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Ermakova, M.

Publications and source records attributed to Ermakova, M..

17 recordsLinked to original sources

PsbS confers limited adaptive benefit to C4 photosynthesis under fluctuating light

Adaptation of plant photosynthesis to dynamic light conditions experienced in natural environments is achieved through specific protective mechanisms. Energy-dependent non-photochemical quenching (qE), regulated by Photosystem II Subunit S (PsbS), is a key process facilitating acclimation to fluctuating light in C3 plants, which operate conventional photosynthesis. C4 plants, which include some of the worlds most productive and agriculturally important crops, have evolved a distinct high-efficiency photosynthetic pathway. Little is known about the role of specific processes, like qE, in acclimation of C4 plants to dynamic light environments. We generated gene-edited lines of the model C4 grass Setaria viridis lacking PsbS, which were found to be deficient in qE. This deficiency resulted in a modest increase in PSII photoinhibition and a CO2 assimilation penalty under light stress in short-term experiments, but photosynthesis and growth under fluctuating light were unaffected. Instead, keeping Photosystem I oxidised through photosynthetic control, negative feedback regulation of the Cytochrome b6f complex, was critical. Therefore, unlike in C3 plants, qE does not provide a significant adaptive advantage to C4 plants under dynamic light conditions. These findings provide important insights into the biology of C4 plants and help prioritise future strategies for improving the productivity and resilience of C4 crops.

plant biology↗

The Role of Phosphoenolpyruvate Carboxylase-Protein Kinase in C4 Photosynthesis: Insights from Zea mays Mutant Analysis

Understanding the regulation of enzyme activity involved in photosynthesis is essential for engineering enhanced carbon fixation in crops. In C4 plants, the enzyme phosphoenolpyruvate carboxylase (PEPC, EC 4.1.1.31) is one of the most abundant leaf enzymes and plays an essential role in photosynthetic carbon dioxide (CO2) fixation. The enzyme also plays a key role in central metabolism (e.g., providing intermediates to the citric acid cycle) and therefore must be highly regulated to coordinate its activity. The regulation of PEPC activity can occur allosterically by glucose 6-phosphate activation and malate inhibition, which is in part influenced by reversible phosphorylation. A specific light-dependent phosphorylation of PEPC at an N-terminal serine residue by the PEPC-protein kinase (PEPC-PK) can regulate its sensitivity to this allosteric regulation. However, the impact of this PEPC phosphorylation has not been tested in a C4 crop. Therefore, we created PEPC-PK mutant lines in Zea mays to assess the impact of PEPC phosphorylation on its allosteric regulation, photosynthesis, and growth. While the maximum PEPC activity was unchanged, PEPC in the PEPC-PK mutant plants was not phosphorylated under light and was more sensitive to malate inhibition. However, gas exchange, electron transport, and field biomass analyses showed no differences in the PEPC-PK mutant plants. These results demonstrate that in Z. mays PEPC phosphorylation affects enzyme sensitivity to malate in vitro but does not substantially alert photosynthetic performance or growth under field conditions suggesting additional regulation of PEPC activity in planta.

plant biology↗

Fitting photosynthetic carbon dioxide and irradiance response curves for C4 leaves

Gas exchange measurements provide crucial insights into the complex mechanisms of photosynthesis. Responses of CO2 assimilation rate (A) to intercellular CO2 partial pressure (Ci) and irradiance (I) link gas exchange measurements to the underlying photosynthetic biochemistry of a leaf. The unique biochemistry and leaf anatomy which distinguish C4 photosynthesis make it necessary to apply models and fitting routines which appropriately parameterise and incorporate these characteristics. Here we provide updates to the C4 photosynthesis model by improving the parameterisation of cyclic electron flow in C4 photosynthesis using experimentally derived values from S. viridis. We additionally describe two fitting routines for assessing C4 photosynthesis based on the updated model. Fitting of a CO2 response curve (A/Ci) provides estimates of maximum PEP carboxylase activity (Vpmax) and maximum Rubisco activity (Vcmax), and calculates the electron transport rate (J) needed to sustain the measured CO2 assimilation rate (A). Fitting of an irradiance response curve (A/I) provides estimates for the maximum electron transport rate (Jmax), day respiration rate (Rd), the quantum yield ({phi}CO2) and light compensation point ({Gamma}light). Values of the above output parameters are provided at both the measurement temperature and at 25 {degrees}C for ease of comparative reporting. The fitting tool has been designed in Microsoft Excel to minimise barriers to entry and enable simplicity of fitting while simultaneously catering to individuals with diverse expertise and experience in C4 gas exchange modelling.

