Search

We use quantum trajectory theory to study the dynamics of the first step in photosynthesis for a single photon interacting with photosystem II (PSII). By considering individual trajectories we are able to look beyond the ensemble average dynamics to compute the PSII system evolution conditioned upon individual photon counting measurements. Measurements of the transmitted photon beam strongly affects the system state, since detection of an outgoing photon confirms that the PSII must be in the electronic ground state, while a null measurement implies it is in an excited electronic state. We show that under ideal conditions, observing the null result transforms a state with a low excited state population to a state with nearly all population contained in the excited states. We study the PSII dynamics conditioned on such photon counting for both a pure excitonic model of PSII and a more realistic model with exciton-phonon coupling to a dissipative phononic environment. In the absence of such coupling, we show that the measured fluorescence rates show oscillations constituting a photon-counting witness of excitonic coherence. Excitonic coupling to the phonon environment has a strong effect on the observed rates of fluorescence, damping the oscillations. Addition of non-radiative decay and incoherent transitions to radical pair states in the reaction center to the phononic model allows extraction of a quantum efficiency of 92.5% from the long-time evolution, consistent with bulk experimental measurements. [ABSTRACT FROM AUTHOR]

Freshwater salinization is an increasing threat to lakes worldwide, but despite being a widespread issue, little is known about its impact on biological communities at the base of the food chain. Here we used a mesocosm set‐up coupled with modern high‐frequency sensor technology to identify short‐ and longer‐term responses of phytoplankton to salinization in an oligotrophic lake. We tested the effects of salinization over a gradient of increasing salt concentrations that can be found in natural lakes exposed to road salt contamination (added salt range: from 0 to 1500 mg Cl− L−1). The high‐frequency chlorophyll‐a (chl‐a) fluorescence measurements showed an increasing divergence of chl‐a concentrations along the salinization gradient over time, with substantially lower concentrations at higher salt levels. At the sub‐daily scale, we found a profound suppression of day–night signal cycles with increasing salinity, which could be related to physiological stress due to the impairment of photosynthesis via effects on the photosystem II or potential changes in the active migration of phytoplankton. Community analyses revealed a similar decline pattern for the total phytoplankton biomass and a collapse of the total zooplankton biomass. Interestingly, we found a loss of phytoplankton diversity coupled with a compositional re‐organization involving the loss of dominant green algae but increased biomass of salt‐tolerant cyanobacteria. Altogether, these results suggest that specific cyanobacterial taxa can benefit from freshwater salinization following the collapse of dominant phytoplankton competitors and zooplankton herbivores. The results also highlight the value of autonomous sensor technology to capture novel, small‐scale ecological responses to freshwater salinization, and thereby to track fast changes in primary producer communities. [ABSTRACT FROM AUTHOR]

Summary The chloroplast genome has considerable potential to enhance crop productivity, but it remains underutilized in breeding because it is difficult to modify. This study elucidates the potential of recently developed chloroplast‐targeted C‐to‐T base editors in facilitating the use of the chloroplast genome for crop breeding. The herbicide metribuzin interferes with photosynthesis by binding to the D1 protein of photosystem II, encoded by the chloroplast genome. Naturally occurring D1 mutants with V219I or A251V substitutions are known to have resistance to some herbicides including metribuzin. Here, using the base editors, we introduced these substitutions and showed that the A251V single mutation and the V219 & A251V double mutations conferred significant metribuzin resistance to Arabidopsis thaliana. The V219I & A251V double mutants exhibited increased metribuzin resistance and grew better than the A251V single mutants. Furthermore, the double mutants grew as well as wild‐type plants in the absence of metribuzin. The single and double mutants, which are a challenge to obtain through traditional mutagenesis and crossbreeding methods, can be relatively easily generated using C‐to‐T base editors. In view of the conservation of V219 and A251 across numerous species, C‐to‐T base editing can potentially confer metribuzin resistance to a wide range of crops. Compared to nuclear genes, chloroplast genes are also less likely to spread into wild populations. Our findings suggest that chloroplast‐targeting C‐to‐T base editors will find many roles in future crop breeding efforts. [ABSTRACT FROM AUTHOR]

Inspired by the direct charge transfer in the natural photosystems, herein, we design covalent triazine frameworks (CTFs) with direct electron transfer by constructing the minimal amount of –donor–acceptor 1–acceptor 2– type moieties in the CTF backbone for photocatalytic hydrogen evolution. By introducing only 0.75% of the acceptor 2, the as-prepared CTF exhibited an enhanced hydrogen evolution rate of 3215 μmol g−1 h−1. [ABSTRACT FROM AUTHOR]

Chloroplast-encoded multi-span thylakoid membrane proteins are crucial for photosynthetic complexes, yet the coordination of their biogenesis remains poorly understood. To identify factors that specifically support the cotranslational biogenesis of the reaction center protein D1 of photosystem (PS) II, we generated and affinity-purified stalled ribosome-nascent chain complexes (RNCs) bearing D1 nascent chains. Stalled RNCs translating the soluble ribosomal subunit uS2c were used for comparison. Quantitative tandem-mass spectrometry of the purified RNCs identified around 140 proteins specifically associated with D1 RNCs, mainly involved in protein and cofactor biogenesis, including chlorophyll biosynthesis, and other metabolic pathways. Functional analysis of STIC2, a newly identified D1 RNC interactor, revealed its cooperation with chloroplast protein SRP54 in the de novo biogenesis and repair of D1, and potentially other cotranslationally-targeted reaction center subunits of PSII and PSI. The primary binding interface between STIC2 and the thylakoid insertase Alb3 and its homolog Alb4 was mapped to STIC2's β-sheet region, and the conserved Motif III in the C-terminal regions of Alb3/4. Synopsis: The biogenesis and maintenance of photosynthetic complexes requires precise coordination of cotranslational maturation, folding, targeting and insertion of their plastid-encoded subunits. This work offers insight into the interactome of photosystem II reaction center-specific ribosome-nascent chain complexes, and identifies a role for STIC2 in their cotranslational protein sorting. Proteins from metabolic, biogenesis, and protein processing pathways associate with D1-translating ribosomes. Knock-out of STIC2 and the targeting factor cpSRP54 in Arabidopsis causes sensitivity to high light and low accumulation of photosystem subunits. STIC2 partially associates with ribosomes and affects chloroplast translation. The C-terminal motif III of the thylakoid membrane proteins Alb3 and Alb4 mediates their interaction within the β-sheet region of STIC2. The chloroplast protein STIC2 associates with ribosomes translating the photosystem II reaction center protein D1 and supports insertion into the thylakoid membrane. [ABSTRACT FROM AUTHOR]

Background: Vegetable soybean is rich in nutrients and has a unique flavor. It is highly preferred by people because of its pharmacological activities, including those that regulate the intestines and lower blood pressure. The pod color of vegetable soybeans is an important quality that indicates their freshness and has a significant impact on their commercialization. Results: In this study, pod color was evaluated in 301 vegetable soybean accessions collected from various regions. Genome-wide association analysis was carried out using the Mixed linear model (MLM), a total of 18 quantitative trait loci including 117 SNPs were detected. Two significant QTLs located on chromosomes 6 (qGPCL4 /qGPCa1/qGPCb2) and 18 (qGPCL10/qGPCb3) were consistently detected across different variables. Based on gene functional annotation, 30 candidate genes were identified in these two candidate intervals. Combined with transcriptome analysis, Glyma.18g241700 has been identified as a candidate gene for regulating pod color in vegetable soybeans. Glyma.18g241700 encodes a chlorophyll photosystem I subunit XI. which localizes to the chloroplast named GmPsaL, qRT-PCR analysis showed that GmPsaL was specifically highly expressed in developing pods. Furthermore, overexpression of GmPsaL in transgenetic Arabidopsis plants produced dark green pods. Conclusions: These findings may be useful for clarifying the genetic basis of the pod color of vegetable soybeans. The identified candidate genes may be useful for the genetic improvement of the appearance quality of vegetable soybeans. [ABSTRACT FROM AUTHOR]

Background: In recent years, more severe droughts have occurred frequently in many parts of the world, drought stress is the primary abiotic stress factor restricting the growth and quality of flue-cured tobacco. Therefore, screening dryland cultivation-compatible flue-cured tobacco varieties will help reduce the negative impact of drought. Methods: Tobacco varieties were selected: Qinyan 96 (Q96), Zhongyan 101 (Z101), Yunyan 87 (Y87), and Yunyan 116 (Y116). A pot experiment was conducted with four water supply gradients: sufficient, mild stress, moderate stress, and severe stress. The aim was to analyze inter-varietal differences in agronomic traits, photosynthetic traits, reactive oxygen species (ROS) metabolism, and antioxidant enzyme system under drought stress. Additionally, the drought resistance of four flue-cured tobacco varieties was evaluated using principal component analysis and membership function analysis. Results: The results showed that drought intensification inhibited seedling growth and development across all varieties, with Q96 showing the least decrease and Y116 the greatest. With the increasing degree of drought stress, photosynthetic rates (Pn), transpiration rate (Tr), and stomatal conduction (Gs) have shown gradually decreasing trends, while substomatal cavity CO2 concentration (Ci) showed a growing trend. Severe drought corresponded with lower chlorophyll content and decreased the maximal photochemical efficiency (Fv/Fm), photosystem II (PSII), and photochemical quenching coefficient (qP) in all varieties, while steady-state non-photochemical quenching (NPQ) increased. Increased drought stress led to significantly higher reactive oxygen species (ROS) and malondialdehyde (MDA) content accumulation in tobacco seedlings. The antioxidant enzyme activities in, Q96, Z101, and Y87 increased under mild drought stress, whereas Y116 showed decreased activity. Conclusion: The drought resistance ranking among the four varieties is as follows: Q96 > Z101 > Y87 > Y116. Therefore, Q96 is a promising drought-tolerant breeding material that can be used as a reference for dryland cultivation of flue-cured tobacco. [ABSTRACT FROM AUTHOR]

