dc.contributor.author | Isik, Kamil | |
dc.contributor.author | Oezdemir-Kocak, Fadime | |
dc.date.accessioned | 2020-06-21T15:08:36Z | |
dc.date.available | 2020-06-21T15:08:36Z | |
dc.date.issued | 2009 | |
dc.identifier.issn | 0944-5013 | |
dc.identifier.uri | https://doi.org/10.1016/j.micres.2006.11.002 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12712/18993 | |
dc.description | Ozdemir Kocak, Fadime/0000-0002-8557-5166; Isik, Kamil/0000-0003-1764-8113 | en_US |
dc.description | WOS: 000263353400007 | en_US |
dc.description | PubMed: 17329088 | en_US |
dc.description.abstract | Nocardia are aerobic, catalase-positive, Gram-positive microorganisms and typically acid-alcohol fast at some stage of the growth cycle. The genus Nocardia, a member of Mycolata group, is clinically important because it is an opportunistic pathogen. The sulfonamide derivative medicines are prefered to cure infection caused by Nocardia, such as nocardiaosis and mycetoma. Antimicrobial activities of seven sulfonamide derivatives have been investigated against some Nocardia species and isolates using the disk diffusion method on Sensitest agar medium (Oxoid). Thirty-six organisms, which consisted of 10 soil isolates selected from different clusters of Aymen study (2003), six clinical isolates provided by Ege University, Medical School, Microbiology and Clinical Microbiology Department, four reference strains, 15 type strains and a control strain of Staphylococcus aureus ATCC 43300 were tested. The strongest inhibition was observed in the cases of IV [N-(2-hydroxy-4-nitro-phenyl)-4-methyl-benzensulfonamid], V (N-(2-hydroxy-5-nitrophenyl)-4-methyl-benzensulfonamid] and III [N-(2-Hydroxy-phenyl)-4-methyl-benzenesulfonamide] against Nocardia. Introducing a hydroxyl group into the ortho position on the ring increased the antimicrobial. activity. Substitution of the electron withdrawing groups such as a nitro group increased the antimicrobial activity remarkably. (C) 2007 Elsevier GmbH. All rights reserved. | en_US |
dc.description.sponsorship | Ondokuz Mayis UniversityOndokuz Mayis University; Science Research Foundation [F356] | en_US |
dc.description.sponsorship | This study was supported by Ondokuz Mayis University, Science Research Foundation Grant No: F356. We are also thankfull. to Y. Bekdemir, H. Kutuk and S. Celik, Department of Chemistry, for providing the sulfonamide derivatives and cordial assistance. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Elsevier Gmbh, Urban & Fischer Verlag | en_US |
dc.relation.isversionof | 10.1016/j.micres.2006.11.002 | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Antimicrobial activity | en_US |
dc.subject | Sulfonamide derivative compounds | en_US |
dc.subject | Nocardia | en_US |
dc.title | Antimicrobial activity screening of some sulfonamide derivatives on some Nocardia species and isolates | en_US |
dc.type | article | en_US |
dc.contributor.department | OMÜ | en_US |
dc.identifier.volume | 164 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.startpage | 49 | en_US |
dc.identifier.endpage | 58 | en_US |
dc.relation.journal | Microbiological Research | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |