Electron Acceptor Of Photosystem II Research Articles

Effects of Novel Photosynthetic Inhibitor [CuL2]Br2 Complex on Photosystem II Activity in Spinach.

The effects of the novel [CuL2]Br2 complex (L = bis{4H-1,3,5-triazino [2,1-b]benzothiazole-2-amine,4-(2-imidazole)}copper(II) bromide complex) on the photosystem II (PSII) activity of PSII membranes isolated from spinach were studied. The absence of photosynthetic oxygen evolution by PSII membranes without artificial electron acceptors, but in the presence of [CuL2]Br2, has shown that it is not able to act as a PSII electron acceptor. In the presence of artificial electron acceptors, [CuL2]Br2 inhibits photosynthetic oxygen evolution. [CuL2]Br2 also suppresses the photoinduced changes of the PSII chlorophyll fluorescence yield (FV) related to the photoreduction of the primary quinone electron acceptor, QA. The inhibition of both characteristic PSII reactions depends on [CuL2]Br2 concentration. At all studied concentrations of [CuL2]Br2, the decrease in the FM level occurs exclusively due to a decrease in Fv. [CuL2]Br2 causes neither changes in the F0 level nor the retardation of the photoinduced rise in FM, which characterizes the efficiency of the electron supply from the donor-side components to QA through the PSII reaction center (RC). Artificial electron donors (sodium ascorbate, DPC, Mn2+) do not cancel the inhibitory effect of [CuL2]Br2. The dependences of the inhibitory efficiency of the studied reactions of PSII on [CuL2]Br2 complex concentration practically coincide. The inhibition constant Ki is about 16 µM, and logKi is 4.8. As [CuL2]Br2 does not change the aromatic amino acids’ intrinsic fluorescence of the PSII protein components, it can be proposed that [CuL2]Br2 has no significant effect on the native state of PSII proteins. The results obtained in the present study are compared to the literature data concerning the inhibitory effects of PSII Cu(II) aqua ions and Cu(II)-organic complexes.

Oxidation of the reaction center chlorophyll of photosystem I is induced via close cooperation of photosystems II and I with progress of drought stress in soybean seedlings

ABSTRACT Drought is a serious abiotic stress that impairs plant productivity. We previously suggested that in rice (Oryza sativa L.) plants, the reaction center chlorophyll of photosystem I (PSI) (P700) is oxidized in response to drought stress via close cooperation of photosystem II (PSII) and PSI to protect PSI, whose fitness is crucial for photosynthesis and plant growth. It has rarely been reported whether such a defense system functions in other plant species. To collect another example, this subject was examined using soybean [Glycine max (L.)]. Irrigation of soil-cultured soybean seedlings was restricted to gradually impose drought stress. A decrease in the quantum efficiency of PSII [Y(II)], induction of non-photochemical quenching (NPQ) of excess light energy at PSII, reduction of the primary quinone electron acceptor of PSII (QA), and P700 oxidation proceeded before severe drought stress led to severe leaf wilting and photoinhibition of PSII and PSI. P700 oxidation, Y(II), and reduction of QA were strongly correlated in this period. These results are in accordance with those observed in rice. In contrast, such correlations disappeared when severely drought-stressed seedlings were included, as P700 oxidation was hampered while Y(II) further decreased in such seedlings. These results suggest that close cooperation of PSII and PSI leading to P700 oxidation functions to protect PSI against drought stress in soybean, and that similar defense system functions in soybean and rice unless drought stress are severe. The drought-stress responses of PSII and PSI are suggested to be regulated by acidification of thylakoid lumen in soybean, according to the changing patterns in the PSII and PSI parameters. Based on the similarity of the photochemistry of soybean and rice in response to drought stress, the effectiveness of P700 oxidation as an index for drought stress diagnosis is discussed. P700 oxidation is affected by factors other than drought stress such as N nutrition levels. However, effects of N nutrition levels are expected to be canceled by using another parameter obtained in P700 measurement as reference, suggesting the suitability of P700 oxidation for drought stress diagnosis.

