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Expression of Four Methionine Sulfoxide Reductases in Staphylococcus aureus

Staphylococcus aureus possesses three MsrA enzymes (MsrA1, MsrA2, MsrA3) that reduce the S-epimer of methionine sulfoxide (MetO) and an MsrB enzyme that reduces R-MetO. The four msr genes are expressed from three different promoters. The msrA1/msrB genes are coexpressed. To determine the expression...

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Detalles Bibliográficos
Autores principales: Singh, Kuldeep, Singh, Vineet K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3261475/
https://www.ncbi.nlm.nih.gov/pubmed/22272204
http://dx.doi.org/10.1155/2012/719594
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author Singh, Kuldeep
Singh, Vineet K.
author_facet Singh, Kuldeep
Singh, Vineet K.
author_sort Singh, Kuldeep
collection PubMed
description Staphylococcus aureus possesses three MsrA enzymes (MsrA1, MsrA2, MsrA3) that reduce the S-epimer of methionine sulfoxide (MetO) and an MsrB enzyme that reduces R-MetO. The four msr genes are expressed from three different promoters. The msrA1/msrB genes are coexpressed. To determine the expression pattern of msr genes, three independent reporter strains were constructed where msr promoter was cloned in front of a promoterless lacZ and the resulting construct was integrated in the chromosome. Using these strains, it was determined that the msrA1/B expression is significantly higher in S. aureus compared to msrA2 or msrA3. Expression of msrA1/B was highest during stationary phase growth, but the expression of msrA2 and msrA3 was highest during the early to midexponential growth phase. Expression of msrA1/B was induced by oxacillin and the expression of msrA3 was upregulated by salt. Expression of msrA2 remained unchanged under all tested conditions.
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spelling pubmed-32614752012-01-23 Expression of Four Methionine Sulfoxide Reductases in Staphylococcus aureus Singh, Kuldeep Singh, Vineet K. Int J Microbiol Research Article Staphylococcus aureus possesses three MsrA enzymes (MsrA1, MsrA2, MsrA3) that reduce the S-epimer of methionine sulfoxide (MetO) and an MsrB enzyme that reduces R-MetO. The four msr genes are expressed from three different promoters. The msrA1/msrB genes are coexpressed. To determine the expression pattern of msr genes, three independent reporter strains were constructed where msr promoter was cloned in front of a promoterless lacZ and the resulting construct was integrated in the chromosome. Using these strains, it was determined that the msrA1/B expression is significantly higher in S. aureus compared to msrA2 or msrA3. Expression of msrA1/B was highest during stationary phase growth, but the expression of msrA2 and msrA3 was highest during the early to midexponential growth phase. Expression of msrA1/B was induced by oxacillin and the expression of msrA3 was upregulated by salt. Expression of msrA2 remained unchanged under all tested conditions. Hindawi Publishing Corporation 2012 2012-01-04 /pmc/articles/PMC3261475/ /pubmed/22272204 http://dx.doi.org/10.1155/2012/719594 Text en Copyright © 2012 K. Singh and V. K. Singh. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Singh, Kuldeep
Singh, Vineet K.
Expression of Four Methionine Sulfoxide Reductases in Staphylococcus aureus
title Expression of Four Methionine Sulfoxide Reductases in Staphylococcus aureus
title_full Expression of Four Methionine Sulfoxide Reductases in Staphylococcus aureus
title_fullStr Expression of Four Methionine Sulfoxide Reductases in Staphylococcus aureus
title_full_unstemmed Expression of Four Methionine Sulfoxide Reductases in Staphylococcus aureus
title_short Expression of Four Methionine Sulfoxide Reductases in Staphylococcus aureus
title_sort expression of four methionine sulfoxide reductases in staphylococcus aureus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3261475/
https://www.ncbi.nlm.nih.gov/pubmed/22272204
http://dx.doi.org/10.1155/2012/719594
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