Distribution Of Photosystem Research Articles

Effects of perfluorooctanoic acid on Microcystis aeruginosa: Stress and self-adaptation mechanisms.

The persistent organic pollutant perfluorooctanoic acid (PFOA) is ubiquitous in aquatic environments. However, little is known about its toxicity to microalgae or the mechanisms by which they may self-adapt to it. We found that growth of the bloom-forming cyanobacterium Microcystis aeruginosa was initially inhibited, with inhibition attenuated after 12 d of PFOA exposure. Growth inhibition gradually decreased and stabilized over time. With increasing PFOA concentration, reactive oxygen species levels and superoxide dismutase and photosystem II activity significantly increased, while respiration, NDH-1 activity, and total carbohydrate content significantly decreased. Self-adaptation mechanisms included antioxidant pathways, energy transfer and distribution of photosystems, and repair of the PSI and NDH complexes. The patterns of change in these parameters were consistent with those of the expression levels of genes in their associated metabolic pathways. Our data suggest that PSII overcompensation might be a strategy by which M. aeruginosa contends with oxidative stress induced by PFOA. Multiple downstream photosynthesis-related proteins were upregulated as a function of PFOA exposure time. These findings may help elucidate physiological, genetic stress and self-adaptive responses of microalgae to PFOA exposure.

Dark-adapted spinach thylakoid protein heterogeneity offers insights into the photosystem II repair cycle

In higher plants, thylakoid membrane protein complexes show lateral heterogeneity in their distribution: photosystem (PS) II complexes are mostly located in grana stacks, whereas PSI and adenosine triphosphate (ATP) synthase are mostly found in the stroma-exposed thylakoids. However, recent research has revealed strong dynamics in distribution of photosystems and their light harvesting antenna along the thylakoid membrane. Here, the dark-adapted spinach (Spinacia oleracea L.) thylakoid network was mechanically fragmented and the composition of distinct PSII-related proteins in various thylakoid subdomains was analyzed in order to get more insights into the composition and localization of various PSII subcomplexes and auxiliary proteins during the PSII repair cycle. Most of the PSII subunits followed rather equal distribution with roughly 70% of the proteins located collectively in the grana thylakoids and grana margins; however, the low molecular mass subunits PsbW and PsbX as well as the PsbS proteins were found to be more exclusively located in grana thylakoids. The auxiliary proteins assisting in repair cycle of PSII were mostly located in stroma-exposed thylakoids, with the exception of THYLAKOID LUMEN PROTEIN OF 18.3 (TLP18.3), which was more evenly distributed between the grana and stroma thylakoids. The TL29 protein was present exclusively in grana thylakoids. Intriguingly, PROTON GRADIENT REGULATION5 (PGR5) was found to be distributed quite evenly between grana and stroma thylakoids, whereas PGR5-LIKE PHOTOSYNTHETIC PHENOTYPE1 (PGRL1) was highly enriched in the stroma thylakoids and practically missing from the grana cores. This article is part of a Special Issue entitled: Photosynthesis Research for Sustainability: Keys to Produce Clean Energy.

Kinetic model for electron and proton transport in chloroplasts with a nonuniform distribution of protein complexes in thylakoid membranes

A mathematical model for describing electron and proton transport in chloroplasts of higher plants with nonuniform distribution of photosystem 1 (PS1) and photosystem 2 (PS2) between granal and stromal thylakoids was proposed. Along with the noncyclic (linear) electron transport from PS2 to terminal acceptor PS1, we considered cyclic electron transport around PS1, ATP synthesis coupled to transmembrane proton transfer through ATP synthase, and ATP consumption in the Calvin cycle. Numerical simulations of the kinetics of the photoinduced redox transformations of the primary PS1 donor (P700) and the behavior of pH in the intrathylakoid space (pHi) and interthylakoid space (pH0), as well as the time evolution of the ATP concentration for various conditions of the functioning of the chloroplast were performed.

Supramolecular photosystem II organization in grana thylakoid membranes: evidence for a structured arrangement.

The distribution of photosystem (PS) II complexes in stacked grana thylakoids derived from electron microscopic images of freeze-fractured chloroplasts are examined for the first time using mathematical methods. These characterize the particle distribution in terms of a nearest neighbor distribution function and a pair correlation function. The data were compared with purely random distributions calculated by a Monte Carlo simulation. The analysis reveals that the PSII distribution in grana thylakoids does not correspond to a random protein mixture but that ordering forces lead to a structured arrangement on a supramolecular level. Neighboring photosystems are significantly more separated than would be the case in a purely random distribution. These results are explained by structural models, in which boundary lipids and light-harvesting complex (LHC) II trimers are arranged between neighboring PSII. Furthermore, the diffusion of PSII was analyzed by a Monte Carlo simulation with a protein density of 80% area occupation (determined for grana membranes). The mobility of the photosystems is severely reduced by the high protein density. From an estimate of the mean migration time of PSII from grana thylakoids to stroma lamellae, it becomes evident that this diffusion contributes significantly to the velocity of the repair cycle of photoinhibited PSII.

