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Biomedical subjects

A B Rubin

Publications and source records attributed to A B Rubin.

At least 127 records · Page 7Linked to original sources

[Mossbauer spectroscopy of cells of cyanobacteria Synechocystis sp. PCC 6803 devoid of photosystem I and containing inactive phycobilisomes].

Mossbauer spectra of the psaAB mutant of Synechocystis sp. PPC 6803 devoid of photosystem I grown in a 57Fe-containing medium were measured. The spectrum is a broadened doublet whose size (about 20%) and parameters (isomeric shift delta = 0.3 mm/s and quadrupole splitting delta = 0.8 mm/s) suggest the presence of abundant nanoclusters of Fe3+ oxides in a superparamagnetic state tightly bound to the membrane. Treatment of cells with EDTA was accompanied by a substantial (tenfold) decrease in the amount of iron nonspecifically bound to the membrane and the appearance of Fe2+ localized, probably, inside cells and/or cell membranes. In addition, the spectrum of washed cells exhibited superfine magnetic splitting due to iron oxide clusters greater in size than nanoclusters present in the membrane prior to EDTA treatment.

Bacterial Proteins↗

[New spatial-temporal dynamics in a reaction-electrodiffusion system].

The properties of a system reaction-electrodiffusion were studied using two-component model of interaction and diffusion of charged particles near membrane in solutions of low ionic strength to which traditional assumptions about local electroneutrality of medium are not applicable. It is shown that the effect of self-consistent electric field leads to bistability, the appearance of localized structures with contrast charge distribution and regimes aperiodical in time and in space.

Algorithms↗

[Damage to macrophage membranes by exposure to middle-wave ultraviolet radiation].

An influence of middle-wave ultraviolet radiation (lambda max = 306 nm) on plasma membranes of mice peritoneal macrophages was studied by microfluorimetry analysis. It was found that a percentage of cells with damaged plasma membranes in the irradiated macrophage population reliably increased with the UVB dose starting with 6 J/cm2. Irradiation of cells with 4.2 J/cm2 UVR dose which does not cause evident damage to plasma membranes led to the latent damage which was detected by treatment with detergent digitonin (4.5 micrograms/ml).

Animals↗

[Modification of damaging effect of ultraviolet radiation on peritoneal macrophage membranes in mice].

Different factors modificating damaging effect of middle-wave ultraviolet radiation (lambda max = 306 nm) on mice peritoneal macrophage plasma membranes were studied. It was shown that damaging effect of ultraviolet declined when the cells were simultaneously treated by red light (lambda max = 713 nm). This protective effect increased when a red component of light became greater and achieved almost 100% when it consisted 28.6%. It was also found that the decrease in intra- and extracellular pH led to the decrease in damaging effect of UVR. The increase of pH bring to an elevation of UVR destructive effect.

Amiloride↗

[Effects of relaxation processes on the temperature dependence of oxidation rate of photooxidized bacteriochlorophyll on the primary quinone in reaction centers of Rhodobacter sphaeroides].

The temperature dependence of the time of dark recombination of charges between photooxidized bacteriochlorophyll and reduced primary quinone acceptor (tau e) in Rhodobacter sphaeroides photosynthetic reaction centers was studied in the temperature range 140-320 K. It was found that the function tau e = tau e(T) is nonmonotonous: in the temperature range from 140 to 290 K, tau e is increased from 40 to 100 ms; however, under further heating to 320 K, tau e decreased to 80 ms. The replacement of H2O by D2O in these preparations caused an acceleration of the recombination process in the range of physiological temperatures, but the nonmonotonous character of the function tau e(T) remained. The theoretical interpretation of the results was made in the framework of the theory of electron-phonon interactions with allowance for the relaxation processes.

Algorithms↗

[Fluorescent photobleaching of endogenous protoporphyrin IX in yeast cells].

Yeast Saccharomyces cerevisiae accumulate in the presence of chelator 2,2'-dipyridyl, two fractions of photosensitizer protoporphyrin IX, which fluoresce with maxima at 625 and 635 nm. The two fractions were found to differ from each other in the dynamics and character of fluorescence photobleaching. In contrast to the protoporphyrin IX that fluoresces with a maximum at 625 nm, the protoporphyrin IX fraction that fluoresces with a maximum at 635 nm is more photolable; in addition, upon photobleaching of its fluorescence, a new maximum at 675 nm appears.

2,2'-Dipyridyl↗

[Kinetic model of primary processes of photosynthesis in chloroplasts. Fast phase of chlorophyll fluorescence induction under light of various intensity].

A kinetic model was developed, which describing the system of generation and consumption of the transmembrane electrochemical proton potential delta mu H+ in primary photosynthetic processes. The model describes the catalytic cycles of photosystems I and II and the cytochrome b/f complex, as well as the ATP synthesis and passive leakage of H+, K+ [symbol: see text] Cl- ions through the thylakoid membrane. The dependence of the electron transfer rates on the value of transmembrane electric potential was taken into account. The model was applied to describe the experimental data on the registration of the fast phase of fluorescence induction. The model gives a realistic description of the fast phase of induction curves at different light intensities (from high to low).