The Anti-Senescence Activity of Cytokinin Arabinosides in Wheat and Arabidopsis Is Negatively Correlated with Ethylene Production.

Leaf senescence, accompanied by chlorophyll breakdown, chloroplast degradation and inhibition of photosynthesis, can be suppressed by an exogenous application of cytokinins. Two aromatic cytokinin arabinosides (6-benzylamino-9-β-d-arabinofuranosylpurines; BAPAs), 3-hydroxy- (3OHBAPA) and 3-methoxy- (3MeOBAPA) derivatives, have recently been found to possess high anti-senescence activity. Interestingly, their effect on the maintenance of chlorophyll content and maximal quantum yield of photosystem II (PSII) in detached dark-adapted leaves differed quantitatively in wheat (Triticum aestivum L. cv. Aranka) and Arabidopsis (Arabidopsis thaliana L. (Col-0)). In this work, we have found that the anti-senescence effects of 3OHBAPA and 3MeOBAPA in wheat and Arabidopsis also differ in other parameters, including the maintenance of carotenoid content and chloroplasts, rate of reduction of primary electron acceptor of PSII (QA) as well as electron transport behind QA, and partitioning of absorbed light energy in light-adapted leaves. In wheat, 3OHBAPA had a higher protective effect than 3MeOBAPA, whereas in Arabidopsis, 3MeOBAPA was the more efficient derivative. We have found that the different anti-senescent activity of 3OHBAPA and 3MeOBAPA was coupled to different ethylene production in the treated leaves: the lower the ethylene production, the higher the anti-senescence activity. 3OHBAPA and 3MeOBAPA also efficiently protected the senescing leaves of wheat and Arabidopsis against oxidative damage induced by both H2O2 and high-light treatment, which could also be connected with the low level of ethylene production.

Effects of low temperature on photoinhibition and singlet oxygen production in four natural accessions of Arabidopsis

Main conclusionsLow temperature decreases PSII damage in vivo, confirming earlier in vitro results. Susceptibility to photoinhibition differs among Arabidopsis accessions and moderately decreases after 2-week cold-treatment. Flavonols may alleviate photoinhibition.The rate of light-induced inactivation of photosystem II (PSII) at 22 and 4 °C was measured from natural accessions of Arabidopsis thaliana (Rschew, Tenela, Columbia-0, Coimbra) grown under optimal conditions (21 °C), and at 4 °C from plants shifted to 4 °C for 2 weeks. Measurements were done in the absence and presence of lincomycin (to block repair). PSII activity was assayed with the chlorophyll a fluorescence parameter Fv/Fm and with light-saturated rate of oxygen evolution using a quinone acceptor. When grown at 21 °C, Rschew was the most tolerant to photoinhibition and Coimbra the least. Damage to PSII, judged from fitting the decrease in oxygen evolution or Fv/Fm to a first-order equation, proceeded more slowly or equally at 4 than at 22 °C. The 2-week cold-treatment decreased photoinhibition at 4 °C consistently in Columbia-0 and Coimbra, whereas in Rschew and Tenela the results depended on the method used to assay photoinhibition. The rate of singlet oxygen production by isolated thylakoid membranes, measured with histidine, stayed the same or slightly decreased with decreasing temperature. On the other hand, measurements of singlet oxygen from leaves with Singlet Oxygen Sensor Green suggest that in vivo more singlet oxygen is produced at 4 °C. Under high light, the PSII electron acceptor QA was more reduced at 4 than at 22 °C. Singlet oxygen production, in vitro or in vivo, did not decrease due to the cold-treatment. Epidermal flavonols increased during the cold-treatment and, in Columbia-0 and Coimbra, the amount correlated with photoinhibition tolerance.

