O-Methylsterigmatocystin

O-Methylsterigmatocystin is a lipid of Polyketides (PK) class.

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There are no associated biomedical information in the current reference collection.

Current reference collection contains 136 references associated with O-Methylsterigmatocystin in LipidPedia. Due to lack of full text of references or no associated biomedical terms are recognized in our current text-mining method, we cannot extract any biomedical terms related to diseases, pathways, locations, functions, genes, lipids, and animal models from the associated reference collection.

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All references with O-Methylsterigmatocystin

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Authors Title Published Journal PubMed Link
pmid:
Lee LW et al. Function of native OmtA in vivo and expression and distribution of this protein in colonies of Aspergillus parasiticus. 2002 Appl. Environ. Microbiol. pmid:12406770
Meyers DM et al. Characterization of aflJ, a gene required for conversion of pathway intermediates to aflatoxin. 1998 Appl. Environ. Microbiol. pmid:9758789
Bhatnagar D et al. Identification of O-methylsterigmatocystin as an aflatoxin B1 and G1 precursor in Aspergillus parasiticus. 1987 Appl. Environ. Microbiol. pmid:3111363
Cleveland TE et al. Conversion of a new metabolite to aflatoxin B2 by Aspergillus parasiticus. 1987 Appl. Environ. Microbiol. pmid:3435144
Prieto R et al. Identification of aflatoxin biosynthesis genes by genetic complementation in an Aspergillus flavus mutant lacking the aflatoxin gene cluster. 1996 Appl. Environ. Microbiol. pmid:8967772
Prieto R and Woloshuk CP ord1, an oxidoreductase gene responsible for conversion of O-methylsterigmatocystin to aflatoxin in Aspergillus flavus. 1997 Appl. Environ. Microbiol. pmid:9143099
Jeenah MS and Dutton MF The conversion of sterigmatocystin to O-methylsterigmatocystin and aflatoxin B1 by a cell-free preparation. 1983 Biochem. Biophys. Res. Commun. pmid:6418171
Bhatnagar D and Cleveland TE Fate of the methyl group during the conversion of sterigmatocystin into O-methylsterigmatocystin and aflatoxin B1 by cell-free preparations of Aspergillus parasiticus. 1988 Biochimie pmid:3139090
Yoshinari T et al. Spiroethers of German chamomile inhibit production of aflatoxin G and trichothecene mycotoxin by inhibiting cytochrome P450 monooxygenases involved in their biosynthesis. 2008 FEMS Microbiol. Lett. pmid:18492060

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