Adenosine Triphosphate↗

[Experimental and theoretical study of processes of cyclical electron transport around photosystem I].

The kinetics of photoinduced EPR I signals at different concentrations of ferredoxin was studied on isolated pea chloroplasts. A kinetic model of ferredoxin-dependent electron transport around photosystem I was suggested. A multiparticle model was constructed, which makes it possible to "directly" model the processes of electron transfer in multiprotein complexes and limited diffusion in different compartments of the system (stroma, lumen, and intermembrane space). A comparison of the kinetic and "direct" models revealed an important role of spatial organization of the system in the kinetics of redox turnover of P700.

Electron Transport↗

[Redistribution of membrane-bound Ca2+ in neurolemma of leech Retzius-neurons during thermostimulation].

Changes in electrical activity, plasma membrane and inner mitochondrial membrane potentials, as well as in the content of membrane-bound calcium and NADH in identified leech ganglion neurons during thermal stimulation were studied by microelectrode and microfluorimetric methods. It was shown that thermal stimulation of skin patches from different regions of leech body causes a reversible increase in the firing rate of pacemaker neurons (Rz neurons). A decrease in the content of membrane-bound calcium in the neurolemma and NADH content in Rz neuron mitochondria, and a depolarization of inner mitochondrial membrane were also observed.

Cell Membrane↗

[Effect of methylmercury on primary photosynthesis processes in green microalgae Chlamydomonas reinhardtii].

The sensitivity of green microalgae Chlamydomonas reinhardtii to methylmercury chloride (MeHg) and chloride mercury (HgCl2) was evaluated by measuring chlorophyll fluorescence parameters by the pulse-amplitude-modulation (PAM) fluorometry. It was shown that MeHg at concentrations above 1 microM decreased the Fv/Fm ratio, which characterizes the maximal efficiency of energy utilization in photosystem II. The degree of inhibition depended on the time of treatment and was always higher under illumination conditions (50 microE.m-2.s-1) than under dark conditions. A similar regularity was observed for the delta F/Fm' ratio, which characterizes the real efficiency of energy storage at the given intensity of the photosynthesis-exciting light. Incubation with 5 microM HgCl2 for 5 h did not affect both ratios. The decrease in Fm at constant F0 as well as changes in the fast fluorescence kinetics after MeHg treatment of algae cells indicated the damage on the donor side of photosystem II and the damage of the electron transfer from QA to QB. The reduction of photochemical fluorescence quenching (qN) under MeHg treatment is also evidence of the increase in the fraction of closed reaction centers (QA-). At the same time, increase in the steady-state level of P700 photooxidation indicated a disturbance of electron transfer between photosystems. The present study demonstrates that methylmercury treatment damaged the photosynthetic electron transfer chain at several sites. The inhibitory effect of methylmercury is much stronger than the effect of mercury chloride on photosynthetic processes.

Animals↗

[Effect of mercuric chloride and methylmercury on photosynthetic activity of the diatom Thalassiosira weissflogii by a fluorescent method].

It was shown by the pulse-amplitude modulation fluorescent method that, at a weak illumination (6 microE m-2.s-1), methylmercury at a concentration of 10(-6)-10(-7) M decreases the photochemical activity of the reaction centers of photosystem II in cells of microalgae Thalassiosira weissflogii after a prolonged lag phase. Cells resistant to methylmercury at these low concentrations were detected by the microfluorimetric method. Chloride mercury decreased the activity of photosystem II of the algae only when at higher concentrations. Both toxicants at a concentration of 10(-6) M decreased the rate of recovery of photoinduced damage of centers of photosystem II and led to an increase in the energization component of nonphotochemical fluorescence quenching. These results indicate that the complex of fluorescent methods can be used to monitor early changes in the photosynthetic apparatus of algae in response to the toxic action of heavy metals.

Diatoms↗

[Regulation of the primary photosynthesis processes].

The mechanisms of primary processes of photosynthesis and macromolecular conformational changes that control the efficiency of primary energy transformation in photosynthesis are discussed. Special attention is focused on the analysis of chlorophyll fluorescence as an integrated parameter indicative of the efficiency and dynamics of primary steps of photosynthesis. Sharp changes in environmental conditions and other unfavorable factors may lead to the distortions of the coupling between consecutive electron transfer steps. As a result, an excess of electrons and/or electronic excitation energy may form at some sites of the electron transport chain. This may lead to the generation of reactive oxygen species responsible for the subsequent oxidative stress. The results of the application of these data in the areas of biotechnology and ecology are demonstrated.

Chlorophyll↗

[Activation of the chloroplast respiration increases chlorophyll fluorescence yield in Chlorella adapted to darkness at higher temperature].