Photosystem II (PSII) has the unique ability to perform water-splitting. With light-harvesting complexes, it forms the PSII supercomplex (PSII-SC) which is a functional unit that can perform efficient energy conversion, as well as photoprotection, allowing photosynthetic organisms to adapt to the naturally fluctuating sunlight intensity. Achieving these functions requires a collaborative energy transfer network between all subunits of the PSII-SC. In this work, we perform kinetic analyses and characterise the energy landscape of the PSII-SC with a structure-based energy transfer model. With first passage time analyses and kinetic Monte Carlo simulations, we are able to map out the overall energy transfer network. We also investigate how energy transfer pathways are affected when individual protein complexes are removed from the network, revealing the functional roles of the subunits of the PSII-SC. In addition, we provide a quantitative description of the flat energy landscape of the PSII-SC. We show that it is a unique landscape that produces multiple kinetically relevant pathways, corresponding to a high pathway entropy. These design principles are crucial for balancing efficient energy conversion and photoprotection. Photosystem II supercomplexes fulfill different functions that require a collaborative energy transfer network. Here, the authors simulate energy-transfer processes in a supercomplex to reveal the functional role of its subunits. [ABSTRACT FROM AUTHOR]

Photosystem II (PSII) is a multi‐subunit protein‐pigment complex with diverse redox‐active cofactors, which enabled the biological availability of O2 on Earth. The substrate specificity and the underlying redox chemistry of the Mn4CaO5 catalytic center are investigated using alternate substrates such as small molecules (ammonia and methanol) and halides (Cl‐, Br‐, I‐) instead of the natural substrate water. Changes in the kinetic profiles of steady‐state O2 evolution and of dichlorophenolindophenol (DCIP) photochemical reduction by PSII as well as the detection of modified sites by proteomic analysis implied the possibility of alternate substrate photooxidation. Of particular interest is the role of two chlorides bound close to the putative water channels in the native system. The mutation of D2‐K317 to alanine is believed to impair the binding of a catalytically relevant chloride, eliminating the chloride requirement for water oxidation catalysis. The efficiency of small molecule photooxidation by the OEC is enhanced by the mutated D2‐K317A PSII complex without the competition from chloride. These results provide insight into the role of bound chloride in native PSII as a filter for enhancing the selectivity of water oxidation. The design principles for PSII may be extended to new strategies for developing highly selective catalysts. [ABSTRACT FROM AUTHOR]

Witches' brooms are abnormal branches that can affect various tree species in the Brazilian savanna, such as Xylopia aromatica. This disease leads to biomass loss and alters growth patterns. This study investigated the anatomical and physiological impacts of witches' broom on X. aromatica, hypothesizing that the disease induces changes in both infected and noninfected branches of the same tree. Measurements included leaf area, chlorophyll content and photosystem II (PSII) functionality in control and infected plants, as well as branch types (control, uninfected and infected branches for infected plants). Water potential was assessed at predawn and midday, and stem samples were analysed for anatomical and vessel element analysis. Witches' broom disease manifests as short brown stems and small yellowish‐green leaves. While infected and uninfected plants showed no significant differences in leaf area and leaf dry biomass, infected branches had reduced leaf number, area and weight. Chlorophyll content and PSII efficiency were significantly reduced in infected branches, indicating photosynthetic disruption. Water potential was lower at predawn in infected plants but normalized by midday, suggesting an adaptive response. Anatomical changes in infected branches included alterations in vessel elements and parenchymatic rays. Overall, X. aromatica displays localized changes due to witches' broom, which aids in water stress adaptation. Despite these findings, long‐term studies are needed to evaluate the impacts on biomass reduction and reproductive investment in Brazilian savanna areas, crucial for understanding the ecological impact and developing survival strategies for affected plants. [ABSTRACT FROM AUTHOR]

Photosynthetic reaction center (RC) proteins are finely tuned molecular systems optimized for solar energy conversion. RCs effectively capture and convert sunlight with near unity quantum efficiency utilizing light-induced directional electron transfer through a series of molecular cofactors embedded within the protein core to generate a long-lived charge separated state with a useable electrochemical potential. Of current interest are new strategies that couple RC chemistry to the direct synthesis of energy-rich compounds. This Feature Article highlights recent work from our lab on RC and RC-inspired hybrid systems that capture the Sun's energy and convert it to chemical energy in the form of H2, a carbon-neutral energy source derived from water. Biohybrids made from the Photosystem I (PSI) RC are among the best photocatalytic H2-producing protein hybrids to date. Targeted self-assembly strategies that couple abiotic catalysts to PSI translate to catalyst incorporation at intrinsic PSI sites within thylakoid membranes to achieve complete solar water-splitting systems. RC-inspired biohybrids interface synthetic photosensitizers and molecular catalysts with small proteins to create photocatalytic systems and enable the spectroscopic discernment of the structural features and electron transfer processes that underpin solar-driven proton reduction. In total, these studies showcase the incredible scientific opportunities photosynthetic biohybrid research provides for harnessing the optimal qualities of both artificial and natural photosynthetic systems and developing materials that capture, convert, and store solar energy as a fuel. [ABSTRACT FROM AUTHOR]

Photosystem I (PSI) forms a large macromolecular complex of ∼580 kDa that resides in the thylakoid membrane and mediates photosynthetic electron transfer. PSI is composed of 18 protein subunits and nearly 200 co-factors. The assembly of the complex in thylakoid membranes requires high spatial and temporal coordination, and is critically dependent on a sophisticated assembly machinery. Here, we report and characterize CO-EXPRESSED WITH PSI ASSEMBLY1 (CEPA1), a PSI assembly factor in Arabidopsis (Arabidopsis thaliana). The CEPA1 gene was identified bioinformatically as being co-expressed with known PSI assembly factors. Disruption of the CEPA1 gene leads to a pale phenotype and retarded plant development but does not entirely abolish photoautotrophy. Biophysical and biochemical analyses revealed that the phenotype is caused by a specific defect in PSI accumulation. We further show that CEPA1 acts at the post-translational level and co-localizes with PSI in nonappressed thylakoid membranes. In native gels, CEPA1 co-migrates with thylakoid protein complexes, including putative PSI assembly intermediates. Finally, protein–protein interaction assays suggest cooperation of CEPA1 with the PSI assembly factor PHOTOSYSTEM I ASSEMBLY3 (PSA3). Together, our data support an important but nonessential role of CEPA1 in PSI assembly. Arabidopsis CO-EXPRESSED WITH PSI ASSEMBLY1 interacts with PHOTOSYSTEM I ASSEMBLY3 and plays an important but nonessential role in assembly of photosystem I. [ABSTRACT FROM AUTHOR]

As an essential intrinsic component of photosystem II (PSII) in all oxygenic photosynthetic organisms, heme-bridged heterodimer cytochrome b559 (Cyt b559) plays critical roles in the protection and assembly of PSII. However, the underlying mechanisms of Cyt b559 assembly are largely unclear. Here, we characterized the Arabidopsis (Arabidopsis thaliana) rph1 (resistance to Phytophthora1) mutant, which was previously shown to be susceptible to the oomycete pathogen Phytophthora brassicae. Loss of RPH1 leads to a drastic reduction in PSII accumulation, which can be primarily attributed to the defective formation of Cyt b559. Spectroscopic analyses showed that the heme level in PSII supercomplexes isolated from rph1 is significantly reduced, suggesting that RPH1 facilitates proper heme assembly in Cyt b559. Due to the loss of RPH1-mediated processes, a covalently bound PsbE–PsbF heterodimer is formed during the biogenesis of PSII. In addition, rph1 is highly photosensitive and accumulates elevated levels of reactive oxygen species under photoinhibitory-light conditions. RPH1 is a conserved intrinsic thylakoid protein present in green algae and terrestrial plants, but absent in Synechocystis, and it directly interacts with the subunits of Cyt b559. Thus, our data demonstrate that RPH1 represents a chloroplast acquisition specifically promoting the efficient assembly of Cyt b559, probably by mediating proper heme insertion into the apo-Cyt b559 during the initial phase of PSII biogenesis. A chloroplast thylakoid protein is involved in the formation of an essential multisubunit protein complex during the initial steps of photosystem II assembly. [ABSTRACT FROM AUTHOR]

