Title of article :
Effect of Curcumin on Aspergillus parasiticus Growth and Expression ofMajor Genes Involved in the Early and Late Stages of Aflatoxin Biosynthesis
Author/Authors :
Jahanshiri, Z Dept. of 1 Mycology and 2 Biochemistry - Faculty of Medical Sciences, Tarbiat Modares University, Tehran , Shams-Ghahfarokhi, M Dept. of 1 Mycology and 2 Biochemistry - Faculty of Medical Sciences, Tarbiat Modares University, Tehran , Allameh, A Dept. of 1 Mycology and 2 Biochemistry - Faculty of Medical Sciences - Tarbiat Modares University, Tehran , Razzaghi-Abyaneh, M Dept. of Mycology - Pasteur Institute of Iran, Tehran
Abstract :
Background: The effect of curcumin as a natural safe compound with different biological activities was examined
on fungal growth and aflatoxin production in Aspergillus parasiticus NRRL 2999.
Methods: The fungus was cultured in presence of serial two-fold concentrations of curcumin (125-2000 μg/ml)
in yeast extract sucrose broth for 3 days at 28°C. Mycelia dry weight was determined as an index of fungal
growth, while aflatoxin production was assessed by high performance liquid chromatography (HPLC). The expression
of ver-1, nor-1, pksA, omtA and aflR genes in aflatoxin biosynthetic pathway was evaluated by real time
PCR.
Results: Curcumin strongly inhibited aflatoxin B1 production in the range of 26.6 to 94.9% by serial two-fold
concentrations from 125 to 2000 μg/ml. Fungal growth was also inhibited by the compound in the range of 34.0
to 60.8%. Analysis of the expression of aflatoxin pathway genes by real time PCR showed that curcumin inhibited
the expression of ver-1, nor-1, pksA, omtA and aflR genes at concentrations of 250 and 1000 μg/ml. In concentration
of 1000 μg/ml, gene expression was reduced by 31.3%, 44.6%, 57.1% 110.9% and 286.7% accordingly.
Reduction in the expression of aflatoxin biosynthesis genes was significant only for aflR. In ferric reducing
ability of plasma (FRAP) assay, curcumin showed strong antioxidant activity at all concentrations tested.
Conclusion: Curcumin may be employed successfully as a good candidate in controlling of toxigenic fungal
growth on food and feed and subsequent contamination with aflatoxins in practice.
Keywords :
Aflatoxin , Aspergillus parasiticus , Curcumin , Gene expression , FRAP , Real-Time PCR
Journal title :
Astroparticle Physics