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Dissertations / Theses on the topic 'Cerevisane'

Author: Grafiati

Published: 7 June 2025

Last updated: 2 August 2025

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1

Gamonet, Franck. "Biosynthèse de la lysine chez la levure Saccharomyces Cerevisiae : rôle(s) des gènes LYS7 et LYS4." Bordeaux 2, 1997. http://www.theses.fr/1997BOR28536.

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2

Cadière, Axelle. "Ingénierie de la voie des pentoses phosphate chez la levure Saccharomyces cerevisiae : applications en œnologie." Thesis, Montpellier, SupAgro, 2010. http://www.theses.fr/2010NSAM0009.

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Il existe un intérêt croissant pour le développement de levures S. cerevisiae œnologiques à rendement abaissé de conversion des sucres en alcool. Nous proposons ici une approche originale basée sur la réorientation du flux carboné vers la voie des pentoses phosphate (VPP). Dans un premier temps, nous avons montré que le flux à travers la VPP est limité par le niveau de réoxydation du NADPH et par la capacité de la voie elle même. Nous avons ensuite mis en évidence le rôle crucial du facteur de transcription Stb5 dans le maintien d'un flux basal à travers la VPP. La surexpression de STB5, coupl

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3

Luz, Juliana Silva da. "Análise estrutural e funcional de cofatores do exossomo em Saccharomyces cerevisiae e Pyrococcus." Universidade de São Paulo, 2006. http://www.teses.usp.br/teses/disponiveis/46/46131/tde-29092006-124545/.

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A síntese ribossomal é uma das maiores atividades em células eucarióticas. Este processo inicia-se no nucléolo e é finalizado após a exportação das subunidades 40S e 60S para o citoplasma. Três dos RNAs ribossomais de eucariotos (18S, 5.8S e 25S) são sintetizados como um transcrito primário de 35S, o qual é processado através de uma complexa e ordenada série de modificações nucleotídicas e clivagens endo e exonucleolíticas. Estas reações dependem de aproximadamente 170 proteínas, 80 small nucleolar RNAs e de seqüências no pré-rRNA. Os fatores trans-atuantes envolvidos no processamento podem s

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4

Kronekova, Zuzana. "Assembly of mitochondrial ubiquinol-cytochrome c oxidoreductase complex in yeast Saccharomyces cerevisiae: The role of Cbp3p and Cbp4p assembly factors." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2005. http://nbn-resolving.de/urn:nbn:de:swb:14-1122027648324-54732.

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Ubiquinol-cytochrome c reductase (complex III) is a central component of the respiratory chain of the inner mitochondrial membrane. It transfers electrons from reduced ubiquinone to ferricytochrome c. Correctly assembled and functional complex III is an essential prerequisite for oxidative energy metabolism. Complex III deficiency has been reported to be associated with several neurodegenerative diseases. Formation and assembly of complex III requires a multitude of specific nuclearly encoded proteins. For example, gene specific translational activators for cytochrome b synthesis as well as th

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5

Ericson, Elke. "High-resolution phenomics to decode : yeast stress physiology /." Göteborg : Göteborg University, Dept. of Cell and Molecular Biology, Faculty of Science, 2006. http://www.loc.gov/catdir/toc/fy0707/2006436807.html.

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6

Eriksson, Peter. "Identification of the two GPD isogenes of saccharomyces cerevisiae and characterization of their response to hyper-osmotic stress." Göteborg : Chalmers Reproservice, 1996. http://catalog.hathitrust.org/api/volumes/oclc/38202006.html.

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7

Pratt, Elizabeth Stratton. "Genetic and biochemical studies of Adr6, a component of the SWI/SNF chromatin remodeling complex /." Thesis, Connect to this title online; UW restricted, 2001. http://hdl.handle.net/1773/10288.

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8

Kerkmann, Katja. "Die genomweite Expressionsanalyse von Deletionsmutanten der Gene NHP6A/B und CDC73 in der Hefe S.cerevisiae." [S.l. : s.n.], 2000. http://deposit.ddb.de/cgi-bin/dokserv?idn=961961651.

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9

Bellahn, Inga. "Biochemische Charakterisierung vakuolärer Vesikel aus Saccharomyces cerevisiae." [S.l. : s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=965643484.

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10

Jestel, Anja. "Strukturelle Charakterisierung des Calpastatin und Untersuchung eines ATP-abhängigen Peptidtransports in S. cerevisiae." [S.l. : s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=966507193.

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11

Anderlund, Mikael. "Redox balancing in recombinant strains of Saccharomyces cerevisiae." Lund : University of Lund, 1998. http://books.google.com/books?id=uc5qAAAAMAAJ.

