Angewandte Chemie International Edition · 2015 · 118 citations · 37 references
PharmacyBiochemistryMolecular BiologyBioorganic ChemistryMetabolic EngineeringNatural Product BiosynthesisCatalytic MechanismsFungal BiotechnologyFungal Natural Product BiosynthesisMetabolic Pathway EngineeringMicrobial Natural Product BiosynthesisTerpenoid BiosynthesisCationic CyclizationDiterpene BiosynthesisFungal Terpenoid BiosynthesisGene DisruptionOxidative Biosynthetic TransformationsOxidative Coupling ReactionsPenitrem Biosynthesis
Penitrem A is one of the most elaborated members of the fungal indole diterpenes. Two separate penitrem gene clusters were identified using genomic and RNA sequencing data, and 13 out of 17 transformations in the penitrem biosynthesis were elucidated by heterologous reconstitution of the relevant genes. These reactions involve 1) a prenylation-initiated cationic cyclization to install the bicyclo[3.2.0]heptane skeleton (PtmE), 2) a two-step P450-catalyzed oxidative processes forming the unique tricyclic penitrem skeleton (PtmK and PtmU), and 3) five sequential oxidative transformations (PtmKULNJ). Importantly, without conventional gene disruption, reconstitution of the biosynthetic machinery provided sufficient data to determine the pathway. It was thus demonstrated that the Aspergillus oryzae reconstitution system is a powerful method for studying the biosynthesis of complex natural products.
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Identification and nomenclature of the genus <i>Penicillium</i>
Cobus M. Visagie, Jos Houbraken, Jens C. Frisvad et al. · Studies in Mycology · 2014 · 902 citations · Full text
Life Sciences, Botany, Microbiology +17
Yi‐Ming Chiang, Edyta Szewczyk, Ashley D. Davidson et al. · Journal of the American Chemical Society · 2009 · 341 citations · Full text
Structure of a cephalosporin synthase
K. Valegård, Anke C. Terwisscha van Scheltinga, Matthew D. Lloyd et al. · Nature · 1998 · 338 citations