Photoreduction Of QA Research Articles

High salicylic acid concentration alters the electron flow associated with photosystem II in barley

In this study, the effects of exogenously applied salicylic acid (0.5 and 5 mM SA) on the rates of photosystem II (PSII) activity was analysed in 4-week-old barley (Hordeum vulgare‘Bahman’ ) seedlings using chlorophyll (Chl) a fluorescence transient (OJIP) measurements. No evident changes in Chl and carotenoid contents as well as chlorophyll fluorescence transient curves were observed in either of the studied concentrations after 24 h of SA application. After 5 d, low SA concentration (0.5 mM) increased PSII activity, Chl b and carotenoid contents in barley seedlings. In contrary, 5 days after 5 mM SA treatment, the maximal quantum efficiency of PSII (Fv/Fm) and the Performance Index (PIABS), as an indicator of PSII structure and functioning, were significantly decreased. This lower Fv/Fm and PIABS coupled with lower levels of Chl b and carotenoids, and lower values of photosynthetic electron transport chain components including the electron transport flux (φEo) and the inferred oxygen evolving complex activity (Fv/Fo). By monitoring the chlorophyll a fluorescence rise kinetics, from the initial “O” level to the “P” (the peak) level, a dramatic increase in “OJ” phase was detected, which coincides with an increased photo-reduction of QA as a result of blockage of electron flow. This study provided the evidence that the high concentration of SA induced damage to different sites of the PSII.

Redox potential of the non-heme iron complex in bacterial photosynthetic reaction center

In bacterial photosynthetic reaction centers (bRC), the electron is transferred from the special pair (P) via accessory bacteriochlorophyll (BA), bacteriopheopytin (HA), the primary quinone (QA) to the secondary quinone (QB). Although the non-heme iron complex (Fe complex) is located between QA and QB, it was generally supposed not to be redox-active. Involvement of the Fe complex in electron transfer (ET) was proposed in recent FTIR studies [A. Remy and K. Gerwert, Coupling of light-induced electron transfer to proton uptake in photosynthesis, Nat. Struct. Biol. 10 (2003) 637–644]. However, other FTIR studies resulted in opposite results [J. Breton, Steady-state FTIR spectra of the photoreduction of QA and QB in Rhodobacter sphaeroides reaction centers provide evidence against the presence of a proposed transient electron acceptor X between the two quinones, Biochemistry 46 (2007) 4459–4465]. In this study, we calculated redox potentials of QA/B (Em(QA/B)) and the Fe complex (Em(Fe)) based on crystal structure of the wild-type bRC (WT-bRC), and we investigated the energetics of the system where the Fe complex is assumed to be involved in the ET. Em(Fe) in WT-bRC is much less pH-dependent than that in PSII. In WT-bRC, we observed significant coupling of ET with Glu-L212 protonation upon oxidation of the Fe complex and a dramatic Em(Fe) downshift by 230 mV upon formation of QA− (but not QB−) due to the absence of proton uptake of Glu-L212. Changes in net charges of the His ligands of the Fe complex appear to be the nature of the redox event if we assume the involvement of the Fe complex in the ET.

The Unusually Strong Hydrogen Bond between the Carbonyl of QAand His M219 in theRhodobacter sphaeroidesReaction Center Is Not Essential for Efficient Electron Transfer from QA-to QB

