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      Diels–Alder Reactions During the Biosynthesis of Sorbicillinoids

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          Abstract

          The sorbicillinoids are a class of biologically active and structurally diverse fungal polyketides arising from sorbicillin. Through co‐expression of sorA, sorB, sorC, and sorD from Trichoderma reesei QM6a, the biosynthetic pathway to epoxysorbicillinol and dimeric sorbicillinoids, which resemble Diels–Alder‐like and Michael‐addition‐like products, was reconstituted in Aspergillus oryzae NSAR1. Expression and feeding experiments demonstrated the crucial requirement of the flavin‐dependent monooxygenase SorD for the formation of dimeric sorbicillinoids, hybrid sorbicillinoids, and epoxysorbicillinol in vivo. In contrast to prior reports, SorD catalyses neither the oxidation of 2′,3′‐dihydrosorbicillin to sorbicillin nor the oxidation of sorbicillinol to oxosorbicillinol. This is the first report that both the intermolecular Diels–Alder and Michael dimerization reactions, as well as the epoxidation of sorbicillinol are catalysed in vivo by SorD.

          Abstract

          One for all: The biosynthetic pathway to dimeric sorbicillinoids and epoxysorbicillinol was reconstituted in Aspergillus oryzae NSAR1. Expression and feeding experiments demonstrated that the flavin‐dependent monooxygenase SorD catalyzes epoxidation, Diels–Alder addition, and Michael addition reactions in vivo.

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          Author and article information

          Contributors
          elizabeth.skellam@oci.uni-hannover.de
          Journal
          Angew Chem Int Ed Engl
          Angew. Chem. Int. Ed. Engl
          10.1002/(ISSN)1521-3773
          ANIE
          Angewandte Chemie (International Ed. in English)
          John Wiley and Sons Inc. (Hoboken )
          1433-7851
          1521-3773
          04 February 2020
          27 March 2020
          : 59
          : 14 ( doiID: 10.1002/anie.v59.14 )
          : 5816-5822
          Affiliations
          [ 1 ] Institute for Organic Chemistry and BMWZ Leibniz University of Hannover Schneiderberg 38 30167 Hannover Germany
          [ 2 ] Biochemistry Department Faculty of Science Zagazig University Zagazig Ash Sharqia Governorate 44519 Egypt
          Author information
          http://orcid.org/0000-0003-4087-0708
          Article
          ANIE201915486
          10.1002/anie.201915486
          7154774
          31943627
          97032261-2912-472d-b3d1-2e4ccfab31c0
          © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.

          This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

          History
          : 04 December 2019
          Page count
          Figures: 9, Tables: 0, References: 42, Pages: 7, Words: 0
          Funding
          Funded by: Deutsche Forschungsgemeinschaft , open-funder-registry 10.13039/501100001659;
          Award ID: INST 187/621-1
          Award ID: INST 187/686-1
          Award ID: CO 1328/5-1
          Funded by: Ministry of Higher Education , open-funder-registry 10.13039/501100002385;
          Award ID: 158473
          Categories
          Research Article
          Research Articles
          Biosynthesis
          Custom metadata
          2.0
          March 27, 2020
          Converter:WILEY_ML3GV2_TO_JATSPMC version:5.8.0 mode:remove_FC converted:14.04.2020

          Chemistry
          biosynthesis,diels–alder reactions,flavin-dependent monooxygenases,polyketides,sorbicillinoids

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