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Light is the source of energy for photosynthetic organisms; when in excess, however, it also drives the formation of reactive oxygen species and, consequently, photoinhibition. Plants and algae have evolved mechanisms to regulate light harvesting efficiency in response to variable light intensity so as to avoid oxidative damage. Nonphotochemical quenching (NPQ) consists of the rapid dissipation of excess excitation energy as heat. Although widespread among oxygenic photosynthetic organisms, NPQ shows important differences in its machinery. In land plants, such as Arabidopsis thaliana, NPQ depends on the presence of PSBS, whereas in the green alga Chlamydomonas reinhardtii it requires a different protein called LHCSR. In this work, we show that both proteins are present in the moss Physcomitrella patens. By generating KO mutants lacking PSBS and/or LHCSR. we also demonstrate that both gene products are active in NPQ. Plants lacking both proteins are more susceptible to high light stress than WT, implying that they are active in photoprotection. These results suggest that NPQ is a fundamental mechanism for survival in excess light and that upon land colonization, photosynthetic organisms evolved a unique mechanism for excess energy dissipation before losing the ancestral one found in algae. [ABSTRACT FROM AUTHOR]

Plants protect themselves against the deleterious effects of high light intensities by inducing a mechanism ubiquitous among plants known as energy dissipation, which safely converts excess light to heat before it can lead to the formation of free radicals. Mutants possessing a deletion of the psbS gene, such as the npq4 mutant, cannot perform energy dissipation and thus offer an opportunity to assess the importance of this process to plant function. In a temperate light environment, greenhouse-grown npq4 mutants of Arcibidopsis thaliana had smaller rosette diameters and leaf numbers. The reduction in size observed in npq4 plants was associated with fewer floral stalks, fewer fruits, lower whole-plant and individual seed masses, and lower germination rates. In the field, npq4 mutants developed fewer fruits. After a controlled exposure to high light stress, both PSI! efficiency and CO2 assimilation were more significantly compromised in npq4 mutants at low light intensities, but not at high light intensities. Thus, the protective nature of energy dissipation manifests in light environments that include periods of high light, which predispose plants to PSII photoinactivation, and periods of low light, when PSII photoinactivation decreases the rate of photosynthesis. [ABSTRACT FROM AUTHOR]

Plants dissipate excess absorbed light energy as heat to protect themselves from photo-oxidative stress. The Arabidopsis thaliana npq6 mutant affected in thermal dissipation was identified by its partial defect in the induction of nonphotochemical quenching of chlorophyll fluorescence (NPQ) by excess light. Positional cloning revealed that npq6 contains a frameshift mutation caused by a single base-pair deletion in the At5g43050 gene, which encodes a member of the hypothetical chloroplast open reading frame 20 (YCF20) family of proteins with unknown function(s). The YCF20 protein family is mostly conserved in oxygenic photosynthetic organisms including cyanobacteria, eukaryotic algae, and plants. Amino acid sequence comparison identified two other genes in Arabidopsis that encode similar proteins to NPQ6: At1g65420 and At3g56830. These three Arabidopsis proteins have functional chloroplast-targeting transit peptides. Using reverse genetics, a mutant with a T-DNA insertion within the At1g65420 gene was identified and shown to exhibit a low NPQ phenotype similar to that of npq6; therefore, At1g65420 was named NPQ7. In contrast, a knockdown mutant in the At3g56830 gene with lower transcript levels showed wild-type levels of NPQ. The npq6 npq7 double mutant had an additive NPQ defect, indicating that the YCF20 family members in Arabidopsis have overlapping functions affecting thermal dissipation. [ABSTRACT FROM AUTHOR]

Two populations of a diatom alga Thallassiosira weisflogii were grown at photon flux densities (PFD) of 0.8 and 8 µmol/(m2 s). For both diatom populations, the recovery of chlorophyll fluorescence parameters ( F0, Fm, Fv/ Fm, and NPQ) was monitored after nondestructive irradiation by visible light at PFD of 40 µmol/(m2 s) and after high-intensity irradiation by visible light (1000–4000 µmol/(m2 s)). The exposure of diatoms to PFD of 40 µmol/(m2 s)—higher than PFD used for algal growth but still nondamaging to photosynthetic apparatus—induced nonphotochemical quenching (NPQ), which was stronger in algae grown at higher PFD (8 µmol/(m2 s)) than in algae grown at low light. After irradiation with high-intensity light, the recovery of chlorophyll fluorescence parameters was more pronounced in algae grown at elevated PFD level. During short-term irradiation of diatoms with high-intensity visible light (1000 µmol/(m2 s)), a stronger NPQ was observed in the culture adapted to high irradiance. After the treatment of algae with dithiothreitol (an inhibitor of carotenoid deepoxidase in the diadinoxanthin cycle) or NH4Cl (an agent abolishing the proton gradient at thylakoid membranes), a short exposure of algae to PFD of 40 µmol/(m2 s) induced hardly any nonphotochemical quenching. The results indicate the dominant contribution of xanthophyll cycle carotenoids to energy-dependent quenching. [ABSTRACT FROM AUTHOR]

Abstract: Nonphotochemical quenching (NPQ) is a fundamental mechanism in photosynthesis by which plants protect themselves against excess excitation energy and which is thus of crucial importance for plant survival and fitness. Recently, carotenoid radical cation (Car•+) formation has been discovered to be a key step in the feedback deexcitation quenching component (qE) of NPQ, whose molecular mechanism and location remains elusive. A recent model for qE suggests that the replacement of violaxanthin (Vio) by zeaxanthin (Zea) in photosynthetic pigment binding pockets can in principle result in qE via the so-called “gear-shift” or electron transfer quenching mechanisms. We performed pump-probe measurements on individual antenna complexes of photosystem II (CP24, CP26 and CP29) upon excitation of the chlorophylls (Chl) into their first excited Qy state at 660 nm when either Vio or Zea was bound to those complexes. The Chl lifetime was then probed by measuring the decay kinetics of the Chl excited state absorption (ESA) at 900 nm. The charge-transfer quenching mechanism, which is characterized by a spectral signature of the transiently formed Zea radical cation (Zea•+) in the near-IR, has also been addressed, both in solution and in light-harvesting complexes of photosystem II (LHC-II). Applying resonant two-photon two-color ionization (R2P2CI) spectroscopy we show here the formation of β-Car•+ in solution, which occurs on a femtosecond time-scale by direct electron transfer to the solvent. The β-Car•+ maxima strongly depend on the solvent polarity. Moreover, our two-color two-photon spectroscopy on CP29 reveals the spectral position of Zea•+ in the near-IR region at 980 nm. [Copyright &y& Elsevier]

