29 research outputs found

    Application of Technical Diagnostic Methods for Ring Rolling Machine

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    Cílem této bakalářské práce je monitoring klíčových prvků rozválcovacího stroje pro výrobu ocelových hladkých kroužků, tvarových kroužků a disků. Nejprve jsou definovány vhodné diagnostické metody, které jsou poté aplikovány na vybrané komponenty. Dalším krokem je zapsání naměřených dat do tabulek a jejich vyhodnocení. Nakonec jsou definována potřebná opatření ke zlepšení provozního stavu stroje. V závěru práce je obsaženo i vyhodnocení časových úspor z hlediska minimalizace neplánovaných odstávek.The goal of this bachelor's thesis is to monitor the key elements of a ring rolling machine designed to produce smooth rings, shaped rings and discs made of steel. First, suitable diagnostic methods are defined, which are then applied to selected components. The next step is to record the measured data in tables and evaluate them. Finally, the necessary measures to improve the operational condition of the machines are defined. The conclusion of the thesis also contains an evaluation of time savings in terms of minimizing unplanned production interruption.340 - Katedra konstruovánívýborn

    Metabolismus a signalizace sirovodíku: úloha proteinů příbuzných k CBS u Caenorhabditis elegans

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    Sirovodík (H2S) je toxický plyn, který ve vysokých koncentracích způsobuje respirační selhání a smrt organismu, zatímco v nízkých koncentracích hraje roli jako vasodilatátor, neuromodulátor, a chrání buňky a tkáně před reperfuzním poškozením, hypoxií, hyperglykémií či dysfunkcí endotelu. Ke studiu fyziologie a signalizace H2S je využíváno hned několik modelových organismů. Hlístice Caenorhabditis elegans je pozoruhodným modelem ke studiu fyziologie, vývojové biologie, a v neposlední řadě i signalizace H2S, nicméně metabolismus sirovodíku v tomto organismu není známý. Cystathionin-beta-synthasa (CBS) je jedním ze tří enzymů produkujících H2S u živočichů. Zajímavé je, že u C. elegans je postulováno hned šest genů kódující homologní proteiny k CBS (cbs-1, cbs-2, cysl-1, cysl -2, cysl -3 a cysl -4). Cílem této práce bylo zjistit funkci těchto genů v metabolismu a signalizaci H2S u C. elegans. Nejprve jsme identifikovali cbs-1 jako gen kódující CBS; rekombinantní purifikovaný protein CBS-1 vykázal CBS aktivitu a RNA interference cbs-1 vedla ke snížené CBS aktivitě a zvýšené hladině homocysteinu v červích homogenátech, což rekapituluje deficit CBS u savců. Je zajímavé, že hlístí a savčí CBS mají odlišnou doménovou architekturu a tedy i posttranslační regulaci. Dále jsme zjistili, že ostatní proteiny...Hydrogen sulfide (H2S) is a toxic gas that causes respiratory failure and death at high concentrations, but at low concentrations, it functions as a signaling molecule in vasodilation and neuromodulation, and it protects cells and tissues from reperfusion injury, hypoxia, hyperglycemia and endothelial dysfunction. Several model organisms have been used to study the physiological roles and signaling pathways of H2S. The roundworm Caenorhabditis elegans is a remarkable model for studying the physiology, developmental biology and signaling of H2S; however, the metabolism of H2S in this animal is largely unknown. Cystathionine beta-synthase (CBS) is one of three H2S-producing enzymes in mammals. Notably, C. elegans possesses 6 genes that encode proteins homologous to CBS, namely cbs- 1, cbs-2, cysl-1, cysl-2, cysl-3 and cysl-4. In this thesis we studied the roles of these genes in H2S metabolism and signaling. First, we identified cbs-1 as the gene encoding CBS in C. elegans; the recombinant purified CBS-1 protein exhibited canonical CBS activity, and RNA interference-mediated silencing of cbs-1 resulted in decreased CBS activity and increased homocysteine levels in worm extracts, recapitulating the phenotypes of CBS deficiency in mammals. Notably, the nematode and human enzymes differ in their domain...Institute of Inherited Metabolic Disorders First Faculty of Medicine Charles University in PragueÚstav dědičných metabolických poruch 1.LF a VFN v PrazeFirst Faculty of Medicine1. lékařská fakult

    Hypoxia Sensing and Responses in Parkinson's Disease.