plant biology↗

A novel PGRL1 paralog refined the control of photoprotection in grasses and facilitated cell specialisation in C4 photosynthesis

The PGR5-PGRL1 pathway protects plants from photodamage by regulating electron flow to maintain Photosystem I in an oxidised state. Grasses possess two PGRL1 paralogs, but their functional roles have remained unknown. Here, we show that the ancestral PGRL1 paralog, PGRL1, which is conserved across algae and land plants, is enriched in the mesophyll cells of grasses that perform the NADP-ME subtype of C4 photosynthesis. In contrast, the grass-specific paralog PGRL1{beta} is enriched in bundle sheath cells. To investigate the functional significance of this cell-specific expression, we generated gene-edited lines of the NADP-ME C4 grass Setaria viridis lacking either PGRL1 paralog. We found that PGRL1{beta} in bundle sheath cells was required for rapid photoprotection, enabling Photosystem I oxidation five seconds faster during transitions from darkness to high light. In contrast, PGRL1 in mesophyll cells was essential for maintaining Photosystem I oxidation under steady-state high-light conditions. We propose that these complementary functions arise from structural differences within the lumen-facing regions of the two paralogs, providing a mechanistic basis for their distinct roles in regulating photoprotection. The conservation of this dual PGRL1 system across grasses suggests that functional specialisation of the paralogs expands the dynamic range of protective responses, enhancing photosynthetic performance under fluctuating and high-light stress conditions.

plant biology↗

PGR5 is needed for redox-dependent regulation of ATP synthase both in chloroplasts and in cyanobacteria

The regulation of proton motive force (pmf) via ATP synthase activity is a critical mechanism by which photosynthetic organisms maintain redox homeostasis and activate photoprotective responses under fluctuating light conditions. Here, we used time-resolved electrochromic shift (ECS) measurements to investigate pmf dynamics across a range of photosynthetic organisms. Our results reveal that ATP synthase is dynamically regulated during light fluctuations, but in Arabidopsis thaliana could this regulation could not be explained by the known light-induced reduction of the CF{square}{gamma} subunit, suggesting alternative control mechanisms. The PROTON GRADIENT REGULATION 5 (PGR5) protein, previously proposed to facilitate cyclic electron transport (CET), also has a potential role in ATP synthase regulation. The physiological role of cyanobacterial Pgr5 has remained elusive. We characterised a {Delta}pgr5 mutant of Synechocystis sp. PCC 6803 and investigated pmf dynamics in pgr5 mutants of Chlamydomonas reinhardtii, Arabidopsis, and the C4 grass Setaria viridis. While PGR5 was not required for CET in Synechocystis, it was needed for downregulating ATP synthase under high irradiance in all tested organisms via a thiol redox state dependent mechanism. Furthermore, interaction between AtPGR5 and AtCF{square}{gamma} suggests that PGR5 functions as a conserved inhibitor of ATP synthase under high light, contributing to pmf retention and photoprotection. HighlightPGR5 is involved in regulation of ATP synthase in fluctuating light conditions across photosynthetic organisms in a manner that depends on the thiol redox state of the chloroplast or cell.

plant biology↗

PGR5 promotes energy-dependent non-photochemical quenching to enable efficient C4 photosynthesis under fluctuating light

PROTON GRADIENT REGULATION 5 (PGR5) is essential for generating proton motive force across thylakoid membranes in C3 plants and supporting photoprotection under fluctuating light conditions. It is proposed that this function is achieved by regulating cyclic electron flow around Photosystem I. During the evolutionary transition from C3 to C4 photosynthesis, the leaf abundance of PGR5 has increased, coinciding with a rise in the cyclic electron flow rate. To investigate the contribution of PGR5 to photoprotection in C4 photosynthesis, we generated model C4 monocot Setaria viridis with null pgr5 alleles. We show that plants lacking PGR5 struggle to establish proton motive force and energy-dependent non-photochemical quenching (qE) at higher irradiances during instantaneous measurements. This leads to a progressive decline in maximum Photosystem I activity when leaves are exposed to repeated cycles of high irradiance. Additionally, plants without PGR5 exhibit severely reduced growth and photosynthesis compared to wild type plants when grown under fluctuating daylight but not under constant daylight. In the absence of PGR5, a slower-relaxing, zeaxanthin-dependent form of non-photochemical quenching supports growth under fluctuating light, albeit at the cost of reduced photochemical efficiency and assimilation rate. Our findings underscore the role of PGR5 in enabling efficient C4 photosynthesis under fluctuating light by establishing proton motive force for the rapid upregulation of qE and preventing photodamage to the electron transport machinery. This study highlights the importance of various non-photochemical quenching mechanisms for C4 photosynthesis and emphasises the role of PGR5 in the evolution of C4 plants.