Cyanobacteria, red algae, and cryptophytes produce 2 classes of proteins for light harvesting: water-soluble phycobiliproteins (PBP) and membrane-intrinsic proteins that bind chlorophylls (Chls) and carotenoids. In cyanobacteria, red algae, and glaucophytes, phycobilisomes (PBS) are complexes of brightly colored PBP and linker (assembly) proteins. To date, 6 structural classes of PBS have been described: hemiellipsoidal, block-shaped, hemidiscoidal, bundle-shaped, paddle-shaped, and far-red-light bicylindrical. Two additional antenna complexes containing single types of PBP have also been described. Since 2017, structures have been reported for examples of all of these complexes except bundle-shaped PBS by cryogenic electron microscopy. PBS range in size from about 4.6 to 18 mDa and can include ∼900 polypeptides and bind >2000 chromophores. Cyanobacteria additionally produce membrane-associated proteins of the PsbC/CP43 superfamily of Chl a/b/d-binding proteins, including the iron-stress protein IsiA and other paralogous Chl-binding proteins (CBP) that can form antenna complexes with Photosystem I (PSI) and/or Photosystem II (PSII). Red and cryptophyte algae also produce CBP associated with PSI but which belong to the Chl a/b-binding protein superfamily and which are unrelated to the CBP of cyanobacteria. This review describes recent progress in structure determination for PBS and the Chl proteins of cyanobacteria, red algae, and cryptophytan algae. [ABSTRACT FROM AUTHOR]

This essay discusses how the ultrastructural changes in chloroplasts, particularly the mechanisms of thylakoid membrane unstacking, help maintain the photosynthetic performance of photosystem II (PSII) under stress conditions. This phenomenon may facilitate the repair of damaged PSII by providing access to the repair machinery. It is argued that this PSII repair mechanism accelerates PSII recovery, optimizing photosynthetic processes in stressed plants. Although some studies demonstrate the relationship between thylakoid membrane unstacking in stress conditions, these studies were developed with model species under controlled conditions. Thus, this essay serves as a validation tool for these previous studies, because it demonstrates that the relationships between ultrastructural changes in chloroplasts and the functioning of PSII are essential acclimative strategies for nonmodel plants to survive the constant edaphoclimatic changes of natural environments. Understanding these subcellular dynamics can significantly inform biologists about the plastic potential of plants, especially in heterogeneous environments. An integrated approach in future studies is necessary, highlighting the importance of exploring plant functional traits at multiple scales, because subcellular characteristics have great potential to understand plant acclimatization. [ABSTRACT FROM AUTHOR]

Single particle cryo electron microscopy (cryo‐EM) is now the major method for the determination of integral membrane protein structure. For the success of a given project the type of membrane mimetic used for extraction from the native cell membrane, purification to homogeneity and finally cryo‐grid vitrification is crucial. Although small molecule amphiphiles – detergents – are the most widely used membrane mimetic, specific tailoring of detergent structure for single particle cryo‐EM is rare and the demand for effective detergents not satisfied. Here, we compare the popular detergent lauryl maltose‐neopentyl glycol (LMNG) with the novel detergent neopentyl glycol‐derived triglucoside‐C11 (NDT‐C11) in its behavior as free detergent and when bound to two types of multisubunit membrane protein complexes – cyanobacterial photosystem I (PSI) and mammalian F‐ATP synthase. We conclude that NDT‐C11 has high potential to become a very useful detergent for single particle cryo‐EM of integral membrane proteins. [ABSTRACT FROM AUTHOR]

Aureococcus anophagefferens forms a model host-virus system with the "giant virus" Kratosvirus quantuckense. Studies to define its ribocell (uninfected) and virocell (virus-infected) forms are needed as these states co-occur during algal blooms. Previously, a link between light-derived energy, virus particle production, and virocell formation was noted. We explored how the time of day (morning, midday, or late day) of virus-host contact shaped virocell ontogeny. In parallel, we explored the dependence on light-derived energy in this mixotrophic plankter by inhibiting photosystem II, testing the role of heterotrophic energy in infection dynamics. Using flow cytometry and photochemical assessments, we examined the physiology of infected cells and controls, and estimated virus particle production. We observed differences between ribocell and virocell response to treatments, including reductions in virus particle production during reduced light duration) and PSII inhibition (i.e. "forced heterotrophy"). This work demonstrates the importance of light in shaping the fate of infected cells and provides insight into factors that constrain in situ blooms. Most significantly, we show that time of the solar day when a virus and host come into contact influences viral particle production, and therefore bloom dynamics; a factor that needs to be considered in bloom modeling work. [ABSTRACT FROM AUTHOR]

Leaf ontogeny of tropical evergreen tree species lasts several months with changes in size, shape, colouration and internal tissue distribution of leaves. Leaf initiation in Saraca asoca generally occurs once in a year during February–April, followed by very limited leafing thereafter. We measured the rate of photosynthesis, chlorophyll a fluorescence, energy quenching and PSII functions during the leaf ontogeny process. Observations were taken up to 35 days after opening of lamina (DAOL). Significant increase in the synthesis and accumulation of photosynthetic pigments but negative net photosynthesis was noticed during initial days of the ontogeny. The leaf moved from heterotrophy to autotrophy with gradual improvement of PSII functions. The ratio of intercellular CO2 (C i) and ambient CO2 (C a) showed significant change at ≥11 DAOL. Increase in the age of the leaf (between 5 and 28 DAOL) caused decrease in O-J rise and corresponding increase in J-I and I-P rise as well as of fluorescence maximum (F M) of the OJIP curve. The improvement of the electron transport components of the donor side of PSII was seen with increase in the functional oxygen evolving complex. The functional improvements of the donor and acceptor side of PSII during leaf ontogeny are discussed. The leaf ontogeny in Saraca asoca usually occurs once in a year and involves variation in PSII function. The developing leaves metabolically switch from heterotrophy to autotrophy. During leaf development, the carotenoids are accumulated earlier than chlorophylls. With the development of leaf, the PSII function improves leading to increased efficiency of oxygen evolving complex and photoelectron transport. [ABSTRACT FROM AUTHOR]

Xero-halophytes are the salt-tolerant plants of dry habitats that adapt efficient strategies to endure extreme salt and water fluctuations. This study elucidated the adaptations related to PSII photochemistry, photoprotection, and photoinhibition in six C4 xero-halophytes (Atriplex stocksii , Haloxylon stocksii , Salsola imbricata, Suaeda fruticosa, Desmostachya bipinnata , and Saccharum griffithii) grown in their native habitats. Chlorophyll a fluorescence quenching measurements suggested that S. imbricata and H. stocksii maintained efficient PSII photochemistry by downregulating heat dissipation and keeping a high fraction of open PSII centres that indicates plastoquinone (PQ) pool oxidation. Fluorescence induction kinetics revealed that S. imbricata demonstrated the highest performance index of PSII excitation to the reduction of end electron acceptors. S. fruticosa sustained photochemical efficiency through enhanced dissipation of excess energy and a low fraction of open PSII centres, indicating PQ reduced state. The large light-harvesting antenna size, deduced from the chlorophyll a / b ratio in S. fruticosa apparently led to the superior performance index of PSII excitation to the reduction of intersystem electron carriers. A. stocksii retained more open PSII centres with responsive non-photochemical quenching to safely dissipate excess energy. Despite maintaining the highest pigment contents and stoichiometry, A. stocksii remained lowest in both performance indices. The grass species D. bipinnata and S. griffithii kept fewer PSII centres open during photoinhibition, as evidenced by downregulation of PSII operating efficiency. The results provide insights into the differential modulation of PSII photochemical efficiency through dynamic control of photoprotective energy dissipation, PQ pool redox states, and photoinhibitory shutdown in these xero-halophytes. Photochemical adaptations of six C4 xero-halophytes reveal diverse strategies to endure salt and water fluctuations in native habitats. Variations in photochemistry, photoprotection, and photoinhibition indicate modulation of PSII photochemical efficiency. Different xero-halophytes exhibit distinct mechanisms for maintaining photochemical efficiency through dynamic control of plastoquinone pool redox states, excess energy dissipation, and shutdown mechanisms in response to environmental challenges. [ABSTRACT FROM AUTHOR]

