Light plays an essential role in photosynthesis; however, its excess can cause damage to cellular components. Photosynthetic organisms thus developed a set of photoprotective mechanisms (e.g., non-photochemical quenching, photoinhibition) that can be studied by a classic biochemical and biophysical methods in cell suspension. Here, we combined these bulk methods with single-cell identification of microdomains in thylakoid membrane during high-light (HL) stress. We used Synechocystis sp. PCC 6803 cells with YFP tagged photosystem I. The single-cell data pointed to a three-phase response of cells to acute HL stress. We defined: (1) fast response phase (0-30 min), (2) intermediate phase (30-120 min), and (3) slow acclimation phase (120-360 min). During the first phase, cyanobacterial cells activated photoprotective mechanisms such as photoinhibition and non-photochemical quenching. Later on (during the second phase), we temporarily observed functional decoupling of phycobilisomes and sustained monomerization of photosystem II dimer. Simultaneously, cells also initiated accumulation of carotenoids, especially ɣ-carotene, the main precursor of all carotenoids. In the last phase, in addition to ɣ-carotene, we also observed accumulation of myxoxanthophyll and more even spatial distribution of photosystems and phycobilisomes between microdomains. We suggest that the overall carotenoid increase during HL stress could be involved either in the direct photoprotection (e.g., in ROS scavenging) and/or could play an additional role in maintaining optimal distribution of photosystems in thylakoid membrane to attain efficient photoprotection.

• MeSH
• bakteriální proteiny genetika   metabolismus   MeSH
• fotosystém I - proteinový komplex genetika   metabolismus   MeSH
• fotosystém II - proteinový komplex genetika   metabolismus   MeSH
• karotenoidy metabolismus   MeSH
• světlo * MeSH
• Synechocystis metabolismus   účinky záření   MeSH
• tylakoidy metabolismus   účinky záření   MeSH
• velikost buňky účinky záření   MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH

Antenna protein aggregation is one of the principal mechanisms considered effective in protecting phototrophs against high light damage. Commonly, it is induced, in vitro, by decreasing detergent concentration and pH of a solution of purified antennas; the resulting reduction in fluorescence emission is considered to be representative of non-photochemical quenching in vivo. However, little is known about the actual size and organization of antenna particles formed by this means, and hence the physiological relevance of this experimental approach is questionable. Here, a quasi-single molecule method, fluorescence correlation spectroscopy (FCS), was applied during in vitro quenching of LHCII trimers from higher plants for a parallel estimation of particle size, fluorescence, and antenna cluster homogeneity in a single measurement. FCS revealed that, below detergent critical micelle concentration, low pH promoted the formation of large protein oligomers of sizes up to micrometers, and therefore is apparently incompatible with thylakoid membranes. In contrast, LHCII clusters formed at high pH were smaller and homogenous, and yet still capable of efficient quenching. The results altogether set the physiological validity limits of in vitro quenching experiments. Our data also support the idea that the small, moderately quenching LHCII oligomers found at high pH could be relevant with respect to non-photochemical quenching in vivo.

• MeSH
• chlorofyl chemie   genetika   účinky záření   MeSH
• fluorescence MeSH
• fluorescenční spektrometrie MeSH
• fotosyntéza genetika   MeSH
• fotosystém II - proteinový komplex genetika   účinky záření   MeSH
• fototrofní procesy genetika   MeSH
• homeodoménový protein Antennapedia chemie   genetika   MeSH
• koncentrace vodíkových iontů MeSH
• proteinové agregáty genetika   MeSH
• shluková analýza MeSH
• světlo škodlivé účinky   MeSH
• světlosběrné proteinové komplexy chemie   genetika   MeSH
• tylakoidy chemie   genetika   účinky záření   MeSH
• zeaxanthiny genetika   MeSH
• Publikační typ
• časopisecké články MeSH

