis> acclimated to temperature and carbon dioxide

Increase in both atmospheric CO₂ concentration [CO₂] and associated warming are likely to alter Earths’ carbon balance and photosynthetic carbon fixation of dominant plant species in a given biome. An experiment was conducted in sunlit, controlled environment chambers to determine effects of atmospheric [CO₂] and temperature on net photosynthetic rate (P _N) and fluorescence (F) in response to internal CO₂ concentration (C _i) and photosynthetically active radiation (PAR) of the C₄ species, big bluestem (Andropogon gerardii Vitman). Ten treatments were comprised of two [CO₂] of 360 (ambient, AC) and 720 (elevated, EC) μmol mol⁻¹ and five day/night temperature of 20/12, 25/17, 30/22, 35/27 and 40/32 °C. Treatments were imposed from 15 d after sowing (DAS) through 130 DAS. Both F-P _N/C _i and F-P _N/PAR response curves were measured on top most fully expanded leaves between 55 and 75 DAS. Plants grown in EC exhibited significantly higher CO₂-saturated net photosynthesis (P _sat), phosphoenolpyruvate carboxylase (PEPC) efficiency, and electron transport rate (ETR). At a given [CO₂], increase in temperature increased P _sat, PEPC efficiency, and ETR. Plants grown at EC did not differ for dark respiration rate (R _D), but had significantly higher maximum photosynthesis (P _max) than plants grown in AC. Increase in temperature increased Pmax, R _D, and ETR, irrespective of the [CO₂]. The ability of PEPC, ribulose-1,5-bisphosphate carboxylase/oxygenase, and photosystem components, derived from response curves to tolerate higher temperatures (>35 °C), particularly under EC, indicates the ability of C₄ species to sustain photosynthetic capacity in future climates.     

Elevated CO2 alleviates the impact of drought on barley improving water status by lowering stomatal conductance and delaying its effects on photosynthesis

We analysed the impact of elevated CO₂ on water relations, water use efficiency and photosynthetic gas exchange in barley (Hordeum vulgare L.) under wet and drying soil conditions. Soil moisture was less depleted under elevated compared to ambient [CO₂]. Elevated CO₂ had no significant effect on the water relations of irrigated plants, except on whole plant hydraulic conductance, which was markedly decreased at elevated compared to ambient CO₂ concentrations. The values of relative water content, water potential and osmotic potential were higher under elevated CO₂ during the entire drought period. The better water status of water-limited plants grown at elevated CO₂ was the result of stomatal control rather than of osmotic adjustment. Despite the low stomatal conductance produced by elevated CO₂, net photosynthesis was higher under elevated than ambient CO₂ concentrations. With water shortage, photosynthesis was maintained for longer at higher rates under elevated CO₂. The reduction of stomatal conductance and therefore transpiration, and the enhancement of carbon assimilation by elevated CO₂, increased instantaneous and whole plant water use efficiency in both irrigated and droughted plants. Thus, the metabolism of barley plants grown under elevated CO₂ and moderate or mild water deficit conditions is benefited by increased photosynthesis and lower transpiration. The reduction in plant water use results in a marked increase in soil water content which delays the onset and severity of water deficit.     

Effect of panicle removal on photosynthetic acclimation under elevated CO<Subscript>2</Subscript> in rice

To examine the role of sink size on photosynthetic acclimation under elevated atmospheric CO₂ concentrations ([CO₂]), we tested the effects of panicle-removal (PR) treatment on photosynthesis in rice (Oryza sativa L.). Rice was grown at two [CO₂] levels (ambient and ambient + 200 μmol mol⁻¹) throughout the growing season, and at full-heading stage, at half the plants, a sink-limitation treatment was imposed by the removal of the panicles. The PR treatment alleviated the reduction of green leaf area, the contents of chlorophyll (Chl) and Rubisco after the full-heading stage, suggesting delay of senescence. Nonetheless, elevated [CO₂] decreased photosynthesis (measured at current [CO₂]) of plants exposed to the PR treatment. No significant [CO₂] × PR interaction on photosynthesis was observed. The decrease of photosynthesis by elevated [CO₂] of plants was associated with decreased leaf Rubisco content and N content. Leaf glucose content was increased by the PR treatment and also by elevated [CO₂]. In conclusion, a sink-limitation in rice improved N status in the leaves, but this did not prevent the photosynthetic down-regulation under elevated [CO₂].     