In native reaction centers (RCs) from photosynthetic purple bacteria the primary quinone (QA) and the secondary quinone (QB) are interconnected via a specific His-Fe-His bridge. In Rhodobacter sphaeroides RCs the C4=O carbonyl of QA forms a very strong hydrogen bond with the protonated Npi of His M219, and the Ntau of this residue is in turn coordinated to the non-heme iron atom. The second carbonyl of QA is engaged in a much weaker hydrogen bond with the backbone N-H of Ala M260. In previous work, a Trp side chain was introduced by site-directed mutagenesis at the M260 position in the RC of Rb. sphaeroides, resulting in a complex that is completely devoid of QA and therefore nonfunctional. A photochemically competent derivative of the AM260W mutant was isolated that contains a Cys side chain at the M260 position (denoted AM260(W-->C)). In the present work, the interactions between the carbonyl groups of QA and the protein in the AM260(W-->C) suppressor mutant have been characterized by light-induced FTIR difference spectroscopy of the photoreduction of QA. The QA-/QA difference spectrum demonstrates that the strong interaction between the C4=O carbonyl of QA and His M219 is lost in the mutant, and the coupled CO and CC modes of the QA- semiquinone are also strongly perturbed. In parallel, a band assigned to the perturbation of the C5-Ntau mode of His M219 upon QA- formation in the native RC is lacking in the spectrum of the mutant. Furthermore, a positive band between 2900 and 2400 cm-1 that is related to protons fluctuating within a network of highly polarizable hydrogen bonds in the native RC is reduced in amplitude in the mutant. On the other hand, the QB-/QB FTIR difference spectrum is essentially the same as for the native RC. The kinetics of electron transfer from QA- to QB were measured by the flash-induced absorption changes at 780 nm. Compared to native RCs the absorption transients are slowed by a factor of about 2 for both the slow phase (in the hundreds of microseconds range) and fast phase (microseconds to tens of microseconds range) in AM260(W-->C) RCs. We conclude that the unusually strong hydrogen bond between the carbonyl of QA and His M219 in the Rb. sphaeroides RC is not obligatory for efficient electron transfer from QA- to QB.

Chloroplast-encoded Polypeptide PsbT Is Involved in the Repair of Primary Electron Acceptor QA of Photosystem II during Photoinhibition in Chlamydomonas reinhardtii

PsbT is a small chloroplast-encoded hydrophobic polypeptide associated with the D1/D2 heterodimer of the photosystem II (PSII) reaction center and is required for the efficient post-translational repair of photodamaged PSII. Here we addressed that role in detail in Chlamydomonas reinhardtii wild type and DeltapsbT cells by analyzing the activities of PSII, the assembly of PSII proteins, and the redox components of PSII during photoinhibition and repair. Strong illumination of cells for 15 min decreased the activities of electron transfer through PSII and Q(A) photoreduction by 50%, and it reduced the amount of atomic manganese by 20%, but it did not affect the steady-state level of PSII proteins, photoreduction of pheophytin (pheo(D1)), and the amount of bound plastoquinone (Q(A)), indicating that the decrease in PSII activity resulted mainly from inhibition of the electron transfer from pheo(D1) to Q(A). In wild type cells, we observed parallel recovery of electron transfer activity through PSII and Q(A) photoreduction, suggesting that the recovery of Q(A) activity is one of the rate-limiting steps of PSII repair. In DeltapsbT cells, the repairs of electron transfer activity through PSII and of Q(A) photoreduction activity were both impaired, but PSII protein turnover was unaffected. Moreover, about half the Q(A) was lost from the PSII core complex during purification. Since PsbT is intimately associated with the Q(A)-binding region on D2, we propose that this polypeptide enhances the efficient recovery of Q(A) photoreduction by stabilizing the structure of the Q(A)-binding region.

Redox states of photosystems I and II in irradiated leaves of wheat seedlings grown under different conditions of nitrogen nutrition

