18 research outputs found
Spectroscopic studies of fluorescence effects in bioactive 4-(5-heptyl-1,3,4-thiadiazol-2-yl)benzene-1,3-diol and 4-(5-methyl-1,3,4-thiadiazol-2-yl)benzene-1,3-diol molecules induced by pH changes in aqueous solutions
Lysosomal exoglycosidases in serum and urine of patients with pancreatic adenocarcinoma.
Spectroscopic Studies of Fluorescence Effects in Bioactive 4-(5-Heptyl-1,3,4-Thiadiazol-2-yl)Benzene-1,3-Diol and 4-(5-Methyl-1,3,4-Thiadiazol-2-yl)Benzene-1,3-Diol Molecules Induced by pH Changes in Aqueous Solutions
Spectroscopic and theoretical studies of fluorescence effects in bio-active: 4-(5-(methyl-1,3,4-thiadiazol-2-yl))benzene-1,3-diol and 4-(5-(methylamino-1,3,4-thiadiazol-2-yl))benzene-1,3-diol compounds : effect of molecular aggregation and amino group position
Recycling of energy dissipated as heat accounts for high activity of Photosystem II
ABSTRACTPhotosystem II (PSII) converts light into chemical energy powering almost entire life on Earth. The primary photovoltaic reaction in the PSII reaction centre requires energy corresponding to 680 nm that is significantly higher than in the case of the low-energy states in the antenna complexes involved in the harvesting of excitations driving PSII. Here we show that despite seemingly insufficient energy, the low-energy excited states can power PSII thanks to the activity of the thermally-driven up-conversion. We demonstrate the operation of this mechanism both in intact leaves and in isolated pigment-protein complex LHCII. A mechanism is proposed, according to which the effective utilization of thermal energy in the photosynthetic apparatus is possible owing to the formation of LHCII supramolecular structures, leading to the coupled energy levels, corresponding to approx. 680 nm and 700 nm, capable of exchanging excitation energy through the spontaneous relaxation and the thermal up-conversion.TOC GRAPHICS</jats:sec
Molecular organisation of dipalmitoylphosphatidylcholine bilayers containing bioactive vompounds 4-(5-heptyl-1,3,4-thiadiazol-2-yl) benzene-1,3-diol and 4-(5-methyl-1,3,4-thiadiazol-2-yl) benzene-1,3-diols
Effect of smoking on activity of N-acetyl-β-hexosaminidase in serum and urine of renal cancer patients
Solvent effects on molecular aggregation in 4-(5-Heptyl-1,3,4-thiadiazol-2-yl) benzene-1,3-diol and 4-(5-Methyl-1,3,4-thiadiazol-2-yl)benzene-1,3-diol
Mechanisms shaping the synergism of zeaxanthin and PsbS in photoprotective energy dissipation in the photosynthetic apparatus of plants
AbstractSafe operation of photosynthesis is vital to plants and is ensured by the activity of numerous processes protecting chloroplasts against photo-damage. The harmless dissipation of excess excitation energy is believed to be the main photoprotective mechanism and is most effective with the simultaneous presence of PsbS protein and zeaxanthin, a xanthophyll accumulated in strong light as a result of the xanthophyll cycle activity. Here we address the problem of specific molecular mechanisms underlying the synergistic effect of zeaxanthin and PsbS. The experiments were conducted with Arabidopsis thaliana, the wild-type and the mutants lacking PsbS (npq4) and affected in the xanthophyll cycle (npq1), with the application of multiple molecular spectroscopy and imaging techniques. Research results lead to the conclusion that PsbS interferes with the formation of tightly packed aggregates of thylakoid membrane proteins, thus enabling the incorporation of xanthophyll cycle pigments into such structures. It was found that xanthophylls trapped within supramolecular structures, most likely in the interfacial protein region, determine their photophysical properties. The structures formed in the presence of violaxanthin are characterized by minimized dissipation of excitation energy. In contrast, the structures formed in the presence of zeaxanthin show enhanced excitation quenching, thus protecting the system against photo-damage.</jats:p
