Discovery and Biosynthesis of Celluxanthenes, Antibacterial Arylpolyene Alkaloids From Diverse Cellulose‐Degrading Anaerobic Bacteria
Abstract
Abstract Cellulose degradation by anaerobic bacteria plays an eminent role in the global carbon cycle and is a critical step in biofuel production. The anaerobic thermophile Clostridium thermocellum (now: Acetivibrio thermocellus ) is particularly efficient at breaking down biomass and produces a “yellow affinity substance” (YAS), a pigment that has been implicated in signaling and conferring higher affinity of the cellulosome to YAS‐loaded cellulose. However, the nature and biosynthetic origin of YAS have remained elusive. Here, we show by isolation and structure elucidation that YAS is a complex of unusual arylpolyene alkaloids (celluxanthenes). Stable isotope labeling experiments reveal all biosynthetic building blocks for celluxanthene assembly. Through a targeted gene deletion, we identify the celluxanthene ( cex ) biosynthesis gene cluster and propose a biosynthetic model in which an arylpolyene generated by an iterative type I polyketide synthase (PKS) undergoes a head‐to‐head fusion with a tryptophan‐derived ketoacid to form a tetronate. Genome mining and metabolic profiling revealed that diverse cellulolytic anaerobes harbor cex gene loci and produce celluxanthene congeners. Celluxanthenes show antibiotic activity against Gram‐positive bacteria including clinically relevant strains. This study solves the long‐standing enigma surrounding the nature of YAS and lays the groundwork for elucidating the precise biological roles of these intricate pigments.
Article Details
Authors (10)
Keishi Ishida
Dept. of Biomolecular Chemistry Leibniz Institute for Natural Product Research and Infection Biology Jena Germany
Jana Krabbe
Department of Biomolecular Chemistry Leibniz Institute for Natural Product Research and Infection Biology (Leibniz‐HKI) Beutenbergstraße 11a 07745 Jena Germany
Philippe R. Meisinger
Department of Biomolecular Chemistry Leibniz Institute for Natural Product Research and Infection Biology (Leibniz‐HKI) Beutenbergstraße 11a 07745 Jena Germany
Gulimila Shabuer
Department of Biomolecular Chemistry Leibniz Institute for Natural Product Research and Infection Biology (Leibniz‐HKI) Beutenbergstraße 11a 07745 Jena Germany
Sebastian Schieferdecker
Department of Biomolecular Chemistry Leibniz Institute for Natural Product Research and Infection Biology (Leibniz‐HKI) Beutenbergstraße 11a 07745 Jena Germany
Michael Cyrulies
BioPilot Plant, Leibniz Institute for Natural Product Research and Infection Biology Leibniz‐HKI 07745 Jena Germany
Cedric Tank
BioPilot Plant, Leibniz Institute for Natural Product Research and Infection Biology Leibniz‐HKI 07745 Jena Germany
Emma Barnes
Department of Biomolecular Chemistry Leibniz Institute for Natural Product Research and Infection Biology (Leibniz‐HKI) Beutenbergstraße 11a 07745 Jena Germany
Christian Paetz
Research Group Biosynthesis/NMR, Max Planck Institute for Chemical Ecology
Christian Hertweck
Department of Biomolecular Chemistry