Photosynthetic characteristics and chlorophyll a fluorescence transient in Lonicera japonica under drought stress

Chlorophyll a fluorescence transient can reveal the degree of thermal damage to plant photosynthetic organs and provide much physiological information about PSII fleetly. However, it is not clear how it reveals photosynthetic mechanisms of plants under decreasing soil moisture. In this paper, the photosynthesis characteristics and photosystem II (PSII) activities in leaves of Lonicera japonica under 11-level soil moisture were explored by gas-exchange analysis and JIP test. Both parameters of net photosynthetic rate (Pn) and water use efficiency (WUE) exhibited an increasing–decreasing trend with the decreasing relative soil water content (RSWC). At 29.7% ≤ RSWC≤ 79.6%, the main reason for Pn decrease was stomatal limitation; at 36.4% ≤ RSWC≤ 55.1%, both Pn and WUE were higher than the average. When RSWC was below 29.7%, Pn, Tr, and WUE significantly decreased. Meanwhile, a JIP-test analysis revealed a distinct K peak with decreases in the quantum yield and energy distribution ratio (ψo or φEo) and increases in the K phase (Wk) and J phase (Vj) at RSWC≤ 29.7%, indicating that severe drought (RSWC≤ 29.7%) damaged the leaf oxygen-evolving complex, caused the accumulation of Q A − in PSII electron acceptors, and, therefore, hindered the progression of the PSII electron transport chain. In addition, at RSWC≤ 29.7%, the absorption flux per CS (ABS/CSo) increased, while the phenomenological energy fluxes for TRo/CSo, ETo/CSo, RC/CSo decreased, indicating that the PSII reaction center was damaged and excessive light energy was accumulated. Therefore, the main reason for the decrease of photosynthetic efficiency was non-stomatal limitation at RSWC≤ 29.7%, and the maximum moisture deficit for the growth of Lonicera japonica is RSWC= 29.7%.

PsbY is required for prevention of photodamage to photosystem II in a PsbM-lacking mutant of Synechocystis sp. PCC 6803

The PsbM (3.9 kDa) and PsbY (4.2 kDa) proteins are membrane-spanning, single-helix, subunits associated with the chlorophyll-binding CP47 pre-complex of photosystem II (PSII). Removal of PsbM resulted in accumulation of PSII pre-assembly complexes and impaired electron transfer between the primary (QA) and secondary (QB) plastoquinone electron acceptors of PSII indicating that the QB-binding site and bicarbonate binding to the non-heme iron were altered in this strain. Removal of PsbY alone had only a minor impact on PSII activity but deleting PsbY in the ΔPsbM background led to additional modification of the acceptor side resulting in ΔPsbM:ΔPsbY cells being susceptible to photodamage and this required protein synthesis for recovery. Addition of bicarbonate was able to compensate for the light-induced damage in ΔPsbM:ΔPsbY cells potentially re-occupying the modified bicarbonate-binding site in the ΔPsbM:ΔPsbY strain and complementation of ΔPsbM:ΔPsbY cells with the psbY gene restored the ΔPsbM phenotype.

Adaptive strategies of Zostera japonica photosynthetic electron transport in response to thermal stress

Seawater warming is emerging as a result of increasing global temperature. In this study, Zostera japonica (Ascherson and Graebner) collected from the intertidal zones of Changdao (37°N, 120°E) were used to investigate the responses of photosynthetic electron transport to thermal exposure in April 2016. As seawater temperature rose from 20 to 32 °C, increases of the relative variable fluorescence at the K-step to the amplitude of F J–F o (W k) and the maximum photochemical efficiency (F v/F m) indicated inhibition of the oxygen-evolving complex (OEC) and photosystem II (PSII) reaction centers, respectively. When exposed to 32 °C for 4 h, both OEC and PSII reaction centers suffered irreversible damage, confirming that 32 °C is the upper critical seawater temperature for Z. japonica photosynthetic electron transport. As a thermal inhibition indicator, PIabs exhibited a time-dependent linear decrease, with irreversible damage of the PSII reaction center occurring once the value of PIabs dropped below 10.60. Based on results of the photosynthetic performance, thermal response strategies were summarized as: (1) an enhancement in the efficiency of the active PSII reaction centers; (2) an increase in the activity of the PSII electron acceptor side; (3) an enhancement in the activities of both PSI and the cyclic electron transport around PSI; (4) the alternation between PSII and PSI. Such adaptive strategies may balance the redox state of electron transport and regulate the distribution of excitation energy between the two photosystems, thereby protecting Z. japonica from ocean warming.