Photosystem II (PSII) is an intrinsic membrane protein complex that functions as a light-driven water:plastoquinone oxidoreductase in oxygenic photosynthesis. Electron transport in PSII is associated with formation of reactive oxygen species (ROS) responsible for oxidative modifications of PSII proteins. In this study, oxidative modifications of the D1 and D2 proteins by the superoxide anion (O2•-) and the hydroxyl (HO•) radicals were studied in WT and a tocopherol cyclase (vte1) mutant, which is deficient in the lipid-soluble antioxidant α-tocopherol. In the absence of this antioxidant, high-resolution tandem mass spectrometry was used to identify oxidation of D1:130E to hydroxyglutamic acid by O2•- at the PheoD1 site. Additionally, D1:246Y was modified to either tyrosine hydroperoxide or dihydroxyphenylalanine by O2•- and HO•, respectively, in the vicinity of the nonheme iron. We propose that α-tocopherol is localized near PheoD1 and the nonheme iron, with its chromanol head exposed to the lipid-water interface. This helps to prevent oxidative modification of the amino acid's hydrogen that is bonded to PheoD1 and the nonheme iron (via bicarbonate), and thus protects electron transport in PSII from ROS damage.

• MeSH
• alfa-tokoferol chemie   metabolismus   MeSH
• aminokyseliny chemie   metabolismus   MeSH
• Arabidopsis enzymologie   genetika   účinky záření   MeSH
• fotosyntéza fyziologie   účinky záření   MeSH
• fotosystém II - proteinový komplex chemie   genetika   metabolismus   MeSH
• hydroxylový radikál chemie   metabolismus   MeSH
• interakční proteinové domény a motivy MeSH
• intramolekulární transferasy chemie   genetika   metabolismus   MeSH
• konformace proteinů, alfa-helix MeSH
• konformace proteinů, beta-řetězec MeSH
• kyslík chemie   metabolismus   MeSH
• molekulární modely MeSH
• mutace MeSH
• oxidace-redukce MeSH
• superoxidy chemie   metabolismus   MeSH
• světlo MeSH
• termodynamika MeSH
• Thermosynechococcus enzymologie   genetika   účinky záření   MeSH
• tylakoidy enzymologie   genetika   účinky záření   MeSH
• vazba proteinů MeSH
• vazebná místa MeSH
• železo chemie   metabolismus   MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH
• Research Support, U.S. Gov't, Non-P.H.S. MeSH

This study presents a mathematical model, which expresses the absorbance of a photosynthetic sample as a non-linear polynomial of selected reference absorbance. The non-linearity is explained by inhomogeneities of a product of pigment concentration and light path length in the sample. The quadratic term of the polynomial reflects the extent of inhomogeneities, and the cubic term is related to deviation of the product distribution from a symmetric one. The model was tested by measurements of suspension of unstacked tobacco thylakoid membranes of different chlorophyll concentrations in cuvettes of different thicknesses. The absorbance was calculated from the diffuse transmittance and reflectance of sample, illuminated by perpendicular collimated light. The evaluated quantity was a sensitivity defined as the relative difference between the sample absorbance and the reference absorbance to the reference absorbance. The non-linearity of sample absorbance was demonstrated by a characteristic deviation of the sensitivity spectrum from a constant value. The absorbance non-linearity decreased on an increase of the product of pigment concentration and cuvette thickness. The model suggests that the sieve and detour effects influence the absorbance in a similar way. The model may be of interest in modeling of leaf or canopy optics including light absorption and scattering.