Citrus crops in the Mediterranean region are often grown in high pH calcareous soils, which promote nutrient imbalances, especially iron deficiency. 'Navelina' trees grafted on eight different citrus rootstocks were assessed in terms of their relative tolerance to these soils. To do so, leaf gas exchange and chlorophyll a fluorescence parameters were measured for 2 consecutive years in leaves without visible injury symptoms. Trees were grown on the rootstocks Carrizo citrange, hybrids of Cleopatra mandarin x Poncirus trifoliata no. 5 (F-A 5), 13 (F-A 13), and 16 (030116), Troyer citrange x common mandarin no. 18 (F-A 418), King mandarin x P. trifoliata no. 7 (F-A 517), 020324 (Troyer citrange x Cleopatra mandarin), and Volkamer lemon x P. trifoliata no. 64 (230164). gS and transpiration rate were clearly lower in leaves of shoots grafted on Carrizo citrange than in those on the other rootstocks assayed, but net photosynthetic flux did not differ. However, leaves of shoots on Carrizo citrange displayed a decline in their maximum quantum yield of PSII photochemistry [variable fluorescence/maximum fluorescence (Fv/Fm) ratio] and other chlorophyll parameters in the steady state such as photochemical quenching (qP) and the quantum efficiency of PSII photochemistry (ΦPSII) as well as an increase in nonphotochemical quenching (qN). Other rootstocks such as 030116, F-A 517 and, especially, F-A 5 showed the highest ΦPSII and Fv/Fm values, whereas F-A 5 had the lowest qN in the steady state. The photosynthetic characteristics observed in leaves on Carrizo citrange showed them to be the least tolerant to these calcareous conditions, whereas photosynthesis of 'Navelina' trees budded on F-A 5 were the most tolerant. [ABSTRACT FROM AUTHOR]

Plants dissipate excess excitation energy as heat by non-photochemical quenching (NPQ). NPQ has been thought to resemble in vitro aggregation quenching of the major antenna complex, light harvesting complex of photosystem II (LHC-II). Both processes are widely believed to involve a conformational change that creates a quenching centre of two neighbouring pigments within the complex. Using recombinant LHC-II lacking the pigments implicated in quenching, we show that they have no particular role. Single crystals of LHC-II emit strong, orientation-dependent fluorescence with an emission maximum at 680 nm. The average lifetime of the main 680 nm crystal emission at 100 K is 1.31 ns, but only 0.39 ns for LHC-II aggregates under identical conditions. The strong emission and comparatively long fluorescence lifetimes of single LHC-II crystals indicate that the complex is unquenched, and that therefore the crystal structure shows the active, energy-transmitting state of LHC-II. We conclude that quenching of excitation energy in the light-harvesting antenna is due to the molecular interaction with external pigments in vitro or other pigment–protein complexes such as PsbS in vivo, and does not require a conformational change within the complex. [ABSTRACT FROM AUTHOR]

Abstract: In a previous study, we found that enhanced CO2 subjected to nodulated alfalfa plants grown at different temperatures (ambient and ambient+4°C) and water availability regimes could protect PSII from photodamage. The main objective of this study was to determine the mechanism(s) involved in the photoprotection of PSII at elevated CO2 levels in this plant. Elevated CO2 reduced carboxylation capacity-induced photosynthetic acclimation and reduced enzymatic and/or nonenzymatic antioxidant activities, suggesting that changes in electron flow did not cause any photooxidative damage (which was also confirmed by H2O2 and lipid peroxidation analyses). Enhanced nonphotochemical quenching and xanthophyll cycle pigments revealed that plants grown at 700μmolmol−1 CO2 compensated for the reduction in energy sink with a larger capacity for nonphotochemical dissipation of excitation energy as heat, i.e., modulating the status of the VAZ components. Elevated CO2 induced the de-epoxidation of violaxanthin to zeaxanthin, facilitating thermal dissipation and protecting the photosynthetic apparatus against the deleterious effect of excess excitation energy. [Copyright &y& Elsevier]

Assessments of nutrient-limitation in microalgae using chl a fluorescence have revealed that nitrogen and phosphorus depletion can be detected as a change in chl a fluorescence signal when nutrient-starved algae are resupplied with the limiting nutrient. This photokinetic phenomenon is known as a nutrient-induced fluorescence transient, or NIFT. Cultures of the unicellular marine chlorophyte Dunaliella tertiolecta Butcher were grown under phosphate starvation to investigate the photophysiological mechanism behind the NIFT response. A combination of low temperature (77 K) fluorescence, photosynthetic inhibitors, and nonphotochemical quenching analyses were used to determine that the NIFT response is associated with changes in energy distribution between PSI and PSII and light-stress-induced nonphotochemical quenching (NPQ). Previous studies point to state transitions as the likely mechanism behind the NIFT response; however, our results show that state transitions are not solely responsible for this phenomenon. This study shows that an interaction of at least two physiological processes is involved in the rapid quenching of chl a fluorescence observed in P-starved D. tertiolecta: (1) state transitions to provide the nutrient-deficient cell with metabolic energy for inorganic phosphate (Pi)-uptake and (2) energy-dependent quenching to allow the nutrient-stressed cell to avoid photodamage from excess light energy during nutrient uptake. [ABSTRACT FROM AUTHOR]

There are at least two photosynthetic cyclic electron transport (CET) pathways in most C3 plants: the NAD(P)H dehydrogenase (NDH)-dependent pathway and a pathway dependent upon putative ferredoxin:plastoquinone oxidoreductase (FQR) activity. While the NDH complex has been identified, and shown to play a role in photosynthesis, especially under stress conditions, less is known about the machinery of FQR-dependent CET. Recent studies indicate that FQR-dependent CET is dependent upon PGR5, a small protein of unknown function. In a previous study we found that overexpression of PGR5 causes alterations in growth and development associated with decreased chloroplast development and a transient increase in nonphotochemical quenching (NPQ) after the shift from dark to light. In the current study we examine the spatiotemporal expression pattern of PGR5, and the effects of overexpression of PGR5 in Arabidopsis under a host of light and stress conditions. To investigate the conserved function of PGR5, we cloned PGR5 from a species which apparently lacks NDH, loblolly pine, and overexpressed it in Arabidopsis. Although greening of cotyledons was severely delayed in overexpressing lines under low light, mature plants survived exposure to high light and drought stress better than wild-type. In addition, PSI was more resistant to high light in the PGR5 overexpressors than in wild-type plants, while PSII was more sensitive to this stress. These complex responses corresponded to alterations in linear and cyclic electron transfer, suggesting that over-accumulation of PGR5 induces pleiotropic effects, probably via elevated CET. We conclude that PGR5 has a developmentally-regulated, conserved role in mediating CET. [ABSTRACT FROM AUTHOR]