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12

Schorling, Stefan. "Ceramidsynthese in Saccharomyces cerevisiae." Diss., lmu, 2001. http://nbn-resolving.de/urn:nbn:de:bvb:19-3658.

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13

Deans, Karen. "Ageing of Saccharomyces cerevisiae." Thesis, Heriot-Watt University, 1997. http://hdl.handle.net/10399/663.

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14

De, Silva-Udawatta Mihiri Nilanthi. "Functional analyses of trehalose-6-phosphate synthase in saccharomyces cerevisiae." free to MU campus, to others for purchase, 1999. http://wwwlib.umi.com/cr/mo/fullcit?p9962518.

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15

Ansell, Ricky. "Redox and osmoregulation in Saccharomyces cerevisiae the role of the two isogenes encoding NAD-dependent glycerol 3-phosphate dehydrogenase /." Göteborg : [Institute of Cell and Molecular Biology, Dept. of General and Marine Microbiology, Lundberg Laboratory, Göteborg University], 1997. http://catalog.hathitrust.org/api/volumes/oclc/38985539.html.

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16

Jaffé, Matthias Benno. "Biochemical studies of the Saccharomyces cerevisae kinetochore." Thesis, Massachusetts Institute of Technology, 1996. http://hdl.handle.net/1721.1/38399.

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17

Kemp, Hilary A. "A complex of six FAR proteins required for pheromone arrest and mating /." view abstract or download file of text, 2003. http://wwwlib.umi.com/cr/uoregon/fullcit?p3113011.

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Thesis (Ph. D.)--University of Oregon, 2003.<br>Typescript. Includes vita and abstract. Includes bibliographical references (leaves 94-104). Also available for download via the World Wide Web; free to University of Oregon users.

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18

Neutzner, Albert. "Termination der Mitose : die Rolle der Phosphatase Cdc14 beim M-G1-Übergang in der Hefe Saccharomyces cerevisiae /." [S.l. : s.n.], 2002. http://www.bsz-bw.de/cgi-bin/xvms.cgi?SWB10252182.

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19

Schauen, Matthias. "Mitochondriale Transportproteine in Saccharomyces cerevisiae." [S.l.] : [s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=965029379.

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20

Schulze, Ulrik. "Anaerobic physiology of Saccharomyces cerevisiae /." Online version, 1995. http://bibpurl.oclc.org/web/20903.

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21

Greig, Duncan. "Sex, species and Saccharomyces cerevisiae." Thesis, University of Oxford, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.301401.

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22

Payne, Thomas. "Protein secretion in Saccharomyces cerevisiae." Thesis, University of Nottingham, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.438772.

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23

Paulo, Jorge Fernando Ferreira de Sousa. "mRNA mistranslation in Saccharomyces cerevisiae." Master's thesis, Universidade de Aveiro, 2012. http://hdl.handle.net/10773/7775.

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Mestrado em Biologia Molecular e Celular<br>The genetic code is defined as a series of biochemical reactions that establish the cellular rules that translate DNA into protein information. It was established more than 3.5 billion years ago and it is one of the most conserved features of life. Over the years, several alterations to the standard genetic code and codon ambiguities have been discovered in both prokaryotes and eukaryotes, suggesting that the genetic code is flexible. However, the molecular mechanisms of evolution of the standard genetic code and the cellular role(s) of codon

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24

Kim, Jae-hyun. "Chromosome segregation in Saccharomyces cerevisiae /." Digital version accessible at:, 1998. http://wwwlib.umi.com/cr/utexas/main.

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25

Caponigro, Giordano Michael. "mRNA decay in Saccharomyces cerevisiae." Diss., The University of Arizona, 1996. http://hdl.handle.net/10150/187472.

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mRNA decay is an important step in the control of gene expression. To study mRNA degradation I have exploited the genetic, biochemical, and molecular tools available in Saccharomyces cerevisiae. These studies provided insight into the signals within individual transcripts which specify their half-lives, the various mechanisms by which mRNAs are degraded, and the trans-acting factors which both perform and control nucleolytic events. I identified a 65 nucleotide segment from the coding region of the unstable MATɑl mRNA which was capable of targeting both the MATɑl and stable PGKI transcripts fo

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26

Dunckley, Travis Lee. "mRNA decapping in Saccharomyces cerevisiae." Diss., The University of Arizona, 2000. http://hdl.handle.net/10150/289165.

