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   <dc:title>A new class of fatty acid allene oxide formed by the DOX-P450 fusion proteins of human and plant pathogenic fungi, C. immitis and Z. tritic</dc:title>
   <dc:creator>Oliw, Ernst H.</dc:creator>
   <dc:creator>Aragó Belenguer, Marc</dc:creator>
   <dc:creator>Chen, Yang</dc:creator>
   <dc:creator>Jernerén, Fredrik</dc:creator>
   <dc:subject>Metabolisme dels lípids</dc:subject>
   <dc:subject>Enzims</dc:subject>
   <dc:subject>Dioxines</dc:subject>
   <dc:subject>Proteïnes</dc:subject>
   <dc:subject>Fongs patògens</dc:subject>
   <dc:subject>Lipid metabolism</dc:subject>
   <dc:subject>Enzymes</dc:subject>
   <dc:subject>Dioxins</dc:subject>
   <dc:subject>Proteins</dc:subject>
   <dc:subject>Pathogenic fungi</dc:subject>
   <dcterms:abstract>Linoleate dioxygenase-cytochrome P450 (DOX-CYP) fusion enzymes are common in pathogenic fungi. The DOX domains form hydroperoxy metabolites of 18:2n-6, which can be transformed by the CYP domains to 1,2- or 1,4-diols, epoxy alcohols, or to allene oxides. We have characterized two novel allene oxide synthases (AOSs), namely, recombinant 8R-DOX-AOS of Coccidioides immitis (causing valley fever) and 8S-DOX-AOS of Zymoseptoria tritici (causing septoria tritici blotch of wheat). The 8R-DOX-AOS oxidized 18:2n-6 sequentially to 8R-hydroperoxy-9Z,12Z-octadecadienoic acid (8R-HPODE) and to an allene oxide, 8R(9)-epoxy-9,12Z-octadecadienoic acid, as judged from the accumulation of the α-ketol, 8S-hydroxy-9-oxo-12Z-octadecenoic acid. The 8S-DOX-AOS of Z. tritici transformed 18:2n-6 sequentially to 8S-HPODE and to an α-ketol, 8R-hydroxy-9-oxo-12Z-octadecenoic acid, likely formed by hydrolysis of 8S(9)-epoxy-9,12Z-octadecadienoic acid. The 8S-DOX-AOS oxidized [8R-2H]18:2n-6 to 8S-HPODE with retention of the 2H-label, suggesting suprafacial hydrogen abstraction and oxygenation in contrast to 8R-DOX-AOS. Both enzymes oxidized 18:1n-9 and 18:3n-3 to α-ketols, but the catalysis of the 8R- and 8S-AOS domains differed. 8R-DOX-AOS transformed 9R-HPODE to epoxy alcohols, but 8S-DOX-AOS converted 9S-HPODE to an α-ketol (9-hydroxy-10-oxo-12Z-octadecenoic acid) and epoxy alcohols in a ratio of ∼1:2. Whereas all fatty acid allene oxides described so far have a conjugated diene impinging on the epoxide, the allene oxides formed by 8-DOX-AOS are unconjugated.</dcterms:abstract>
   <dcterms:issued>2018-10-09T11:53:41Z</dcterms:issued>
   <dcterms:issued>2018-10-09T11:53:41Z</dcterms:issued>
   <dcterms:issued>2016-08</dcterms:issued>
   <dcterms:issued>2018-10-09T11:53:41Z</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:relation>Reproducció del document publicat a: https://doi.org/10.1194/jlr.M068981</dc:relation>
   <dc:relation>Journal of Lipid Research, 2016, vol. 57, num. 8, p. 1518-1528</dc:relation>
   <dc:relation>https://doi.org/10.1194/jlr.M068981</dc:relation>
   <dc:rights>(c) American Society for Biochemistry and Molecular Biology, 2016</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>American Society for Biochemistry and Molecular Biology</dc:publisher>
   <dc:source>Articles publicats en revistes (Ciències Fisiològiques)</dc:source>
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