Intense sunlight is dangerous for photosynthetic organisms. Cyanobacteria, like plants, protect themselves from light-induced stress by dissipating excess absorbed energy as heat. Recently, it was discovered that a soluble orange carotenoid protein, the OCP, is essential for this photoprotective mechanism. Here we show that the OCP is also a member of the family of photoactive proteins; it is a unique example of a photoactive protein containing a carotenoid as the photoresponsive chromophore. Upon illumination with blue-green light, the OCP undergoes a reversible transformation from its dark stable orange form to a red "active" form. The red form is essential for the induction of the photoprotective mechanism. The illumination induces structural changes affecting both the carotenoid and the protein. Thus, the OCP is a photoactive protein that senses light intensity and triggers photoprotection. [ABSTRACT FROM AUTHOR]

The efficiency of light harvesting in higher plant photosynthesis is regulated in response to external environmental conditions. Under conditions of excess light, the normally highly efficient light-harvesting system of photosystem II is switched into a state in which unwanted, potentially harmful, energy is dissipated as heat. This process, known as nonphotochemical quenching, occurs by the creation of energy quenchers following conformational change in the light-harvesting complexes, which is initiated by the build up of the thylakoid pH gradient and controlled by the xanthophyll cycle. In the present study, the evidence to support the notion that this regulatory mechanism is dependent upon the organization of the different antenna subunits in the stacked grana membranes is reviewed. We postulate that nonphotochemical quenching occurs within a structural locus comprising the PsbS subunit and components of the light-harvesting antenna, CP26, CP24, CP29 and LHCIIb (the major trimeric light-harvesting complex), formed in response to protonation and controlled by the xanthophyll cycle carotenoids. [ABSTRACT FROM AUTHOR]

Effects of inhibitors and cofactors of cyclic and noncyclic electron transport on nonphotochemical quenching of chlorophyll fluorescence induced by action potential (AP) was investigated in Chara corallina cells. Under control conditions, energy-dependent quenching (q E) develops upon the increase in photosynthetically active radiation (PAR); it also arises and reversibly disappears after AP generation at moderate irradiances. The treatment of cells with diuron (DCMU) completely eliminated q E established at high irradiances and q E induced by AP generation. The activation of cyclic electron transport by DCMU in combination with phenazine methosulfate restored q E at high irradiances but did not restore q E imposed after AP generation. The presence in the medium of a PSI acceptor, methyl viologen at concentrations from 100 μM to 0.83 mM had no effect on fluorescence and photosynthetic activity of chloroplasts until the application of a single excitatory stimulus. Once a single AP was generated in the presence of methyl viologen, it induced irreversible q E at a wide range of irradiances, which indicates the AP-triggered redirection of a part of electron flow from the main pathway to the artificial acceptor. It is concluded that AP generation opens access for permeation of a divalent cation methyl viologen from the medium to the chloroplast stroma across two membrane barriers, the plasmalemma and the inner membrane of the chloroplast envelope. [ABSTRACT FROM AUTHOR]

Although populations of cyanobacteria are usually considered to be clonal, their capacity to survive environmental changes suggests intrapopulation genetic variation. We therefore estimated the genetic variability on the basis of two processes important for any photoautotroph – photochemical and nonphotochemical quenching – as well as photosynthetic pigment concentrations. For this purpose, two parameters related to photochemical and nonphotochemical quenching were measured using specific experimental and statistical procedures, in 25 strains of the cyanobacterium Microcystis aeruginosa, along with their contents of chlorophyll a, total carotenoids and phycocyanin. The experimental procedure allowed discrimination between genetic and nongenetic (or residual) variability among strains. The high genetic variability found in photosynthetic pigments and both photosynthetic parameters denotes large differences even among strains isolated from the same community. The high genetic diversity within a population could be important for the evolutionary success of cyanobacteria. [ABSTRACT FROM AUTHOR]

Abstract: Changes in in situ xanthophyll activity were compared in symbiotic dinoflagellates within the reef-building corals, Montastraea faveolata, Montastraea annularis, and Acropora cervicornis over a daily light cycle from morning until dusk on a shallow (4 m) patch reef. Examination of algae collected from the tops and sides of M. faveolata and M. annularis revealed typical inter-conversion of diadinoxanthin and diatoxanthin, with the greatest abundance of diatoxanthin noted by the mid-morning to afternoon, correlating to daily reduction in the effective quantum yield of photosystem II (ΔF / F m′) for the respective colony location. A. cervicornis had the highest proportion of diatoxanthin relative to the total xanthophyll pool, yet it also displayed the least amount of total daily xanthophyll cycling which did not correlate well with patterns of change in ΔF / F m′. For intraspecific comparisons, no significant difference in daily xanthophyll activity was noted between the different locations in each coral species, while differences in ΔF / F m′ were detected. In some cases temporal trends in nonphotochemical quenching (NPQ) of chlorophyll fluorescence did not match patterns in xanthophyll activity when peak xanthophyll cycling tended to lag behind the immediate light intensity measured in the mid-morning at some colony locations. Genetic characterization of symbionts using polymerase chain reaction-denaturing gradient electrophoresis of the rDNA internal transcribed spacer 2 region (ITS2) revealed that M. faveolata and M. annularis hosted the type B1 symbiont at all locations, while the type A3 symbiont was noted throughout A. cervicornis. Results indicate that while xanthophyll cycling appears to be largely a ubiquitous phenomenon in symbiotic dinoflagellates, the degree of cycling can be quite different between coral species at the same depth and that other biochemical pathways for daily photoprotection may predominate some host–symbiont combinations. [Copyright &y& Elsevier]

Abstract: Cells of characean algae exposed to illumination arrange plasma-membrane H+ fluxes and photosynthesis in coordinated spatial patterns (bands). This study reveals that H+ transport and photosynthesis patterns in these excitable cells are affected not only by light conditions but also by electric excitation of the plasma membrane. It is shown that generation of action potential (AP) temporally eliminates alkaline bands, suppresses O2 evolution, and differentially affects primary reactions of photosystem II (PSII) in different cell regions. The quantum yield of PSII electron transport decreased after AP in the alkaline but not in acidic cell regions. The effects of electric excitation on fluorescence and the PSII electron flow were most pronounced at light-limiting conditions. Evidence was obtained that the shift in chlorophyll fluorescence after AP is due to the increase in ΔpH at thylakoid membranes. It is concluded that the AP-triggered pathways affecting ion transport and photosynthetic energy conversion are linked but not identical. [Copyright &y& Elsevier]