Photosynthetic water splitting by the Mn4Ca2+OX catalyst of photosystem II: its structure, robustness and mechanism.

The biological energy cycle of our planet is driven by photosynthesis whereby sunlight is absorbed by chlorophyll and other accessory pigments. The excitation energy is then efficiently transferred to a reaction centre where charge separation occurs in a few picoseconds. In the case of photosystem II (PSII), the energy of the charge transfer state is used to split water into oxygen and reducing equivalents. This is accomplished by the relatively low energy content of four photons of visible light. PSII is a large multi-subunit membrane protein complex embedded in the lipid environment of the thylakoid membranes of plants, algae and cyanobacteria. Four high energy electrons, together with four protons (4H+), are used to reduce plastoquinone (PQ), the terminal electron acceptor of PSII, to plastoquinol (PQH2). PQH2 passes its reducing equivalents to an electron transfer chain which feeds into photosystem I (PSI) where they gain additional reducing potential from a second light reaction which is necessary to drive CO2 reduction. The catalytic centre of PSII consists of a cluster of four Mn ions and a Ca2+ linked by oxo bonds. In addition, there are seven amino acid ligands. In this Article, I discuss the structure of this metal cluster, its stability and the probability that an acid-base (nucleophilic-electrophilic) mechanism catalyses the water splitting reaction on the surface of the metal-cluster. Evidence for this mechanism is presented from studies on water splitting catalysts consisting of organo-complexes of ruthenium and manganese and also by comparison with the enzymology of carbon monoxide dehydrogenase (CODH). Finally the relevance of our understanding of PSII is discussed in terms of artificial photosynthesis with emphasis on inorganic water splitting catalysts as oxygen generating photoelectrodes.

In vivo assessment of effect of phytotoxin tenuazonic acid on PSII reaction centers

Tenuazonic acid (TeA), a phytotoxin produced by the fungus Alternaria alternata isolated from diseased croftonweed (Ageratina adenophora), exhibits a strong inhibition in photosystem II (PSII) activity. In vivo chlorophyll fluorescence transients of the host plant croftonweed, show that the dominant effect of TeA is not on the primary photochemical reaction but on the biochemical reaction after QA. The most important action site of TeA is the QB site on the PSII electron-acceptor side, blocking electron transport beyond QA− by occupying the QB site in the D1 protein. However, TeA does not affect the antenna pigments, the energy transfer from antenna pigment molecules to reaction centers (RCs), and the oxygen-evolving complex (OEC) at the donor side of PSII. TeA severely inactivated PSII RCs. The fraction of non-QA reducing centers and non-QB reducing centers show a time- and concentration-dependent linear increase. Conversely, the amount of active QA or QB reducing centers declined sharply in a linear way. The fraction of non-QB reducing centers calculated from data of fluorescence transients is close to the number of PSII RCs with their QB site filled by TeA. An increase of the step-J level (VJ) in the OJIP fluorescence transients attributed to QA− accumulation due to TeA bound to the QB site is a typical characteristic response of the plants leaf with respect to TeA penetration.

