<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Matern, Andreas</dc:creator>
  <dc:creator>Böttcher, Christoph</dc:creator>
  <dc:creator>Eschen-Lippold, Lennart</dc:creator>
  <dc:creator>Westermann, Bernhard</dc:creator>
  <dc:creator>Smolka, Ulrike</dc:creator>
  <dc:creator>Döll, Stefanie</dc:creator>
  <dc:creator>Trempel, Fabian</dc:creator>
  <dc:creator>Aryal, Bibek</dc:creator>
  <dc:creator>Scheel, Dierk</dc:creator>
  <dc:creator>Geisler, Markus</dc:creator>
  <dc:creator>Rosahl, Sabine</dc:creator>
  <dc:date>2019-04-26</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Nonhost resistance of Arabidopsis thaliana against Phytophthora infestans, a  filamentous eukaryotic microbe and the causal agent of potato late blight, is based on  a multilayered defense system. Arabidopsis thaliana controls pathogen entry through  the penetration-resistance genes PEN2 and PEN3, encoding an atypical myrosinase  and an ABC transporter, respectively, required for synthesis and export of unknown  indole compounds. To identify pathogen-elicited leaf surface metabolites and further  unravel nonhost resistance in Arabidopsis, we performed untargeted metabolite  profiling by incubating a P. infestans zoospore suspension on leaves of WT or pen3  mutant Arabidopsis plants. Among the plant-secreted metabolites, 4-methoxyindol-3- yl-methanol and S-(4-methoxy-indol-3-yl-methyl) cysteine were detected in spore  suspensions recollected from WT plants, but at reduced levels from the pen3 mutant  plants. In both whole-cell and microsome-based assays, 4-methoxyindol-3-yl- methanol was transported in a PEN3-dependent manner, suggesting that this  compound is a PEN3 substrate. The syntheses of both compounds were dependent  on functional PEN2 and phytochelatin synthase 1. None of these compounds inhibited  mycelial growth of P. infestans in vitro. Of note, exogenous application of 4- methoxyindol-3-yl methanol slightly elevated cytosolic Ca2+ levels and enhanced  callose deposition in hydathodes of seedlings treated with a bacterial pathogen- associated molecular pattern (PAMP), flagellin (flg22). Loss of flg22-induced callose  deposition in leaves of pen3 seedlings was partially reverted by the addition of 4- methoxyindol-3-yl methanol. In conclusion, we have identified a specific indole  compound that is a substrate for PEN3 and contributes to the plant defense response  against microbial pathogens.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/307898</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307898/files/gei_sat.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307898/files/gei_sat_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1074/jbc.RA119.007676</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Journal of Biological Chemistry. - 2019, vol. 294, no. 17, p. 6857–6870</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">A substrate of the ABC transporter PEN3 stimulates bacterial flagellin (flg22)-induced callose deposition in Arabidopsis thaliana</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
