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      Chemical composition and antibacterial activity of the essential oils of Ferula vesceritensis Coss et Dur. leaves, endemic in Algeria

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          Abstract

          Background

          The biological importance of members of genus Ferula promoted us to investigate the leaves of Ferula vesceritensis Coss et Dur. (endemic plant) previously not investigated. This study presents the chemical composition and antibacterial activities of the hydrodistilled oils.

          Results

          Volatile components of the leaves of F. vesceritensis have been studied by gas chromatography–mass spectrometry to afford 23 compounds. The major components were found to be 5,9-tetradecadiyne (24.72%), germacrene D (24.51%), farnesene (8.57%), and α-bisabolene (8.57%). The antimicrobial activities of the essential oils were evaluated by disk diffusion method and tested against Gram-positive and Gram-negative bacteria. The volatile oil showed a strong antibacterial activity against Staphylococcus aureus, Escherichia coli, and Klebsiella pneumonia.

          Conclusions

          These results reinforce the previous studies showing that the genus Ferula is considered as a good source of essential oils. The results presented here can be considered as the first information on the antimicrobial properties of F. vesceritensis.

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          Most cited references14

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          Sesquiterpene coumarins and sesquiterpenes from Ferula sinaica

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            Coumarins.

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              Ferulenol specifically inhibits succinate ubiquinone reductase at the level of the ubiquinone cycle.

              The natural compound ferulenol, a sesquiterpene prenylated coumarin derivative, was purified from Ferula vesceritensis and its mitochondrial effects were studied. Ferulenol caused inhibition of oxidative phoshorylation. At low concentrations, ferulenol inhibited ATP synthesis by inhibition of the adenine nucleotide translocase without limitation of mitochondrial respiration. At higher concentrations, ferulenol inhibited oxygen consumption. Ferulenol caused specific inhibition of succinate ubiquinone reductase without altering succinate dehydrogenase activity of the complex II. This inhibition results from a limitation of electron transfers initiated by the reduction of ubiquinone to ubiquinol in the ubiquinone cycle. This original mechanism of action makes ferulenol a useful tool to study the physiological role and the mechanism of electron transfer in the complex II. In addition, these data provide an additional mechanism by which ferulenol may alter cell function and demonstrate that mitochondrial dysfunction is an important determinant in Ferula plant toxicity.
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                Author and article information

                Journal
                Org Med Chem Lett
                Org Med Chem Lett
                Organic and Medicinal Chemistry Letters
                Springer
                2191-2858
                2012
                3 September 2012
                : 2
                : 31
                Affiliations
                [1 ]Laboratory of Biomolecules and Plant Breeding, Life Science and Nature Department, Faculty of Exact Science and Life Science and Nature, University of Larbi Ben Mhidi, Oum El Bouaghi, Algeria
                [2 ]Laboratory of Natural Products and Organic Synthesis, Department of Chemistry, Faculty of Science, University of Mentouri-Constantine, Constantine, Algeria
                Article
                2191-2858-2-31
                10.1186/2191-2858-2-31
                3517384
                22937773
                9601889c-ec32-43ed-8d8c-5d1875b2fef1
                Copyright ©2012 Zellagui et al.; licensee Springer.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 24 December 2011
                : 17 April 2012
                Categories
                Original Article

                Pharmaceutical chemistry
                antimicrobial activity,volatile oils,ferula vesceritensis,gc-ms
                Pharmaceutical chemistry
                antimicrobial activity, volatile oils, ferula vesceritensis, gc-ms

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