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Investigations on the essential oil of Lippia rugosa from Cameroon for its potential use as antifungal agent against Aspergillus flavus Link ex. Fries
Authors:NL Tatsadjieu  PM Jazet Dongmo  MB Ngassoum  F-X Etoa  CMF Mbofung
Affiliation:1. Department of Food Science and Nutrition, National Advanced School of Agro-Industrial Sciences, University of Ngaoundere, P.O. Box 454, Ngaoundere, Adamaoua, Cameroon;2. Department of Applied Chemistry, National Advanced School of Agro-Industrial Sciences, University of Ngaoundere, P.O. Box 454, Ngaoundere, Adamaoua, Cameroon;3. Department of Biochemistry, Faculty of Science, University of Yaounde I, P.O. Box 812, Yaounde, Centre, Cameroon;1. School of Pharmacy and Bioengineering, Chengdu University, Chengdu 610106, PR China;2. Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100193, PR China;3. School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, PR China
Abstract:Lippia rugosa essential oil was tested for its effectiveness against Aspergillus flavus on artificial growth media. The chemical composition of the oil was determined by gas chromatography–mass spectrometry (GC–MS). Geraniol (51.5%), nerol (18.6%) and geranial (10.4%) were the main components of Lippia oil. After 8 days of incubation on essential oil supplemented medium, mycelium growth of A. flavus was totally inhibited by 1000 mg l?1 of L. rugosa essential oil. The effect of essential oil on aflatoxin B1 synthesis was evaluated in SMKY broth. The medium supplemented with different essential oil concentrations, was inoculated with A. flavus mycelium and incubated at 25 °C. After 2, 4, 6 and 8 days, aflatoxin B1 (AFB1) was quantified in the supernatant using Enzyme Linked Immuno-Sorbent Assay (ELISA). Results showed that aflatoxin B1 synthesis was inhibited by 1000 mg l?1 of L. rugosa essential oil after 8 days of incubation. The effect of the EO on the H+-ATPase pumping membrane was also evaluated in the presence of several concentrations of oil (200–2000 mg l?1) by monitoring glucose-induced acidification of the external medium. L. rugosa essential oil at the concentration of 2000 mg l?1 completely inhibited the activity of this enzyme. These data suggest that the essential oil of L. rugosa is a fungicidal for A. flavus and its possible cellular target include the H+-ATPase.Results obtained in the present study indicate the possibility of exploiting Lippia rugosa essential oil in the fight against strains of A. flavus responsible for biodeterioration of stored foods products.
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