Sri Lankan cassava mosaic virus (SLCMV) poses a significant threat to global food security by affecting the production of cassava (Manihot esculenta) in South‐east Asia. It causes mosaic patterns on the leaves, disrupts photosynthesis and respiration, and alters carbohydrate accumulation in the tubers. This study aimed to identify proteins associated with cassava mosaic disease symptoms in three cassava cultivars: resistant (TMEB419), tolerant (Kasetsart 50, KU50) and susceptible (Rayong 11, R11) to SLCMV. These cultivars were inoculated with SLCMV using top‐cleft grafting and monitored at 21, 32 and 67 days post‐inoculation (dpi). The disease severity differed among the cultivars following SLCMV inoculation. Liquid chromatography–tandem mass spectrometry (LC–MS/MS)‐based proteomics analysis identified 541 differentially expressed proteins (DEPs), including photosynthesis‐ and respiration‐associated proteins such as RuBisCO large subunit‐binding protein α (LSBP), chlorophyll a‐b binding protein, photosystem I reaction centre subunit III (PSI‐F), glyceraldehyde‐3‐phosphate dehydrogenase (GAPDH) and fructose‐bisphosphate aldolase (FBA). A protein–protein interaction network revealed interactions among PSI, PSII, cytochrome complex proteins and electron transporter proteins. Chlorophyll(ide) b reductase NYC1, upregulated in R11 (susceptible) at 21 and 32 dpi, interacted with chlorophyllase‐related proteins, suggesting that it has a role in altering chlorophyll metabolism. Reverse transcription‐quantitative PCR gene expression analysis confirmed upregulation of genes related to photosynthesis and respiration in KU50 and R11, predominantly at 21 or 32 dpi. These findings provide valuable insights into cassava responses to SLCMV infection, especially at the protein level and are key for developing resistant cultivars and effective disease management strategies in future research. [ABSTRACT FROM AUTHOR]

Climate‐driven changes in temperature and high nutrient inputs from anthropogenic activities significantly impact the interactions between submerged macrophytes and phytoplankton, potentially causing regime shifts in shallow freshwater lakes. Cyanobacteria, in particular, are predicted to become dominant among the phytoplankton under climate change, contributing to the collapse of submerged macrophytes. This study aimed to explore how submerged macrophytes and phytoplankton respond to rising temperatures and nutrient addition, how the presence of submerged macrophytes influences the photosynthetic activity of cyanobacteria, and how submerged macrophytes adapt their morphology and physiology to cope with excess phytoplankton. We conducted a fully factorial experiment consisting of two temperature conditions (low and high temperature), two nutrient conditions (with and without nutrient addition) and two plant conditions (plant presence and absence). We analysed changes in phytoplankton biomass and diversity (taxonomic and functional) in response to rising temperatures and nutrient addition. The maximum photochemical efficiency of the photosystem II (Fv/Fm) and the maximum relative electron transport rates (rETRmax) of cyanobacteria were determined. We measured the response of macrophytes to environmental changes by measuring antioxidant enzymes, such as superoxide dismutase (SOD) and catalase (CAT), as well as morphological indicators like plant height, weight, and the relative growth rate. In the absence of submerged macrophytes, rising temperatures led to higher total phytoplankton biomass and cyanobacteria dominance alongside reduced taxonomic and functional diversity. Conversely, when submerged macrophytes were present and no nutrients were added, rising temperatures did not lead to increased phytoplankton biomass. Macrophytes can suppress undesirable cyanobacterial proliferation by competing for nutrients and inhibiting Fv/Fm. Furthermore, under conditions of environmental stress, such as high chlorophyll a concentrations due to nutrient inputs, submerged macrophytes adapted by increasing height and the activity of antioxidant enzymes, such as SOD and CAT. Within the context of climate warming and increased nutrient inputs, phytoplankton growth, especially of cyanobacteria, may be favoured. However, our study demonstrated the critical role of submerged macrophytes in inhibiting phytoplankton, especially when nutrients were controlled. By using these physiological indicators to assess the life activity of organisms, our research provided new insights into macrophyte‐phytoplankton relationships during regime shifts in aquatic ecosystems. [ABSTRACT FROM AUTHOR]

Forage legumes face simultaneous abiotic and biotic stresses, causing substantial yield losses. This study explores the combined impacts of drought and Phoma medicaginis infection on the growth and photosynthetic activity of Medicago truncatula contrasting lines TN6.18 and F83005.5. The tolerant TN6.18 line exhibits superior tolerance to combined drought and P. medicaginis infection, manifesting in minimal leaf area reduction, the highest number of healthy leaves, increased carotenoids content, a consistently high and stable photosynthesis rate, and enhanced performance of photosystems PSI and PSII. On the contrary, the sensitive F83005.5 line shows pronounced leaf chlorosis, particularly under drought stress, and decreased pigment levels under the combination of drought and P. medicaginis infection stresses (combined stress). Moreover, the drought-stressed F83005.5, experiences reduced hydration and photosynthetic performance, linked to diminished gas exchange and chlorophyll fluorescence parameters. Chlorophyll fluorescence revealed more severe PSI impairment than PSII under combined stress. In conclusion, understanding the Pm8 infection-drought interaction enhances insights into M. truncatula resistance mechanisms to the combination of these stresses. [ABSTRACT FROM AUTHOR]

Singe‐turnover active chlorophyll a fluorometry (STAF) can be used to assess phytoplankton photosynthetic rates in terms of the photosystem II photochemical flux (JVPII, μmol e− m−3 s−1) instantaneously, autonomously, and at high resolution. While JVPII provides an upper limit to rates of phytoplankton primary productivity in units of carbon fixation, the conversion between these two rates is variable, limiting our ability to utilize high‐resolution JVPII data to monitor phytoplankton primary productivity. Simultaneous measurements of JVPII and 14C‐fixation help in understanding the factors controlling the variable ratio between the two rates. However, to date, methodological inconsistencies, including differences in incubation lengths and light quality, have greatly inhibited practical assessment of such electron to carbon ratios (Φe,C, mol e− mol C−1). We here present data from a range of dual‐incubation experiments in northeast Atlantic waters during which JVPII and 14C‐fixation were measured simultaneously on the same sample. Time‐course experiments show how Φe,C increases with incubation length, likely reflecting the transition from gross to net 14C‐fixation. Dual‐incubation experiments conducted under different light levels show a tendency for increased Φe,C under (super‐)saturating light. Finally, data from a diurnal experiment demonstrate how Φe,C increases over the course of a day, due to downregulation of 14C‐fixation. We provide a detailed description of our methodological approach, including a critical discussion of improvements to the calculation of JVPII implemented in the LabSTAF instrument used for active fluorescence measurements and the limitations of the well‐established 14C‐fixation approach. [ABSTRACT FROM AUTHOR]

Introduction: Plants in the environment are affected by various stresses, depending on the duration, intensity and growth stage of the plant, these stresses can reduce the process of photosynthesis and affect their growth and performance. However, traditional methods, even technically advanced ones such as the measurements of photosynthetic rates through the gas exchange (CO2, H2O, and O2), are timeconsuming and provide incomplete information on overall photosynthetic function. The development of knowledge in the field of chlorophyll fluorescence shows that this indicator has a high ability to study the photochemical efficiency of plant photosynthesis. Methods: For measuring the chlorophyll fluorescence in plants, leaves were dark-adapted for 30 minutes using leaf clips provided by the producer of handy-PEA. Measurements were performed on the middle of plant leaves following the standard protocol with illumination with continuous red light (peak in 650 nm wavelength; the spectral line half-width of 22 nm) provided by an array of three light-emitting diodes. The light pulse intensity used was 3500 μmol(photon).m-2s-1 and the duration of the light pulse was 1 s. The measured data were used for the calculation of the photosynthetic parameters using Biolyzer v. 3.06 HP software (a software provided with handy-PEA). Some of the parameters we discussed in this article due to their significance are FO = minimum fluorescence, FM = maximum fluorescence, FO/FM = The maximum quantum yield of basal non-photochemical energy losses, FV/FM = the maximum quantum efficiency of PSII, VJ = the relative variable fluorescence in step J after 2 ms, VI = the relative variable fluorescence in step I after 30 ms, N = the number of QA redox turnovers until FM, SM = the pool size of the electron acceptors on the reducing side of PSII, PIABS = performance index. Main Findings: The study of chlorophyll fluorescence can analyze with high detail the function and state of PSII reaction centres, and light-harvesting complexes. This index has a high correlation with other physiological parameters under different environmental stresses. In this article, an overview of the results of chlorophyll fluorescence analysis of crops underenvironmental stressesis given, and the key steps to stresses are presented. Under drought stress the ratio of active reaction centers in chlorophyll, primary photochemical reactions, and electron transfer are affected. By salinity stress in crops, the values of variable and, maximum fluorescence, the energy required to close the reaction centers, and the photosynthetic efficiency index decrease, while the time required to reach the maximum fluorescence increases. Under cold stress conditions, electron transfer flow per reactive centers, the quantum performance of photosystem II, and the efficiency of the water splitting complex in photosystem II decrease. Potassium affects light-dependent steps such as the size of receiving antennae and the electron connection of photosystem II reaction centers. The electron acceptor part of photosystem II is the main site of inhibition of photosynthetic electron transfer under the application of herbicides. Conclusion and Implications: This article has provided an overview of the information about the wide opportunities of using the chlorophyll fluorescence technique in plant science, agriculture and ecological research. The measured parameters of chlorophyll fluorescence are called the JIP-test and its analysis can be used to evaluate the effects of environmental stresses on plants. This technique requires more practical studies in biotic and even non-biotic stress conditions to provide reliable information to investigate the growth and development of plants, and this leads to an increase in our knowledge of the physiological basis of crop photosynthesis under stress conditions. [ABSTRACT FROM AUTHOR]