Changes in the redox states of photosystem I (PSI) and PSII in irradiated wheat leaves were studied after growing seedlings on a nitrogen-free medium or media containing either nitrate or ammonium. The content of P700, the primary electron donor of PSI was quantified using the maximum magnitude of absorbance changes at 830 nm induced by saturating white light. The highest content of P700 in leaves was found for seedlings grown on the ammonium-containing medium, whereas its lowest content was observed on seedlings grown in the presence of nitrate. At all irradiances of actinic light, the smallest accumulation of reduced QA was observed in leaves of ammonium-grown plants. Despite variations in light-response curves of P700 photooxidation and QA photoreduction, the leaves of all plants exposed to different treatments demonstrated similar relationships between steady-state levels of P700+ and QA−. The accumulation of oxidized P700 up to 40% of total P700 content was not accompanied by significant QA photoreduction. At higher extents of P700 photooxidation, a linear relationship was found between the steady-state levels of P700+ and QA−. The leaves of all treatments demonstrated biphasic patterns of the kinetics of P700+ dark reduction after irradiation by far-red light exciting specifically PSI. The halftimes of corresponding kinetic components were found to be 2.6–4 s (fast component) and 17–22 s (slow component). The two components of P700+ dark reduction were related to the existence of two PSI populations with different rates of electron input from stromal reductants. The magnitudes of these components differed for plants grown in the presence of nitrate, on the one hand, and plants grown either in the presence of ammonium or in the absence of nitrogen, on the other hand. This indicates the possible influence of nitrogen nutrition on synthesis of different populations of PSI in wheat leaves. The decrease in far-red light irradiance reduced the relative contribution of the fast component to P700+ reduction. The fast component completely disappeared at low irradiances. This finding indicates that the saturating far-red light must be applied to determine correctly the relative content of each PSI population in wheat leaves.

Conformational heterogeneity of the bacteriopheophytin electron acceptor HA in reaction centers from Rhodopseudomonas viridis revealed by Fourier transform infrared spectroscopy and site-directed mutagenesis.

The light-induced Fourier transform infrared (FTIR) difference spectra corresponding to the photoreduction of either the HA bacteriopheophytin electron acceptor (HA-/HA spectrum) or the QA primary quinone (QA-/QA spectrum) in photosynthetic reaction centers (RCs) of Rhodopseudomonas viridis are reported. These spectra have been compared for wild-type (WT) RCs and for two site-directed mutants in which the proposed interactions between the carbonyls on ring V of HA and the RC protein have been altered. In the mutant EQ(L104), the putative hydrogen bond between the protein and the 9-keto C=O of HA should be affected by changing Glu L104 to a Gln. In the mutant WF(M250), the van der Waals interactions between Trp M250 and the 10a-ester C=O of HA should be modified. The characteristic effects of both mutations on the FTIR spectra support the proposed interactions and allow the IR modes of the 9-keto and 10a-ester C=O of HA and HA- to be assigned. Comparison of the HA-/HA and QA-/QA spectra leads us to conclude that the QA-/QA IR signals in the spectral range above 1700 cm-1 are largely dominated by contributions from the electrostatic response of the 10a-ester C=O mode of HA upon QA photoreduction. A heterogeneity in the conformation of the 10a-ester C=O mode of HA in WT RCs, leading to three distinct populations of HA, appears to be related to differences in the hydrogen-bonding interactions between the carbonyls of ring V of HA and the RC protein. The possibility that this structural heterogeneity is related to the observed multiexponential kinetics of electron transfer and the implications for primary processes are discussed. The effect of 1H/2H exchange on the QA-/QA spectra of the WT and mutant RCs shows that neither Glu L104 nor any other exchangeable carboxylic residue changes appreciably its protonation state upon QA reduction.

Electrostatic influence of QA reduction on the IR vibrational mode of the 10a-ester C==O of HA demonstrated by mutations at residues Glu L104 and Trp L100 in reaction centers from Rhodobacter sphaeroides.