Variations in phytoplankton photo-physiology and productivity in a dynamic eutrophic ecosystem: a fast repetition rate fluorometer-based study

We investigated the photoacclimation state and photosynthetic rate of cells in the highly eutrophic upper Gulf of Thailand (UGOT), using fast repetition rate (FRR) fluorometry. Observations revealed differences in photosystem II (PSII) parameters: the maximum photochemical quantum efficiency of PSII (Fv/Fm), the functional absorption cross-section of PSII (σPSII) and the rate of reoxidation of the primary PSII electron acceptor (1/τQa), which were dependent on the hydrographic structure of the water column. FRR-derived parameters were used to estimate the chlorophyll a-normalized, photosynthetic rate (PB); the photosynthesis vs. irradiance (P–E) curves were derived from in situ PB profiles. The P–E parameters differed markedly between the upper stratified waters and the mixed water column; that is, the maximum photosynthetic rate |$P_{{\rm max}}^{\rm B} $| and the light saturation parameter (Ek) were higher in the upper stratified waters, while the initial slope of the P–E curve (α) was higher in the mixed waters. This indicates that cells acclimated to relatively bright light dominated the upper stratified waters, while cells acclimated to lower light dominated the mixed waters. A significant, positive relationship was found between the average PB in the euphotic zone and surface photosynthetically available radiation, from all profiles at both sampling sites, which suggests that phytoplankton photosynthesis in the UGOT was controlled primarily by irradiance. Furthermore, as stress from nutrient-limitation is unlikely in the UGOT, cells might realize their photosynthetic potential by means of photoacclimation, even under the different light regimes present in the UGOT.

Dissection of photosynthetic electron transport process in sweet sorghum under heat stress.

Plant photosynthesis and photosystem II (PSII) are susceptible to high temperature. However, photosynthetic electron transport process under heat stress remains unclear. To reveal this issue, chlorophyll a fluorescence and modulated 820 nm reflection were simultaneously detected in sweet sorghum. At 43°C, J step in the chlorophyll a fluorescence transient was significantly elevated, suggesting that electron transport beyond primary quinone of PSII (QA) (primary quinone electron acceptor of PSII) was inhibited. PSI (Photosystem I) photochemical capacity was not influenced even under severe heat stress at 48°C. Thus, PSI oxidation was prolonged and PSI re-reduction did not reach normal level. The inhibition of electron transport between PSII and PSI can reduce the possibility of PSI photoinhibition under heat stress. PSII function recovered entirely one day after heat stress at 43°C, implying that sweet sorghum has certain self-remediation capacity. When the temperature reached 48°C, the maximum quantum yield for primary photochemistry and the electron transport from PSII donor side were remarkably decreased, which greatly limited the electron flow to PSI, and PSI re-reduction suspended. The efficiency of an electron transferred from the intersystem electron carrier (plastoquinol, PQH2) to the end electron acceptors at the PSI acceptor side increased significantly at 48°C, and the reason was the greater inhibition of electron transport before PQH2. Thus, the fragment from QA to PQH2 is the most heat sensitive in the electron transport chain between PSII and PSI in sweet sorghum.

Natural Variants of Photosystem II Subunit D1 Tune Photochemical Fitness to Solar Intensity *

Photosystem II (PSII) is composed of six core polypeptides that make up the minimal unit capable of performing the primary photochemistry of light-driven charge separation and water oxidation in all oxygenic phototrophs. The D1 subunit of this complex contains most of the ligating amino acid residues for the Mn(4)CaO(5) core of the water-oxidizing complex (WOC). Most cyanobacteria have 3-5 copies of the psbA gene coding for at least two isoforms of D1, whereas algae and plants have only one isoform. Synechococcus elongatus PCC 7942 contains two D1 isoforms; D1:1 is expressed under low light conditions, and D1:2 is up-regulated in high light or stress conditions. Using a heterologous psbA expression system in the green alga Chlamydomonas reinhardtii, we have measured growth rate, WOC cycle efficiency, and O(2) yield as a function of D1:1, D1:2, or the native algal D1 isoform. D1:1-PSII cells outcompete D1:2-PSII cells and accumulate more biomass in light-limiting conditions. However, D1:2-PSII cells easily outcompete D1:1-PSII cells at high light intensities. The native C. reinhardtii-PSII WOC cycles less efficiently at all light intensities and produces less O(2) than either cyanobacterial D1 isoform. D1:2-PSII makes more O(2) per saturating flash than D1:1-PSII, but it exhibits lower WOC cycling efficiency at low light intensities due to a 40% faster charge recombination rate in the S(3) state. These functional advantages of D1:1-PSII and D1:2-PSII at low and high light regimes, respectively, can be explained by differences in predicted redox potentials of PSII electron acceptors that control kinetic performance.

