Evidence map›Paper›PMID 42892638›Full record

ArticleCommunications chemistry2026

Targeted pathway mining reveals novel modified hexapeptides from the demiguisin family.

Tanya Decker, Marie Dayras, Lena Schweizer, Sari Rasheed, Franziska Fries, Bulisa Iova, Kasun H Bodawatta, Knud Andreas Jønsson, Rolf Müller, Christine Beemelmanns

Abstract read
In one paragraph

Article in Communications chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Tanya DeckerHelmholtz Institute for Pharmaceutical Research Saarland (HIPS), Saarbrücken, Germany.
Marie DayrasHelmholtz Institute for Pharmaceutical Research Saarland (HIPS), Saarbrücken, Germany.ORCID http://orcid.org/0000-0002-2598-7943
Lena SchweizerHelmholtz Institute for Pharmaceutical Research Saarland (HIPS), Saarbrücken, Germany.ORCID http://orcid.org/0000-0003-1296-5486
Sari RasheedHelmholtz Institute for Pharmaceutical Research Saarland (HIPS), Saarbrücken, Germany.ORCID http://orcid.org/0000-0002-9700-0474
Franziska FriesHelmholtz Institute for Pharmaceutical Research Saarland (HIPS), Saarbrücken, Germany.ORCID http://orcid.org/0009-0009-6485-8317
Bulisa IovaPNG National Museum and Art Gallery, Port Moresby, Papua New Guinea.
Kasun H BodawattaSection for Molecular Ecology and Evolution, Globe Institute, University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-6095-9059
Knud Andreas JønssonDepartment of Bioinformatics and Genetics, Swedish Museum of Natural History, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-1875-9504
Rolf MüllerHelmholtz Institute for Pharmaceutical Research Saarland (HIPS), Saarbrücken, Germany.ORCID http://orcid.org/0000-0002-1042-5665
Christine BeemelmannsHelmholtz Institute for Pharmaceutical Research Saarland (HIPS), Saarbrücken, Germany. Christine.beemelmanns@helmholtz-hips.de.ORCID http://orcid.org/0000-0002-9747-3423

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Following the discovery of the piperazic acid (Piz)-containing hexapeptide demiguisin A from a toxic bird-associated Amycolatopsis strain, we aimed to investigate the structural diversity and bioactive potential of this natural product family. Here, we used the dmg biosynthetic gene cluster from Amycolatopsis sp. PS_44_ISF1 as a pathway mining probe to search for alternative demiguisin A producers. A global search identified only one other soil-derived Amycolatopsis sp. NBC_01488, encoding a highly syntenic pathway. Under feather-mimicking conditions, PS_44_ISF1 demonstrated enhanced growth and metabolite production relative to NBC_01488. Despite phylogenomic distance, both strains produced shared metabolites, while NBC_01488 yielded more abundant demiguisins, enabling the isolation of five novel derivatives characterized by two Piz-moieties with different hydroxylation patterns and glycine truncation. Two congeners displayed potent activity against the avian pathogen Mycobacterium intracellulare and moderate activity against Mycobacterium tuberculosis. These findings show that targeted pathway mining guided the expansion of the chemical diversity of Piz-modifications and demiguisin congeners with promising anti-Mycobacterium activity.

Identifiers

PMID42892638
PMCPMC13676617

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.