• MeSH
• chlorofyl metabolismus   MeSH
• fotosyntéza účinky záření   MeSH
• listy rostlin fyziologie   účinky záření   MeSH
• pigmentace účinky záření   MeSH
• světlo MeSH
• tabák fyziologie   účinky záření   MeSH
• technologie dálkového snímání MeSH
• teoretické modely * MeSH
• tylakoidy účinky záření   MeSH
• Publikační typ
• časopisecké články MeSH

In the model cyanobacterium Synechocystis sp. PCC 6803, the terminal enzyme of chlorophyll biosynthesis, chlorophyll synthase (ChlG), forms a complex with high light-inducible proteins, the photosystem II assembly factor Ycf39 and the YidC/Alb3/OxaI membrane insertase, co-ordinating chlorophyll delivery with cotranslational insertion of nascent photosystem polypeptides into the membrane. To gain insight into the ubiquity of this assembly complex in higher photosynthetic organisms, we produced functional foreign chlorophyll synthases in a cyanobacterial host. Synthesis of algal and plant chlorophyll synthases allowed deletion of the otherwise essential native cyanobacterial gene. Analysis of purified protein complexes shows that the interaction with YidC is maintained for both eukaryotic enzymes, indicating that a ChlG-YidC/Alb3 complex may be evolutionarily conserved in algae and plants.

• MeSH
• bakteriální proteiny genetika   metabolismus   MeSH
• fotosyntéza účinky záření   MeSH
• fotosystém II - proteinový komplex genetika   metabolismus   MeSH
• fylogeneze MeSH
• ligasy tvořící vazby C-O klasifikace   genetika   metabolismus   MeSH
• proteiny huseníčku genetika   metabolismus   MeSH
• světlo MeSH
• Synechocystis genetika   metabolismus   MeSH
• tylakoidy metabolismus   účinky záření   MeSH
• vazba proteinů účinky záření   MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH

A model was constructed which includes electron transport (linear and cyclic and Mehler type reaction) coupled to proton translocation, counter ion movement, ATP synthesis, and Calvin-Benson cycle. The focus is on modeling of the light-induced total electric potential difference (ΔΨ) which in this model originates from the bulk phase electric potential difference (ΔΨb), the localized electric potential difference (ΔΨc), as well as the surface electric potential difference (ΔΨs). The measured dual wavelength transmittance signal (ΔA515-560nm, electrochromic shift) was used as a proxy for experimental ΔΨ. The predictions for theoretical ΔΨ vary with assumed contribution of ΔΨs, which might imply that the measured ΔA515-560nm trace on a long time scale reflects the interplay of the ΔΨ components. Simulations also show that partitioning of proton motive force (pmf) to ΔΨb and ΔpH components is sensitive to the stoichiometric ratio of H(+)/ATP, energy barrier for ATP synthesis, ionic strength, buffer capacity and light intensity. Our model shows that high buffer capacity promotes the establishment of ΔΨb, while the formation of pHi minimum is not 'dissipated' but 'postponed' until it reaches the same level as that for low buffer capacity. Under physiologically optimal conditions, the output of the model shows that at steady state in light, the ΔpH component is the main contributor to pmf to drive ATP synthesis while a low ΔΨb persists energizing the membrane. Our model predicts 11mV as the resting electric potential difference across the thylakoid membrane in dark. We suggest that the model presented in this work can be integrated as a module into a more comprehensive model of oxygenic photosynthesis.

• MeSH
• biologické modely * MeSH
• časové faktory MeSH
• koncentrace vodíkových iontů účinky záření   MeSH
• listy rostlin metabolismus   účinky záření   MeSH
• membránové potenciály účinky záření   MeSH
• počítačová simulace MeSH
• protonmotorická síla účinky záření   MeSH
• protony MeSH
• pufry MeSH
• světlo * MeSH
• transport elektronů MeSH
• tylakoidy metabolismus   účinky záření   MeSH
• uhlík metabolismus   MeSH
• Publikační typ
• časopisecké články MeSH