Short flashes and continuous light have similar photoinhibitory efficiency in intact leaves

Lincomycin-treated pumpkin leaves were illuminated with either continuous light or saturating single-turnover xenon flashes to study the dependence of photoinactivation of photosystem II (PSII) on the mode of delivery of light. The flash energy and the time interval between the flashes were varied between the experiments, and photoinactivation was measured with oxygen evolution and the ratio of variable to maximum fluorescence (Fv/Fm). The photoinhibitory efficiency of saturating xenon flashes was found to be directly proportional to flash energy and independent of the time interval between the flashes. These findings indicate that a low-light-specific mechanism, based on charge recombination between PSII electron acceptors and the oxygen-evolving complex, is not the main cause of photoinactivation caused by short flashes in vivo. Furthermore, the relationship between the rate constant of photoinactivation and photon flux density was similar for flashes and continuous light when Fv/Fm was used to quantify photoinactivation, suggesting that continuous-light photoinactivation has a mechanism in which the quantum yield does not depend on the mode of delivery of light. A similar quantum yield of photoinhibition for flashes and continuous light is compatible with the manganese-based photoinhibition mechanism and with mechanisms in which singlet oxygen, produced via a direct photosensitization reaction, is the agent of damage. However, the classical acceptor-side and donor-side mechanisms do not predict a similar quantum yield for flashes and continuous light.

Characterization of photosystem II photochemistry in transgenic tobacco plants with lowered Rubisco activase content

Rubisco activase plays an important role in the regulation of CO 2 assimilation. However, it is unknown how activase regulates photosystem II (PSII) photochemistry. To investigate the effects of Rubisco activase on PSII photochemistry, we obtained transgenic tobacco ( Nicotiana tabacum) plants with 50% (i7), 25% (i28), and 5% (i46) activase levels as compared to wild type plants by using a gene encoding tobacco activase for the RNAi construct. Both CO 2 assimilation and PSII activity were significantly reduced only in transgenic i28 and i46 plants, suggesting that activase deficiency led to decreased PSII activity. Flash-induced fluorescence kinetics indicated that activase deficiency resulted in a slow electron transfer between Q A (primary quinine electron acceptor of PSII) and Q B (secondary quinone electron acceptor of PSII). Thermoluminescence measurements revealed that activase deficiency induced a shift of S 2Q A − and S 2Q B − recombinations to higher temperatures in parallel, and a decrease in the intensities of the thermoluminescence emissions. Activase deficiency also dampened the period-four oscillation of the thermoluminescence B-band. Protein gel blot analysis showed that activase deficiency resulted in a significant decrease in the content of D1, D2, CP43, CP47, and PsbO proteins. Transmission electron microscopy analysis demonstrated that activase deficiency induced a significant decrease in the number of grana stacks per chloroplast and discs per grana stack. Our results suggest that activase plays an important role in maintaining PSII function and chloroplast development.

The different effects of chilling stress under moderate light intensity on photosystem II compared with photosystem I and subsequent recovery in tropical tree species

Tropical plants are sensitive to chilling temperatures above zero but it is still unclear whether photosystem I (PSI) or photosystem II (PSII) of tropical plants is mainly affected by chilling temperatures. In this study, the effect of 4 degrees C associated with various light densities on PSII and PSI was studied in the potted seedlings of four tropical evergreen tree species grown in an open field, Khaya ivorensis, Pometia tomentosa, Dalbergia odorifera, and Erythrophleum guineense. After 8 h chilling exposure at the different photosynthetic flux densities of 20, 50, 100, 150 micromol m(-2) s(-1), the maximum quantum yield of PSII (F (v) /F (m)) in all of the four species decreased little, while the quantity of efficient PSI complex (P (m)) remained stable in all species except E. guineense. However, after chilling exposure under 250 micromol m(-2) s(-1) for 24 h, F (v) /F (m) was severely photoinhibited in all species whereas P (m) was relative stable in all plants except E. guineense. At the chilling temperature of 4 degrees C, electron transport from PSII to PSI was blocked because of excessive reduction of primary electron acceptor of PSII. F (v) /F (m) in these species except E. guineense recovered to approximately 90% after 8 h recovery in low light, suggesting the dependence of the recovery of PSII on moderate PSI and/or PSII activity. These results suggest that PSII is more sensitive to chilling temperature under the moderate light than PSI in tropical trees, and the photoinhibition of PSII and closure of PSII reaction centers can serve to protect PSI.

On the approaches applied in formulation of a kinetic model of photosystem II: Different approaches lead to different simulations of the chlorophyll a fluorescence transients

Chlorophyll a fluorescence rise (O–J–I–P transient) was in literature simulated using models describing reactions occurring solely in photosystem II (PSII) and plastoquinone (PQ) pool as well as using complex models which described, in addition to the above, also subsequent electron transport occurring beyond the PQ pool. However, there is no consistency in general approach how to formulate a kinetic model and how to describe particular reactions occurring even in PSII only. In this work, simple kinetic PSII models are considered always with the same electron carriers and same type of reactions but some reactions are approached in different ways: oxygen evolving complex is considered bound to PSII or “virtually” separated from PSII; exchange of doubly reduced secondary quinone PSII electron acceptor, Q B, with PQ molecule from the PQ pool is described by one second order reaction or by two subsequent reactions; and all possible reactions or only those which follow in logical order are considered. By combining all these approaches, eight PSII models are formulated which are used for simulations of the chlorophyll a fluorescence transients. It is shown that the different approaches can lead to qualitatively different results. The approaches are compared with other models found elsewhere in the literature and therefore this work can help the readers to better understand the other models and their results.

A Novel Nucleus-Encoded Chloroplast Protein, PIFI, Is Involved in NAD(P)H Dehydrogenase Complex-Mediated Chlororespiratory Electron Transport in Arabidopsis

A transient rise in chlorophyll fluorescence after turning off actinic light reflects nonphotochemical reduction of the plastoquinone (PQ) pool. This process is dependent on the activity of the chloroplast NAD(P)H dehydrogenase (NDH) complex, which mediates electron flow from stromal reductants to the PQ pool. In this study, we characterized an Arabidopsis (Arabidopsis thaliana) T-DNA insertion mutant pifi (for postillumination chlorophyll fluorescence increase), which possesses an intact NDH complex, but lacks the NDH-dependent chlorophyll fluorescence increase after turning off actinic light. The nuclear gene PIFI (At3g15840) containing the T-DNA insertion encodes a chloroplast-targeted protein localized in the stroma and is annotated as a protein of unknown function. The pifi mutant exhibited a lower capacity for nonphotochemical quenching, but similar CO(2) assimilation rates, photosystem II (PSII) quantum efficiencies (PhiPSII), and reduction levels of the primary electron acceptor of PSII (1 - qL) as compared with the wild type. The pifi mutant grows normally under optimal conditions, but exhibits greater sensitivity to photoinhibition and long-term mild heat stress than wild-type plants, which is consistent with lower capacity of nonphotochemical quenching. We conclude that PIFI is a novel component essential for NDH-mediated nonphotochemical reduction of the PQ pool in chlororespiratory electron transport.

