Bioprospecting for Trichothecene 3-O-Acetyltransferases in the Fungal GenusFusariumYields Functional Enzymes with Different Abilities To Modify the Mycotoxin Deoxynivalenol
ABSTRACTThe trichothecene mycotoxin deoxynivalenol (DON) is a common contaminant of small grains, such as wheat and barley, in the United States. New strategies to mitigate the threat of DON need to be developed and implemented. TRI101 and TRI201 are trichothecene 3-O-acetyltransferases that are able to modify DON and reduce its toxicity. Recent work has highlighted differences in the activities of TRI101 from two different species ofFusarium(F. graminearumandF. sporotrichioides), but little is known about the relative activities of TRI101/TRI201 enzymes produced by other species ofFusarium. We clonedTRI101orTRI201genes from seven different species ofFusariumand found genetic identity between sequences ranging from 66% to 98%.In vitrofeeding studies using transformed yeast showed that all of the TRI101/TRI201 enzymes tested were able to acetylate DON; conversion of DON to 3-acetyl-deoxynivalenol (3ADON) ranged from 50.5% to 100.0%, depending on theFusariumspecies from which the gene originated. A time course assay showed that the rate of acetylation varied from species to species, with the gene fromF. sporotrichioideshaving the lowest rate. Steady-state kinetic assays using seven purified enzymes produced catalytic efficiencies for DON acetylation ranging from 6.8 × 104M−1·s−1to 4.7 × 106M−1·s−1. Thermostability measurements for the seven orthologs ranged from 37.1°C to 43.2°C. Extended sequence analysis of portions ofTRI101/TRI201from 31 species ofFusarium(including known trichothecene producers and nonproducers) suggested that other members of the genus may contain functionalTRI101/TRI201genes, some with the potential to outperform those evaluated in the present study.