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    Parkinson's disease (PD) is associated with various deficits in sensing and responding to reductions in oxygen availability (hypoxia). Here we summarize the evidence pointing to a central role of hypoxia in PD, discuss the relation of hypoxia and oxygen dependence with pathological hallmarks of PD, including mitochondrial dysfunction, dopaminergic vulnerability, and alpha-synuclein-related pathology, and highlight the link with cellular and systemic oxygen sensing. We describe cases suggesting that hypoxia may trigger Parkinsonian symptoms but also emphasize that the endogenous systems that protect from hypoxia can be harnessed to protect from PD. Finally, we provide examples of preclinical and clinical research substantiating this potential

    Conserved roles of C. elegans and human MANFs in sulfatide binding and cytoprotection.

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    Mesencephalic astrocyte-derived neurotrophic factor (MANF) is an endoplasmic reticulum (ER) protein that can be secreted and protects dopamine neurons and cardiomyocytes from ER stress and apoptosis. The mechanism of action of extracellular MANF has long been elusive. From a genetic screen for mutants with abnormal ER stress response, we identified the gene Y54G2A.23 as the evolutionarily conserved C. elegans MANF orthologue. We find that MANF binds to the lipid sulfatide, also known as 3-O-sulfogalactosylceramide present in serum and outer-cell membrane leaflets, directly in isolated forms and in reconstituted lipid micelles. Sulfatide binding promotes cellular MANF uptake and cytoprotection from hypoxia-induced cell death. Heightened ER stress responses of MANF-null C. elegans mutants and mammalian cells are alleviated by human MANF in a sulfatide-dependent manner. Our results demonstrate conserved roles of MANF in sulfatide binding and ER stress response, supporting sulfatide as a long-sought lipid mediator of MANF's cytoprotection

    Novel structural arrangement of nematode cystathionine β-synthases: characterization of Caenorhabditis elegans CBS-1

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    CBSs (cystathionine β-synthases) are eukaryotic PLP (pyridoxal 5 *-phosphate)-dependent proteins that maintain cellular homocysteine homoeostasis and produce cystathionine and hydrogen sulfide. In the present study, we describe a novel structural arrangement of the CBS enzyme encoded by the cbs-1 gene of the nematode Caenorhabditis elegans. The CBS-1 protein contains a unique tandem repeat of two evolutionarily conserved catalytic regions in a single polypeptide chain. These repeats include a catalytically active C-terminal module containing a PLP-binding site and a less conserved N-terminal module that is unable to bind the PLP cofactor and cannot catalyse CBS reactions, as demonstrated by analysis of truncated variants and active-site mutant proteins. In contrast with other metazoan enzymes, CBS-1 lacks the haem and regulatory Bateman domain essential for activation by AdoMet (S-adenosylmethionine) and only forms monomers. We determined the tissue and subcellular distribution of CBS-1 and showed that cbs-1 knockdown by RNA interference leads to delayed development and to an approximately 10-fold elevation of homocysteine concentrations in nematode extracts. The present study provides the first insight into the metabolism of sulfur amino acids and hydrogen sulfide in C. elegans and shows that nematode CBSs possess a structural feature that is unique among CBS proteins

    Domain Organization, Catalysis and Regulation of Eukaryotic Cystathionine Beta-Synthases