The light-induced QA-/QA FTIR difference spectrum of the photoreduction of the primary quinone (QA) in reaction centers (RCs) from Rhodobacter sphaeroides exhibits a set of complex differential bands between 1750 and 1715 cm(-1). Several of these features correspond in frequency to bands that bleach in the HA-/HA FTIR difference spectra of the photoreduction of the bacteriopheophytin electron acceptor (HA). Since the 10a-ester C==O from HA and the side chains of protonated carboxylic acids would be expected to contribute in this spectral region, mutations were designed at Trp L100 and Glu L104, which have been proposed to form hydrogen bonds to the 10a-ester and the 9-keto carbonyls on ring V of HA, respectively. The QA/-/QA spectra measured in IH2O and 2H2O of RCs from wild type (WT) were compared to those of RCs with the mutation Trp to Phe at L100 [WF(L100)], Glu to Leu at L104 [EL(L104)], or both mutations [EL(L104)/WF(L100)]. The spectra of the mutants in the 1800-1400 cm(-1) frequency range exhibit only limited perturbations compared to those of WT, indicating the absence of significant structural changes due to the mutations. Part of a differential signal centered around 1732 cm(-1) in the spectrum of WT RCs is downshifted by approximately 7 cm(-1) in EL(L104), while it is upshifted by approximately 11 cm(-1) in WF(L100). This upshift of the differential signal is assigned to the frequency change of the 10a-ester C==O of HA induced by the rupture of the hydrogen bond with Trp L100. The 1H2O-minus-2H2O double-difference spectrum of WT RCs exhibits a characteristic differential signal positive at 1730 cm-1 and negative at 1724 cm-1 that is absent in the corresponding spectra of EL(L104) and of the double mutant, implicating Glu L104 in the QA-/QA spectral changes. This differential signal is strongly modified in frequency and amplitude in the 1H2O-minus-2H2O spectrum of WF(L100), indicating that it does not correspond to a direct response of the C==O mode of the Glu L104 side chain upon QA reduction. Instead, perturbation of the hydrogen bond of the 9-keto C==O with Glu L104 is proposed to induce a change of electron density on ring V of HA, thereby altering the frequency of the 10a-ester C==O that is in partial conjugation with ring V. The loss of the hydrogen bond to the 9-keto C==O of HA due to the Glu L104 to Leu mutation or the alteration of the strength of the hydrogen bond by 1H/2H exchange on Glu L104 appears to produce such effects. Thus, the QA-/QA spectra above 1700 cm-1 are dominated by contributions from the 10a-ester C==O of HA, with most of the differential signals assigned to a small frequency downshift of the 10a-ester C==O of HA in response to QA reduction. The complexity of the signals implies a structural heterogeneity of the conformation and hydrogen bonding of the 10a-ester C==O of HA, which may be related to the functional heterogeneity observed in electron transfer kinetics. The present FTIR results show that the reduction of QA can induce a pronounced electrostatic effect on molecular vibrations of chemical groups located about 10 A away from QA. They also demonstrate that, within experimental limits, the proton uptake observed at pH 7 upon QA photoreduction [McPherson, P. H., Okamura, M. Y., & Feher, G. (1988) Biochim. Biophys. Acta 934, 348-368] involves none of the exchangeable carboxylic groups of the RC.

Stoichiometries of Photosystem I and Photosystem II in Rice Mutants Differently Deficient in Chlorophyll b

Stoichiometries of photosystem I (PSI) and photosystem II (PSII) reaction centers in a cultivar of rice, Norin No. 8, and three chlorophyll b-deficient mutants derived from the cultivar were investigated. Quantitation of PSI by photooxidation of P-700 and chromatographic assay of vitamin K1 showed that, on the basis of chlorophyll, the mutants have higher concentrations of PSI than the wildtype rice. Greater increases were observed in the PSII contents measured by photoreduction of QA, binding of a radioactive herbicide and atomic absorption spectroscopy of Mn. Consequently, the PSII to PSI ratio increased from 1.1–1.3 in the wild-type rice to 1.8 in chlorina 2, which contains no Chl b, and to 2.0–3.3 in chlorina 11 and chlorina 14, which have chlorophyll a/b ratios of 9 and 13, respectively. Measurement of oxygen evolution with saturating single-turnover flashes revealed that, whereas at most 20% of PSII centers are inactive in oxygen evolution in the wildtype rice, the non-functional PSII centers amount to about 50% in the three mutant strains. The fluorescence induction kinetics was also analyzed to estimate proportions of the inactive PSII in the mutants. The data obtained suggest that plants have an ability to adjust the stoichiometry of the two photosystems and the functional organization of PSII in response to the genetically induced deficiency of chlorophyll b.