In the chloroplast, the 54 kDa subunit of the signal recognition particle (cpSRP54) is involved in the post-translational transport of the light-harvesting chlorophyll a / b -binding proteins (LHCPs) and the co-translational transport of plastid-encoded subunits of the photosynthetic complexes to the thylakoid membrane. It forms a high-affinity complex with plastid-specific cpSRP43 for post-translational transport, while a ribosome-associated pool coordinates its co-translational function. CpSRP54 constitutes a conserved multidomain protein, comprising a GTPase (NG) and a methionine-rich (M) domain linked by a flexible region. It is further characterized by a plastid-specific C-terminal tail region containing the cpSRP43-binding motif. To characterize the physiological role of the various regions of cpSRP54 in thylakoid membrane protein transport, we generated Arabidopsis cpSRP54 knockout (ffc1-2) lines producing truncated cpSRP54 variants or a GTPase point mutation variant. Phenotypic characterization of the complementation lines demonstrated that the C-terminal tail region of cpSRP54 plays an important role exclusively in post-translational LHCP transport. Furthermore, we show that the GTPase activity of cpSRP54 plays an essential role in the transport pathways for both nuclear as well as plastid-encoded proteins. In addition, our data revealed that plants expressing cpSRP54 without the C-terminal region exhibit a strongly increased accumulation of a photosystem I assembly intermediate. [ABSTRACT FROM AUTHOR]

Volvox sect. Volvox is a group of green algae with unique morphological features (thick cytoplasmic bridges between somatic cells and spiny zygote walls) and a worldwide distribution. Despite research interest in the diversity of organisms in ancient lakes, Volvox sect. Volvox from ancient lakes worldwide has not been identified to the species level. Here, we established clonal cultures of two species of this group originating from Lake Biwa, an ancient lake in Japan, and performed identification based on morphological and molecular data. One was identified as Volvox kirkiorum based on the nuclear ribosomal DNA internal spacer region (ITS) sequence, bisexual (monoicous or monoecious) spheroids, and zygote morphology. The other showed genetic separation from related species based on the secondary structure of the ITS and results of phylogenetic analysis of a combined data set from the nuclear actin gene, ITS, and two plastid genes (large subunit of RuBisCO and photosystem II CP43 apoprotein gene); it represented a new phylogenetic lineage within Volvox sect. Volvox, suggesting possible endemism in Lake Biwa. This species produced bisexual spheroids with different zygote morphology and zygote number from other species with bisexual spheroids in Volvox sect. Volvox. Therefore, Volvox biwakoensis Nozaki et H. Yamaguchi sp. nov. is described herein. This is the first endemic species of the genus Volvox described from an ancient lake. [ABSTRACT FROM AUTHOR]

Summary We explored the adaptive mechanisms of Ostreococcus tauri, a marine picophytoplankton with a ubiquitous ocean presence. We aimed to understand its photosynthetic acclimation, as featured in the cryo‐EM structure of its photosystem I (PSI) supercomplex. This structure revealed a unique composition involving a phosphorylated Lhcp trimer bound to the PSI core along with two additional Lhcp trimers, suggesting potential state transitions for photoacclimation. To investigate this hypothesis, we conducted a series of biochemical and physiological experiments. We analyzed absorption spectra to differentiate between PSI and PSII, particularly focusing on blue–green wavelengths, and examined the effects of specific excitation of Lhcp with green light, including its phosphorylation and the formation of the PSI‐LHCI‐Lhcp supercomplex. Our experiments clarified the distinctive effects attributable to absorption by pigments associated with Lhcp. Exciting Lhcp with green light induced its phosphorylation, leading to the formation of the PSI‐LHCI‐Lhcp supercomplex. Notably, the functional antenna size of PSI could reversibly expand in response to green light, demonstrating its state transition capability. These findings not only highlight the unique photosynthetic acclimation adapted to the marine environment but also suggest a possible ancestral role of state transitions in green plants, given the phylogenetic position of Prasinophyceae. [ABSTRACT FROM AUTHOR]

Smooth crabgrass [Digitaria ischaemum (Schreb.) Schreb. ex Muhl.] is one of the most troublesome summer annual weeds in cool‐season turfgrass. Field experiments demonstrated a strong relationship between spring photosynthetic active radiation reaching the soil surface and the resulting smooth crabgrass cover in Kentucky bluegrass (Poa pratensis L.) 2/3 months later in summer. Both smooth crabgrass and canopy penetrating light were consistently reduced by higher mowing heights. Follow‐up experiments in controlled environments were initiated to improve our understanding of how light quality and quantity influence smooth crabgrass germination and growth. Smooth crabgrass germination was ≥99% following exposure to blue, red (R), far red (FR), both R and FR light pulses, or complete darkness treatments. A second germination experiment examined six levels of turfgrass canopy shade (0%, 24%, 44%, 77%, 90%, and 100% photosynthetic photon flux density [PPFD] reduction) and found that smooth crabgrass germination was ≥99% for all treatments. These experiments indicate that light quality and quantity do not affect smooth crabgrass germination. A greenhouse experiment examined five levels of turfgrass canopy shade (0%, 44%, 59%, 81%, and 91% PPFD reduction). Smooth crabgrass quantum and PSII (Photosystem II) operating efficiency increased in response to shade, while leaf number and thickness, specific leaf weight, tillering, mass, electron transport rate, and stomatal conductance decreased with increasing shade. Overall, the results demonstrate that smooth crabgrass is able to germinate regardless of canopy density, but seedling growth, development, and plant function are diminished in a dense turfgrass canopy shade. [ABSTRACT FROM AUTHOR]

Photosystem I is a key component of primary energy conversion in oxygenic photosynthesis. Electron transfer reactions in Photosystem I take place across two parallel electron transfer chains that converge after a few electron transfer steps, sharing both the terminal electron acceptors, which are a series of three iron–sulphur (Fe-S) clusters known as F X , F A , and F B , and the terminal donor, P 700 . The two electron transfer chains show kinetic differences which are, due to their close geometrical symmetry, mainly attributable to the tuning of the physicochemical reactivity of the bound cofactors, exerted by the protein surroundings. The factors controlling the rate of electron transfer between the terminal Fe-S clusters are still not fully understood due to the difficulties of monitoring these events directly. Here we present a discussion concerning the driving forces associated with electron transfer between F X and F A as well as between F A and F B , employing a tunnelling-based description of the reaction rates coupled with the kinetic modelling of forward and recombination reactions. It is concluded that the reorganisation energy for F X − oxidation shall be lower than 1 eV. Moreover, it is suggested that the analysis of mutants with altered F A redox properties can also provide useful information concerning the upstream phylloquinone cofactor energetics. [ABSTRACT FROM AUTHOR]

This study investigates the immobilization of cyanobacterial photosystem I (PSI) from Synechocystis sp. PCC 6803 onto fluorine-doped tin oxide (FTO) conducting glass plates to create photoelectrodes for biohybrid solar cells. The fabrication of these PSI–FTO photoelectrodes is based on two immobilization processes: rapid electrodeposition driven by an external electric field and slower adsorption during solvent evaporation, both influenced by gravitational sedimentation. Deposition and performance of photoelectrodes was investigated by UV–Vis absorption spectroscopy and photocurrent measurements. We investigated the efficiency of PSI immobilization under varying conditions, including solution pH, applied electric field intensity and duration, and electrode polarization, with the goals to control (1) the direction of migration and (2) the orientation of the PSI particles on the substrate surface. Variation in the pH value of the PSI solution alters the surface charge distribution, affecting the net charge and the electric dipole moment of these proteins. Results showed PSI migration to the positively charged electrode at pH 6, 7, and 8, and to the negatively charged electrode at pH 4.4 and 5, suggesting an isoelectric point of PSI between 5 and 6. At acidic pH, the electrophoretic migration was largely hindered by protein aggregation. Notably, photocurrent generation was consistently cathodic and correlated with PSI layer thickness, and no conclusions can be drawn on the orientation of the immobilized proteins. Overall, these findings suggest mediated electron transfer from FTO to PSI by the used electrolyte containing 10 mM sodium ascorbate and 200 μM dichlorophenolindophenol. [ABSTRACT FROM AUTHOR]

The rice, like other plants, undergoes photoprotection mode by increasing nonphotochemical quenching (NPQ) in high light intensity (> 1200 µmol m− 2s− 1 PPFD), which attenuates photosystem II yield (φPSII) drastically. The plant remains in photoprotection mode even after light intensity becomes not stressful for an extended period. While there are significant differences in the time it takes for photoprotection to recover among different genotypes, its use is limited in plant breeding because measuring the chlorophyll fluorescence parameters in progressive actinic light after dark adaptation takes more than forty-five minutes per genotype. The study finds that instantly measured A400/A1800 ratio by five minutes in flag leaves of 25 diverse genotypes strongly associated with the φPSII400 differences between theoretical and actual, qPd400 and NPQ400 with R2 values 0.74, 0.65 and 0.60, respectively. In two consecutive years, GWAS of A400/A1800 ratio identified the regions with genes reported earlier for plant photoprotection recovery. Additionally, QTL analysis in a RIL population also identified the regions carrying known genes related to photoprotection. Thus, the A400/A1800 ratio can quickly phenotype many plants for easier introgression of the traits in popular cultivars. The identified genotypes, genes, and QTLs can be used to improve yield potential and allele mining. [ABSTRACT FROM AUTHOR]

