Academic literature on the topic 'Bioenergetic; Sulphur'

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Journal articles on the topic "Bioenergetic; Sulphur"

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Sheeran, Freya L., and Salvatore Pepe. "Posttranslational modifications and dysfunction of mitochondrial enzymes in human heart failure." American Journal of Physiology-Endocrinology and Metabolism 311, no. 2 (August 1, 2016): E449—E460. http://dx.doi.org/10.1152/ajpendo.00127.2016.

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Deficiency of energy supply is a major complication contributing to the syndrome of heart failure (HF). Because the concurrent activity profile of mitochondrial bioenergetic enzymes has not been studied collectively in human HF, our aim was to examine the mitochondrial enzyme defects in left ventricular myocardium obtained from explanted end-stage failing hearts. Compared with nonfailing donor hearts, activity rates of complexes I and IV and the Krebs cycle enzymes isocitrate dehydrogenase, malate dehydrogenase, and aconitase were lower in HF, as determined spectrophotometrically. However, activity rates of complexes II and III and citrate synthase did not differ significantly between the two groups. Protein expression, determined by Western blotting, did not differ between the groups, implying posttranslational perturbation. In the face of diminished total glutathione and coenzyme Q10levels, oxidative modification was explored as an underlying cause of enzyme dysfunction. Of the three oxidative modifications measured, protein carbonylation was increased significantly by 31% in HF ( P < 0.01; n = 18), whereas levels of 4-hydroxynonenal and protein nitration, although elevated, did not differ. Isolation of complexes I and IV and F1FoATP synthase by immunocapture revealed that proteins containing iron-sulphur or heme redox centers were targets of oxidative modification. Energy deficiency in end-stage failing human left ventricle involves impaired activity of key electron transport chain and Krebs cycle enzymes without altered expression of protein levels. Augmented oxidative modification of crucial enzyme subunit structures implicates dysfunction due to diminished capacity for management of mitochondrial reactive oxygen species, thus contributing further to reduced bioenergetics in human HF.
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Kovács, Á. T., G. Rákhely, J. Balogh, G. Maróti, A. Fülöp, and K. L. Kovács. "Anaerobic regulation of hydrogenase transcription in different bacteria." Biochemical Society Transactions 33, no. 1 (February 1, 2005): 36–38. http://dx.doi.org/10.1042/bst0330036.

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Hydrogen metabolism is closely related to other important metabolic and energetic processes of bacterial cells, such as photosynthesis, anaerobic respiration and sulphur metabolism. Even small environmental changes influence these networks through different regulatory systems. The presence or absence of oxygen is one of the most important signals; how the cascades evolved to transmit this signal in different bacteria is summarized. In many instances, hydrogen is released only under anoxic conditions, because of bioenergetic considerations. Most [NiFe] hydrogenases are inactivated by oxygen, but many of them can be re-activated under reducing conditions. In addition to direct inactivation of the hydrogenases, oxygen can also regulate their expression. The global regulatory systems [FNR (fumarate and nitrate reduction regulator), ArcAB (aerobic respiratory control) and RegAB], which respond to alterations in oxygen content and redox conditions of the environment, have an important role in hydrogenase regulation of several bacteria. FNR-like proteins were shown to be important for the regulation of hydrogenases in Escherichia coli, Thiocapsa roseopersicina and Rhizobium leguminosarum, whereas RegA protein modulates the expression of hupSL genes in Rhodobacter capsulatus.
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Icka, Pirro, Robert Damo, and Engjëllushe Icka. "Paulownia Tomentosa, a Fast Growing Timber." Annals ”Valahia” University of Targoviste - Agriculture 10, no. 1 (October 1, 2016): 14–19. http://dx.doi.org/10.1515/agr-2016-0003.