Abstract: Photocalorimetry has rarely been employed to investigate the processes in photosynthesis. Yet, especially when complemented by simultaneous oxygen polarographic measurements, it can probe: (i) the light-excited decay of chlorophyll molecules to the ground state by the photochemical process in photosynthesis; (ii) light emission as fluorescence; and (iii) thermal dissipation. The possibility of detecting the latter two was examined by these methods. The halotolerant chlorophytic microalga, Dunaliella maritima, was grown routinely at 25μmolphotonm−2 s−1 incident light and in the experiments it was exposed to higher light intensity and salinity in order to observe the energetic consequences of stress in terms of the net heat and oxygen fluxes. The results showed that at 50 and 90μmolphotonm−2 s−1 the net heat flow varied from rapidly negative (endothermic) to sharply positive (exothermic). This was different to the simultaneous data from the oxygen polarographic sensor that always showed oxygen evolution in the light. Energy balances to correct for the slight imbalance in the response to incident radiant light and to convert the oxygen evolution to energy values by the oxycaloric equivalent for glucose (−470kJmol−1 O2) revealed an extra source of heat at 15.5±3.3 (S.E.) and at 9.4±3.2pW per cell for the control and treated cells, respectively, at 90μmolphotonm−2 s−1. This was thought to be due mainly to nonphotochemical quenching (NPQ), characteristically with a small contribution from chlorophyll fluorescence. There was an insignificant (paired t-test: P = 0.131) difference in dark oxygen flux of the control (1% saline) and osmotically stressed (3%) cells, meaning that respiration could provide no more ATP to pump the greater quantity of Na+ ions from the cell at higher salinity. Evidence is provided that cells in the higher salinity had a lower specific growth rate, which may have been due to the ATP being diverted from the synthesis of biomass to the Na+, K+-ATPase pump. The dark heat flux was significantly (P = 0.036) greater in the 3% treatment than in the 1% control, whereas the dark oxygen flux was similar for both of them. This meant that the calorimetric/respirometric (CR) ratio in the control was more negative than the oxycaloric equivalent, and indicated the presence of an anaerobic pathway, presumably the glycolytic synthesis of glycerol that increased with higher salinity. [Copyright &y& Elsevier]

Biochemical and physiological acclimation to different light environments is crucial for plant growth and survival. In high light (HL), feedback de-excitation (qE) is a well-known photoprotective mechanism that dissipates excess excitation energy in the light-harvesting antenna of photosystem II (PSII) and relieves excitation pressure in the photosynthetic electron transport chain. The xanthophylls zeaxanthin (Z) and lutein (L) function in qE, but also have roles as antioxidants. Although several studies have shown that qE is important during short-term fluctuations in light intensity, here we show that it is not required for the growth of Arabidopsis thaliana in prolonged HL conditions in the laboratory. Mutants that are deficient in qE alone, qE and Z synthesis, or in qE, Z synthesis and also L synthesis were able to grow at 1800 µmol photons m−2 s−1 and exhibited no major symptoms of photooxidative stress. The mutants (and wild type) acclimated to HL by increasing photosynthetic capacity and decreasing light harvesting, which together rendered qE less important for photoprotection. At a metabolite level, the HL-grown mutants appeared to compensate for their remaining qE deficit with increased α-tocopherol and ascorbate levels compared to the wild type. The specificity of this response provides insight into the relationship between qE and the antioxidant network in plants. [ABSTRACT FROM AUTHOR]

Under excess illumination, plant photosystem Il dissipates excess energy through the quenching of chlorophyll fluorescence, a process known as nonphotochemical quenching. Activation of nonphotochemical quenching has been linked to the conversion of a carotenoid with a conjugation length of nine double bonds (violaxanthin) into an 11-double-bond carotenoid (zeaxanthin). It has been suggested that the increase in the conjugation length turns the carotenoid from a nonquencher into a quencher of chlorophyll singlet excited states, but unequivocal evidence is lacking. Here, we present a transient absorption spectroscopic study on a model system made up of a zinc phthalocyanine (Pc) molecule covalently linked to carotenoids with 9, 10. or 11 conjugated carbon-carbon double bonds. We show that a carotenoid can act as an acceptor of Pc excitation energy, thereby shortening its singlet excited-state lifetime. The conjugation length of the carotenoid is critical to the quenching process. Remarkably, the addition of only one double bond can turn the carotenoid from a nonquencher into a very strong quencher. By studying the solvent polarity dependence of the quenching using target analysis of the time-resolved data, we show that the quenching proceeds through energy transfer from the excited Pc to the optically forbidden S1 state of the carotenoid, coupled to an intramolecular charge-transfer state. The mechanism for excess energy dissipation in photosystem II is discussed in view of the insights obtained on this simple model system. [ABSTRACT FROM AUTHOR]

Abstract: Leaves and chloroplasts from Arabidopsis plants with increased amounts of PsbS protein showed the same percentage increase in nonphotochemical quenching in comparison to the wild type both in the presence and absence of zeaxanthin. The absorption change at 525–535nm was also more pronounced in both cases. It is suggested that PsbS alone can cause the quenching, supporting the model in which zeaxanthin acts as an allosteric activator and is not the primary cause of the process. It is proposed that PsbS acts as a trigger of the conformational change that leads to the establishment of nonphotochemical quenching. [Copyright &y& Elsevier]

When exposed to light, the cells of characean algae produce intermittent regions of H+ extrusion and H+ absorption, featuring different photosynthetic activities. Methods for local measurements of outer pH, O2 content, and photochemical activity of photosystem II (PSII) were applied to examine microscopic regions of Chara coralline Klein ex Willd. internodes. The results show that the functional spatial heterogeneity of these excitable cells is controlled not only by light but also by electric excitation of the plasma membrane. Generation of a single action potential (AP) induced a reversible transition to the state with homogenous pH distribution and had different effects on photosynthesis in cell regions producing alkaline and acid zones. The effective quantum yield of PSII primary processes and the maximal chlorophyll fluorescence decreased after AP in the alkaline cell regions but were almost unaffected in the acidic cell regions. The suppression of photosynthesis after AP was also evident in the decrease of photosynthetic O2 evolution. The results provide evidence that electric signals arising at the plasmalemma are transmitted to the level of thylakoid membranes. The effects of electric excitation on fluorescence and the quantum yield of PSII photochemistry were best pronounced at low light intensities and low level of nonphotochemical quenching. The sensitivity of chlorophyll fluorescence in resting and excited cells to light intensity and protonophores indicates that the AP-induced fluorescence changes derive from the increase in pH gradient at the thylakoid membrane. The temporal elimination of alkaline zones and inhibition of photosynthesis apparently arise from parallel operational sequences that have a common initial stage. A possible role of cytosolic Ca2+ rise in the mechanism of photosynthesis suppression after electric excitation of the plasma membrane is discussed. [ABSTRACT FROM AUTHOR]

