Abstract

Resting cultures of Aspergillus parasiticus were treated with sorbic acid (200 ppm), Nα-palmitoyl-l-lysyl-l-lysine ethyl ester dihydrochloride (PLL) (300 ppm), nisin (30 ppm), nystatin (30 U/ml), dichlorvos (9 ppm), butylated hydroxyanisole (BHA) (30 ppm) and isoprothiolane (30 ppm). Incorporation of [14C]acetate into aflatoxins B1 and G1 by the mold in the presence of these antifungal agents was measured after 12 h of agitated incubation at 28°C. Nystatin and BHA effectively inhibited incorporation of the label into aflatoxin B1 (73.1 and 56.9%) and G1 (68.9 and 91.6%), respectively, whereas PLL and nisin, at the levels used, were less effective. Sorbic acid caused greater inhibition of de novo synthesis of aflatoxin B1 than of G1 while isoprothiolane exhibited the opposite effect. Because the compounds tested had dissimilar physical, chemical and antimicrobial properties, it is likely that they inhibited synthesis of aflatoxin by different mechanisms. Generally, inhibition of aflatoxin synthesis by the test chemicals under resting conditions was more pronounced than what was reported earlier when the same chemicals (at the same levels) were tested with growing cultures of the mold.

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