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      Crowdsourcing natural products discovery to access uncharted dimensions of fungal metabolite diversity.

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          Abstract

          A fundamental component for success in drug discovery is the ability to assemble and screen compounds that encompass a broad swath of biologically relevant chemical-diversity space. Achieving this goal in a natural-products-based setting requires access to a wide range of biologically diverse specimens. For this reason, we introduced a crowdsourcing program in which citizen scientists furnish soil samples from which new microbial isolates are procured. Illustrating the strength of this approach, we obtained a unique fungal metabolite, maximiscin, from a crowdsourced Alaskan soil sample. Maximiscin, which exhibits a putative combination of polyketide synthase (PKS), non-ribosomal peptide synthetase (NRPS), and shikimate pathway components, was identified as an inhibitor of UACC-62 melanoma cells (LC50=0.93 μM). The metabolite also exhibited efficacy in a xenograft mouse model. These results underscore the value of building cooperative relationships between research teams and citizen scientists to enrich drug discovery efforts.

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          Author and article information

          Journal
          Angew. Chem. Int. Ed. Engl.
          Angewandte Chemie (International ed. in English)
          1521-3773
          1433-7851
          Jan 13 2014
          : 53
          : 3
          Affiliations
          [1 ] Department of Chemistry and Biochemistry, Stephenson Life Sciences Research Center, University of Oklahoma, 101 Stephenson Parkway Norman, OK 73019-5251 (USA); Natural Products Discovery Group and Institute for Natural Products Applications and Research Technologies, University of Oklahoma (USA).
          Article
          NIHMS547952
          10.1002/anie.201306549
          24285637
          85d0a4fe-a115-49ce-bb61-7170189c1c96
          Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
          History

          antitumor agents,biosynthesis,crowdsourcing,drug discovery,epigenetics

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