Discovery and Biosynthesis of Celluxanthenes, Antibacterial Arylpolyene Alkaloids From Diverse Cellulose‐Degrading Anaerobic Bacteria

K Keishi Ishida (Dept. of Biomolecular Chemistry Leibniz Institute for Natural Product Research and Infection Biology Jena Germany) J Jana Krabbe (Department of Biomolecular Chemistry Leibniz Institute for Natural Product Research and Infection Biology (Leibniz‐HKI) Beutenbergstraße 11a 07745 Jena Germany) P Philippe R. Meisinger (Department of Biomolecular Chemistry Leibniz Institute for Natural Product Research and Infection Biology (Leibniz‐HKI) Beutenbergstraße 11a 07745 Jena Germany) G Gulimila Shabuer (Department of Biomolecular Chemistry Leibniz Institute for Natural Product Research and Infection Biology (Leibniz‐HKI) Beutenbergstraße 11a 07745 Jena Germany) S Sebastian Schieferdecker (Department of Biomolecular Chemistry Leibniz Institute for Natural Product Research and Infection Biology (Leibniz‐HKI) Beutenbergstraße 11a 07745 Jena Germany) M Michael Cyrulies (BioPilot Plant, Leibniz Institute for Natural Product Research and Infection Biology Leibniz‐HKI 07745 Jena Germany) C Cedric Tank (BioPilot Plant, Leibniz Institute for Natural Product Research and Infection Biology Leibniz‐HKI 07745 Jena Germany) E Emma Barnes (Department of Biomolecular Chemistry Leibniz Institute for Natural Product Research and Infection Biology (Leibniz‐HKI) Beutenbergstraße 11a 07745 Jena Germany) C Christian Paetz (Research Group Biosynthesis/NMR, Max Planck Institute for Chemical Ecology) C Christian Hertweck (Department of Biomolecular Chemistry)

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

Volume / Issue Vol. 64, Issue 24
Published June 10, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

K

Keishi Ishida

Dept. of Biomolecular Chemistry Leibniz Institute for Natural Product Research and Infection Biology Jena Germany

J

Jana Krabbe

Department of Biomolecular Chemistry Leibniz Institute for Natural Product Research and Infection Biology (Leibniz‐HKI) Beutenbergstraße 11a 07745 Jena Germany

P

Philippe R. Meisinger

Department of Biomolecular Chemistry Leibniz Institute for Natural Product Research and Infection Biology (Leibniz‐HKI) Beutenbergstraße 11a 07745 Jena Germany

G

Gulimila Shabuer

Department of Biomolecular Chemistry Leibniz Institute for Natural Product Research and Infection Biology (Leibniz‐HKI) Beutenbergstraße 11a 07745 Jena Germany

S

Sebastian Schieferdecker

Department of Biomolecular Chemistry Leibniz Institute for Natural Product Research and Infection Biology (Leibniz‐HKI) Beutenbergstraße 11a 07745 Jena Germany

M

Michael Cyrulies

BioPilot Plant, Leibniz Institute for Natural Product Research and Infection Biology Leibniz‐HKI 07745 Jena Germany

C

Cedric Tank

BioPilot Plant, Leibniz Institute for Natural Product Research and Infection Biology Leibniz‐HKI 07745 Jena Germany

E

Emma Barnes

Department of Biomolecular Chemistry Leibniz Institute for Natural Product Research and Infection Biology (Leibniz‐HKI) Beutenbergstraße 11a 07745 Jena Germany

C

Christian Paetz

Research Group Biosynthesis/NMR, Max Planck Institute for Chemical Ecology

C

Christian Hertweck

Department of Biomolecular Chemistry