plant biology↗

NDH complex-mediated cyclic electron flow in bundle sheath cells enables C4 photosynthesis

The superior productivity of C4 plants is achieved via a metabolic C4 cycle which acts as a CO2 pump across mesophyll and bundle sheath (BS) cells and requires an additional input of energy in the form of ATP. Chloroplast NADH dehydrogenase-like complex (NDH) increases ATP production in C3 plants by operating cyclic electron flow (CEF) around Photosystem I (PSI), and its importance for C4 photosynthesis has been proposed from evolutionary and reverse genetics studies. We used the gene-edited C4 species Setaria viridis with null ndhO alleles lacking NDH to study a contribution of the complex to the cell-level electron transport. Our results indicate that NDH is the primary PSI electron acceptor mediating the majority of CEF in BS cells whilst the contribution of the complex to CEF in mesophyll cells is minimal. Moreover, the reduced leaf CO2 assimilation rate and growth of plants lacking the complex cannot be rescued by supplying additional CO2, indicating that NDH is essential for generating ATP required for CO2 fixation by the C3 cycle. Hereby we resolve a cell-level mechanism for the contribution of NDH to supporting high CO2 assimilation rates in C4 photosynthesis.

plant biology↗

Faster responses of photosynthesis to light transitions increase biomass and grain yield in transgenic Sorghum bicolor overexpressing Rieske FeS

Sorghum is one of the most important crops providing food and feed in many of the worlds harsher environments. Sorghum utilises the C4 pathway of photosynthesis in which a biochemical carbon concentrating mechanism results in high CO2 assimilation rates. Overexpressing the Rieske subunit of the Cytochrome b6f complex was previously shown to increase the rate of photosynthetic electron transport and stimulate CO2 assimilation in the model C4 plant Setaria viridis. To test whether productivity of C4 crops could be improved by Rieske overexpression, we created transgenic Sorghum bicolor plants with increased Rieske content. The transgenic plants showed no marked changes in abundance of other photosynthetic proteins or chlorophyll content. Increases in yield of Photosystem II and CO2 assimilation rate as well as faster responses of non-photochemical quenching during transient photosynthetic responses were observed as a result of an elevated in vivo Cytochrome b6f activity in plants overexpressing Rieske. The steady-state rates of electron transport and CO2 assimilation did not differ between transgenic and control plants, suggesting that Cytochrome b6f is not the only factor limiting electron transport in sorghum at high light and high CO2. Nevertheless, more agile responses of photosynthesis to light transitions led to increases in biomass and grain yield in plants overexpressing Rieske. Our results indicate that increasing Rieske content could boost productivity of C4 crops by improving the efficiency of light utilisation and conversion to biomass.

plant biology↗

A cross-scale analysis to understand and quantify effects of photosynthetic enhancement on crop growth and yield

Photosynthetic manipulation provides new opportunities for enhancing crop yield. However, understanding and quantifying effectively how the seasonal growth and yield dynamics of target crops might be affected over a wide range of environments is limited. Using a state-of-the-art cross-scale model we predicted crop-level impacts of a broad list of promising photosynthesis manipulation strategies for C3 wheat and C4 sorghum. The manipulation targets have varying effects on the enzyme-limited (Ac) and electron transport-limited (Aj) rates of photosynthesis. In the top decile of seasonal outcomes, yield gains with the list of manipulations were predicted to be modest, ranging between 0 and 8%, depending on the crop type and manipulation. To achieve the higher yield gains, large increases in both Ac and Aj are needed. This could likely be achieved by stacking Rubisco function and electron transport chain enhancements or installing a full CO2 concentrating system. However, photosynthetic enhancement influences the timing and severity of water and nitrogen stress on the crop, confounding yield outcomes. Strategies enhancing Ac alone offers more consistent but smaller yield gains across environments, Aj enhancement alone offers higher gains but is undesirable in less favourable environments. Understanding and quantifying complex cross-scale interactions between photosynthesis and crop yield will challenge and stimulate photosynthesis and crop research. Summary StatementLeaf-canopy-crop prediction using a state-of-the-art cross-scale model improves understanding of how photosynthetic manipulation alters wheat and sorghum growth and yield dynamics. This generates novel insights for quantifying impacts of photosynthetic enhancement on crop yield across environments.