New insights into the cellular mechanisms of plant growth at elevated atmospheric carbon dioxide concentrations

Rising atmospheric carbon dioxide concentration ([CO₂]) significantly influences plant growth, development, and biomass. Increased photosynthesis rate, together with lower stomatal conductance, has been identified as the key factors that stimulate plant growth at elevated [CO₂] (e[CO₂]). However, variations in photosynthesis and stomatal conductance alone cannot fully explain the dynamic changes in plant growth. Stimulation of photosynthesis at e[CO₂] is always associated with post‐photosynthetic secondary metabolic processes that include carbon and nitrogen metabolism, cell cycle functions, and hormonal regulation. Most studies have focused on photosynthesis and stomatal conductance in response to e[CO₂], despite the emerging evidence of e[CO₂]'s role in moderating secondary metabolism in plants. In this review, we briefly discuss the effects of e[CO₂] on photosynthesis and stomatal conductance and then focus on the changes in other cellular mechanisms and growth processes at e[CO₂] in relation to plant growth and development. Finally, knowledge gaps in understanding plant growth responses to e[CO₂] have been identified with the aim of improving crop productivity under a CO₂ rich atmosphere.     

The F<Subscript>O</Subscript>F<Subscript>1</Subscript> ATP synthase: from atomistic three-dimensional structure to the rotary-chemical function

There are numerous studies describing how growth conditions influence the efficiency of C₄ photosynthesis. However, it remains unclear how changes in the biochemical capacity versus leaf anatomy drives this acclimation. Therefore, the aim of this study was to determine how growth light and nitrogen availability influence leaf anatomy, biochemistry and the efficiency of the CO₂ concentrating mechanism in Miscanthus × giganteus. There was an increase in the mesophyll cell wall surface area but not cell well thickness in the high-light (HL) compared to the low-light (LL) grown plants suggesting a higher mesophyll conductance in the HL plants, which also had greater photosynthetic capacity. Additionally, the HL plants had greater surface area and thickness of bundle-sheath cell walls compared to LL plants, suggesting limited differences in bundle-sheath CO₂ conductance because the increased area was offset by thicker cell walls. The gas exchange estimates of phosphoenolpyruvate carboxylase (PEPc) activity were significantly less than the in vitro PEPc activity, suggesting limited substrate availability in the leaf due to low mesophyll CO₂ conductance. Finally, leakiness was similar across all growth conditions and generally did not change under the different measurement light conditions. However, differences in the stable isotope composition of leaf material did not correlate with leakiness indicating that dry matter isotope measurements are not a good proxy for leakiness. Taken together, these data suggest that the CO₂ concentrating mechanism in Miscanthus is robust under low-light and limited nitrogen growth conditions, and that the observed changes in leaf anatomy and biochemistry likely help to maintain this efficiency.     

The interaction of biotic and abiotic factors at multiple spatial scales affects the variability of CO<Subscript>2</Subscript> fluxes in polar environments

