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Bactericidal and antioxidant effects of essential oils from Satureja montana L., Myristica fragrans H. and Cymbopogon flexuosus
Authors:DAdCS Rezende  CD Oliveira  LR Batista  VRF Ferreira  RM Brandão  ARS Caetano  MVP Alves  MG Cardoso
Institution:1. Departmento de Química, Universidade Federal de Lavras - MG, Lavras, Brazil;2. Departmento de Ciência dos Alimentos, Universidade Federal de Lavras - MG, Lavras, Brazil
Abstract:The extraction and characterization of the essential oils (EO) from Satureja montana L., Myristica fragrans H. and Cymbopogon flexuosus and the determination of their antibacterial and antioxidant activities were achieved. The EO were identified by gas chromatography/mass spectrometry and quantified by gas chromatography using a flame ionization detector. The antibacterial potential against Escherichia coli and Staphylococcus aureus was evaluated by cell susceptibility assays and by scanning electron microscopy. The antioxidant activity was evaluated by the 2,2-diphenyl-1-picrylhydrazyl assay, by β-carotene bleaching and by determining the reducing power. Borneol (36·18%), γ-terpineol (12·66%) and carvacrol (11·07%) were the principal components in the EO from S. montana, and sabinene (49·23%) and α-pinene (13·81%) were found in the EO from M. fragrans. Geranial (59·66%) and neral (38·98%) isomers were the only major components in the EO from C. flexuosus. The EO from S. montana was effective against E. coli, with minimum inhibitory and bactericidal concentrations (MIC and MBC) of 6·25 µl ml?1, whereas bactericidal potential against both was observed for the EO from M. fragrans; MIC = 6·25 µl ml?1 for S. aureus and MBC = 12·5 µl ml?1 for E. coli. A significant protective role on lipid substrates in the β-carotene bleaching assay was seen for the EO from S. montana and M. fragrans. Overall, such EO can be promising agents against pathogenic bacteria and for protecting biomolecules during oxidative stress.
Keywords:essential oils  natural antibiotics  natural products  oxidative stress  Satureja montana L    secondary metabolites
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