EVIDENCE FOR A LACK OF PHOTOSYSTEM SEGREGATION IN CHLAMYDOMONAS REINHARDTII (CHLOROPHYCEAE)

The distribution of photosystems I and II (PSI and PSII) in cells of Chlamydomonas reinhardtii Dangeard was studied by immunogold electron microscopy using cultures grown autotrophically at moderate irradiance and harvested in the middle of the light period. Sections of Lowicryl‐embedded cells were labeled with monospecific heterologous antisera raised against the reaction center proteins of PSI (CP1‐e) or the core antenna proteins of PSII (CP40 and CP47). All three antisera labeled both the appressed and the nonappressed thylakoid membranes at essentially similar densities. Labeling with both PSI and PSII antisera was slightly more concentrated over the outer nonappressed membranes of the thylakoid bands (1.7‐ to 2.4‐fold with anti‐CP1‐ e and 1.5‐ to 1.8‐fold with anti‐CP47 and anti‐CP40). However, since appressed membranes comprised 73% of the total thylakoid membranes, 50%–62% of the PSI and 58%–65% of the PSII labeling were localized on appressed membranes. We conclude that photosystem distribution in C. reinhardtii is similar to that reported for other algae and different from the lateral heterogeneity observed in higher plants.

Cytochemical Localization of Photosystem I in Relation to Differentiation of the Thylakoid Membranes during Greening of Barley Leaves

Changes in distribution of photosystem I (PS I) in the developing thylakoid membranes of greening barley (Hordeum vulgare L. cv. Amagi-Nijo) chloroplasts were studied by a cytochemical method using 3,3'-diaminobenzidine (DAB). The activity was detected on the thylakoid of etiochloroplasts after 1 h of greening. Stacks of a few thylakoids (thought to be an initiation of grana) appeared at about 2-3 h of greening. Until 4 h, the DAB reaction was observed uniformly throughout the whole thylakoid system (stroma and grana thylakoids). After 6 h of greening, The DAB reaction was detected heterogeneously in the etiochloroplasts; more intense on the stroma thylakoid and peripheral grana thylakoid. Further illumination led to more distinct heterogeneity of the DAB reaction. Thus, redistribution of PS I proceeded differentially after onset of grana formation in the developing etiochloroplasts. Measurements of chlorophyll content, light saturation of PS I activity and fluorescence emission spectra of greening barley leaves suggest that redistribution of PS I may reflect developmental changes in assembly of the PS I complex with light-harvesting chlorophyll-protein complex.

The distribution of Photosystem I and Photosystem II polypeptides between the cytoplasmic and thylakoid membranes of cyanobacteria

In a previous study we found that the 33 kDa extrinsic polypeptide of Photosystem II is present in both the cytoplasmic and thylakoid membranes of cyanobacteria, but forms part of a functional complex only in the latter [Smith et al. (1987) Mol. Microbiol. 6, 1821–1827]. In order to determine if this phenomenon is restricted to the 33 kDa polypeptide we have extended this study in Anacystis nidulans to include a number of other polypeptides of Photosystem I and Photosystem II. We have found that D1 and possibly PsaC are present in both membranes, CP43 and CP47 are confined to the thylakoid membranes, and the distribution of PsaD and PsaE is dependent upon the growth stage of the cyanobacteria.

The distribution of Photosystem I and Photosystem II polypeptides between the cytoplasmic and thylakoid membranes of cyanobacteria

In a previous study we found that the 33 kDa extrinsic polypeptide of Photosystem II is present in both the cytoplasmic and thylakoid membranes of cyanobacteria, but forms part of a functional complex only in the latter [Smith et al. (1987) Mol. Microbiol. 6, 1821–1827]. In order to determine if this phenomenon is restricted to the 33 kDa polypeptide we have extended this study in Anacystis nidulans to include a number of other polypeptides of Photosystem I and Photosystem II. We have found that D1 and possibly PsaC are present in both membranes, CP43 and CP47 are confined to the thylakoid membranes, and the distribution of PsaD and PsaE is dependent upon the growth stage of the cyanobacteria.

