Evidence map›Paper›PMID 41822988›Full record

ReviewEssays in biochemistry2026

Transposon mutagenesis in bacterial natural product discovery.

Mega F Warsito, Napawit Nonthakaew, Marina Suppi, Liam K R Sharkey, Justin Nodwell, Sacha J Pidot

Abstract readReview
In one paragraph

Review in Essays in biochemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Bacterial biosynthetic gene clusters.Essays in biochemistry · 2026
    Review
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

6 authors.

Mega F Warsito *Department of Microbiology and Immunology at the Doherty Institute, University of Melbourne, Melbourne, 3000, Australia.
Napawit Nonthakaew *Department of Microbiology and Immunology at the Doherty Institute, University of Melbourne, Melbourne, 3000, Australia.
Marina Suppi *Department of Microbiology and Immunology at the Doherty Institute, University of Melbourne, Melbourne, 3000, Australia.
Liam K R SharkeyDepartment of Microbiology and Immunology at the Doherty Institute, University of Melbourne, Melbourne, 3000, Australia.ORCID 0000-0001-9324-8678
Justin NodwellDepartment of Biochemistry, Temerty Faculty of Medicine, University of Toronto, Ontario M5G 1M1, Canada.ORCID 0000-0001-7909-1803
Sacha J PidotDepartment of Microbiology and Immunology at the Doherty Institute, University of Melbourne, Melbourne, 3000, Australia.ORCID 0000-0003-1202-6614

Funding

Department of Education and Training | Australian Research Council (ARC) DP2201000905Department of Education and Training | Australian Research Council (ARC) DP230102668DHAC | National Health and Medical Research Council (NHMRC) GNT2021638
6 · The paper itself

Abstract

Transposon mutagenesis has re-emerged as a powerful and versatile strategy for discovering and characterising specialised metabolites encoded by biosynthetic gene clusters (BGCs). While genomics has revealed an enormous diversity of putative BGCs across bacteria, many remain silent, weakly expressed, or genetically intractable, necessitating experimental tools that can link genotype to chemical output. Transposons provide an unbiased and broadly applicable platform for disrupting, activating, or modulating gene expression without relying on homologous recombination, making them particularly valuable in challenging microbial hosts. Here, we review the major applications of transposon mutagenesis in natural product discovery, providing examples that highlight discoveries made using phenotype- and bioactivity-guided screens, phenotype-independent strategies, and transposon-based engineering of heterologous expression platforms. Transposon technologies provide flexible and scalable tools for activating, characterising, and engineering microbial BGCs. As genome mining continues to unearth rich seams of unexplored metabolic potential, these tools will remain essential for converting genetic predictions into chemical discovery.

Indexed as

BacteriaBiological ProductsDNA Transposable ElementsMutagenesisMultigene FamilyBiological ProductsDNA Transposable Elementsbiotechnologymicrobiologytransposons

Identifiers

PMID41822988
PMCPMC13500788

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.