A tenfold increase in chlororespiration during dark incubation of Chlorella perynoidosa Chick at high temperature doubled the initial chlorophyll fluorescence yield (F0). The presence of iodacetamide or unmetabolizable glucose analog 2-deoxy-D-glucose prevented increase in both chlororespiration and F0 yield. The rates of chlororespiration and F0 yield growth demonstrated a similar pattern of temperature dependence. Inhibition of electron transport between QA and plastoquinone prevented increase in F0 during dark respiration of the cells at high temperature. Apparently, a pool of plastoquinone was restored in the chlororespiratory chain during the dark incubation at 37.5-41 degrees C and plastoquinone exchanged electrons with QA. This is the cause of QA reduction and subsequent increase in F0 yield.

Adaptation, Physiological↗

[The photochemical activity of photosystem II in sulfur-deprived Chlamydomonas reinhardtii cells depends on the redox state of the quinone pool during the transition to anaerobiosis].

Measurements with a PAM fluorometer showed that the photochemical activity of photosystem II (PS II) in sulfur-deprived Chlamydomonas reinhardtii cells (media TAP-S) decreases slowly under aerobic conditions. In a closed cultivator, when the rate of O2 photosynthetic evolution declines below the rate of respiration, the cell culture is under anaerobic conditions in which the activation of hydrogenase and the production of hydrogen take place. We found that the slow decrease in PS II activity is followed by an abrupt inactivation of PS II centers just after the onset of anaerobiosis. This fast PS II inactivation is reversed by aeration of the media and is accompanied by an increase in the fluorescence parameter Ft. Moreover, the rate of the abrupt PS II inactivation diminished after the addition into the medium of electron acceptors such as CO2 (carbonate-bicarbonate buffer), NO3- and SO4(2-) , the assimilation of which in chloroplasts requires a lot of reductants. We suggest that the PS II inactivation is due to the overreduction of the plastoquinone pool after the onset of anaerobiosis.

Anaerobiosis↗

[The temperature dependence of high-resolution 1H NMR spectra of Rhodobacter sphaeroides photosynthetic reaction centres in a temperature range of 25-40 degrees C].

High-resolution 1H-NMR spectra registered within a temperature range of 25-40 degrees C revealed a nonmonotonous dome-shaped temperature dependence of the ratio between integral NMR signal intensities determined at ppm intervals 2.5-4.5 and 0.2-2.5 with a maximum at 30 degrees C. This may be due to RC structural changes accompanying the temperature rise and accelerating the recombination reaction between oxidized bacteriochlorophyll and reduced primary quinone at temperatures above 30 degrees C.

Electron Transport↗

[Effect of methylmercury chloride on the primary photosynthetic activity of higher plants].

The effect of methylmercury chloride (MeHg) on the fluorescence characteristics of pea seedling leaves and thylakoids isolated from these leaves was studied by the pulse-amplitude-modulation (PAM) fluorometric method. In 3-4 days after the addition of MeHg (20 microM) to the nutritious solution, the maximal (Fv/Fm) and real (under steady state actinic light illumination) (deltaF/F'm) quantum photochemical yield of PS II decreased. The nonphotochemical fluorescence quenching coefficient in control (qN) decreased after its maximum value has been reached. In MeHg-treated samples, this decrease was not observed, possibly due to the disturbance of delta pH energy transducing processes in ATP synthase. This was confirmed by the results of experiments on isolated thylakoids. After MeHg (5 microM) treatment of thylakoids, the photophosphorylation rate and light-triggered Mg2+-dependent H+-ATPase activity were suppressed by 20-40%, depending on the duration of MeHg exposure. However, in experiments with isolated thylakoids, no decrease either in the electron transport rate or in the Fv/Fm ratio was observed. In total, the results obtained allow one to assume that MeHg at concentrations and time duration used directly damages the coupling complex. The PS II inactivation in leaves and algae cells may be a result of the oxidative stress processes.

Chloroplast Proton-Translocating ATPases↗

[A kinetic model of the cytochrome bf complex. Evaluation of kinetic parameters].

A kinetic model of the cytochrome bf complex was developed on the assumption that the Q-cycle operates. The bf complex was considered as a membrane enzyme catalyzing the electron transfer from plastoquinol to plastocyanine, which is coupled with proton translocation from the chloroplast stroma to the thylakoid lumen. The dependence of the electron transfer rates on the value of the transmembrane electric potential was taken into account. The model was applied to describe the experimental data on the flash-induced turnover of cytochromes b, plastocyanine, and the kinetics of proton deposition in the thylakoid lumen. The estimation of model parameters was performed.

Cytochrome b6f Complex↗

[Calculation of local Hurst exponents in the Ca(2+)-activated K(+)-channel dwell time].

A novel method based on the maximum overlap wavelet transform of dwell time series is proposed. Information on local multifractal properties of the series, namely local Hurst exponents or Holder exponents, was obtained. The results confirm the presence of multifractality and intrinsic correlations in the Ca(2+)-activated K+ channel dwell time series. The data on the local multifractal structure of the series can be interpreted in terms of processes having self-organized criticality. The proposed approach allows one to widen the store of methods for the analysis of single ion channel activity.

Algorithms↗