plant biology↗

Rieske FeS overexpression in tobacco provides increased abundance and activity of Cytochrome b6f

Photosynthesis is fundamental for plant growth and yield. The Cytochrome b6f complex catalyses a rate-limiting step in thylakoid electron transport and therefore represents an important point of regulation of photosynthesis. Here we show that overexpression of a single core subunit of Cytochrome b6f, the Rieske FeS protein, led to up to a 40% increase in the abundance of the complex in Nicotiana tabacum (tobacco) and was accompanied by an enhanced in vitro Cytochrome f activity, indicating a full functionality of the complex. Analysis of transgenic plants overexpressing Rieske FeS by the light-induced fluorescence transients technique revealed a more oxidised primary quinone acceptor of Photosystem II (QA) and plastoquinone pool and a faster electron transport from the plastoquinone pool to Photosystem I upon changes in irradiance, compared to control plants. A faster establishing of qE, the energy-dependent component of non-photochemical quenching, in transgenic plants suggested a more rapid build-up of the transmembrane proton gradient, also supporting the increased in vivo Cytochrome b6f activity. However, there was no consistent increase in steady-state rates of electron transport or CO2 assimilation in plants overexpressing Rieske FeS grown in either laboratory conditions or in field trials, suggesting that the in vivo activity of the complex was only transiently increased upon changes in irradiance. Our results show that overexpression of Rieske FeS in tobacco enhances abundance of functional Cytochrome b6f and electron transport capacity and may have a potential to increase plant productivity if combined with other traits. One-sentence summaryIncreased abundance of Cytochrome b6f complex leads to transient increases in photosynthetic electron transport rate in tobacco.

plant biology↗

Increased sedoheptulose-1,7-bisphosphatase content in the C4 species Setaria viridis does not affect photosynthesis

Sedoheptulose-1,7-bisphosphatase (SBPase) is one of the rate-limiting enzymes of the Calvin cycle, and, in C3 plants, increasing the abundance of SBPase is known to provide higher photosynthetic rates and stimulate biomass and yield. C4 plants usually have higher photosynthetic rates because they operate a biochemical CO2 concentrating mechanism between mesophyll and bundle sheath cells. In the C4 system, SBPase and other enzymes of Calvin cycle are localised to the bundle sheath cells. Here we tested what effect increasing abundance of SBPase would have on C4 photosynthesis. Using Setaria viridis, a model C4 plant of NADP-ME subtype, we created transgenic plants with 1.5 to 3.2-times higher SBPase content, compared to wild type plants. Transcripts of the transgene were found predominantly in the bundle sheaths suggesting the correct cellular localisation of the protein. Abundance of RBCL, the large subunit of Rubisco, was not affected in transgenic plants overexpressing SBPase, and neither was relative chlorophyll content or photosynthetic electron transport parameters. We found no correlation between SBPase content in S. viridis and saturating rates of CO2 assimilation. Moreover, detailed analysis of CO2 assimilation rates at different CO2 partial pressure, irradiance and leaf temperature, showed no improvement of photosynthesis in plants overexpressing SBPase. We discuss potential implications of these results for understanding the regulation of C4 photosynthesis.

plant biology↗

Flv3A facilitates O2 photoreduction and affects H2 photoproduction independently of Flv1A in diazotrophic Anabaena filaments

