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Regioselective Halogenation of Lavanducyanin by a Site-Selective Vanadium-Dependent Chloroperoxidase

Jackson T. Baumgartner, Shaun M. K. McKinnie

2024Organic Letters15 citationsDOIOpen Access PDF

Abstract

High Resolution Image Download MS PowerPoint Slide Halogenated phenazine meroterpenoids are a structurally unusual family of marine actinobacterial natural products that exhibit antibiotic, antibiofilm, and cytotoxic bioactivities. Despite a lack of established phenazine halogenation biochemistry, genomic analysis of Streptomyces sp. CNZ-289, a prolific lavanducyanin and C2-halogenated derivative producer, suggested the involvement of vanadium-dependent haloperoxidases. We subsequently discovered lavanducyanin halogenase (LvcH), characterized it in vitro as a regioselective vanadium-dependent chloroperoxidase, and applied it in late-stage chemoenzymatic synthesis.

Topics & Concepts

PhenazineHalogenationChemistryRegioselectivityVanadiumCombinatorial chemistryOrganic chemistryStereochemistryCatalysisVanadium and Halogenation ChemistryMarine Sponges and Natural ProductsOxidative Organic Chemistry Reactions
Regioselective Halogenation of Lavanducyanin by a Site-Selective Vanadium-Dependent Chloroperoxidase | Litcius