Energy coupling, membrane lipids and structure of thylakoids of Lupin plants submitted to water stress

Bioenergetic properties of thylakoids from plants submitted to a water stress stress (watering stopped for 6-15 days) have been measured in two lupin genotypes characterized as resistant or susceptible to drought. This energy coupling was assessed by flow-force relationships relating the phosphorylation rate to the magnitude of the proton gradient % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXafv3ySLgzGmvETj2BSbqef0uAJj3BZ9Mz0bYu% H52CGmvzYLMzaerbd9wDYLwzYbItLDharqqr1ngBPrgifHhDYfgasa% acOqpw0xe9v8qqaqFD0xXdHaVhbbf9v8qqaqFr0xc9pk0xbba9q8Wq% Ffea0-yr0RYxir-Jbba9q8aq0-yq-He9q8qqQ8frFve9Fve9Ff0dme% GabaqaaiGacaGaamqadaabaeaafiaakabbaaa6daaahjxzL5gapeqa% aiabgs5aenaaxacabaGaeqiVd0galeqabaGaaiOFaaaakmaaBaaale% aacaWGibWaaWbaaWqabeaacqGHRaWkaaaaleqaaaaa!4D55!\[\Delta \mathop \mu \limits^\~ _{H^ + } \]. The fluorescent probe 9-aminoacridine was used to express, as a ΔpH, the whole % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXafv3ySLgzGmvETj2BSbqef0uAJj3BZ9Mz0bYu% H52CGmvzYLMzaerbd9wDYLwzYbItLDharqqr1ngBPrgifHhDYfgasa% acOqpw0xe9v8qqaqFD0xXdHaVhbbf9v8qqaqFr0xc9pk0xbba9q8Wq% Ffea0-yr0RYxir-Jbba9q8aq0-yq-He9q8qqQ8frFve9Fve9Ff0dme% GabaqaaiGacaGaamqadaabaeaafiaakabbaaa6daaahjxzL5gapeqa% aiabgs5aenaaxacabaGaeqiVd0galeqabaGaaiOFaaaakmaaBaaale% aacaWGibWaaWbaaWqabeaacqGHRaWkaaaaleqaaaaa!4D55!\[\Delta \mathop \mu \limits^\~ _{H^ + } \] by calibrating fluorescence quenching against the phosphate potential ΔGp in 'state 4', i.e., when ATP synthesis is strictly balanced by its hydrolysis. This calibration procedure was shown to be unaffected by treatments. At equal energization (iso-ΔpH), ATP synthesis was halved by a medium stress and disappeared for a more severe stress, whereas ΔpH at equal energy input (light) declined only under a severe drought. For an identical ΔpH, PS 1-driven phosphorylation is always more efficient than PS 2, both in control and stressed plants. Thus, uncoupling is not the cause of the phosphorylation decline; moreover, retention of a 'micro-chemiosmotic' type of coupling implies that the distribution of photosystems and ATPases is unchanged. Parallel to these functional alterations, the lipid content of thylakoids dramatically dropped. As galactolipids fell strongly, neutral lipids rose slightly. Fatty acids decreased then increased with stress, yet phosphorylation did not recover in the latter case and membrane permeability to protons remained unaffected. Overall, these observations suggest a preserved thylakoid structure and this was indeed observed on electron micrographs, even for a severe stress. Therefore, the membrane integrity is probably preserved more by the protein network than by the lipid matrix and the loss of the phosphorylating activity mainly reflects a loss of ATPases or at least their inactivation, possibly due to their altered lipid environment. Finally, from the bioenergetic point of view, the susceptible genotype was unexpectedly less affected by drought than the resistant.

Distribution of intrinsic and extrinsic subunits of the PS II protein complex between appressed and non-appressed regions of the thylakoid membrane: an immunocytochemical study

The distribution of photosystem (PS) II centers between appressed and non-appressed domains of the thylakoid membranes has been investigated, using immunogold labeling, in C. reinhardtii and in spinach. We have used antibodies directed against the two main intrinsic subunits of the PS II center and against two extrinsic subunits of the O 2-evolving site. 90% of the two intrinsic PS II antigens are located in the appressed membranes, in a density 3–3.5-fold higher than in the non-appressed regions. The same distribution is observed for the two extrinsic antigens. This result suggests that the O 2-evolving system is associated with the PS II center, both in appressed and in non-appressed regions of the thylakoid membrane.

