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dc.contributor.authorChemsa, A.E.
dc.contributor.authorZellagui, A.
dc.contributor.authorÖztürk, Mehmet
dc.contributor.authorErol, E.
dc.contributor.authorCeylan, O.
dc.contributor.authorDuru, M.E.
dc.contributor.authorGherraf, N.
dc.date.accessioned2020-11-20T16:48:13Z
dc.date.available2020-11-20T16:48:13Z
dc.date.issued2016
dc.identifier.issn2028-2508
dc.identifier.urihttps://hdl.handle.net/20.500.12809/5992
dc.description.abstractThe essential oil obtained from the aerial parts of Marrubium deserti de Noé. (Lamiaceae), growing in the North fringe of the Algerian Sahara, was analyzed by GC-MS. Thirty-eight compounds were identified, representing 99.70% of the total oils. The GC-MS analysis revealed the presence of tetracosane, germacrene D, ?-cadinene, a-cadinol and t-cadinol as the main constituents, representing 31.11%, 7.91%, 6.52%, 6.26% and 5.81%, respectively. Minimum inhibitory concentrations (MICs) of essential oil and methanol extract were calculated by microtitre broth dilution method, and antibiofilm effects by microplate biofilm assay. The highest antibiofilm activity was found to be 69.31% against Micrococcus luteus NRRL B-4375 at 25 mg/mL for methanol extract and 36.62% against Candida albicans ATCC 10239 at 25 ?L/mL concentration for essential oil. The antioxidant activity was determined using three complementary tests namely: ?-carotene-linoleic acid, DPPHfree radical scavenging, and CUPRAC assays. In ?-carotene-linoleic acid assay, both the oil and the extract exhibited good lipid peroxidation inhibition activity, demonstrating 76.81 ± 0.59 and 86.33 ± 0.27% at 200 ?g/mL concentration, respectively. In DPPH and CUPRAC assays, however, the methanol extract exhibited high antioxidant activity; however, the essential oil showed weak activity. The in vitro anticholinesterase activity, was carried out against acetylcholinesterase and butyrylcholinesterase enzymes spectrophotometrically using Elman method. Methanol extract showed weak acetylcholinesterase and butyrylcholinesterase inhibitory activities, while the essential oil was inactive against both enzymes.en_US
dc.item-language.isoengen_US
dc.publisherMohammed Premier Universityen_US
dc.item-rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAntibiofilmen_US
dc.subjectAnticholinesteraseen_US
dc.subjectAntioxidanten_US
dc.subjectEssential oilen_US
dc.subjectMarrubium desertien_US
dc.titleAntibiofilm formation, antioxidant and anticholinesterase activities of essential oil and methanol extract of Marrubium deserti de Noéen_US
dc.item-typearticleen_US
dc.contributor.departmenten_US
dc.contributor.departmentTempChemsa, A.E., Department of Biology, Faculty of Life and Natural Sciences, El Oued University, Algeria, Laboratory of Biomolecules and Plant Breeding, Faculty of Exact Science and Life Science and Nature, University of Larbi Ben Mhidi, Oum El Bouaghi, Algeria, Department of Chemistry, Faculty of Science, MuglaSitkiKocman University, Mugla, Turkey; Zellagui, A., Laboratory of Biomolecules and Plant Breeding, Faculty of Exact Science and Life Science and Nature, University of Larbi Ben Mhidi, Oum El Bouaghi, Algeria; Öztürk, M., Department of Chemistry, Faculty of Science, MuglaSitkiKocman University, Mugla, Turkey; Erol, E., Department of Chemistry, Faculty of Science, MuglaSitkiKocman University, Mugla, Turkey; Ceylan, O., Department of Plant and Animal Breeding, Ula Ali Kocman Vocational School, MuglaSitkiKocman University, Mugla, Turkey; Duru, M.E., Department of Chemistry, Faculty of Science, MuglaSitkiKocman University, Mugla, Turkey; Gherraf, N., Laboratory of Biomolecules and Plant Breeding, Faculty of Exact Science and Life Science and Nature, University of Larbi Ben Mhidi, Oum El Bouaghi, Algeriaen_US
dc.identifier.volume7en_US
dc.identifier.issue3en_US
dc.identifier.startpage993en_US
dc.identifier.endpage1000en_US
dc.relation.journalJournal of Materials and Environmental Scienceen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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