Search results for "electron transport chain"
showing 10 items of 82 documents
The Impact of a Finite Waveguide Work Function on Resonant Tunneling
2021
To describe electron transport in a waveguide, we assume that the electron wave functions vanish at the waveguide boundary. This means that, being in the waveguide, an electron can not cross the waveguide boundary because of the infinite potential barrier. In reality, the assumption has never been fulfilled: generally, electrons can penetrate through the waveguide boundary and go some distance away from the waveguide. Therefore, we have to clarify how this phenomenon affects the resonant tunneling.
Spatial fluctuations of the chemical potential in case of nearly coherent transport along an ordered chain
1991
The Landauer-Buttiker approach is used to describe electron transport along a chain of scatterers which allow elastic as well as inelastic processes. The inelastic scattering takes place via side branches coupling the chain to electron reservoirs which serve as a heat bath. For small inelastic coupling of the scatterers to the heat bath strong interference effects lead to spatial fluctuations of the charge density. The corresponding oscillations of the chemical potential are discussed in view of phase-sensitive experiments measuring the four-probe resistance.
Proteomics evaluation of enniatins acute toxicity in rat liver
2021
Abstract Enniatins (ENs) are emerging mycotoxins produced by Fusarium fungi which are cytotoxic also at low concentrations due to its ionophoric properties. The aim of this study was to evaluate the hepatic toxicity of ENs exposure at different concentrations in Wistar rats through a proteomic approach. Animals were intoxicated by oral gavage with medium (EN A 256, ENA1 353, ENB 540, ENB1 296 μg/mL) and high concentrations (ENA 513, ENA1 706, ENB 1021, ENB1 593 μg/mL) of an ENs mixture and sacrificed after 8 h. Protein extraction was performed using powdered liver. Peptides were analyzed using a liquid chromatography coupled with a quadrupole time-of-flight mass spectrometer. Proteins were …
Synthesis of pyrido[2,1-a]isoquinolin-4-ones and oxazino[2,3-a]isoquinolin-4-ones: New inhibitors of mitochondrial respiratory chain
2013
International audience; Benzo[a]quinolizine is an important heterocyclic framework that can be found in numerous bioactive compounds. The general scheme for the synthesis of these compounds was based on the preparation of the appropriate dihydroisoquinolines by Bischler-Napieralski cyclization with good yields, followed by the Pemberton method to form the oxazinones or pyridones derivatives via acyl-ketene imine cyclocondensation. All the synthesized compounds were assayed in vitro for their ability to inhibit mitochondrial respiratory chain. Most of the tested compounds were able to inhibit the integrated electron transfer chain, measured as NADH oxidation, which includes complexes I, III …
Cherimolin-1, New Selective Inhibitor of the First Energy-Coupling Site of the NADH:Ubiquinone Oxidoreductase (Complex I)
1997
The mechanism linking electron transport to proton translocation in the NADH:ubiquinone oxidoreductase (complex I of the mitochondrial respiratory chain) is still unclear. Inhibitors acting at different sites of the enzyme are powerful tools to clarify this mechanism. Up to now, a unique inhibitor, the Annonaceous acetogenin rolliniastatin-2, selectively blocks the most internal proton-translocation site. This study introduces cherimolin-1, a new acetogenin that inhibits the complex I with this special mode of action, which is more easily available from the plant material. Moreover, the mode of action of this scarce type of complex I inhibitor is further characterized.
Bisbenzyltetrahydroisoquinolines, a New Class of Inhibitors of the Mitochondrial Respiratory Chain Complex I
2004
Four bisbenzyltetrahydroisoquinoline alkaloids (-)-medelline, (+)-antioquine, (+)-aromoline, and (+)-obamegine were isolated from the fruits of Xylopia columbiana. These compounds, the previously isolated alkaloids (+)-thaligrisine and (+)-isotetrandrine, as well as their O-acetylated derivatives were assayed on submitochondrial particles from beef heart as inhibitors of the mammalian respiratory chain. The results revealed that these alkaloids act as selective inhibitors of mitochondrial complex I in a 0.15 - 4.71 microM range. O-Acetylation, which increases their lipophilicity, considerably increased the inhibitory potency.
Biotechnological potential of respiring Zymomonas mobilis: a stoichiometric analysis of its central metabolism.
2013
The active, yet energetically inefficient electron transport chain of the ethanologenic bacterium Zymomonas mobilis could be used in metabolic engineering for redox-balancing purposes during synthesis of certain products. Although several reconstructions of Z. mobilis metabolism have been published, important aspects of redox balance and aerobic catabolism have not previously been considered. Here, annotated genome sequences and metabolic reconstructions have been combined with existing biochemical evidence to yield a medium-scale model of Z. mobilis central metabolism in the form of COBRA Toolbox model files for flux balance analysis (FBA). The stoichiometric analysis presented here sugges…
Inhibitory Effects of the Insecticides Allethrin, Lindane, and Jacutin-Fogetten Sublimate on Photosynthetic Electron Transport
1979
Abstract The inhibitory effects of the insecticides Allethrin, Lindane, and Jacutin-Fogetten sublimate on photosynthetic electron transport of broken chloroplasts were tested. 50 μmol l-1 Allethrin caused an inhibition of 80% of the benzoquinone and ferricyanide Hill-reactions. 39 μmol l-1 Lindane inhibited the basal, coupled and uncoupled electron transport to ferricyanide up to 35%. The precipitate formed by the sublimation of Jauctin-Fogetten containing Lindane depressed electron transport much more than pure Lindane. 50 μg ml-1 of the sublimate led to an 80% inhibition of ferricyanide Hill-reaction.
The paradoxical cyanide-stimulated respiration of Zymomonas mobilis: cyanide sensitivity of alcohol dehydrogenase (ADH II)
2003
The respiratory inhibitor cyanide stimulates growth of the ethanologenic bacteriumZymomonas mobilis, perhaps by diverting reducing equivalents from respiration to ethanol synthesis, thereby minimizing accumulation of toxic acetaldehyde. This study sought to identify cyanide-sensitive components of respiration. In aerobically grown, permeabilizedZ. mobiliscells, addition of 200 μM cyanide caused gradual inhibition of ADH II, the iron-containing alcohol dehydrogenase isoenzyme, which, in aerobic cultures, might be oxidizing ethanol and supplying NADH to the respiratory chain. In membrane preparations, NADH oxidase was inhibited more rapidly, but to a lesser extent, than ADH II. The time-cours…
Retene, pyrene and phenanthrene cause distinct molecular-level changes in the cardiac tissue of rainbow trout (Oncorhynchus mykiss) larvae, part 1 – …
2020
Polycyclic aromatic hydrocarbons (PAHs) are contaminants of concern that impact every sphere of the environment. Despite several decades of research, their mechanisms of toxicity are still poorly understood. This study explores the mechanisms of cardiotoxicity of the three widespread model PAHs retene, pyrene and phenanthrene in the rainbow trout (Oncorhynchus mykiss) early life stages. Newly hatched larvae were exposed to each individual compound at sublethal doses causing no significant increase in the prevalence of deformities. Changes in the cardiac transcriptome were assessed after 1, 3, 7 and 14 days of exposure using custom Salmo salar microarrays. The highest number of differentiall…