Capillary microelectrodes and pulse amplitude-modulated microfluorometry were used to study light-triggered changes in cell membrane potential, chlorophyll fluorescence, and photochemical yield of PSII in chloroplasts of a hornwort Anthoceros sp. The action potential was generated by illuminating the plant sample for a few seconds. It was accompanied by a reversible decrease in quantum efficiency of PSII and by nonphotochemical quenching of fluorescence that continued as long as 10 min after the light stimulus. The presence of ammonium ions (2 mM) enhanced the amplitude and prolonged the duration of dark changes of fluorescence parameters in accordance with the reported increase in duration and amplitude of the light-triggered action potential in the presence of NH. A rapid retardation of PSII activity within the first seconds of illumination was also evident from absorbance changes at 810 nm reflecting the redox conversions of chlorophyll P700. The PSII-dependent stage of reduction in the induction curves of P700 absorbance was strongly suppressed, and the amplitudes of signals induced by white and far-red light (717 nm) differed insignificantly. It is concluded that a short-term irradiation triggers the generation of ΔpH at the thylakoid membranes, which is accompanied by inhibition of the plasma membrane H+ pump and by reversible inactivation of PSII due to increased thermal dissipation of chlorophyll excitations. [ABSTRACT FROM AUTHOR]

Determining the spatial and temporal diversity of photosynthetic processes in forest canopies presents a challenge to the evaluation of biological feedbacks needed for improvement of carbon and climate models. Limited access with portable instrumentation, especially in the outer canopy, makes remote sensing of these processes a priority in experimental ecosystem and climate change research. Here, we describe the application of a new, active, chlorophyll fluorescence measurement system for remote sensing of light use efficiency, based on analysis of laser-induced fluorescence transients (LIFT). We used mature stands of Populus grown at ambient (380 ppm) and elevated CO2 (1220 ppm) in the enclosed agriforests of the Biosphere 2 Laboratory (B2L) to compare parameters of photosynthetic efficiency, photosynthetic electron transport, and dissipation of excess light measured by LIFT and by standard on-the-leaf saturating flash methods using a commercially available pulse-modulated chlorophyll fluorescence instrument (Mini-PAM). We also used LIFT to observe the diel courses of these parameters in leaves of two tropical forest dominants, Inga and Pterocarpus, growing in the enclosed model tropical forest of B2L. Midcanopy leaves of both trees showed the expected relationships among chlorophyll fluorescence-derived photosynthetic parameters in response to sun exposure, but, unusually, both displayed an afternoon increase in nonphotochemical quenching in the shade, which was ascribed to reversible inhibition of photosynthesis at high leaf temperatures in the enclosed canopy. Inga generally showed higher rates of photosynthetic electron transport, but greater afternoon reduction in photosynthetic efficiency. The potential for estimation of the contribution of outer canopy photosynthesis to forest CO2 assimilation, and assessment of its response to environmental stress using remote sensing devices such as LIFT, is briefly discussed. [ABSTRACT FROM AUTHOR]

The relationship between the fluorescence lifetime (τ) and yield (Φ) obtained in phase and modulation fluorometry at 54 MHz during the chlorophyll fluorescence induction in dark-adapted leaves under low actinic light has been investigated. Three typical phases have been identified: (i) linear during the OI photochemical rise, (ii) convex curvature during the subsequent IP thermal rise, and (iii) linear during the PS slow decay. A similar relationship has been obtained in the fluorescence induction for the fluorescence yield measured at 685 nm plotted versus the fluorescence yield measured at 735 nm. A spectrally resolved analysis shows that the curvature of the τ–Φ relationship is not due to chlorophyll fluorescence reabsorption effects. Several other hypotheses are discussed and we conclude that the curvature of the τ–Φ relationship is due to a variable and transitory nonphotochemical quenching. We tentatively propose that this quenching results from a conformational change of a pigment–protein complex of Photosystem II core antenna during the IP phase and could explain both spectral and temporal transitory changes of the fluorescence. A variable blue shift of the 685 nm peak of the fluorescence spectrum during the IP phase has been observed, supporting this hypothesis. [Copyright &y& Elsevier]

The electric-field induced absorption changes (Stark effect) of reconstituted light-harvesting complex II (LHCII) in different oligomerisation states—monomers and trimers—with different xanthophyll content have been probed at 77 K. The Stark spectra of the reconstituted control samples, containing the xanthophylls lutein and neoxanthin, are very similar to previously reported spectra of native LHCII. Reconstituted LHCII, containing lutein but no neoxanthin, shows a similar electrooptical response in the Chl a region, but the Stark signal of Chl b around 650 nm amounts to at most ∼25% of that of the control samples. We conclude that neoxanthin strongly modifies the electronic states of the nearby Chl b molecules causing a large electrooptical response at 650 nm stemming from one or more Chls b in the control samples. Ambiguities about the assignment of several bands in the Soret region [Biochim. Biophys. Acta 1605 (2003) 83] are resolved and the striking difference in electric field response between the two lutein molecules is confirmed. The Stark effect in the carotenoid spectral region in both control and neoxanthin-deficient samples is almost identical, showing that the neoxanthin Stark signal is small and much less intense than the lutein Stark signal. [Copyright &y& Elsevier]

© New Phytologist (2004) doi: 10.1111/j.1469-8137.2004.00996.x [ABSTRACT FROM AUTHOR]

When cells of the green alga Chlorella vulgaris Beij. are transferred from growth at 5 °C and an irradiance of 150 μmol photons m-2 s-1 to 27 °C and the same irradiance, they undergo what is normally considered a high-light to low-light phenotypic change. This involves a 3-fold increase in cellular chlorophyll content with a concomitant increase in light-harvesting complex polypeptide levels. This process appears to occur in response to the cellular capacity to utilize the products of photosynthesis, with the redox state of the plastoquinone pool sensing the cellular energy balance. The phenotypic adjustment can be enhanced or blocked using chemical inhibitors that modulate the redox state of the plastoquinone pool. The functional changes in the photosynthetic apparatus that occurred during the high-light to low-light acclimation were examined with special consideration paid to the paradox that 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU)-treated cells, with non-functional photosystem II (PSII), accumulate light-harvesting polypeptides. At the structural and basic functional levels, the light-harvesting complex of the cells treated with DCMU was indistinguishable from that of the untreated, control cells. To examine how PSII was protected in the DCMU-treated cells, we measured the content of xanthophyll-cycle pigments. It appeared that a zeaxanthin-dependent nonphotochemical quenching process was involved in PSII protection during greening in the presence of DCMU. Metabolic inhibitors of mitochondrial respiration were used to examine how the change in cellular energy balance regulates the greening process. Apparently, the mitochondrion acts to supply energy to the chloroplast during greening, and inhibition of mitochondrial respiration diminishes chlorophyll accumulation apparently through an increase in the redox state of the plastoquinone pool. [ABSTRACT FROM AUTHOR]

