An Unprecedented Cyclization Mechanism in the Biosynthesis of Carbazole Alkaloids in Streptomyces. (13th August 2019)

• Record Type: Journal Article
• Authors: Kobayashi, Masaya; Tomita, Takeo; Shin‐ya, Kazuo; Nishiyama, Makoto; Kuzuyama, Tomohisa
• Is Part Of: Angewandte Chemie. Volume 131:Number 38(2019)
• Page Start: 13483
• Page End: 13487
• Publication Date: 2019-08-13
• Subjects: Biosynthese -- Carbazole -- Cyclisierung -- Enzyme -- Proteinstruktur; Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.201906864
• Languages: English
• ISSNs: 0044-8249

Abstract

Abstract: Carquinostatin A (CQS), a potent neuroprotective substance, is a unique carbazole alkaloid with both an ortho ‐quinone function and an isoprenoid moiety. We identified the entire gene cluster responsible for CQS biosynthesis in Streptomyces exfoliatus through heterologous production of CQS and gene deletion. Biochemical characterization of seven CQS biosynthetic gene products (CqsB1–7) established the total biosynthetic pathway of CQS. Reconstitution of CqsB1 and CqsB2 showed that the synthesis of the carbazole skeleton involves CqsB1‐catalyzed decarboxylative condensation of an α‐hydroxyl‐β‐keto acid intermediate with 3‐hydroxybutyryl‐ACP followed by CqsB2‐catalyzed oxidative cyclization. Based on crystal structures and mutagenesis‐based biochemical assays, a detailed mechanism for the unique deprotonation‐initiated cyclization catalyzed by CqsB2 is proposed. Finally, analysis of the substrate specificity of the biosynthetic enzymes led to the production of novel carbazoles. Abstract : Die glorreichen Sieben : Der gesamte Biosynthesepfad des Carbazolalkaloids Carquinostatin A (CQS) wurde durch die biochemische Charakterisierung der sieben biosynthetischen CQS‐Genprodukte CqsB1–7 aufgeklärt. Die Kristallstruktur von CqsB2, das den Cyclisierungsschritt katalysiert, liefert mechanistische Einblicke in die komplizierten Reaktionen in der enzymatischen Synthese von Carbazolen.