Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/2857
Title: Functional analysis of free methionine-R-sulfoxide reductase from saccharomyces cerevisiae
Authors: Le, Dung Tien
Lee, Byung Cheon
Marino, Stefano M.
Zhang, Yan
Fomenko, Dmitri E.
Kaya, Alaattin
Hacıoğlu, Elise
Kwak, Geun-Hee
Koç, Ahmet
Kim, Hwa-Young
Gladyshev, Vadim N.
Hacıoğlu, Elise
Koç, Ahmet
Izmir Institute of Technology. Molecular Biology and Genetics
Keywords: Catalytic activity
Saccharomyces cerevisiae
Methionine sulfoxide
Methionine sulfoxide reductase
Yeast cell
Enzyme activity
Issue Date: Feb-2009
Publisher: American Society for Biochemistry and Molecular Biology
Source: Le, D. T., Lee, B. C., Marino, S. M., Zhang, Y., Fomenko, D. E., Kaya, A., Hacıoğlu, E., Kwak, G. H., Koç, A., Kim, H. Y. and Gladyshev, V. N. (2009). Functional analysis of free methionine-R-sulfoxide reductase from saccharomyces cerevisiae. Journal of Biological Chemistry, 248(7), 4354-4364. doi:10.1074/jbc.M805891200
Abstract: Methionine sulfoxide reductases (Msrs) are oxidoreductases that catalyze thiol-dependent reduction of oxidized methionines. MsrA and MsrB are the best known Msrs that repair methionine S-sulfoxide (Met-S-SO) and methionine-R-sulfoxide (Met-R-SO) residues in proteins, respectively. In addition, an Escherichia coli enzyme specific for free Met-R-SO, designated fRMsr, was recently discovered. In this work, we carried out comparative genomic and experimental analyses to examine occurrence, evolution, and function of fRMsr. This protein is present in single copies and two mutually exclusive subtypes in about half of prokaryotes and unicellular eukaryotes but is missing in higher plants and animals. A Saccharomyces cerevisiae fRMsr homolog was found to reduce free Met-R-SO but not free Met-S-SO or dabsyl-Met-R-SO. fRMsr was responsible for growth of yeast cells on Met-R-SO, and the double fRMsr/MsrA mutant could not grow on a mixture of methionine sulfoxides. However, in the presence of methionine, even the triple fRMsr/MsrA/MsrB mutant was viable. In addition, fRMsr deletion strain showed an increased sensitivity to oxidative stress and a decreased life span, whereas overexpression of fRMsr conferred higher resistance to oxidants. Molecular modeling and cysteine residue targeting by thioredoxin pointed to Cys101 as catalytic and Cys125 as resolving residues in yeast fRMsr. These residues as well as a third Cys, resolving Cys91, clustered in the structure, and each was required for the catalytic activity of the enzyme. The data show that fRMsr is the main enzyme responsible for the reduction of free Met-R-SO in S. cerevisiae.
URI: http://dx.doi.org/10.1074/jbc.M805891200
http://hdl.handle.net/11147/2857
ISSN: 0021-9258
0021-9258
Appears in Collections:Molecular Biology and Genetics / Moleküler Biyoloji ve Genetik
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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