Antenna Sizes of Photosystem I and Photosystem II in Chlorophyll b-Deficient Mutants of Rice. Evidence for an Antenna Function of Photosystem II Centers That are Inactive in Electron Transport

Light-harvesting capacities of photosystem I (PSI) and photosystem II (PSII) in a wild-type and three chlorophyll 6-deficient mutant strains of rice were determined by measuring the initial slope of light-respons e curve of PSI and PSII electron transport and kinetics of light-induced redox changes of P-700 and QA, respectively. The light-harvesting capacity of PSI determined by the two methods was only moderately reduced by chlorophyll 6-deficiency. Analysis of the fluorescence induction that monitors time course of QA photoreduction showed that both relative abundance and antenna size of PSIIa decrease with increasing deficiency of chlorophyll b and there is only PSII,, in chlorina 2 which totally lacks chlorophyll b. The numbers of antenna chlorophyll molecules associated with the mutant PSII centers were, therefore, three to five times smaller than that of PSII a in the wild type rice. Rates of PSII electron transport determined on the basis of PSII centers in the three mutants were 60-70% of that in the normal plant at all photon flux densities examined, indicating that substantial portions of the mutant PSII centers are inactive in electron transport. The initial slopes of light-respons e curves of PSII electron transport revealed that the functional antenna sizes of the active populations of PSII centers in the mutants correspond to about half that of PSII a in the wild type rice. Thus, the numbers of chlorophyll molecules that serve as antenna of the oxygen-evolving PSII centers in the mutants are significantly larger than those that are actually associated with each PSII center. It is proposed that the inactive PSII serves as an antenna of the active PSII in the three chlorophyll ^-deficient mutants of rice. In spite of the reduced antenna size of PSII, therefore, the total light-harvesting capacity of PSII approximately matches that of PSI in the mutants.

Effects of bicarbonate and formate on the donor side of Photosystem 2

Sodium formate at concentration of 5-20 μM suppresses electron flow on the donor side of Photosystem 2 (PS 2) in pea subchloroplast membranes (DT-20) which is revealed by inhibition of photoinduced changes of chlorophyll fluorescence yield related to photoreduction of QA and pheophytin (the primary and intermediary electron acceptors) and oxygen evolution and the increase of absorbance changes related to photooxidation of P680, the primary electron donor, under continuous illumination. These activities are also inhibited upon partial depletion of bicarbonate in the medium and restored by the addition of 0.1-10 mM NaHCO3. At concentrations higher than 20 μM formate induces the known bicarbonate effect on the acceptor side of PS 2 which dominates at millimolar concentrations of the agent. In Tris-treated (Mn-depleted) DT-20 the restoration of electron flow with 0.2 μM MnCl2 (4 Mn atoms per one PS 2 reaction center) in the medium depleted of bicarbonate is efficient only after the addition of 5 mM NaHCO3. The restoration in the presence of NaHCO3 is accompanied by an increased functional binding of Mn(2+) to PS 2 membranes which is confirmed by experiments on removal of added Mn(2+) by either sedimentation or the addition of EDTA. Pre-illumination increases the Mn binding in the presence of bicarbonate. The data show that the bicarbonate effect on the donor side of PS 2 is related to a relatively low-affinity bound pool of bicarbonate. It is suggested that bicarbonate takes part in the formation of the Mn-cluster capable of water oxidation as an obligatory ligand or through modification of the binding site(s) of Mn.

Light-harvesting chlorophyll a-b complex requirement for regulation of Photosystem II photochemistry by non-photochemical quenching

Recently, it has been suggested (Horton et al. 1992) that aggregation of the light-harvesting a-b complex (LHC II) in vitro reflects the processes which occur in vivo during fluorescence induction and related to the major non-photochemical quenching (qE). Therefore the requirement of this chlorophyll a-b containing protein complex to produce qN was investigated by comparison of two barley mutants either lacking (chlorina f2) or depressed (chlorina(104)) in LHC II to the wild-type and pea leaves submitted to intermittent light (IL) and during their greening in continuous light.It was observed that qN was photoinduced in the absence of LHC II, i.e. in IL grown pea leaves and the barley mutants. Nevertheless, in these leaves qN had no (IL, peas) or little (barley mutants) inhibitory effect on the photochemical efficiency of QA reduction measured by flash dosage response curves of the chlorophyll fluorescence yield increase induced by a single turn-over flashDuring greening in continuous light of IL pea leaves, an inhibitory effect on QA photoreduction associated to qN developed as Photosystem II antenna size increased with LHC II synthesis. Utilizing data from the literature on connectivity between PS II units versus antenna size, the following hypothesis is put forward to explain the results summarized above. qN can occur in the core antenna or Reaction Center of a fraction of PS II units and these units will not exhibit variable fluorescence. Other PS II units are quenched indirectly through PS II-PS II exciton transfer which develops as the proportion of connected PS II units increases through LHC II synthesis.