Summary: 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. The importance of chloroplast NADH dehydrogenase‐like complex (NDH) operating cyclic electron flow (CEF) around Photosystem I (PSI) for C4 photosynthesis has been shown in reverse genetics studies but the contribution of CEF and NDH to cell‐level electron fluxes remained unknown.We have created gene‐edited Setaria viridis with null ndhO alleles lacking functional NDH and developed methods for quantification of electron flow through NDH in BS and mesophyll cells.We show that CEF accounts for 84% of electrons reducing PSI in BS cells and most of those electrons are delivered through NDH while the contribution of the complex to electron transport in mesophyll cells is minimal. A decreased leaf CO2 assimilation rate and growth of plants lacking NDH cannot be rescued by supplying additional CO2.Our results indicate that NDH‐mediated CEF is the primary electron transport route in BS chloroplasts highlighting the essential role of NDH in generating ATP required for CO2 fixation by the C3 cycle in BS cells. [ABSTRACT FROM AUTHOR]

To understand the physiological responses of seedlings to mechanical wounding, we analyzed photosynthesis, chlorophyll fluorescence, and endogenous hormones in tomato (Solanum lycopersicum L.) subjected to varying levels of mechanical pressure. The results showed that, at 4 h after wounding, excess excitation energy was dissipated as thermal energy through the reduction in the photosystem II (PSII) opening degree and the increase in non-photochemical quenching. Photodamage was avoided, and stomatal closure was the most prominent factor in photosynthesis inhibition. However, 12 h after wounding, the photoprotective mechanism was insufficient to mitigate the excess excitation energy caused by the wound, leading to photochemical damage to physiological processes. Meanwhile, the non-stomatal factor became the most prominent limiting factor for photosynthesis at 80 N pressure. At 12 and 36 h after wounding, the concentrations of abscisic acid (ABA), methyl jasmonate (MeJA), indole-3-acetic acid (IAA), zeatin riboside (ZR), and gibberellic acid (GA3) in the stems showed a trend towards being increased, which promoted wound healing. However, after mechanical wounding, the ratio of stress- to growth-promoting hormones first increased and then decreased. This pattern can enhance stress resistance and promote cell division, respectively. Comprehensive analysis showed that the fluorescence parameter, photochemical quenching coefficient (Qp_Lss), was the most suitable indicator for evaluating mechanical wounding conditions. [ABSTRACT FROM AUTHOR]

Agriophyllum squarrosum (L.) Moq. is a highly prevalent xerophytic species found throughout northern China. It is suitable for cultivation in semi-arid sandy environments and may establish roots in arid desert locations. This species plays a pioneering and exploratory role in the colonization of desert plants. In this study, we selected A. squarrosum from the Urat desert steppe (UD) and Horqin sandy land (HS) to explore their adaptation mechanisms to drought and rehydration environments by using the pot weighing control method to simulate an arid environment. The findings showed that the control (watering to 60–65% of field capacity) exceeded its required amount and the leaves turned yellow. The chlorophyll content was lower than those under moderate and severe drought, and rehydration caused a decrease. However, the contents of malondialdehyde, soluble sugar, and proline in the drought treatment were higher than those in the control. Under moderate and severe drought, the chlorophyll content and the quantum efficiency of photosystem II (Fv/Fm) of A. squarrosum from UD were higher than those from HS. During drought and rehydration processes, the proline content was relatively lower, while the activities of peroxidase (POD), superoxide dismutase (SOD), and catalase (CAT) and the content of soluble sugar and soluble protein were higher. However, antioxidant enzymes and osmoregulators from UD were higher than those from HS. The results suggest that the stronger ability of A. squarrosum to endure drought environments in UD is due to the high level of antioxidant enzymes and osmoregulators, which are conducive to relieving cell membrane damage when subjected to drought and rehydration. [ABSTRACT FROM AUTHOR]

Melatonin (MT) is considered as an antistress molecule that plays a constructive role in the acclimation of plants to both biotic and abiotic stress conditions. In the present study, we assessed the impact of 10 and 100 μM MT foliar spray, on chlorophyll content, and photosystem II (PSII) function, under moderate drought stress, on oregano (Origanum vulgare L.) plants. Our aim was to elucidate the molecular mechanism of MT action on the photosynthetic electron transport process. Foliar spray with 100 μM MT was more effective in mitigating the negative impact of moderate drought stress on PSII function, compared to 10 μM MT. MT foliar spray significantly improved the reduced efficiency of the oxygen-evolving complex (OEC), and PSII photoinhibition (Fv/Fm), which were caused by drought stress. Under moderate drought stress, foliar spray with 100 μM MT, compared with the water sprayed (WA) leaves, increased the non-photochemical quenching (NPQ) by 31%, at the growth irradiance (GI, 205 μmol photons m−2 s−1), and by 13% at a high irradiance (HI, 1000 μmol photons m−2 s−1). However, the lower NPQ increase at HI was demonstrated to be more effective in decreasing the singlet-excited oxygen (1O2) production at HI (−38%), in drought-stressed oregano plants sprayed with 100 μM MT, than the corresponding decrease in 1O2 production at the GI (−20%), both compared with the respective WA-sprayed leaves under moderate drought. The reduced 1O2 production resulted in a significant increase in the quantum yield of PSII photochemistry (ΦPSII), and the electron transport rate (ETR), in moderate drought-stressed plants sprayed with 100 μM MT, compared with WA-sprayed plants, but only at the HI (+27%). Our results suggest that the enhancement of PSII functionality, with 100 μM MT under moderate drought stress, was initiated by the NPQ mechanism, which decreased the 1O2 production and increased the fraction of open PSII reaction centers (qp), resulting in an increased ETR. [ABSTRACT FROM AUTHOR]

The short-term effects of UV radiation and low temperature on ultrastructure, photosynthetic activity (measured as the maximal photochemical quantum yield of photosystem II: Fv/Fm), chlorophyll-a (Chl-a) contents, and UV-absorbing compounds on the carpospores of Iridaea cordata from a sub-Antarctic population were investigated. Exposure to both photosynthetically active radiation (PAR) and PAR + UV for 4 h caused ultrastructural modifications in all treatments. Under PAR + UV at 2 °C, a disruption of the chloroplast's internal organization was observed. Plastoglobuli were often found in carpospores exposed to 2 °C. 'Electron dense particles', resembling physodes of brown algae, were detected for the first time in cells exposed to PAR and PAR + UV at 8 °C. Fv/Fm decreased following 4 h exposure at 2 °C under PAR + UV (64%) and PAR (25%). At 8 °C, Fv/Fm declined by 21% only under PAR + UV. The photosynthesis of carpospores previously treated with UV partially recovered after a 4 h exposure under dim light. UV-absorbing compounds were degraded in all radiation and temperature treatments without recovery after a 4 h dim light period. Chl-a did not change, whereas total carotenoids increased under PAR at 8 °C The study indicates that although carpospores of I. cordata exhibit photoprotective mechanisms, UV radiation strongly damages their ultrastructure and physiology, which were exacerbated under low temperatures. [ABSTRACT FROM AUTHOR]

Although graphene oxide (GO) has extensive recognized application prospects in slow-release fertilizer, plant pest control, and plant growth regulation, the incorporation of GO into nano herbicides is still in its early stages of development. This study selected a pair of sweet corn sister lines, nicosulfuron (NIF)-resistant HK301 and NIF-sensitive HK320, and sprayed them both with 80 mg kg–1 of GO-NIF, with clean water as a control, to study the effect of GO-NIF on sweet corn seedling growth, photosynthesis, chlorophyll fluorescence, and antioxidant system enzyme activity. Compared to spraying water and GO alone, spraying GO-NIF was able to effectively reduce the toxic effect of NIF on sweet corn seedlings. Compared with NIF treatment, 10 days after of spraying GO-NIF, the net photosynthetic rate (A), stomatal conductance (Gs), transpiration rate (E), photosystem II photochemical maximum quantum yield (Fv/Fm), photochemical quenching coefficient (qP), and photosynthetic electron transfer rate (ETR) of GO-NIF treatment were significantly increased by 328.31%, 132.44%, 574.39%, 73.53%, 152.41%, and 140.72%, respectively, compared to HK320. Compared to the imbalance of redox reactions continuously induced by NIF in HK320, GO-NIF effectively alleviated the observed oxidative pressure. Furthermore, compared to NIF treatment alone, GO-NIF treatment effectively increased the activities of superoxide dismutase (SOD), guaiacol peroxidase (POD), catalase (CAT), and ascorbate peroxidase (APX) in both lines, indicating GO induced resistance to the damage caused by NIF to sweet corn seedlings. This study will provides an empirical basis for understanding the detoxification promoting effect of GO in NIF and analyzing the mechanism of GO induced allogeneic detoxification in cells. [ABSTRACT FROM AUTHOR]

ABSTRACT Although it powers photosynthesis, ultraviolet‐A1 radiation (UV‐A1) is usually not defined as photosynthetically active radiation (PAR). However, the quantum yield (QY) with which UV‐A1 drives net photosynthesis rate (A) is unknown, as are the kinetics of A and chlorophyll fluorescence under constant UV‐A1 exposure. We measured A in leaves of six genotypes at four spectra peaking at 365, 385, 410 and 450 nm, at intensities spanning 0–300 μmol m s−1. All treatments powered near‐linear increases in A in a wavelength‐dependent manner. QY at 365 and 385 nm was linked to the apparent concentration of flavonoids, implicating the pigment in reductions of photosynthetic efficiency under UV‐A1; in several genotypes, A under 365 and 385 nm was negative regardless of illumination intensity, suggesting very small contributions of UV‐A1 radiation to CO2 fixation. Exposure to treatment spectra for 30 min caused slow increases in nonphotochemical quenching, transient reductions in A and dark‐adapted maximum quantum yield of photosystem II, that depended on wavelength and intensity, but were generally stronger the lower the peak wavelength was. We conclude that UV‐A1 generally powers A, but its definition as PAR requires additional evidence of its capacity to significantly increase whole‐canopy carbon uptake in nature. [ABSTRACT FROM AUTHOR]

Due to anthropogenic input of nutrients and emissions of greenhouse gases, macroalgae inhabiting coastal areas often experience drastic fluctuations in nutrients and seawater warming. In this work, we investigated the photosynthetic performance and antioxidant response of the commercially important red macroalgae Gracilariopsis lemaneiformis under four different nutrient conditions at 20°C and 23°C. Our results showed that the enrichment of NO3- and PO43- (high concentrations of nitrogen (N) and phosphorus (P), denoted as HNHP) significantly enhanced photosynthesis and growth by up to 42% and 66% for net photosynthesis rate and 83% and 134% for relative growth rate (RGR) under 20°C and 23°C, respectively, compared with natural seawater (low concentrations of N and P, denoted as LNLP). However, enriching only with PO43- (low concentration of N and high concentration of P, denoted as LNHP) or NO3- (high concentration of N and low concentration of P, denoted as HNLP) brought no significant change in RGR. A two-way ANOVA analysis revealed an interaction between nutrient variations and temperature, with elevated temperature intensifying the inhibition observed under HNLP conditions. To further elucidate this interaction, we assessed the damage and recovery processes of the photosynthetic apparatus, along with the antioxidant activities. The increased damage (k) and reduced recovery (r) rates of photosystem II (PSII) in both LNLP and HNLP conditions indicated a heightened susceptibility to photoinhibition in G. lemaneiformis, leading to reactive oxygen species (ROS) accumulation and exacerbated oxidative stress, culminating in decreased photosynthesis and growth rates. At higher temperatures, these phosphorus deficiency-induced inhibitions were amplified, as evidenced by increases in k values and ROS contents, coupled with a decrease in r values. In summary, our data suggest that the photosynthetic performance and growth of G. lemaneiformis are vulnerable to phosphorus deficiency, particularly in the context of future ocean warming. Consequently, phosphorus fertilization during cultivation warrants more attention. [ABSTRACT FROM AUTHOR]

Clothianidin (CL) is a neonicotinoid insecticide widely used in crop protection against insect pests. However, its effects on photosynthesis remain largely unknown. Here, by investigating the influence of CL at the concentrations of 22 and 110 μg/L on the primary processes of photosynthesis, membrane fluidity and structural changes of pea chloroplasts, we located several primary binding sites of this pesticide. Similar dynamics were observed for both concentrations. However, statistically significant differences were only found at 110 μg/L for all methods used. The light saturated rate of linear electron flow decreased mainly due to the disturbance of electron flow on the acceptor side of photosystem II (PSII) associated with the appearance of QB‐nonreducing centers and empty QB binding sites of PSII. The functioning of the donor side of PSII, the activity of photosystem I (PSI) and the maximum quantum yield of PSII photochemistry (Fv/Fm) were not found to be significantly altered. Increased membrane fluidity and structural alterations of the thylakoid membrane led to a decrease in the development of the proton gradient ΔрН and membrane energization processes. [ABSTRACT FROM AUTHOR]

Flavodiiron proteins (FLVs) catalyze the reduction of oxygen to water by using electrons from Photosystem I (PSI). In several photosynthetic organisms such as cyanobacteria, green algae, mosses and gymnosperms, FLV-dependent electron flow protects PSI from over-reduction and consequent damage especially under fluctuating light conditions. In this work we investigated biochemical and structural properties of FLVA and FLVB from the model moss Physcomitrium patens. The two proteins, expressed and purified from Escherichia coli, bind both iron and flavin cofactors and show NAD(P)H oxidase activity as well as oxygen reductase capacities. Moreover, the co-expression of both FLVA and FLVB, coupled to a tandem affinity purification procedure with two different affinity tags, enabled the isolation of the stable and catalytically active FLVA/B hetero tetrameric protein complex with cooperative nature. The multimeric organization was shown to be stabilized by inter-subunit disulfide bonds. This investigation provides valuable new information on the biochemical properties of FLVs, with new insights into their in vivo activity. [ABSTRACT FROM AUTHOR]

Plants have evolved various photosynthetic adaptations and photoprotective mechanisms to survive in fluctuating and extreme light environments. Many light-activated photosynthetic proteins and enzymes adjust to plant leaf anatomy and leaf pigments to facilitate these processes. Under excessive amounts of light, plants use non-photochemical quenching (NPQ) mechanisms to dissipate excess absorbed light energy as heat to prevent photoinhibition and, therefore, mitigate damage to the plant's photosystems. In this study, we examined photosynthetic adaptations to the light environment in common beans using representative genotypes of the Andean (Calima) and the Mesoamerican (Jamapa) gene pools. We estimated their leaf chlorophyll fluorescence characteristics using dark- and light-adapted mature leaves from three-week-old plants. Our results indicated a higher chlorophyll fluorescence of the light-adapted leaves in the Mesoamerican genotype. NPQ induction was early and extended in the Andean genotype. A similar response in the Mesoamerican counterpart required high light intensity (≥1500 PAR). The NPQ relaxation was rapid in the Mesoamerican genotype (t1/2: 6.76 min) but sluggish in the Andean genotype (t1/2: 9.17 min). These results indicated variable adaptation to light environments between the two common bean genotypes and suggested different strategies for surviving fluctuating light environments that can be exploited for developing plants with environmentally efficient photosynthesis under light limitations. [ABSTRACT FROM AUTHOR]

The development of methods to detect plant stress is not only a scientific challenge, but is also of great importance for agriculture and forestry. However, at present, stress diagnostics based on plant spectral characteristics has several limitations: (1) the high dependence of stress assessment on plant species identity; (2) the poor differentiation of different types of stress; and (3) the difficulty of detecting stress before visible symptoms appear. In this regard, the development of plant spectral metrics represents a significant area of research. Ficus elastica plants were exposed under the photosynthetic photon flux density (PPFD) from 0 to 1200 μmol photons m−2s−1. Exposure of F. elastica leaves to excess light (EL) (≥400 μmol photons m−2s−1) resulted in an increase in reflectance in the yellow-green region (522–594 nm) and a decrease in reflectance in the red region (666–682 nm) of the spectrum, accompanied by a shift of the red edge point toward the longer wavelength. These changes were revealed using the previously proposed light stress index (LSI = mean(R666:682)/mean(R522:594)). Based on the results obtained, two new vegetation indices (VIs) were proposed: LSIRed = R674/R654 and LSINorm = (R674 − R654)/(R674 + R654), indicating light stress by changes in the red region of the spectrum. The results of the study showed that LSI, LSIRed, and LSINorm have a high degree of coupling strength with maximal quantum yields of photosystem II values. The plant response to EL exposure, as assessed by the values of these three VIs, was well expressed regardless of the PPFD levels. The effect of EL at non-stressful PPFDs (50–200 μmol photons m−2s−1) was found to disappear within one hour after cessation of exposure. In contrast, the effect of the stressful PPFD (800 μmol photons m−2s−1) was found to persist for at least 80 h after cessation of exposure. The results of the study indicate the need to consider light history in spectral monitoring of vegetation. [ABSTRACT FROM AUTHOR]

