Ralfuranone thioether production by the plant pathogen Ralstonia solanacearum
Julia Pauly1, Dieter Spiteller, Jeanine Linz
1Friedrich-Schiller-Universität, Department of Pharmaceutical Biology at the Hans-Knöll-Institut, Beutenbergstrasse 11a, 07745 Jena (Germany).
Abstract:
Ralfuranones are aryl-substituted furanone secondary metabolites of the Gram-negative plant pathogen Ralstonia solanacearum. New sulfur-containing ralfuranone derivatives were identified, including the methyl thioether-containing ralfuranone D. Isotopic labeling in vivo, as well as headspace analyses of volatiles from R. solanacearum liquid cultures, established a mechanism for the transfer of an intact methylthio group from L-methionine or α-keto-γ-methylthiobutyric acid. The methylthio acceptor molecule ralfuranone I, a previously postulated biosynthetic intermediate in ralfuranone biosynthesis, was isolated and characterized by NMR. The highly reactive Michael acceptor system of this intermediate readily reacts with various thiols, including glutathione.
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