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OxaD: A Versatile Indolic Nitrone Synthase from the Marine-Derived Fungus Penicillium oxalicum F30.
Newmister, Sean A; Gober, Claire M; Romminger, Stelamar; Yu, Fengan; Tripathi, Ashootosh; Parra, Lizbeth Lorena L; Williams, Robert M; Berlinck, Roberto G S; Joullié, Madeleine M; Sherman, David H.
Afiliación
  • Gober CM; Department of Chemistry, University of Pennsylvania , 231 South 34th Street, Philadelphia, Pennsylvania 19104, United States.
  • Parra LL; Instituto de Química de São Carlos, Universidade de São Paulo , CP 780, São Carlos, São Paulo CEP 13560-970, Brazil.
  • Williams RM; Department of Chemistry, Colorado State University , Fort Collins, Colorado 80523, United States.
  • Berlinck RG; University of Colorado Cancer Center , Aurora, Colorado 80045, United States.
  • Joullié MM; Instituto de Química de São Carlos, Universidade de São Paulo , CP 780, São Carlos, São Paulo CEP 13560-970, Brazil.
  • Sherman DH; Department of Chemistry, University of Pennsylvania , 231 South 34th Street, Philadelphia, Pennsylvania 19104, United States.
J Am Chem Soc ; 138(35): 11176-84, 2016 09 07.
Article en En | MEDLINE | ID: mdl-27505044
ABSTRACT
Indole alkaloids are a diverse class of natural products known for their wide range of biological activities and complex chemical structures. Rarely observed in this class are indolic nitrones, such as avrainvillamide and waikialoid, which possess potent bioactivities. Herein the oxa gene cluster from the marine-derived fungus Penicillium oxalicum F30 is described along with the characterization of OxaD, a flavin-dependent oxidase that generates roquefortine L, a nitrone-bearing intermediate in the biosynthesis of oxaline. Nitrone functionality in roquefortine L was confirmed by spectroscopic methods and 1,3-dipolar cycloaddition with methyl acrylate. OxaD is a versatile biocatalyst that converts an array of semisynthetic roquefortine C derivatives bearing indoline systems to their respective nitrones. This work describes the first implementation of a nitrone synthase as a biocatalyst and establishes a novel platform for late-stage diversification of a range of complex natural products.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Oxigenasas / Penicillium / Indoles / Óxidos de Nitrógeno Idioma: En Revista: J Am Chem Soc Año: 2016 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Oxigenasas / Penicillium / Indoles / Óxidos de Nitrógeno Idioma: En Revista: J Am Chem Soc Año: 2016 Tipo del documento: Article