Climate change may turn Arctic biomes from carbon sinks into sources and vice versa, depending on the balance between gross ecosystem photosynthesis, ecosystem respiration (ER) and the resulting net ecosystem exchange (NEE). Photosynthetic capacity is species specific, and thus, it is important to quantify the contribution of different target plant species to NEE and ER. At Ny Ålesund (Svalbard archipelago, Norway), we selected different Arctic tundra plant species and measured CO₂ fluxes at plot scale and photosynthetic capacity at leaf scale. We aimed to analyze trends in CO₂ fluxes during the transition seasons (beginning vs. end of the growing season) and assess which abiotic (soil temperature, soil moisture, PAR) and biotic (plot type, phenology, LAI, photosynthetic capacity) factors influenced CO₂ emissions. NEE and ER differed between vegetation communities. All communities acted as CO₂ sources, with higher source strength at the beginning than at the end of the growing season. The key factors affecting NEE were soil temperature, LAI and species-specific photosynthetic capacities, coupled with phenology. ER was always influenced by soil temperature. Measurements of photosynthetic capacity indicated different responses among species to light intensity, as well as suggesting possible gains in response to future increases in atmospheric CO₂ concentrations. Species-specific adaptation to low temperatures could trigger significant feedbacks in a climate change context. Our data highlight the need to quantify the role of dominant species in the C cycle (sinks or sources), as changes of vegetation composition or species phenology in response to climate change may have great impact on the regional CO₂ balance.     

Elevated Atmospheric CO<Subscript>2</Subscript> Increases Root Exudation of Carbon in Wetlands: Results from the First Free-Air CO<Subscript>2</Subscript> Enrichment Facility (FACE) in a Marshland

Experiments employing free-air CO₂ enrichment (FACE) facilities have indicated that elevated atmospheric carbon dioxide (eCO₂) stimulates growth in diverse terrestrial ecosystems. Studies of the effects of eCO₂ on wetland plants have indicated a similar response, but these studies were mostly performed in growth chambers. We conducted a 2-year FACE experiment [CO₂ ≈ 582 µmol mol^?1] in a marsh in Spain to test whether the common reed (Phragmites australis) responds to carbon enrichment, as previously reported in other macrophytes. More specifically, we tested the effect of eCO₂ on P. australis growth, photosynthesis, transpiration, and biomass, its effect on modifying plant and soil ratios of carbon, nitrogen, and phosphorus, and whether the strong environmental variability of this wetland modulates these responses. Our findings show that effects of eCO₂ in this wetland environment are more complex than previously believed, probably due to hydrological effects. The effects of eCO₂ on reed plants were cumulative and manifested at the end of the growing season as increased 38–44% instantaneous transpiration efficiency (ratio of net photosynthesis to transpiration), which was dependent on plant age. However, this increase did not result in a significant increase in biomass, because of excessive root exudation of carbon. These observations contrast with previous observations of wetland plants to increased atmospheric CO₂ in growth chambers and shed new light on the role of wetland plants as a carbon sink in the face of global climate change. The combined effects of water stress, eCO₂, and soil carbon processes must be considered when assessing the function of wetlands as a carbon sink under global change scenarios.     

CO<Subscript>2</Subscript>-concentrating mechanism in cyanobacterial photosynthesis: organization,physiological role,and evolutionary origin

The cellular and molecular organization of the CO₂-concentrating mechanism (CCM) of cyanobacteria is reviewed. The primary processes of uptake, translocation, and accumulation of inorganic carbon (C_i) near the active site of carbon assimilation by the enzyme ribulose-1,5-bisphosphate carboxylase in the C₃ cycle in cyanobacteria are described as one of the specialized forms of CO₂ concentration which occurs in some photoautotrophic cells. The existence of this form of CO₂ concentration expands our understanding of photosynthetic C_i assimilation. The means of supplying C_i to the C₃ cycle in cyanobacteria is not by simple diffusion into the cell, but it is the result of coordinated functions of high-affinity systems for the uptake of CO₂ and bicarbonate, as well as intracellular CO₂/HCO₃ ^? interconversions by carbonic anhydrases. These biochemical events are under genetic control, and they serve to maintain cellular homeostasis and adaptation to CO₂ limitation. Here we describe the organization of the CCM in cyanobacteria with a special focus on the CCM of relict halo- and alkaliphilic cyanobacteria of soda lakes. We also assess the role of the CCM at the levels of the organism, the biosphere, and evolution.     