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The major pathway of mRNA degradation in yeast occurs through deadenylation, decapping and subsequent 5' to 3' exonucleolytic decay of the transcript body. The products of the DCP1 and DCP2 genes are required for mRNA decapping. DCP1 encodes a conserved mRNA decapping enzyme. Dcp2p is a highly conserved protein that is required for the activation of Dcp1p. The Dcp2p contains a functional Muff motif that is required for its decapping function, suggesting that Dcp2p encodes a pyrophosphatase. These results suggest that Dcp2p hydrolyzes a specific pyrophosphate bond that either directly activates

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27

Schaefer, Jonathan Brook. "Regulation of G1 exit by the Swi6p transcription factor /." Thesis, Connect to this title online; UW restricted, 2007. http://hdl.handle.net/1773/5080.

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28

Van, Dyk Dewald 1975. "Genetic analysis of a signal transduction pathway : the regulation of invasive growth and starch degradation in Saccharomyces cerevisiae." Thesis, Stellenbosch : Stellenbosch University, 2004. http://hdl.handle.net/10019.1/49972.

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Dissertation (PhD)--University of Stellenbosch, 2004.<br>ENGLISH ABSTRACT: Cells of the yeast Saccharomyces cerevisiae are able to change their morphological appearance in response to a variety of extracellular and intracellular signals. The processes involved in morphogenesis are well characterised in this organism, but the exact mechanism by which information emanating from the environment is integrated into the regulation of the actin cytoskeleton and the yeast cell cycle, is still not clearly understood. Considerable progress has, however, been made. The processes are investigated o

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29

Tan, Yves S. H. "Regulation of the type 1 protein phosphatase in saccharomyces cerevisiae." free to MU campus, to others for purchase, 2001. http://wwwlib.umi.com/cr/mo/fullcit?p3013031.

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30

Gagiano, Marco 1971. "The molecular characterisation of Mss11p, a transcriptional activator of the Saccharomyces cerevisiae MUC1 and STA1-3 genes." Thesis, Stellenbosch : Stellenbosch University, 2002. http://hdl.handle.net/10019.1/53138.

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Thesis (PhD)--University of Stellenbosch, 2002<br>ENGLISH ABSTRACT: Upon nutrient limitation, normal cells of the budding yeast, Saccharomyces cerevisiae, undergo a transition from ovoid cells that bud in an axial (haploid) or bipolar (diploid) fashion to elongated cells that bud in a unipolar fashion. The daughter cells stay attached to the mother cells, resulting in chains of cells referred to as pseudohyphae. These filaments can grow invasively into the growth substrate (haploid), or away from the colony (diploid), and are hypothesised to be an adaptation of yeast cells that enables t

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31

Luban, Cornelia. "Systematische Identifizierung und Analyse mitochondrialer Spleissfaktoren der Bäckerhefe Saccharomyces cerevisiae." Berlin mbv, 2008. http://d-nb.info/990627039/04.

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32

Sullivan, David Patrick. "Intracellular sterol transport and distribution in saccharomyces cerevisiae /." Access full-text from WCMC, 2009. http://proquest.umi.com/pqdweb?did=1692359491&sid=3&Fmt=2&clientId=8424&RQT=309&VName=PQD.

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33

Sherman, James. "Proteome-scale kinetic processes : methods and applications /." Thesis, Connect to this title online; UW restricted, 2005. http://hdl.handle.net/1773/10284.

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34

Börlin, Marine. "Diversité et structure de population des levures Saccharomyces cerevisiae à l’échelle du vignoble bordelais : Impact de différents facteurs sur la diversité." Thesis, Bordeaux, 2015. http://www.theses.fr/2015BORD0273/document.

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Saccharomyces cerevisiae est l’acteur principal de la fermentation du moût de raisin, mais l’influence de facteurs sur sa distribution dans les vignobles est peu connue. La région bordelaise, par son histoire et ses appellations, est une région d’intérêt pour étudier la diversité de S.cerevisiae. Au total, 2422 isolats de S.cerevisiae provenant de prélèvements de raisins et de cuves en fermentation spontanées sur deux années consécutives ont été analysés par 15 à 17 marqueurs microsatellites. Une très grande diversité génétique est mise en évidence, supérieure en mode de conduite conventionnel

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35

Strässle, Christoph A. "Modell zur Spontansynchronisation von Saccharomyces cerevisiae /." [S.l.] : [s.n.], 1988. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=8598.

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36

Deckers, Markus. "Charakterisierung peroxisomaler Proteine aus Saccharomyces cerevisiae." [S.l.] : [s.n.], 2007. http://deposit.ddb.de/cgi-bin/dokserv?idn=985178043.

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37

Stüer, Heike. "Wahrnehmung von Biotinmangel durch Saccharomyces cerevisiae." kostenfrei, 2009. http://www.opus-bayern.de/uni-regensburg/volltexte/2009/1353/.