Polyunsaturated lipids are important components of photosynthetic membranes. Xanthophylls are the main photoprotective agents, can assist in protection against light stress, and are crucial in the recovery from photoinhibition. We generated the xanthophyll- and polyunsaturated lipid-deficient ROAD mutant of Synechocystis sp. PCC6803 (Synechocystis) in order to study the little-known cooperative effects of lipids and carotenoids (Cars). Electron microscopic investigations confirmed that in the absence of xanthophylls the S-layer of the cellular envelope is missing. In wild-type (WT) cells, as well as the xanthophyll-less (RO), polyunsaturated lipid-less (AD), and the newly constructed ROAD mutants the lipid and Car compositions were determined by MS and HPLC, respectively. We found that, relative to the WT, the lipid composition of the mutants was remodeled and the Car content changed accordingly. In the mutants the ratio of non-bilayer-forming (NBL) to bilayer-forming (BL) lipids was found considerably lower. Xanthophyll to β-carotene ratio increased in the AD mutant. In vitro and in vivo methods demonstrated that saturated, monounsaturated lipids and xanthophylls may stabilize the trimerization of Photosystem I (PSI). Fluorescence induction and oxygen-evolving activity measurements revealed increased light sensitivity of RO cells compared to those of the WT. ROAD showed a robust increase in light susceptibility and reduced recovery capability, especially at moderate low (ML) and moderate high (MH) temperatures, indicating a cooperative effect of xanthophylls and polyunsaturated lipids. We suggest that both lipid unsaturation and xanthophylls are required for providing the proper structure and functioning of the membrane environment that protects against light and temperature stress.

• MeSH
• beta-karoten metabolismus   účinky záření   MeSH
• buněčná membrána genetika   metabolismus   účinky záření   ultrastruktura   MeSH
• časové faktory MeSH
• fenotyp MeSH
• fotosyntéza genetika   účinky záření   MeSH
• fotosystém I - proteinový komplex genetika   metabolismus   účinky záření   MeSH
• fyziologická adaptace MeSH
• fyziologický stres * MeSH
• genotyp MeSH
• membránové lipidy metabolismus   účinky záření   MeSH
• metabolismus lipidů genetika   účinky záření   MeSH
• mutace MeSH
• světlo * MeSH
• Synechocystis genetika   metabolismus   účinky záření   ultrastruktura   MeSH
• teplota * MeSH
• tylakoidy metabolismus   účinky záření   MeSH
• xanthofyly genetika   metabolismus   účinky záření   MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH
• Research Support, N.I.H., Extramural MeSH
• Research Support, U.S. Gov't, Non-P.H.S. MeSH

Thylakoid biogenesis is an intricate process requiring accurate and timely assembly of proteins, pigments and other cofactors into functional, photosynthetically competent membranes. PSII assembly is studied in particular as its core protein, D1, is very susceptible to photodamage and has a high turnover rate, particularly in high light. PSII assembly is a modular process, with assembly steps proceeding in a specific order. Using aqueous two-phase partitioning to separate plasma membranes (PM) and thylakoid membranes (TM), we studied the subcellular localization of the early assembly steps for PSII biogenesis in a Synechocystis sp. PCC6803 cyanobacterium strain lacking the CP47 antenna. This strain accumulates the early D1-D2 assembly complex which was localized in TM along with associated PSII assembly factors. We also followed insertion and processing of the D1 precursor (pD1) by radioactive pulse-chase labeling. D1 is inserted into the membrane with a C-terminal extension which requires cleavage by a specific protease, the C-terminal processing protease (CtpA), to allow subsequent assembly of the oxygen-evolving complex. pD1 insertion as well as its conversion to mature D1 under various light conditions was seen only in the TM. Epitope-tagged CtpA was also localized in the same membrane, providing further support for the thylakoid location of pD1 processing. However, Vipp1 and PratA, two proteins suggested to be part of the so-called 'thylakoid centers', were found to associate with the PM. Together, these results suggest that early PSII assembly steps occur in TM or specific areas derived from them, with interaction with PM needed for efficient PSII and thylakoid biogenesis.