The model heterocyst-forming filamentous cyanobacterium, Anabaena sp. PCC 7120 (Anabaena) represents multicellular organisms capable of simultaneously performing oxygenic photosynthesis in vegetative cells and the O2-sensitive N2-fixation inside the heterocysts. The flavodiiron proteins (FDPs) have been shown to participate in photoprotection of photosynthesis by driving excess electrons to O2 (Mehler-like reaction). Here, we addressed the physiological relevance of the vegetative cell-specific Flv1A and Flv3A on the bioenergetic processes occurring in diazotrophic Anabaena under variable CO2. We demonstrate that both Flv1A and Flv3A are required for proper induction of the Mehler-like reaction upon a sudden increase in light intensity, which is likely important for the activation of carbon-concentrating mechanisms (CCM) and CO2 fixation. Under ambient CO2 diazotrophic conditions, Flv3A is capable of mediating moderate O2 photoreduction, independently of Flv1A, but in coordination with Flv2 and Flv4. Strikingly, the lack of Flv3A resulted in strong downregulation of the heterocyst-specific uptake hydrogenase, which led to enhanced H2 photoproduction under both oxic and micro-oxic conditions. These results reveal a novel regulatory network between the Mehler-like reaction and the diazotrophic metabolism, which is of great interest for future biotechnological applications.

plant biology↗

Expression of a CO2-permeable aquaporin enhances mesophyll conductance in the C4 species Setaria viridis

A fundamental limitation of photosynthetic carbon fixation is the availability of CO4. In C4 plants, primary carboxylation occurs in mesophyll cytosol, and little is known about the role of CO2 diffusion in facilitating C4 photosynthesis. We have examined the expression, localization, and functional role of selected plasma membrane intrinsic aquaporins (PIPs) from Setaria italica (foxtail millet) and discovered that SiPIP2;7 is CO2-permeable. When ectopically expressed in mesophyll cells of S. viridis (green foxtail), SiPIP2;7 was localized to the plasma membrane and caused no marked changes in leaf biochemistry. Gas-exchange and C18O16O discrimination measurements revealed that targeted expression of SiPIP2;7 enhanced the conductance to CO2 diffusion from the intercellular airspace to the mesophyll cytosol. Our results demonstrate that mesophyll conductance limits C4 photosynthesis at low pCO2 and that SiPIP2;7 is a functional CO2 permeable aquaporin that can improve CO2 diffusion at the airspace/mesophyll interface and enhance C4 photosynthesis.

plant biology↗

Resolving leaf level metabolism of C4 Setaria viridis acclimated to low light through a biochemical model

When C4 leaves are exposed to low light, CO2 concentration in the bundle sheath (BS) cells decreases, causing an increase in photorespiration relative to assimilation, and a consequent reduction in biochemical efficiency. These effects can be mitigated by complex acclimation syndromes, which are of primary importance for crop productivity, but not well studied. We unveil an acclimation strategy involving regulation of electron transport processes. Firstly, we characterise anatomy, gas-exchange and electron transport of C4 Setaria viridis grown under low light. Through a purposely developed biochemical model, we resolve the photon fluxes and reaction rates to explain how the concerted acclimation strategies sustain photosynthetic efficiency. Our results show that a smaller BS in low light-grown plants limited leakiness (the ratio of CO2 leak rate out of the BS over the rate of supply via C4 acid decarboxylation) but sacrificed light harvesting and ATP production. To counter ATP shortage and maintain high assimilation rates, plants facilitated light penetration through the mesophyll and upregulated cyclic electron flow in the BS. This shade tolerance mechanism based on optimisation of light reactions is potentially more efficient than the known mechanisms involving the rearrangement of carbon metabolism, and can potentially lead to innovative strategies for crop improvement. SignificanceWe mechanistically link the optical cross-section of leaf compartments with the rate of electron transport, the engagement of cyclic electron flow, the relative rate of ATP and NADPH generation, and fluxes through the carbon metabolism. The striking capacity of Setaria viridis to counter the decrease in light absorption in the bundle sheath with an increase of cyclic electron flow presents perhaps the most efficient mechanism of shade acclimation.

plant biology↗

Up-regulation of bundle sheath electron transport capacity under limiting light in C4 Setaria viridis

C4 photosynthesis is a biochemical pathway that operates across mesophyll and bundle sheath (BS) cells to increase CO2 concentration at the site of CO2 fixation. C4 plants benefit from high irradiance but their efficiency decreases under shade causing a loss of productivity in crop canopies. We investigated shade acclimation responses of a model NADP-ME monocot Setaria viridis focussing on cell-specific electron transport capacity. Plants grown under low light (LL) maintained CO2 assimilation rates similar to high light plants but had an increased chlorophyll and light-harvesting-protein content, predominantly in BS cells. Photosystem II (PSII) protein abundance, oxygen-evolving activity and the PSII/PSI ratio all increased in LL BS cells indicating a higher capacity for linear electron flow. PSI, ATP synthase, Cytochrome b6f and the chloroplastic NAD(P) dehydrogenase complex, which constitute the BS cyclic electron flow machinery, were all upregulated in LL plants. A decline in PEP carboxylase activity in mesophyll cells and a consequent shortage of reducing power in BS chloroplasts was associated with the more oxidised redox state of the plastoquinone pool in LL plants and the formation of PSII - light-harvesting complex II supercomplexes with an increased oxygen evolution rate. Our results provide evidence of a redox regulation of the supramolecular composition of Photosystem II in BS cells in response to shading. This newly identified link contributes to understanding the regulation of PSII activity in C4 plants and will support strategies for crop improvement including the engineering of C4 photosynthesis into C3 plants. Significance statementThe efficiency of C4 photosynthesis decreases under low irradiance causing a loss of productivity in crop canopies. We investigate shade acclimation of a model NADP-ME monocot, analysing cell-specific protein expression and electron transport capacity. We propose a regulatory pathway controlling abundance and activity of Photosystem II in bundle sheath cells in response to irradiance.

plant biology↗

Flavodiiron proteins and NDH-1 cooperate to maintain photosynthetic redox poise in Synechocystis

In oxygenic photosynthetic organisms excluding angiosperms, flavodiiron proteins (FDPs) catalyze light-dependent reduction of O2 to H2O. This alleviates electron pressure on the photosynthetic apparatus and protects it from photodamage. In Synechocystis sp. PCC 6803, four FDP isoforms function as hetero-oligomers of Flv1 and Flv3 and/or Flv2 and Flv4. An alternative electron transport pathway mediated by the NAD(P)H dehydrogenase-like complex (NDH-1) also contributes to redox hemostasis and the photoprotection of photosynthesis. Four NDH-1 types haven been characterized in cyanobacteria: NDH-11 and NDH-12, which function in respiration; and NDH-13 and NDH-14, which function in CO2 uptake. All four types are involved in cyclic electron transport. Along with single FDP mutants ({Delta}flv1 and {Delta}flv3) and the double NDH-1 mutants ({Delta}d1d2, which is deficient in NDH-11,2 and {Delta}d3d4, which is deficient in NDH-13,4), we studied triple mutants lacking either one of Flv1 or Flv3, and NDH-11,2 or NDH-13,4. We show that the presence of either Flv1/3 or NDH-11,2, but not NDH-13,4, is indispensable for survival during changes in growth conditions from high CO2 /moderate light to low CO2 / high light. Our results suggest functional redundancy and crosstalk between FDPs and NDH-11,2 under the studied conditions, and demonstrate that the functions of FDPs and NDH-11,2 are dynamically coordinated for the efficient oxidation of PSI and for photoprotection under variable CO2 and light availability. One sentence summaryFlavodiiron proteins and NDH-1 complex ensure survival of cyanobacterial cells by cooperatively safeguarding the photosynthetic apparatus against excessive reduction

plant biology↗

Overexpression of the Rieske FeS protein of the Cytochrome b6f complex increases C4 photosynthesis

C4 plants contribute 20% to the global primary productivity despite representing only 4% of higher plant species. Their CO2 concentrating mechanism operating between mesophyll and bundle sheath cells increases CO2 partial pressure at the site of Rubisco and hence photosynthetic efficiency. Electron transport chains in both cell types supply ATP and NADPH for C4 photosynthesis. Since Cytochrome b6f is a key point of control of electron transport in C3 plants, we constitutively overexpressed the Rieske FeS subunit in Setaria viridis to study the effects on C4 photosynthesis. Rieske FeS overexpression resulted in a higher content of Cytochrome b6f in both mesophyll and bundle sheath cells without marked changes in abundances of other photosynthetic complexes and Rubisco. Plants with higher Cytochrome b6f abundance showed better light conversion efficiency in both Photosystems and could generate higher proton-motive force across the thylakoid membrane. Rieske FeS abundance correlated with CO2 assimilation rate and plants with a 10% increase in Rieske FeS content showed a 10% increase in CO2 assimilation rate at ambient and saturating CO2 and high light. Our results demonstrate that Cytochrome b6f controls the rate of electron transport in C4 plants and that removing electron transport limitations can increase the rate of C4 photosynthesis.

plant biology↗