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38

Großmann, Guido. "Plasma membrane compartmentation in Saccharomyces cerevisiae." kostenfrei, 2008. http://www.opus-bayern.de/uni-regensburg/volltexte/2009/1152/.

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39

London, Markus Konrad Justin. "Regulation der Proteasombiogenese in Saccharomyces cerevisiae." [S.l. : s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=974673315.

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40

Beck, Karsten. "Das Dhh1 Protein aus Saccharomyces cerevisiae." Diss., lmu, 2002. http://nbn-resolving.de/urn:nbn:de:bvb:19-7362.

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41

Widlund, Per Olov Ingvar. "The Saccharomyces cerevisiae chromosomal passenger, Bir1 /." Thesis, Connect to this title online; UW restricted, 2006. http://hdl.handle.net/1773/9202.

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42

Thompson, C. L. "Interaction of pentamidine with Saccharomyces cerevisiae." Thesis, University of Hull, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.377415.

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43

Reithinger, Johannes. "Membrane Protein Biogenesis in Saccharomyces cerevisiae." Doctoral thesis, Stockholms universitet, Institutionen för biokemi och biofysik, 2013. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-95376.

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Membranes are hydrophobic barriers that define the outer boundaries and internal compartments of living cells. Membrane proteins are the gates in these barriers, and they perform vital functions in the highly regulated transport of matter and information across membranes. Membrane proteins destined for the endoplasmic reticulum are targeted either co- or post-translationally to the Sec61 translocon, the major translocation machinery in eukaryotic cells, which allows for lateral partitioning of hydrophobic segments into the lipid bilayer. This thesis aims to acquire insights into the mechanism

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44

Spalding, A. C. "Host-plasmid interactions in Saccharomyces cerevisiae." Thesis, University of Kent, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.383082.

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45

Jenkins, F. "Development of thermotolerance in Saccharomyces cerevisiae." Thesis, Bucks New University, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.234851.

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46

Pearce, Amanda K. "Regulation of glycolysis in Saccharomyces cerevisiae." Thesis, University of Aberdeen, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.301297.

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This thesis extends the work of Crimmins (1995) on the control of glycolytic flux in yeast by the enzymes 6-phosphofructo-1-kinase and pyruvate kinase (Pyk1p). This study also examines the influence of Pf1kp and Pyk1p upon yeast resistance to the weak acid preservative, benzoic acid. In <I>Saccharomyces cerevisiae</I>, Pyk1p is encoded by <I>PYK1</I>, and the α and β subunits of Pf1kp are encoded by <I>PFK1</I> and <I>PFK2</I>, respectively. To test the influence of these genes upon glycolytic control, an isogenic set of <I>S. cerevisiae</I> mutants were utilised in which <I>PYK1, PFK1</I> and

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47

Hatton, Lee S. "Gluconeogenic gene regulation in Saccharomyces cerevisiae." Thesis, University of Aberdeen, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.387524.

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The yeast <I>FBP1 </I>and <I>PCK1</I> genes and the gluconeogenic enzymes that they encode, fructose-1,6-<I>bis</I>phosphatase and phosphoenolpyruvate carboxykinase, are subject to multiple levels of regulation by glucose. It has been reported that transcriptional repression of these genes is exceptionally sensitive to glucose, being triggered by glucose concentrations of less than 0.005% (0.25 mM). It was shown here that in addition at transcriptional repression, the <I>FBP1 </I>and <I>PCK1</I> and mRNAs are destabilised about 2-fold upon addition of the same low levels of glucose. Low levels

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48

Rowley, Neil K. "Studies on the Saccharomyces cerevisiae genome." Thesis, University of Cambridge, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.361615.

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49

Zealey, Gavin Ross. "Plasmid copy number in Saccharomyces cerevisiae." Thesis, University of Bath, 1985. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.333232.

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Studies were made of 2 mum based chimaeric plasmid copy number in Saccharomyces cerevisiae. A plasmid (pAYE56) containing three selectable genes in yeast (yeast LEU2, bacterial CAT and HSV-1 - TK) was constructed to reflect changes in copy number. Yeast transformants could be grown under three selection regimes and plasmid copy number estimated. During selective growth for the LEU2 gene there are about 20 plasmids per cell. This increases to about 100 during selective growth for the TK gene and furthermore the copy number can be controlled by the stringency of selection. Simultaneous selection

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50

Gimeno, Carlos Joaquín. "Characterization of Saccharomyces cerevisiae pseudohyphal development." Thesis, Massachusetts Institute of Technology, 1994. http://hdl.handle.net/1721.1/33506.

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