Rui Oliveira

Dr. Rui Oliveira

1. Department of Biology, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal
+3
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Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 January 2023 in Nature Protocols
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ACAndrew Collins
Andrew Collins
PMPETER MOLLER
PETER MOLLER
Goran GajskiGoran Gajski
Goran Gajski
SVSoňa Vodenková
Soňa Vodenková
AAAbdulhadi Abdulwahed
Abdulhadi Abdulwahed
Amaya AzquetaAmaya Azqueta
Amaya Azqueta

1 April 2005 in Molecular Biology of the Cell
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CFCélia Ferreira
Célia Ferreira
FVFrank van Voorst
Frank van Voorst
AMAntónio Martins
António Martins
LNLuisa Neves
Luisa Neves
RORui Oliveira
Rui Oliveira
ABAnders Brandt
Anders Brandt
Glycerol and other polyols are used as osmoprotectants by many organisms. Several yeasts and other fungi can take up glycerol by proton symport. To identify genes involved in active glycerol uptake in Saccharomyces cerevisiae we screened a deletion mutant collection comprising 321 genes encoding proteins with 6 or more predicted transmembrane domains for impaired growth on glycerol medium. Deletion of STL1, which encodes a member of the sugar transporter family, eliminates active glycerol transport. Stl1p is present in the plasma membrane in S. cerevisiae during conditions where glycerol symport is functional. Both the Stl1 protein and the active glycerol transport are subject to glucose-induced inactivation, following identical patterns. Furthermore, the Stl1 protein and the glycerol symporter activity are strongly but transiently induced when cells are subjected to osmotic shock. STL1 was heterologously expressed in Schizosaccharomyces pombe, a yeast that does not contain its own active glycerol transport system. In S. pombe, STL1 conferred the ability to take up glycerol against a concentration gradient in a proton motive force-dependent manner. We conclude that the glycerol proton symporter in S. cerevisiae is encoded by STL1.


1 July 2000 in Molecular Microbiology
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BHBjørn Holst
Bjørn Holst
CLChristina Lunde
Christina Lunde
FLFernanda Lages
Fernanda Lages
RORui Oliveira
Rui Oliveira
CLCândida Lucas
Cândida Lucas
MKMorten Kielland-Brandt
Morten Kielland-Brandt
Many yeast species can utilize glycerol, both as a sole carbon source and as an osmolyte. In Saccharomyces cerevisiae, physiological studies have previously shown the presence of an active uptake system driven by electrogenic proton symport. We have used transposon mutagenesis to isolate mutants affected in the transport of glycerol into the cell. Here we present the identification of YGL084c, encoding a multimembrane‐spanning protein, as being essential for proton symport of glycerol into S. cerevisiae. The gene is named GUP1 (glycerol uptake) and, for growth on glycerol, is important as a carbon and energy source. In addition, in strains deficient in glycerol production it also provides osmotic protection by the addition of glycerol. Another open reading frame (ORF), YPL189w, presenting a high degree of homology to YGL084c, similarly appears to be involved in active glycerol uptake in salt‐containing glucose‐based media in strains deficient in glycerol production. Analogously, this gene is named GUP2. To our knowledge, this is the first report on a gene product involved in active transport of glycerol in yeasts. Mutations with the same phenotypes occurred in two other ORFs of previously unknown function, YDL074c and YPL180w.


1 May 2007 in Tetrahedron
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RBRosa Batista
Rosa Batista
SCSusana Costa
Susana Costa
EMElisabeth L. Malheiro
Elisabeth L. Malheiro
MBMichael Scott Belsley
Michael Scott Belsley
Maria RaposoMaria Raposo
Maria Raposo