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24 S. Marín et al.control A. flavus, A. niger, A. terreus, F. oxysporum, F. roseum, P. italicum, Cladosporiumcladosporioides and Alt. alternata. The m<strong>in</strong>imum <strong>in</strong>hibitory concentrationof extracts aga<strong>in</strong>st A. flavus and A. niger were superior to those of twocommonly used synthetic fungicides (Shukla et al., 2008).The essential oil of Amomum subulatum exhibited a fungitoxic spectrumaga<strong>in</strong>st a wide range of moulds such as A. niger, A. flavus, A. terreus,A. fumigatus, Alt. alternata, Cladosporium herbarum, Curvularia lunata, F. oxysporum,Helm<strong>in</strong>thosporium oryzae and Trichoderma viride. Their mycelial growthwas significantly <strong>in</strong>hibited at 750 μg/ml (S<strong>in</strong>gh et al., 2008a).An <strong>in</strong> vitro <strong>in</strong>itial screen<strong>in</strong>g of a range of 37 essential oils (<strong>in</strong>clud<strong>in</strong>gc<strong>in</strong>namon leaf, Cynnamomum zeylanicum; clove, Syzygium aromaticum; lemongrass,Cymbopogon citrates; oregano, Origanum vulgare; and palma rose,Cymbopogon mart<strong>in</strong>ii) on <strong>in</strong>hibition of mycelial growth of toxigenic stra<strong>in</strong>s ofF. verticillioides, F. proliferatum and F. gram<strong>in</strong>earum under different temperatures(20–30°C) and water activities (a w) (0.95–0.995) was made. The basicmedium was a 3% maize meal extract agar. The agar medium was modifiedwith glycerol <strong>in</strong> order to get the assayed water activity and the essential oilswere <strong>in</strong>corporated at different concentrations (0, 500, 1000 μg/ml). Althoughwater activity was determ<strong>in</strong>ant for the growth of the isolates, <strong>in</strong> general, thepreservative effects of the oils were not l<strong>in</strong>ked to a w. However, a trend to ahigher <strong>in</strong>hibition by the oils when a wwas low was observed. Temperaturehad a m<strong>in</strong>or importance <strong>in</strong> the <strong>in</strong>hibitory effect of the essential oils (Vellutiet al., 2004a).Essential oils of both c<strong>in</strong>namon and clove were shown to effectively<strong>in</strong>hibit growth of both A. flavus and P. islandicum by direct contact, and <strong>in</strong> thevapour phase. In the atmosphere generated by these two essential oils eugenolwas the major compound, while other essential oils with low levels ofeugenol proved to be <strong>in</strong>effective, suggest<strong>in</strong>g that eugenol was the antimicrobialagent (López et al., 2005).Guynot et al. (2003) proved that the volatile fractions of c<strong>in</strong>namon leaf,clove, bay (Laurus nobilis), lemongrass and thyme (Thymus vulgaris) showedpotential antifungal activity aga<strong>in</strong>st A. flavus and A. niger.In vitro assays for the <strong>in</strong>hibition of mycotox<strong>in</strong> productionSpecies <strong>in</strong> Aspergillus section Flavi, ma<strong>in</strong>ly A. flavus and A. parasiticus areamong the most commonly occurr<strong>in</strong>g spoilage fungi. Some stra<strong>in</strong>s of thesespecies have the ability to produce aflatox<strong>in</strong>s. These fungi <strong>in</strong>vade agriculturalcommodities such as corn, peanuts and cottonseed, and herbal drugs,the result<strong>in</strong>g contam<strong>in</strong>ation with aflatox<strong>in</strong> often mak<strong>in</strong>g these pro ducts unfitfor consumption. Moreover, these mycotox<strong>in</strong>s are considered carc<strong>in</strong>ogenicsubstances and their presence is a health concern, so their control is one ofthe aims <strong>in</strong> order to obta<strong>in</strong> safe <strong>products</strong>. Little attention has been paid, however,to the efficacy of essential oils <strong>in</strong> <strong>in</strong>hibit<strong>in</strong>g aflatox<strong>in</strong> production.Recently, work has been carried out to study the effect of these <strong>products</strong> asanti-aflatoxigenic agents.

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