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Abstract The fast growing woody crops are a very important source for the generation of the bioenergetics biomass. Paulownia sp. Is a plant part of this group, and because of its fast growth, multiple values and high adaptability with climate conditions, is set recently in the centre of the intention. Paulownia is one of the fastest growing species in the world with low concentration of ash, sulphur and nitrogen and high calorific energy from its wood. It is considered as an energetic crop adequate for the production of the solid biocarburants and the bioethanol. The cultivation of the Paulownia because of the high absorption of CO2 from the air, to support the fast growth of the biomass, is considered as an effective mean to soften the climacteric changes. The plant is also considered as suitable to improve the abandoned lands when its cultivation is concentrated to the biomass production. The genus of Paulownia (Scrophulariaceae) is autochthones species of China and East Asia and as such is not found naturally in Albania. To study the regionalization possibilities of this species in the Korça climacteric conditions, aiming its cultivation according the fast growth coppice system were planted in 2014 in Cangonj (Devoll) 300 seedlings of P. tomentosa in a distance of 1 x 1 m. during the year 2015 were planted other 400 seedlings prepared with seeds. This article deals with the preliminary data of the regionalization performance of this high energetic value crop.
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Richardson, Katherine H., John J. Wright, Mantas Šimėnas, Jacqueline Thiemann, Ana M. Esteves, Gemma McGuire, William K. Myers, et al. "Functional basis of electron transport within photosynthetic complex I." Nature Communications 12, no. 1 (September 10, 2021). http://dx.doi.org/10.1038/s41467-021-25527-1.

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AbstractPhotosynthesis and respiration rely upon a proton gradient to produce ATP. In photosynthesis, the Respiratory Complex I homologue, Photosynthetic Complex I (PS-CI) is proposed to couple ferredoxin oxidation and plastoquinone reduction to proton pumping across thylakoid membranes. However, little is known about the PS-CI molecular mechanism and attempts to understand its function have previously been frustrated by its large size and high lability. Here, we overcome these challenges by pushing the limits in sample size and spectroscopic sensitivity, to determine arguably the most important property of any electron transport enzyme – the reduction potentials of its cofactors, in this case the iron-sulphur clusters of PS-CI (N0, N1 and N2), and unambiguously assign them to the structure using double electron-electron resonance. We have thus determined the bioenergetics of the electron transfer relay and provide insight into the mechanism of PS-CI, laying the foundations for understanding of how this important bioenergetic complex functions.
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Bonifácio, Vasco D. B., Sofia A. Pereira, Jacinta Serpa, and João B. Vicente. "Cysteine metabolic circuitries: druggable targets in cancer." British Journal of Cancer, November 23, 2020. http://dx.doi.org/10.1038/s41416-020-01156-1.

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AbstractTo enable survival in adverse conditions, cancer cells undergo global metabolic adaptations. The amino acid cysteine actively contributes to cancer metabolic remodelling on three different levels: first, in its free form, in redox control, as a component of the antioxidant glutathione or its involvement in protein s-cysteinylation, a reversible post-translational modification; second, as a substrate for the production of hydrogen sulphide (H2S), which feeds the mitochondrial electron transfer chain and mediates per-sulphidation of ATPase and glycolytic enzymes, thereby stimulating cellular bioenergetics; and, finally, as a carbon source for epigenetic regulation, biomass production and energy production. This review will provide a systematic portrayal of the role of cysteine in cancer biology as a source of carbon and sulphur atoms, the pivotal role of cysteine in different metabolic pathways and the importance of H2S as an energetic substrate and signalling molecule. The different pools of cysteine in the cell and within the body, and their putative use as prognostic cancer markers will be also addressed. Finally, we will discuss the pharmacological means and potential of targeting cysteine metabolism for the treatment of cancer.
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Dissertations / Theses on the topic "Bioenergetic; Sulphur"

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Camba, Acosta Raul O. "Reaction mechanisms of iron-sulfur proteins studied by protein-film voltammetry." Thesis, University of Oxford, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.365860.

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