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Please use this identifier to cite or link to this item:
http://hdl.handle.net/10174/14566
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Title: | Antimicrobial Activity and Chemical Composition of the Essential Oils of Portuguese Foeniculum vulgare Fruits |
Authors: | Mota, Ana Martins, M. Rosário Arantes, Silvia Lopes, Violeta Bettencourt, Eliseu Pombal, Sofia Gomes, Arlindo Silva, Lúcia |
Keywords: | Foeniculum vulgare Essential oils Fruits Chemical composition Chemotypes, Antimicrobial activity. Chemotypes Antimicrobial activity |
Issue Date: | Feb-2015 |
Citation: | Mota A.S., Martins M.R., Arantes S., Lopes V.R., Bettencourt E., Pombal S., Gomes A.C. Silva L.A. (2015) Antimicrobial Activity and Chemical Composition of the Essential Oils of Portuguese Foeniculum vulgare Fruits. Natural Product Communications, 10 (4):673-676. |
Abstract: | The aim of this study was to investigate the chemical composition and antimicrobial activity of essential oils obtained by hydrodistillation from fruits of six
fennel accessions collected from wild populations occurring in the centre and south of Portugal. Composition of essential oils was established by Gas
Chromatography-Flame Ionization Detector (GC-FID) and Gas Chromatography-Mass Spectrometry (GC-MS) analysis. The obtained yields of the essential
oils were found to vary greatly in the range of 1.1 to 2.9% (v/w) and the chemical composition varied with the region of collection. A total of 16 compounds
were identified. The main compounds were fenchone (16.9 – 34.7%), estragole (2.5 – 66.0%) and trans-anethole (7.9 – 77.7%). The percentages of these three
main compounds were used to determine the relationship between the different oil samples and to group them into four different chemotypes:
anethole/fenchone; anethole; estragole and anethole/estragole. Antifungal activity of essential oils was evaluated against six food spoilage fungi: Aspergillus
niger, A. japonicus, A. oryzae, Fusarium oxysporum, Rhizophus oryzae and R. stolonifer. Antibacterial activity was assessed against three Gram-positive
strains: Enterococcus faecalis ATCC 29212, Staphylococcus epidermidis ATCC 12228 and S. aureus ATCC 28213; and against six Gram-negative strains:
Escherichia coli ATCC 25922; Morganella morganii LFG 08; Proteus mirabilis LFG 04; Salmonella enteritidis LFG 05; S. entiritidis serovar typhimurium
LFG 06 and Pseudomonas aeruginosa ATCC 27853 by the disc diffusion agar method; the minimal inhibitory concentration (MIC) was determined using
the broth macro-dilution method. The MIC values varied from 62.5 (E. coli ATCC 25922) to 2000 μg/mL (P. aeruginosa ATCC 27853). |
URI: | http://hdl.handle.net/10174/14566 |
ISSN: | 1934-578X |
Type: | article |
Appears in Collections: | MED - Publicações - Artigos em Revistas Internacionais Com Arbitragem Científica
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