The oxidation/reduction kinetics of the plastoquinone pool controls the appearance of the I-peak in the O–J–I–P chlorophyll fluorescence rise: Effects of various electron acceptors

Quantitative analysis of the fluorescence induction (FI) rise was used in this study to elucidate the complex effects of N, N, N′, N′-tetramethyl- p-phenylenediamine (TMPD) on thylakoids. Reduced TMPD molecules, responsible for the ADRY agent effect, caused an increase in the amplitude of the O–J rise. Also, only oxidized TMPD molecules were shown to have the ability to bind the Q B pocket of photosystem II (PSII). On the other hand, the I–P rise was slowed in proportion with the oxidized TMPD concentration, inducing the clear appearance of the I-peak. While this property was previously thought to be unique to TMPD, this study shows that some artificial electron acceptors of PSII, silicomolybdate, 2,5-dichloro- p-benzoquinone, and phenyl- p-benzoquinone, have a similar effect. These results demonstrated a major role of the oxido-reduction kinetics of the PQ-pool in the resolution of J–I and I–P phases in the FI of isolated thylakoids.

The polyphasic chlorophyll a fluorescence rise measured under high intensity of exciting light.

Chlorophyll a fluorescence rise caused by illumination of photosynthetic samples by high intensity of exciting light, the O-J-I-P (O-I1-I2-P) transient, is reviewed here. First, basic information about chlorophyll a fluorescence is given, followed by a description of instrumental set-ups, nomenclature of the transient, and samples used for the measurements. The review mainly focuses on the explanation of particular steps of the transient based on experimental and theoretical results, published since a last review on chlorophyll a fluorescence induction [Lazár D (1999) Biochimica et Biophysica Acta 1412, 1-28]. In addition to 'old' concepts (e.g. changes in redox states of electron acceptors of photosystem II (PSII), effect of the donor side of PSII, fluorescence quenching by oxidised plastoquinone pool), 'new' approaches (e.g. electric voltage across thylakoid membranes, electron transport through the inactive branch in PSII, recombinations between PSII electron acceptors and donors, electron transport reactions after PSII, light gradient within the sample) are reviewed. The K-step, usually detected after a high-temperature stress, and other steps appearing in the transient (the H and G steps) are also discussed. Finally, some applications of the transient are also mentioned.

Chlorophyll a fluorescence induction kinetics in leaves predicted from a model describing each discrete step of excitation energy and electron transfer associated with Photosystem II

Chlorophyll a fluorescence induction (FI) is widely used as a probe for studying photosynthesis. On illumination, fluorescence emission rises from an initial level O to a maximum P through transient steps, termed J and I. FI kinetics reflect the overall performance of photosystem II (PSII). Although FI kinetics are commonly and easily measured, there is a lack of consensus as to what controls the characteristic series of transients, partially because most of the current models of FI focus on subsets of reactions of PSII, but not the whole. Here we present a model of fluorescence induction, which includes all discrete energy and electron transfer steps in and around PSII, avoiding any assumptions about what is critical to obtaining O J I P kinetics. This model successfully simulates the observed kinetics of fluorescence induction including O J I P transients. The fluorescence emission in this model was calculated directly from the amount of excited singlet-state chlorophyll in the core and peripheral antennae of PSII. Electron and energy transfer were simulated by a series of linked differential equations. A variable step numerical integration procedure (ode15s) from MATLAB provided a computationally efficient method of solving these linked equations. This in silico representation of the complete molecular system provides an experimental workbench for testing hypotheses as to the underlying mechanism controlling the O J I P kinetics and fluorescence emission at these points. Simulations based on this model showed that J corresponds to the peak concentrations of Q(-)AQB (QA and QB are the first and second quinone electron acceptor of PSII respectively) and Q(-)AQ(-)B and I to the first shoulder in the increase in concentration of Q(-)AQ(2-)B. The P peak coincides with maximum concentrations of both Q(-)AQ(2-)B and PQH2. In addition, simulations using this model suggest that different ratios of the peripheral antenna and core antenna lead to differences in fluorescence emission at O without affecting fluorescence emission at J, I and P. An increase in the concentration of QB-nonreducing PSII centers leads to higher fluorescence emission at O and correspondingly decreases the variable to maximum fluorescence ratio (F v/F m).