Deletion Mutagenesis of the Cytochrome b559 Protein Inactivates the Reaction Center of Photosystem II.

In green plant-like photosynthesis, oxygen evolution is catalyzed by a thylakoid membrane-bound protein complex, photosystem II. Cytochrome b559, a protein component of the reaction center of this complex, is absent in a genetically engineered mutant of the cyanobacterium, Synechocystis 6803 [Pakrasi, H.B., Williams, J.G.K., and Arntzen, C.J. (1988). EMBO J. 7, 325-332]. In this mutant, the genes psbE and psbF, encoding cytochrome b559, were deleted by targeted mutagenesis. Two other protein components, D1 and D2 of the photosystem II reaction center, are also absent in this mutant. However, two chlorophyll-binding proteins, CP47 and CP43, as well as a manganese-stabilizing extrinsic protein component of photosystem II are stably assembled in the thylakoids of this mutant. Thus, this deletion mutation destabilizes the reaction center of photosystem II only. The mutant also lacks a fluorescence maximum peak at 695 nm (at 77 K) even though the CP47 protein, considered to be the origin of this fluorescence peak, is present in this mutant. We propose that the fluorescence at 695 nm originates from an interaction between the reaction center of photosystem II and CP47. The deletion mutant shows the absence of variable fluorescence at room temperature, indicating that its photosystem II complex is photochemically inactive. Also, photoreduction of QA, the primary acceptor quinone in photosystem II, could not be detected in the mutant. We conclude that cytochrome b559 plays at least an essential structural role in the reaction center of photosystem II.

Thermodynamics of the charge recombination in photosystem II

The temperature dependence of the electric field-induced chlorophyll luminescence in photosystem II was studied in Tris-washed, osmotically swollen spinach chloroplasts (blebs). The system II reaction centers were brought in the state Z(+)P(+)-QA (-)QB (-) by preillumination and the charge recombination to the state Z(+)PQAQB (-) was measured at various temperatures and electrical field strengths. It was found that the activation enthalpy of this back reaction was 0.16 eV in the absence of an electrical field and diminished with increasing field strength. It is argued that this energy is the enthalpy difference between the states IQA (-) and I(-)QA and accounts for about half of the free energy difference between these states. The redox state of QB does not influence this free energy difference within 150 μs after the photoreduction of QA. The consequences for the interpretation of thermodynamic properties of QA are discussed.

Mechanism of photoinhibition: photochemical reaction center inactivation in system II of chloroplasts

Photoinhibition of photosynthesis is manifested at the level of the leaf as a loss of CO2 fixation and at the level of the chloroplast thylakoid membrane as a loss of photosystem II electron-transport capacity. At the photosystem II level, photoinhibition is manifested by a lowered chlorophyll a variable fluorescence yield, by a lowered amplitude of the light-induced absorbance change at 320 nm (ΔA320) and 540-minus-550 nm (ΔA540-550), attributed to inhibition of the photoreduction of the primary plastoquinone QA molecule. A correlation of the kinetics of variable fluorescence yield loss with the inhibition of QA photoreduction suggested that photoinhibited reaction centers are incapable of generating a stable charge separation but are highly efficient in the trapping and non-photochemical dissipation of absorbed light. The direct effect of photoinhibition on primary photochemical parameters of photosystem II suggested a permanent reaction center modification the nature of which remains to be determined.