The Distribution of Photosynthetic Reactions in the Chloroplast Lamellar System

Chloroplast fragmentation, ATPase, Proton pump, Cyclic Phosphorylation, NH4Cl-uncoupling Cyclic phosphorylation and latent ATPase follow the distribution of photosystem I in the chloroplast membrane. Both activities are found higher in stroma lamellae than in grana. The extent of proton uptake is found to be higher in the grana. Since this uptake depends on internal volume and buffer capacity besides proton pump activity, the distribution of the proton pump proper remains to be elucidated. Any fragmentation of the large inner compartment of the chlorolast lamellar system into smaller vesicles results in decreased sensitivity of cyclic phosphorylation to uncoupling by ammonium chloride. Consequently both, isolated grana and stroma lamellae, show decreased uncoupling by ammonium chloride. The effect can be explained by the action of a membrane potential in photophosphorylation which builds up during illumination and might be more stable in a system with the larger number of individual compartments just for statistical reasons. No assumption on changes in specific ion permeabilities during fragmentation of chloroplasts are needed.

Distribution of photosystems 1 and 2 in the chloroplast lamellar structure.

Research Article| June 01 1972 Distribution of photosystems 1 and 2 in the chloroplast lamellar structure P V Sane P V Sane Search for other works by this author on: This Site PubMed Google Scholar Biochem J (1972) 128 (1): 33P. https://doi.org/10.1042/bj1280033Pb Views Icon Views Article contents Figures & tables Video Audio Supplementary Data Peer Review Share Icon Share Twitter LinkedIn Cite Icon Cite Get Permissions Citation P V Sane; Distribution of photosystems 1 and 2 in the chloroplast lamellar structure. Biochem J 1 June 1972; 128 (1): 33P. doi: https://doi.org/10.1042/bj1280033Pb Download citation file: Ris (Zotero) Reference Manager EasyBib Bookends Mendeley Papers EndNote RefWorks BibTex toolbar search Search Dropdown Menu nav search search input Search input auto suggest search filter All ContentAll JournalsBiochemical Journal Search Advanced Search This content is only available as a PDF. © 1972 London: The Biochemical Society1972 Article PDF first page preview Close Modal You do not currently have access to this content.

Spectral, Physical, and Electron Transport Activities in the Photosynthetic Apparatus of Mesophyll Cells and Bundle Sheath Cells of Digitaria sanguinalis (L.) Scop.

Isolated mesophyll cells and bundle sheath cells of Digitaria sanguinalis were used to study the light-absorbing pigments and electron transport reactions of a plant which possesses the C(4)-dicarboxylic acid cycle of photosynthesis. Absorption spectra and chlorophyll determinations are presented showing that mesophyll cells have a chlorophyll a-b ratio of about 3.0 and bundle sheath cells have a chlorophyll a-b ratio of about 4.5. The absorption spectrum of bundle sheath cells has a greater absorption in the 700 nm region at liquid nitrogen temperature, and there is a relatively greater amount of a pigment absorbing at 670 nm in the bundle sheath cells compared to the mesophyll cells. Fluorescence emission spectra, at liquid nitrogen temperature, of mesophyll cells have a fluorescence 730 nm-685 nm ratio of about 0.82 and bundle sheath cells have a ratio of about 2.84. The reversible light-induced absorption change in the region of P(700) absorption is similar in both cell types but bundle sheath cells exhibit about twice as much total P(700) change as mesophyll cells on a total chlorophyll basis. The delayed light emission of bundle sheath cells is about one-half that of mesophyll cells. Both mesophyll cells and bundle sheath cells evolve oxygen in the presence of Hill oxidants with the mesophyll cells exhibiting about twice the activity of bundle sheath cells, and both activities are inhibited by 1 muM 3-(3,4-dichlorophenyl)-1, 1-dimethylurea. Ferredoxin nicotinamide adenine dinucleotide phosphate reductase is present in both cells although it is about 3- or 4-fold higher in mesophyll cells than in bundle sheath cells. Glyceraldehyde 3-P dehydrogenases, both nicotinamide adenine dinucleotide and nicotinamide adenine dinucleotide phosphate, are equally distributed in the two cell types on a chlorophyll basis. Malic enzyme is localized in the bundle sheath cells.We interpret the data as evidence for the presence of a complete chloroplast electron transport system from oxygen evolution to pyridine nucleotide reduction in both mesophyll and bundle sheath cells. However, there is a quantitative difference in the distribution of photosystem I and photosystem II components in the two photosynthetic cells with about a 3-fold higher photosystem I-II ratio in the bundle sheath cells than in the mesophyll cells. A scheme is proposed to accommodate photosynthetic CO(2) fixation and electron transport activities in the mesophyll cells via a beta-carboxylation and in the bundle sheath cells via carboxylation of ribulose-1, 5-diphosphate.