The response of the photosynthetic apparatus to high irradiance illumination (440–2200 W/m2) was studied in the diatom Thallassiosira weisflogii by fluorescence methods. Changes in the photosynthetic apparatus were monitored by measuring characteristics of chlorophyll fluorescence F0, Fm, Fv / Fm, and qN for several hours after illumination of the alga with high-intensity light. Incubation of the alga with 2 mM DTT, an inhibitor of de-epoxidase of carotenoids in the diadinoxanthin cycle, led to a decrease in the nonphotochemical quenching of chlorophyll fluorescence and a drop in the Fv / Fm ratio, a characteristic that reflects the quantum efficiency of the functioning of the photosynthetic apparatus. Light-induced absorption changes associated with transformations of carotenoids of diadinoxanthin cycle were recorded in vivo in algal suspensions in the absence and in the presence of DTT. Using the microfluorometric method, we measured cell distribution over the efficiency of the primary processes of photosynthesis ( Fv / Fm) after illumination. We found cells with a high tolerance of their photosynthetic apparatus to photooxidative damage. The relatively high tolerance of a portion of the cell population to high-light illumination can be related to light-induced transformation of carotenoids and to the functioning of other protective systems of the photosynthetic apparatus in diatoms. [ABSTRACT FROM AUTHOR]

Lobaria pulmonaria (L.) Hoffm. survives large changes in ambient light and temperature between winter and summer in temperate deciduous forests. Potential photosystem II (PSII) electron transport, measured at 20°C using chlorophyll fluorescence analysis, was consistent in thallus samples taken in March and August from a temperate deciduous forest, while the potential for nonphotochemical quenching (NPQ) was higher in March than in August. NPQ was, however, similar in March and August in a population from a coniferous site with a permanently closed canopy. Thalli measured at a typical March field temperature showed a depression of PSII electron transport, q[sub p] and gross CO[sub 2] uptake and a rise in realized NPQ. Xanthophyll cycle pigments were more abundant in the March than in the August samples in the deciduous forest populations but did not change significantly in the permanently closed-canopy population. In August, relatively low NPQ correlated with xanthophyll pool size in the deciduous forest samples. The more intense NPQ derived from low temperature and low CO[sub 2] -electron demand in the March samples, however, was not correlated with xanthophyll pool size. Thus, most of the NPQ observed in the high light exposure March samples was not explained by variation in xanthophyll pool size.Key words: carotenoids, excitation quenching, lichen, nonphotochemical quenching, PSII electron transport.Dans les forêts décidues tempérées, le Lobaria pulmonaria (L.) Hoffm. survit à de grands écarts de température et de luminosité du milieu ambiant entre l'hiver et l'été. Le transport potentiel d'électron photosystème II (PSII), mesuré par analyse à 20°C de la fluorescence de la chlorophylle, est congruent dans des échantillons de thalles prélevés en mars et en août dans une forêt décidue tempérée, alors que le potentiel du quenching non-photochimique (QNP) est plus élevée en mars qu'en août. Cependant, le QNP est semblable en mars et en août chez une population venant d'une forêt coniférienne voisine, avec une canopée fermée en permanence. Les mesures effectuées sur des thalles à une température typique du terrain en mars, montre une dépression du transport d'électron PSII, du q[sub p] et de l'absorption brute en CO[sub 2] , ainsi qu'une augmentation du QNP réalisé. Les pigments du cycle des xanthophylles sont plus abondants dans les échantillons de mars que ceux d'août, dans les populations de forêts décidues. En août, le QNP relativement faible est corrélé avec la dimension du pool des xanthophylles dans les échantillons provenant de forêts décidues. Cependant, le QNP plus intense dérivé d'une basse température et d'une faible demande en CO[sub 2] dans les échantillons de mars n'est pas corrélé avec la dimension du pool des xanthophylles. Ainsi, la majeure partie du QNP observé sous haute intensité lumineuse dans les échantillons de mars ne s'explique pas par la variation de la dimension du pool des xanthophylles.Mots clés : Caroténoïdes, quenching par excitation, lichen, quenching non-photochimique, transport d'électron PSII.[Traduit par la Rédaction] [ABSTRACT FROM AUTHOR]

We characterized the photosynthetic properties of the pmgA mutant of Synechocystis PCC 6803, which cannot change its photosystem stoichiometry under a high-light condition (200 µmol m–2 s–1), in order to clarify the physiological significance of the regulation of photosystem stoichiometry. We found that (1) PSII activity was inhibited more in wild-type cells on the first day under the high-light conditions than in mutant cells. (2) The growth of the mutants following the initial imposition of high light was faster than that of wild-type cells. (3) However, growth was severely inhibited in the mutants after the third day of exposure to high light. (4) The growth inhibition in the mutants under the extended high-light conditions was reversed by the addition of sublethal concentrations of 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU), which seemed to mimic photoinhibition of PSII. These results suggest that the main role of adjusting the photosystem stoichiometry with respect to light intensity is not to maintain efficient photosynthesis, but to down regulate electron transfer. Failure to down regulate electron flow leads to cell death under prolonged exposure to high light in this cyanobacterium. [ABSTRACT FROM PUBLISHER]

When light absorption by a plant exceeds its capacity for light utilization, photosynthetic light harvesting is rapidly downregulated by photoprotective thermal dissipation, which is measured as nonphotochemical quenching of chlorophyll fluorescence (NPQ). To address the involvement of specific xanthophyll pigments in NPQ, we have analyzed mutants affecting xanthophyll metabolism in Arabidopsis thaliana. An npq1 lut2 double mutant was constructed, which lacks both zeaxanthin and lutein due to defects in the violaxanthin de-epoxidase and lycopene ∈-cyclase genes. The npq1 lut2 strain had normal Photosystem II efficiency and nearly wild-type concentrations of functional Photosystem II reaction centers, but the rapidly reversible component of NPQ was completely inhibited. Despite the defects in xanthophyll composition and NPQ, the npq1 lut2 mutant exhibited a remarkable ability to tolerate high light. [ABSTRACT FROM AUTHOR]