New horizons for building pyrenoid-based CO2-concentrating mechanisms in plants to improve yields

Many photosynthetic species have evolved CO₂-concentrating mechanisms (CCMs) to improve the efficiency of CO₂ assimilation by Rubisco and reduce the negative impacts of photorespiration. However, the majority of plants (i.e. C3 plants) lack an active CCM. Thus, engineering a functional heterologous CCM into important C3 crops, such as rice (Oryza sativa) and wheat (Triticum aestivum), has become a key strategic ambition to enhance yield potential. Here, we review recent advances in our understanding of the pyrenoid-based CCM in the model green alga Chlamydomonas reinhardtii and engineering progress in C3 plants. We also discuss recent modeling work that has provided insights into the potential advantages of Rubisco condensation within the pyrenoid and the energetic costs of the Chlamydomonas CCM, which, together, will help to better guide future engineering approaches. Key findings include the potential benefits of Rubisco condensation for carboxylation efficiency and the need for a diffusional barrier around the pyrenoid matrix. We discuss a minimal set of components for the CCM to function and that active bicarbonate import into the chloroplast stroma may not be necessary for a functional pyrenoid-based CCM in planta. Thus, the roadmap for building a pyrenoid-based CCM into plant chloroplasts to enhance the efficiency of photosynthesis now appears clearer with new challenges and opportunities.

Research on pyrenoid formation has led to key advances toward engineering an algal CO₂-concentrating mechanism into C3 land plants, and a recent model predicts an optimized pathway for future work.     

Exploiting leaf starch synthesis as a transient sink to elevate photosynthesis, plant productivity and yields

Improvements in plant productivity (biomass) and yield have centered on increasing the efficiency of leaf CO₂ fixation and utilization of products by non-photosynthetic sink organs. We had previously demonstrated a correlation between photosynthetic capacity, plant growth, and the extent of leaf starch synthesis utilizing starch-deficient mutants. This finding suggested that leaf starch is used as a transient photosynthetic sink to recycle inorganic phosphate and, in turn, maximize photosynthesis. To test this hypothesis, Arabidopsis thaliana and rice (Oryza sativa L.) lines were generated with enhanced capacity to make leaf starch with minimal impact on carbon partitioning to sucrose. The Arabidopsis engineered plants exhibited enhanced photosynthetic capacity; this translated into increased growth and biomass. These enhanced phenotypes were displayed by similarly engineered rice lines. Manipulation of leaf starch is a viable alternative strategy to increase photosynthesis and, in turn, the growth and yields of crop and bioenergy plants.     

Elevated CO<Subscript>2</Subscript> reduces stomatal and metabolic limitations on photosynthesis caused by salinity in <Emphasis Type="Italic">Hordeum vulgare</Emphasis>

The future environment may be altered by high concentrations of salt in the soil and elevated [CO₂] in the atmosphere. These have opposite effects on photosynthesis. Generally, salt stress inhibits photosynthesis by stomatal and non-stomatal mechanisms; in contrast, elevated [CO₂] stimulates photosynthesis by increasing CO₂ availability in the Rubisco carboxylating site and by reducing photorespiration. However, few studies have focused on the interactive effects of these factors on photosynthesis. To elucidate this knowledge gap, we grew the barley plant, Hordeum vulgare (cv. Iranis), with and without salt stress at either ambient or elevated atmospheric [CO₂] (350 or 700 μmol mol⁻¹ CO₂, respectively). We measured growth, several photosynthetic and fluorescence parameters, and carbohydrate content. Under saline conditions, the photosynthetic rate decreased, mostly because of stomatal limitations. Increasing salinity progressively increased metabolic (photochemical and biochemical) limitation; this included an increase in non-photochemical quenching and a reduction in the PSII quantum yield. When salinity was combined with elevated CO₂, the rate of CO₂ diffusion to the carboxylating site increased, despite lower stomatal and internal conductance. The greater CO₂ availability increased the electron sink capacity, which alleviated the salt-induced metabolic limitations on the photosynthetic rate. Consequently, elevated CO₂ partially mitigated the saline effects on photosynthesis by maintaining favorable biochemistry and photochemistry in barley leaves.