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ARS Home » Pacific West Area » Albany, California » Western Regional Research Center » Foodborne Toxin Detection and Prevention Research » Research » Publications at this Location » Publication #237082

Title: Biological activity and property of a biopesticide, Pichia anomala

Author
item Hua, Sui Sheng
item PARFITT, DAN - University Of California
item HOLTZ, BRENT - University Of California - Cooperative Extension Service
item Sarreal, Siov

Submitted to: Annual Meeting Horticultural Society
Publication Type: Abstract Only
Publication Acceptance Date: 2/15/2009
Publication Date: N/A
Citation: N/A

Interpretive Summary:

Technical Abstract: Aspergillus flavus is a globally distributed fungus. It causes disease in human and crop plants due to the production of numerous conidia dispersed by air movement and possibly by insects. The fungus is an economically important food contaminant because it produces the most potent natural carcinogenic compounds known as “aflatoxins” in agricultural crops and food products such as corn, peanuts, cotton and tree nuts. The genes directly involved in aflatoxin (AF) production have been identified in an 82kb cluster. Genetic studies of AF biosynthesis led to the cloning of 29 genes responsible for enzymatic reactions. Aflatoxin concentrations produced by different strains of A. flavus in the same nutrient medium vary greatly. Concentrations of aflatoxin in high producers can be 100 fold over the low producers. The factors underlying different levels of aflatoxin production among these strains are not well understood. We resorted to real time RT-PCR assays of genes involved in aflatoxin biosynthesis. The expression of several well defined genes, aflJ, aflR, omtB, pksA in these isolates was analyzed. The transcriptional levels of aflJ and pksA were higher in all the isolates of high aflatoxin production compared to strain CA18, a low produce of aflatoxin. Levels of omtB gene expression showed a wide variation among isolates. The AF cluster genes, aflJ, aflR, pksA, omtB was expressed at very high levels in afltoxingenic isolates in comparison to strains which do not produce aflatoxin (strain CA88). It appears that expression of pksA and aflJ positively influenced the quantity of aflatoxin production in various isolates found in food products.