High light stress induced not only a sustained form of xanthophyll cycle-dependent energy dissipation but also sustained thylakoid protein phosphorylation. The effect of protein phosphatase inhibitors (fluoride and molybdate ions) on recovery from a 1-h exposure to a high PFD was examined in leaf discs of Parthenocissus quinquefolia (Virginia creeper). Inhibition of protein dephosphorylation induced zeaxanthin retention and sustained energy dissipation (NPQ) upon return to low PFD for recovery, but had no significant effects on pigment and Chl fluorescence characteristics under high light exposure. In addition, whole plants of Monstera deliciosa and spinach grown at low to moderate PFDs were transferred to high PFDs, and thylakoid protein phosphorylation pattern (assessed with anti-phosphothreonine antibody) as well as pigment and Chl fluorescence characteristics were examined over several days. A correlation was obtained between dark-sustained D1/D2 phosphorylation and dark-sustained zeaxanthin retention and maintenance of PS II in a state primed for energy dissipation in both species. The degree of these dark-sustained phenomena was more pronounced in M. deliciosa compared with spinach. Moreover, M. deliciosa but not spinach plants showed unusual phosphorylation patterns of Lhcb proteins with pronounced dark-sustained Lhcb phosphorylation even under low PFD growth conditions. Subsequent to the transfer to a high PFD, dark-sustained Lhcb protein phosphorylation was further enhanced. Thus, phosphorylation patterns of D1/D2 and Lhcb proteins differed from each other as well as among plant species. The results presented here suggest an association between dark-sustained D1/D2 phosphorylation and sustained retention of zeaxanthin and energy dissipation (NPQ) in light-stressed, and particularly ‘photoinhibited’, leaves. Functional implications of these observations are discussed. [ABSTRACT FROM AUTHOR]

We have isolated very high light resistant nuclear mutants ( VHLR) in Chlamydomonas reinhardtii, that grow in 1500–2000 μmol photons m−2 s−1 (VHL) lethal to wildtype. Four nonallelic mutants have been characterized in terms of Photosystem II (PS II) function, nonphotochemical quenching (NPQ) and xanthophyll pigments in relation to acclimation and survival under light stress. In one class of VHLR mutants isolated from wild type ( S4 and S9), VHL resistance was accompanied by slower PS II electron transfer, reduced connectivity between PS II centers and decreased PS II efficiency. These lesions in PS II function were already present in the herbicide resistant D1 mutant A251L ( L*) from which another class of VHLR mutants ( L4 and L30) were isolated, confirming that optimal PS II function was not critical for survival in very high light. Survival of all four VHLR mutants was independent of CO2 availability, whereas photoprotective processes were not. The de-epoxidation state (DPS) of the xanthophyll cycle pigments in high light (HL, 600 μmol photons m−2 s−1) was strongly depressed when all genotypes were grown in 5% CO2. In S4 and S9 grown in air under HL and VHL, high DPS was well correlated with high NPQ. However when the same genotypes were grown in 5% CO2, high DPS did not result in high NPQ, probably because high photosynthetic rates decreased thylakoid ΔpH. Although high NPQ lowered the reduction state of PS II in air compared to 5% CO2 at HL in wildtype, S4 and S9, this did not occur during growth of S4 and S9 in VHL. L* and VHLR mutants L4 and L30, also showed high DPS with low NPQ when grown air or 5% CO2, possibly because they were unable to maintain sufficiently high ΔpH due to constitutively impaired PS II electron transport. Although dissipation of excess photon energy through NPQ may contribute to VHL resistance, there is little evidence that the different genes conferring the VHLR phenotype affect this form of photoprotection. Rather, the decline of chlorophyll per biomass in all VHLR mutants grown under VHL suggests these genes may be involved in regulating antenna components and photosystem stoichiometries. [ABSTRACT FROM AUTHOR]

Photosynthetic organisms use sunlight as the primary energy source to fix CO 2 . However, in nature, light energy is highly variable, reaching levels of saturation for periods ranging from milliseconds to hours. In the green microalga Chlamydomonas reinhardtii, safe dissipation of excess light energy by nonphotochemical quenching (NPQ) is mediated by light-harvesting complex stress-related (LHCSR) proteins and redistribution of light-harvesting antennae between the photosystems (state transition). Although each component underlying NPQ has been documented, their relative contributions to NPQ under fluctuating light conditions remain unknown. Here, by monitoring NPQ in intact cells throughout high light/dark cycles of various illumination periods, we find that the dynamics of NPQ depend on the timescales of light fluctuations. We show that LHCSRs play a major role during the light phases of light fluctuations and describe their role in growth under rapid light fluctuations. We further reveal an activation of NPQ during the dark phases of all high light/dark cycles and show that this phenomenon arises from state transition. Finally, we show that LHCSRs and state transition synergistically cooperate to enable NPQ response during light fluctuations. These results highlight the dynamic functioning of photoprotection under light fluctuations and open a new way to systematically characterize the photosynthetic response to an ever-changing light environment., (© 2022 The Authors. Plant, Cell & Environment published by John Wiley & Sons Ltd.)

Improvement of crop climate resilience will require an understanding of whole-plant adaptation to specific local environments. This review places features of plant form and function related to photosynthetic productivity, as well as associated gene-expression patterns, into the context of the adaptation of Arabidopsis thaliana ecotypes to local environments with different climates in Sweden and Italy. The growth of plants under common cool conditions resulted in a proportionally greater emphasis on the maintenance of photosynthetic activity in the Swedish ecotype. This is compared to a greater emphasis on downregulation of light-harvesting antenna size and upregulation of a host of antioxidant enzymes in the Italian ecotype under these conditions. This differential response is discussed in the context of the climatic patterns of the ecotypes' native habitats with substantial opportunity for photosynthetic productivity under mild temperatures in Italy but not in Sweden. The Swedish ecotype's response is likened to pushing forward at full speed with productivity under low temperature versus the Italian ecotype's response of staying safe from harm (maintaining redox homeostasis) while letting productivity decline when temperatures are transiently cold. It is concluded that either strategy can offer directions for the development of climate-resilient crops for specific locations of cultivation. [ABSTRACT FROM AUTHOR]

Drought is one of the most important abiotic stress factors limiting maize production worldwide. The objective of this study was to investigate whether photoprotection of PSII was associated with the degree of drought tolerance and yield in three maize hybrids (30Y87, 31R88, P3939). To do this, three maize hybrids were subjected to three cycles of drought, and we measured the activities of photosystem II (PSII) and photosystem I (PSI). In a second field experiment, three maize hybrids were subjected to drought by withholding irrigation, and plant water status, yield and yield attributes were measured. Drought stress decreased leaf water potential (ΨL) in three maize hybrids, and this reduction was more pronounced in hybrid P3939 (−40%) compared to that of 30Y87 (−30%). Yield and yield attributes of three maize hybrids were adversely affected by drought. The number of kernels and 100-kernel weight was the highest in maize hybrid 30Y87 (−56%, −6%), whereas these were lowest in hybrid P3939 (−88%, −23%). Drought stress reduced the quantum yield of PSII [Y(II)], photochemical quenching (qP), electron transport rate through PSII [ETR(II)] and NPQ, except in P3939. Among the components of NPQ, drought increased the Y(NPQ) with concomitant decrease in Y(NO) only in P3939, whereas Y(NO) increased in drought-stressed plants of hybrid 30Y87 and 31R88. However, an increase in cyclic electron flow (CEF) around PSI and Y(NPQ) in P3939 might have protected the photosynthetic machinery but it did not translate in yield. However, drought-stressed plants of 30Y87 might have sufficiently downregulated PSII to match the energy consumption in downstream biochemical processes. Thus, changes in PSII and PSI activity and development of NPQ through CEF are physiological mechanisms to protect the photosynthetic apparatus, but an appropriate balance between these physiological processes is required, without which plant productivity may decline. [ABSTRACT FROM AUTHOR]