SUMMARY: HSP90Cs are essential molecular chaperones localized in the plastid stroma that maintain protein homeostasis and assist the import and thylakoid transport of chloroplast proteins. While HSP90C contains all conserved domains as an HSP90 family protein, it also possesses a unique feature in its variable C‐terminal extension (CTE) region. This study elucidated the specific function of this HSP90C CTE region. Our phylogenetic analyses revealed that this intrinsically disordered region contains a highly conserved DPW motif in the green lineages. With biochemical assays, we showed that the CTE is required for the chaperone to effectively interact with client proteins PsbO1 and LHCB2 to regulate ATP‐independent chaperone activity and to effectuate its ATP hydrolysis. The CTE truncation mutants could support plant growth and development reminiscing the wild type under normal conditions except for a minor phenotype in cotyledon when expressed at a level comparable to wild type. However, higher HSP90C expression was observed to correlate with a stronger response to specific photosystem II inhibitor DCMU, and CTE truncations dampened the response. Additionally, when treated with lincomycin to inhibit chloroplast protein translation, CTE truncation mutants showed a delayed response to PsbO1 expression repression, suggesting its role in chloroplast retrograde signaling. Our study therefore provides insights into the mechanism of HSP90C in client protein binding and the regulation of green chloroplast maturation and function, especially under stress conditions. [ABSTRACT FROM AUTHOR]

Pinus massoniana Lamb. is an evergreen conifer; however, some current-year seedlings exhibit "winter reddening" at the onset of winter. The biological significance of this reddening is unclear. We examine the physiological responses of needles during the reddening process and explore the relationships between physiological traits and seeding cold resistance. Based on needle color, we recognize non-reddened, partially reddened, and fully reddened needle stages. As reddening progresses, chlorophyll fluorescence parameters (maximum light energy conversion efficiency of photosystem II (PSII) photochemistry, PSII potential activity, effective photosynthetic quantum yield, non-photochemical and photochemical quenching coefficients, and actual quantum yield of PSII photochemistry) decrease, reducing photosynthetic efficiency. Concurrently, the proportion of regulated energy dissipation in quantum yield of PSII decreases, and that of PSII non-regulated energy dissipation increases. Antioxidant enzyme activities (catalase and peroxidase) and osmoregulatory substances (soluble sugars and proteins and proline) increase, and malondialdehyde levels and relative cell damage at 4 °C and −10 °C gradually increase. Although P. massoniana seedlings adapt to low-temperature environments as their needles redden by increasing antioxidant enzyme activities and osmoregulatory substances and by adjusting photosynthetic efficiency and light energy distribution, cell membrane damage persists. Cold resistance in P. massoniana seedlings is not fully established during winter reddening. [ABSTRACT FROM AUTHOR]

Phytoplankton photosynthesis is the first step of energy capture in the open ocean and is therefore fundamental for global biogeochemical processes and ecosystem functioning. High‐resolution methods are required to fully capture the variability of marine photosynthesis and its environmental drivers. Here, we combine two high‐resolution underway methods to study phytoplankton photophysiology, Fast Repetition Rate fluorometry and Flow Cytometry, along a transect in the North‐East Atlantic Ocean from the polar circle to the equator. Significant spatial distinctions in photophysiological strategies were found between biogeographical provinces. The most pronounced distinction was present between the subarctic North Atlantic and the oligotrophic subtropical gyre, where the latter was typified by high photosystem II (PSII) turnover rates, low pigment‐to‐cell volume ratios, low PSII quantum efficiency and low absorption cross sections for photochemistry in PSII. Small‐scale variability along the transect results from varying diel cycles in photophysiology, possibly governed by light availability and cell metabolism. In general, we found that variability in PSII photochemistry was associated with variability in sea surface temperature, whereas the median mixed layer irradiance could explain more of the variation in the light harvesting capacity of the phytoplankton community. This implies that the expected climate change driven shoaling of the mixed layer may impact phytoplankton light harvesting strategies. Plain Language Summary: Marine photosynthesis is the basis of life in the ocean and therefore plays a fundamental role in the worlds' largest ecosystem. Phytoplankton adjust their photosynthesis to different environmental conditions, such as nutrients and light. Here, we combine data from two high‐resolution methods to study phytoplankton in the eastern North Atlantic Ocean from the polar circle to the equator. We show that the photosynthesis of phytoplankton differs between oceanographic regions and that daily cycles as well as environmental drivers play a role in the observed variability in marine photosynthesis. These insights are important to improve our predictions and understanding of the effects of climate change on marine ecosystems and biological productivity. Key Points: Combining underway methods on a small sailing sampling platform allows for high‐resolution characterization of phytoplankton photophysiologyDistinct photophysiological adaptation per marine biogeographical province reflects prevailing geochemical conditions across spatio‐temporal scalesNon‐linear relationships between photophysiology and environmental variables were present with superimposed diel trends [ABSTRACT FROM AUTHOR]

Optimizing photosynthesis is considered an important strategy for improving crop yields to ensure food security. To evaluate the potential of using photosynthesis-related parameters in crop breeding programs, we measured chlorophyll fluorescence along with growth-related and morphological traits of 23 barley inbred lines across different developmental stages in field conditions. The photosynthesis-related parameters were highly variable, changing with light intensity and developmental progression of plants. Yet, the variation in photosystem II quantum yield observed among the inbred lines in the field largely reflected the variation in CO2 assimilation properties in controlled climate chamber conditions, confirming that the chlorophyll fluorescence-based technique can provide proxy parameters of photosynthesis to explore genetic variation under field conditions. Heritability (⁠ H 2 ⁠) of the photosynthesis-related parameters in the field ranged from 0.16 for the quantum yield of non-photochemical quenching to 0.78 for the fraction of open photosystem II center. Two parameters, the maximum photosystem II efficiency in the light-adapted state (⁠ H 2 =0.58) and the total non-photochemical quenching (⁠ H 2 =0.53), showed significant positive and negative correlations, respectively, with yield-related traits (dry weight per plant and net straw weight) in the barley inbred lines. These results indicate the possibility of improving crop yield through optimizing photosynthetic light use efficiency by conventional breeding programs. [ABSTRACT FROM AUTHOR]

Plant thioredoxins (TRXs) are involved in numerous metabolic and signalling pathways, such as light‐dependent regulation of photosynthesis. The atypical TRX CDSP32, chloroplastic drought‐induced stress protein of 32 kDa, includes two TRX‐fold domains and participates in responses to oxidative stress as an electron donor to other thiol reductases. Here, we further characterised potato lines modified for CDSP32 expression to clarify the physiological roles of the TRX. Upon high salt treatments, modified lines displayed changes in the abundance and redox status of CDSP32 antioxidant partners, and exhibited sensitivity to combined saline‐alkaline stress. In non‐stressed plants overexpressing CDSP32, a lower abundance of photosystem II subunits and ATP‐synthase γ subunit was noticed. The CDSP32 co‐suppressed line showed altered chlorophyll a fluorescence induction and impaired regulation of the transthylakoid membrane potential during dark/light and light/dark transitions. These data, in agreement with the previously reported interaction between CDSP32 and ATP‐synthase γ subunit, suggest that CDSP32 affects the redox regulation of ATP‐synthase activity. Consistently, modelling of protein complex 3‐D structure indicates that CDSP32 could constitute a suitable partner of ATP‐synthase γ subunit. We discuss the roles of the TRX in the regulation of both photosynthetic activity and enzymatic antioxidant network in relation with environmental conditions. [ABSTRACT FROM AUTHOR]

The fusion of hydrogenases and photosynthetic reaction centers (RCs) has proven to be a promising strategy for the production of sustainable biofuels. Type I (iron-sulfur-containing) RCs, acting as photosensitizers, are capable of promoting electrons to a redox state that can be exploited by hydrogenases for the reduction of protons to dihydrogen (H2). While both [FeFe] and [NiFe] hydrogenases have been used successfully, they tend to be limited due to either O2 sensitivity, binding specificity, or H2 production rates. In this study, we fuse a peripheral (stromal) subunit of Photosystem I (PS I), PsaE, to an O2-tolerant [FeFe] hydrogenase from Clostridium beijerinckii using a flexible [GGS]4 linker group (CbHydA1-PsaE). We demonstrate that the CbHydA1 chimera can be synthetically activated in vitro to show bidirectional activity and that it can be quantitatively bound to a PS I variant lacking the PsaE subunit. When illuminated in an anaerobic environment, the nanoconstruct generates H2 at a rate of 84.9 ± 3.1 µmol H2 mgchl -1 h-1. Further, when prepared and illuminated in the presence of O2, the nanoconstruct retains the ability to generate H2, though at a diminished rate of 2.2 ± 0.5 µmol H2 mgchl -1 h-1. This demonstrates not only that PsaE is a promising scaffold for PS I-based nanoconstructs, but the use of an O2-tolerant [FeFe] hydrogenase opens the possibility for an in vivo H2 generating system that can function in the presence of O2. [ABSTRACT FROM AUTHOR]

Photosystem I (PSI) light-harvesting antenna complexes LHCI contain spectral forms that absorb and emit photons of lower energy than that of its primary electron donor, P700. The most red-shifted fluorescence is associated with the Lhca4 complex. It has been suggested that this red emission is related to the inter-chlorophyll charge transfer (CT) states. In this work we present a systematic quantum-chemical study of the CT states in Lhca4, accounting for the influence of the protein environment by estimating the electrostatic interactions. We show that significant energy shifts result from these interactions and propose that the emission of the Lhca4 complex is related not only to the previously proposed a603+-a608-state, but also to the a602+-a603-state. We also investigate how different protonation patterns of protein amino acids affect the energetics of the CT states. [ABSTRACT FROM AUTHOR]