EFS12- Book of abstracts - Contact
EFS12- Book of abstracts - Contact
EFS12- Book of abstracts - Contact
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SESSION 6: FUTURE CHALLENGE FOR EUROPE AND WORLDWIDE<br />
P137 - A role for carboxylesterases in the chemotype<br />
shift in F. graminearum populations?<br />
C. Schmeitzl 1 , F. Berthiller 2 , M. Shams 2 , J. A. Torres-Acosta 1 , G.<br />
Wiesenberger 1 , M. Lemmens 3 , P. Spörhase 1 , G. Adam 1<br />
University <strong>of</strong> Natural Resources and Life Sciences (BOKU); 1 Department <strong>of</strong> Applied Genetics and Cell<br />
Biology, A-1190 Vienna, Austria; 2 Department for Agrobiotechnology, IFA Tulln, Center <strong>of</strong> Analytical<br />
Chemistry; 3 Biotechnology in Plant Production, A-3430 Tulln, Austria<br />
E-mail: clemens.schmeitzl@boku.ac.at<br />
A shift in F. graminearum populations, favoring the 3-Acetyl-DON (3-ADON) over<br />
the 15-Acetyl-DON (15–ADON) chemotype, has been observed in many parts <strong>of</strong><br />
the world. In a wheat germ coupled in vitro transcription and translation system<br />
the order <strong>of</strong> toxicity was determined to be 15 ADON > DON >>> 3-ADON. So it is<br />
unclear why maintaining the 3-acetyl-group (which is used for self-protection<br />
during toxin synthesis <strong>of</strong> Fusarium) could be <strong>of</strong> advantage. Our hypothesis is that<br />
the C3-acetyl group prevents detoxification <strong>of</strong> DON to DON-3-O-glucoside by<br />
cytosolic plant UDP-glucosyltransferases. There is evidence that this is the mode<br />
<strong>of</strong> action <strong>of</strong> the now widely deployed resistance gene Fhb1 <strong>of</strong> wheat (Lemmens et<br />
al. 2005). Yet, the toxin has to be deacetylated eventually, to be able to interact<br />
with the ribosomal target. The deacetylation reactions are not only catalyzed by<br />
seemingly cell surface associated extracellular Fusarium Tri8 protein but also by<br />
currently uncharacterized plant carboxylesterases. Deacetylation <strong>of</strong> 3-ADON was<br />
observed in different tissues <strong>of</strong> Arabidopsis thaliana and the monocot model<br />
system Brachypodium distachyon, and in crop plants like wheat and maize.<br />
Especially wheat ears can efficiently deacetylate 3-ADON into DON. Based on<br />
sequence similarity with the carboxylesterase gene family <strong>of</strong> A. thaliana, we have<br />
identified candidate genes in B. distachyon. The cellular localization <strong>of</strong> the gene<br />
products is unknown, but some seem to be localized to the endoplasmatic<br />
reticulum (ER) based on bioinformatics tools. If deacetylation takes place in the<br />
ER, the released DON (protected there from cytosolic UGTs) might preferentially<br />
target ribosomes at the rough ER. Some <strong>of</strong> the candidate Brachypodium<br />
carboxylesterase genes were found to be induced upon 3-ADON treatment. We<br />
have started to test the carboxylesterase activity by expressing candidate genes<br />
in yeast and performing in vivo feeding assays.<br />
Keywords: Fusarium, carboxylesterase, plant pathogen interaction<br />
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