Photosynthesis is an important remaining opportunity for further improvement in the genetic yield potential of our major crops. Measurement, analysis, and improvement of leaf CO 2 assimilation ( A ) have focused largely on photosynthetic rates under light-saturated steady-state conditions. However, in modern crop canopies of several leaf layers, light is rarely constant, and the majority of leaves experience marked light fluctuations throughout the day. It takes several minutes for photosynthesis to regain efficiency in both sun-shade and shade-sun transitions, costing a calculated 10-40% of potential crop CO 2 assimilation. Transgenic manipulations to accelerate the adjustment in sun-shade transitions have already shown a substantial productivity increase in field trials. Here, we explore means to further accelerate these adjustments and minimize these losses through transgenic manipulation, gene editing, and exploitation of natural variation. Measurement andanalysis of photosynthesis in sun-shade and shade-sun transitions are explained. Factors limiting speeds of adjustment and how they could be modified to effect improved efficiency are reviewed, specifically nonphotochemical quenching (NPQ), Rubisco activation, and stomatal responses.

The orange carotenoid protein (OCP) is responsible for nonphotochemical quenching (NPQ) in cyanobacteria, a defense mechanism against potentially damaging effects of excess light conditions. This soluble two-domain protein undergoes profound conformational changes upon photoactivation, involving translocation of the ketocarotenoid inside the cavity followed by domain separation. Domain separation is a critical step in the photocycle of OCP because it exposes the N-terminal domain (NTD) to perform quenching of the phycobilisomes. Many details regarding the mechanism and energetics of OCP domain separation remain unknown. In this work, we apply metadynamics to elucidate the protein rearrangements that lead to the active, domain-separated, form of OCP. We find that translocation of the ketocarotenoid canthaxanthin has a profound effect on the energetic landscape and that domain separation only becomes favorable following translocation. We further explore, characterize, and validate the free energy surface (FES) using equilibrium simulations initiated from different states on the FES. Through pathway optimization methods, we characterize the most probable path to domain separation and reveal the barriers along that pathway. We find that the free energy barriers are relatively small (<5 kcal/mol), but the overall estimated kinetic rate is consistent with experimental measurements (>1 ms). Overall, our results provide detailed information on the requirement for canthaxanthin translocation to precede domain separation and an energetically feasible pathway to dissociation., (© 2022 The Protein Society.)

Diatoms are successful phytoplankton clades able to acclimate to changing environmental conditions, including e.g. variable light intensity. Diatoms are outstanding at dissipating light energy exceeding the maximum photosynthetic electron transfer (PET) capacity via the nonphotochemical quenching (NPQ) process. While the molecular effectors of NPQ as well as the involvement of the proton motive force (PMF) in its regulation are known, the regulators of the PET/PMF relationship remain unidentified in diatoms. We generated mutants of the H + /K + antiporter KEA3 in the model diatom Phaeodactylum tricornutum. Loss of KEA3 activity affects the PET/PMF coupling and NPQ responses at the onset of illumination, during transients and in steady-state conditions. Thus, this antiporter is a main regulator of the PET/PMF coupling. Consistent with this conclusion, a parsimonious model including only two free components, KEA3 and the diadinoxanthin de-epoxidase, describes most of the feedback loops between PET and NPQ. This simple regulatory system allows for efficient responses to fast (minutes) or slow (e.g. diel) changes in light environment, thanks to the presence of a regulatory calcium ion (Ca 2+ )-binding domain in KEA3 modulating its activity. This circuit is likely tuned by the NPQ-effector proteins, LHCXs, providing diatoms with the required flexibility to thrive in different ocean provinces., (© 2022 The Authors New Phytologist © 2022 New Phytologist Foundation.)

Photosynthetic pigments are an integral and vital part of all photosynthetic machinery and are present in different types and abundances throughout the photosynthetic apparatus. Chlorophyll, carotenoids and phycobilins are the prime photosynthetic pigments which facilitate efficient light absorption in plants, algae, and cyanobacteria. The chlorophyll family plays a vital role in light harvesting by absorbing light at different wavelengths and allowing photosynthetic organisms to adapt to different environments, either in the long-term or during transient changes in light. Carotenoids play diverse roles in photosynthesis, including light capture and as crucial antioxidants to reduce photodamage and photoinhibition. In the marine habitat, phycobilins capture a wide spectrum of light and have allowed cyanobacteria and red algae to colonise deep waters where other frequencies of light are attenuated by the water column. In this review, we discuss the potential strategies that photosynthetic pigments provide, coupled with development of molecular biological techniques, to improve crop yields through enhanced light harvesting, increased photoprotection and improved photosynthetic efficiency., (© 2021. The Author(s), under exclusive licence to Springer Nature B.V.)

Sun-induced fluorescence in the far-red region (SIF) is increasingly used as a remote and proximal-sensing tool capable of tracking vegetation gross primary production (GPP). However, the use of SIF to probe changes in GPP is challenged during extreme climatic events, such as heatwaves. Here, we examined how the 2018 European heatwave (HW) affected the GPP-SIF relationship in evergreen broadleaved trees with a relatively invariant canopy structure. To do so, we combined canopy-scale SIF measurements, GPP estimated from an eddy covariance tower, and active pulse amplitude modulation fluorescence. The HW caused an inversion of the photosynthesis-fluorescence relationship at both the canopy and leaf scales. The highly nonlinear relationship was strongly shaped by nonphotochemical quenching (NPQ), that is, a dissipation mechanism to protect from the adverse effects of high light intensity. During the extreme heat stress, plants experienced a saturation of NPQ, causing a change in the allocation of energy dissipation pathways towards SIF. Our results show the complex modulation of the NPQ-SIF-GPP relationship at an extreme level of heat stress, which is not completely represented in state-of-the-art coupled radiative transfer and photosynthesis models., (© 2021 The Authors. New Phytologist © 2021 New Phytologist Foundation.)