• MeSH
• bakteriální proteiny metabolismus   MeSH
• buněčná membrána metabolismus   MeSH
• fotosyntéza účinky záření   MeSH
• fotosystém II - proteinový komplex metabolismus   MeSH
• světlo MeSH
• Synechocystis metabolismus   účinky záření   MeSH
• tylakoidy metabolismus   účinky záření   MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH

Spatial segregation of photosystems in the thylakoid membrane (lateral heterogeneity) observed in plants and in the green algae is usually considered to be absent in photoautotrophs possessing secondary plastids, such as diatoms. Contrary to this assumption, here we show that thylakoid membranes in the chloroplast of a marine diatom, Phaeodactylum tricornutum, contain large areas occupied exclusively by a supercomplex of photosystem I (PSI) and its associated Lhcr antenna. These membrane areas, hundreds of nanometers in size, comprise hundreds of tightly packed PSI-antenna complexes while lacking other components of the photosynthetic electron transport chain. Analyses of the spatial distribution of the PSI-Lhcr complexes have indicated elliptical particles, each 14 × 17 nm in diameter. On larger scales, the red-enhanced illumination exerts a significant effect on the ultrastructure of chloroplasts, creating superstacks of tens of thylakoid membranes.

• MeSH
• chloroplasty metabolismus   účinky záření   ultrastruktura   MeSH
• fotosystém I - proteinový komplex metabolismus   MeSH
• fotosystém II - proteinový komplex metabolismus   MeSH
• multiproteinové komplexy metabolismus   ultrastruktura   MeSH
• rozsivky metabolismus   účinky záření   ultrastruktura   MeSH
• světlo MeSH
• světlosběrné proteinové komplexy metabolismus   MeSH
• transmisní elektronová mikroskopie MeSH
• tylakoidy metabolismus   účinky záření   ultrastruktura   MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH

Gymnosperms, unlike angiosperms, are able to synthesize chlorophyll and form photosystems in complete darkness. Photosystem I (PSI) formed under such conditions is fully active, but photosystem II (PSII) is present in its latent form with inactive oxygen evolving complex (OEC). In this work we have studied light-induced gradual changes in PSII function in dark-grown cotyledons of Norway spruce (Picea abies) via the measurement of chlorophyll a fluorescence rise, absorption changes at 830 nm, thermoluminescence glow curves (TL) and protein analysis. The results indicate that in dark-grown cotyledons, alternative reductants were able to act as electron donors to PSII with inactive OEC. Illumination of cotyledons for 5 min led to partial activation of PSII, which was accompanied by detectable oxygen evolution, but still a substantial number of PSII centers remained in the so called PSII-Q(B)-non-reducing form. Interestingly, even 24 h long illumination was not sufficient for the full activation of PSII centers. This was evidenced by a weak attachment of PsbP protein and the absence of PsbQ protein in PSII particles, the absence of PSII supercomplexes, the suboptimal maximum yield of PSII photochemistry, the presence of C band in TL curve and also the presence of up-shifted Q band in TL in DCMU-treated cotyledons. This slow light-induced activation of PSII in dark-grown cotyledons could contribute to the prevention of PSII overexcitation before the light-induced increase in PSI/PSII ratio allows effective operation of linear electron flow.

• MeSH
• chlorofyl chemie   metabolismus   MeSH
• fotosyntéza účinky záření   MeSH
• fotosystém I - proteinový komplex metabolismus   MeSH
• fotosystém II - proteinový komplex metabolismus   MeSH
• kotyledon růst a vývoj   metabolismus   účinky záření   MeSH
• kyslík metabolismus   MeSH
• luminiscenční měření metody   MeSH
• rostlinné proteiny metabolismus   MeSH
• semenáček růst a vývoj   metabolismus   účinky záření   MeSH
• smrk růst a vývoj   metabolismus   účinky záření   MeSH
• světlo * MeSH
• teplota MeSH
• tma * MeSH
• transport elektronů účinky záření   MeSH
• tylakoidy metabolismus   účinky záření   MeSH
• western blotting MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH