Evidence map›Paper›PMID 40178295›Full record

ArticleAngewandte Chemie (International ed. in English)2025

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

Keishi Ishida, Jana Krabbe, Philippe R Meisinger, Gulimila Shabuer, Sebastian Schieferdecker, Michael Cyrulies, Cedric Tank, Emma Barnes, Christian Paetz, Christian Hertweck

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Keishi Ishida *Department of Biomolecular Chemistry, Leibniz Institute for Natural Product Research and Infection Biology (Leibniz-HKI), Beutenbergstraße 11a, 07745, 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 MeisingerDepartment of Biomolecular Chemistry, Leibniz Institute for Natural Product Research and Infection Biology (Leibniz-HKI), Beutenbergstraße 11a, 07745, Jena, Germany.
Gulimila ShabuerDepartment of Biomolecular Chemistry, Leibniz Institute for Natural Product Research and Infection Biology (Leibniz-HKI), Beutenbergstraße 11a, 07745, Jena, Germany.
Sebastian SchieferdeckerDepartment of Biomolecular Chemistry, Leibniz Institute for Natural Product Research and Infection Biology (Leibniz-HKI), Beutenbergstraße 11a, 07745, Jena, Germany.
Michael CyruliesBioPilot Plant, Leibniz Institute for Natural Product Research and Infection Biology, Leibniz-HKI, 07745, Jena, Germany.
Cedric TankBioPilot Plant, Leibniz Institute for Natural Product Research and Infection Biology, Leibniz-HKI, 07745, Jena, Germany.
Emma BarnesDepartment of Biomolecular Chemistry, Leibniz Institute for Natural Product Research and Infection Biology (Leibniz-HKI), Beutenbergstraße 11a, 07745, Jena, Germany.
Christian PaetzResearch Group Biosynthesis/NMR, Max Planck Institute for Chemical Ecology, 07745, Jena, Germany.
Christian HertweckDepartment of Biomolecular Chemistry, Leibniz Institute for Natural Product Research and Infection Biology (Leibniz-HKI), Beutenbergstraße 11a, 07745, Jena, Germany.

Funding

European Regional Development Fund (ERDF) (MassNat)European Research Council Advanced Grant ERC AdG 101141624 - AnoxyGen
6 · The paper itself

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.

Indexed as

Acetivibrio thermocellusAlkaloidsAnti-Bacterial AgentsBacteria, AnaerobicCelluloseAlkaloidsAnti-Bacterial AgentsCelluloseAlkaloidsBiosynthesisNatural ProductsPolyenesPolyketides

Identifiers

PMID40178295
PMCPMC12144888

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.