Screening for microorganisms that inhibit aflatoxin production from environments showed that inhibited aflatoxin production by . The inhibitory substance in the culture medium of was confirmed to be citrinin (CTN). RT-PCR analyses showed that CTN did not inhibit expressions of aflatoxin biosynthetic genes (, , and ) of , whereas feeding experiments using showed that CTN inhibited the in vivo conversion of dihydrosterigmatocystin to AFB·AFG. These results suggest that CTN inhibits a certain post-transcriptional step in aflatoxin biosynthesis. CTN in the culture medium of was found to be decreased or lost with time, suggesting that a certain metabolite produced by is the cause of the CTN decrease; we then purified, characterized, and then analyzed the substance. Physico-chemical analyses confirmed that the metabolite causing a decrease in CTN fluorescence was kojic acid (KA) and the resulting product was identified as a novel substance: (1,3,4)-3,4-dihydro-6,8-dihydroxy-1-(3-hydroxy-6-(hydroxymethyl)-4-oxo-4-pyran-2-yl)-3,4,5-trimethyl-1-isochromene-7-carboxylic acid, which was named "CTN-KA adduct". Our examination of the metabolites' toxicities revealed that unlike CTN, the CTN-KA adduct did not inhibit aflatoxin production by . These results indicate that CTN's toxicity was alleviated with KA by converting CTN to the CTN-KA adduct.

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