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Here, we report that <jats:styled-content style=\"fixed-case\"><jats:italic>ugt73b3<\/jats:italic><\/jats:styled-content>, <jats:styled-content style=\"fixed-case\"><jats:italic>ugt73b5<\/jats:italic><\/jats:styled-content> and <jats:styled-content style=\"fixed-case\"><jats:italic>ugt73b3 ugt73b5<\/jats:italic> T\u2010DNA<\/jats:styled-content> insertion mutants exhibited an accumulation of reactive oxygen species (<jats:styled-content style=\"fixed-case\">ROS<\/jats:styled-content>), an enhanced cell death during the <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content> to <jats:styled-content style=\"fixed-case\"><jats:italic>Pst\u2010AvrRpm1<\/jats:italic><\/jats:styled-content>, whereas glutathione levels increased in the single mutants. <jats:italic>In silico<\/jats:italic> analyses indicate that <jats:styled-content style=\"fixed-case\"><jats:italic>UGT73B3<\/jats:italic><\/jats:styled-content> and <jats:styled-content style=\"fixed-case\"><jats:italic>UGT73B5<\/jats:italic><\/jats:styled-content> belong to the <jats:italic>early salicylic acid (<jats:styled-content style=\"fixed-case\">SA<\/jats:styled-content>)<\/jats:italic>\u2010<jats:italic>induced<\/jats:italic> genes whose pathogen\u2010induced expression is co\u2010regulated with genes related to cellular redox homeostasis and general detoxification. Analyses of metabolic alterations in <jats:styled-content style=\"fixed-case\"><jats:italic>ugt<\/jats:italic><\/jats:styled-content> mutants reveal modification of <jats:styled-content style=\"fixed-case\">SA<\/jats:styled-content> and scopoletin contents which correlate with redox perturbation, and indicate quantitative modifications in the pattern of tryptophan\u2010derived <jats:styled-content style=\"fixed-case\">SM<\/jats:styled-content> accumulation after <jats:styled-content style=\"fixed-case\"><jats:italic>Pst\u2010AvrRpm1<\/jats:italic><\/jats:styled-content> inoculation. Our data suggest that <jats:styled-content style=\"fixed-case\"><jats:roman>UGT73B3<\/jats:roman><\/jats:styled-content> and <jats:styled-content style=\"fixed-case\"><jats:roman>UGT73B5<\/jats:roman><\/jats:styled-content> participate in regulation of redox status and general detoxification of <jats:styled-content style=\"fixed-case\">ROS<\/jats:styled-content>\u2010reactive <jats:styled-content style=\"fixed-case\">SMs<\/jats:styled-content> during the <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content> to <jats:styled-content style=\"fixed-case\"><jats:italic>Pst\u2010AvrRpm1<\/jats:italic><\/jats:styled-content>, and that decreased resistance to <jats:styled-content style=\"fixed-case\"><jats:italic>Pst\u2010AvrRpm1<\/jats:italic><\/jats:styled-content> in <jats:styled-content style=\"fixed-case\"><jats:italic>ugt<\/jats:italic><\/jats:styled-content> mutants is tightly linked to redox 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