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dc.contributor.authorGraminha, Marcia A. S.
dc.contributor.authorRocha, Eleusa M. F.
dc.contributor.authorPrade, Rolf A.
dc.contributor.authorMartinez-Rossi, Nilce M.
dc.date.accessioned2018-08-15T12:44:22Z
dc.date.available2018-08-15T12:44:22Z
dc.date.issued2004-09
dc.identifieroksd_graminha_terbinafineresi_2004
dc.identifier.citationGraminha, M. A. S., Rocha, E. M. F., Prade, R. A., & Martinez-Rossi, N. M. (2004). Terbinafine resistance mediated by salicylate 1-monooxygenase in Aspergillus nidulans. Antimicrobial Agents and Chemotherapy, 48(9), 3530-3535. https://doi.org/10.1128/AAC.48.9.3530-3535.2004
dc.identifier.urihttps://hdl.handle.net/11244/301413
dc.description.abstractResistance to antifungal agents is a recurring and growing problem among patients with systemic fungal infections. UV-induced Aspergillus nidulans mutants resistant to terbinafine have been identified, and we report here the characterization of one such gene. A sib-selected, 6.6-kb genomic DNA fragment encodes a salicylate 1-monooxygenase (salA), and a fatty acid synthase subunit (fasC) confers terbinafine resistance upon transformation of a sensitive strain. Subfragments carrying salA but not fasC confer terbinafine resistance. salA is present as a single-copy gene on chromosome VI and encodes a protein of 473 amino acids that is homologous to salicylate 1-monooxygenase, a well-characterized naphthalene-degrading enzyme in bacteria. salA transcript accumulation analysis showed terbinafine-dependent induction in the wild type and the UV-induced mutant Terb7, as well as overexpression in a strain containing the salA subgenomic DNA fragment, probably due to the multicopy effect caused by the transformation event. Additional naphthalene degradation enzyme-coding genes are present in fungal genomes, suggesting that resistance could follow degradation of the naphthalene ring contained in terbinafine.
dc.formatapplication/pdf
dc.languageen_US
dc.publisherAmerican Society for Microbiology
dc.rightsThis material has been previously published. In the Oklahoma State University Library's institutional repository this version is made available through the open access principles and the terms of agreement/consent between the author(s) and the publisher. The permission policy on the use, reproduction or distribution of the material falls under fair use for educational, scholarship, and research purposes. Contact Digital Resources and Discovery Services at lib-dls@okstate.edu or 405-744-9161 for further information.
dc.titleTerbinafine resistance mediated by salicylate 1-monooxygenase in Aspergillus nidulans
osu.filenameoksd_graminha_terbinafineresi_2004.pdf
dc.description.peerreviewPeer reviewed
dc.identifier.doi10.1128/AAC.48.9.3530-3535.2004
dc.description.departmentMicrobiology and Molecular Genetics
dc.type.genreArticle
dc.type.materialText
dc.subject.keywordsantifungal agents
dc.subject.keywordsaspergillus nidulans
dc.subject.keywordschromosome mapping
dc.subject.keywordsculture media
dc.subject.keywordsdna fragmentation
dc.subject.keywordsdna primers
dc.subject.keywordsdrug resistance
dc.subject.keywordsfatty acid synthases
dc.subject.keywordsgene library
dc.subject.keywordsmixed function oxygenases
dc.subject.keywordsnaphthalenes


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