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Appl. Environ. Microbiol., Feb 1996, 353-359, Vol 62, No. 2
SP McCormick, TM Hohn and AE Desjardins
An acetyltransferase gene (Tri3) was isolated from Fusarium
sporotrichioides by complementation of a previously identified Tri3- mutant
and shown to be closely linked to three other trichothecene biosynthetic
pathway genes. Comparison of the Tri3 sequence with its cDNA revealed the
presence of four introns. The Tri3 cDNA contains a 1,539-bp open reading
frame that encodes a protein with a molecular mass of 57,418 Da. Regulation
of Tri3 transcription in liquid cultures appeared identical to that of
other trichothecene pathway genes. Disruption of the Tri3 gene resulted in
the accumulation of deacetylated calonectrins rather than T-2 toxin. The
results of whole- cell feeding experiments with Tri3- strains suggested
that 15-O- acetylation is blocked. Cell-free feeding experiments confirmed
that Tri3- strains are able to acetylate a trichothecene C-3 hydroxyl group
but are unable to acetylate a trichothecene C-15 hydroxyl group. Our
results show that Tri3 encodes an acetyltransferase that converts 15-
decalonectrin to calonectrin.
Copyright © 1996, American Society for Microbiology
Isolation and characterization of Tri3, a gene encoding 15-O- acetyltransferase from Fusarium sporotrichioides
Mycotoxin Research Unit, National Center for Agricultural Utilization Research, Peoria, Illinois 61604, USA. mccormsp@ncaur1.ncaur.gov
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