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    Cystathionine beta-synthase (CBS) is a key regulator of sulfur amino acid metabolism diverting homocysteine, a toxic intermediate of the methionine cycle, via the transsulfuration pathway to the biosynthesis of cysteine. Although the pathway itself is well conserved among eukaryotes, properties of eukaryotic CBS enzymes vary greatly. Here we present a side-by-side biochemical and biophysical comparison of human (hCBS), fruit fly (dCBS) and yeast (yCBS) enzymes. Preparation and characterization of the full-length and truncated enzymes, lacking the regulatory domains, suggested that eukaryotic CBS exists in one of at least two significantly different conformations impacting the enzyme’s catalytic activity, oligomeric status and regulation. Truncation of hCBS and yCBS, but not dCBS, resulted in enzyme activation and formation of dimers compared to native tetramers. The dCBS and yCBS are not regulated by the allosteric activator of hCBS, S-adenosylmethionine (AdoMet); however, they have significantly higher specific activities in the canonical as well as alternative reactions compared to hCBS. Unlike yCBS, the heme-containing dCBS and hCBS showed increased thermal stability and retention of the enzyme’s catalytic activity. The mass-spectrometry analysis and isothermal titration calorimetry showed clear presence and binding of AdoMet to yCBS and hCBS, but not dCBS. However, the role of AdoMet binding to yCBS remains unclear, unlike its role in hCBS. This study provides valuable information for understanding the complexity of the domain organization, catalytic specificity and regulation among eukaryotic CBS enzymes.This work was supported by Postdoctoral Fellowship 0920079G from the American Heart Association (to TM), by National Institutes of Health Grant HL065217, by American Heart Association Grant In-Aid 09GRNT2110159, by a grant from the Jerome Lejeune Foundation (all to JPK) and by a research contract RYC2009-04147 (to ALP). In addition, grant support (P11-CTS-07187, CSD2009-00088 and BIO2012-34937) to Dr. Jose M. Sanchez-Ruiz (University of Granada) and SGIker technical and human support (UPV/EHU, MICINN, GV/EJ, ESF) are gratefully acknowledged

    The Trial with K. H. Frank in front of the Extraordinary People's Court

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    In my Master's thesis I described in detail the historical process of war criminal Karl Hermann Frank. He was a man who had been influencing the main events in the Czech lands for many years. I divided the thesis in ten chapters. The first chapter is devoted to the personality of K. H. Frank. I tried to briefly describe all the life's milestones of a man justly sentenced to death for his crimes against the Czechoslovak state. In the second and third chapter I focused on two men who played a very important role in the process and extradition of K. H. Frank, Kamill Resler and Bohuslav Ečer. In subsequent chapters I fully dealt with the process itself, from the very start through the daily courses of the trial to the verdict. In conclusion I summarized findings from the process and answer the question about the objectivity of proceedings against the accused

    The metabolism and signaling of hydrogen sulfide: the role of CBS-related proteins in Caenorhabditis elegans

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    Hydrogen sulfide (H2S) is a toxic gas that causes respiratory failure and death at high concentrations, but at low concentrations, it functions as a signaling molecule in vasodilation and neuromodulation, and it protects cells and tissues from reperfusion injury, hypoxia, hyperglycemia and endothelial dysfunction. Several model organisms have been used to study the physiological roles and signaling pathways of H2S. The roundworm Caenorhabditis elegans is a remarkable model for studying the physiology, developmental biology and signaling of H2S; however, the metabolism of H2S in this animal is largely unknown. Cystathionine beta-synthase (CBS) is one of three H2S-producing enzymes in mammals. Notably, C. elegans possesses 6 genes that encode proteins homologous to CBS, namely cbs- 1, cbs-2, cysl-1, cysl-2, cysl-3 and cysl-4. In this thesis we studied the roles of these genes in H2S metabolism and signaling. First, we identified cbs-1 as the gene encoding CBS in C. elegans; the recombinant purified CBS-1 protein exhibited canonical CBS activity, and RNA interference-mediated silencing of cbs-1 resulted in decreased CBS activity and increased homocysteine levels in worm extracts, recapitulating the phenotypes of CBS deficiency in mammals. Notably, the nematode and human enzymes differ in their domain..
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