Evidence map›Paper›PMID 42720419›Full record

ArticleJournal of industrial microbiology & biotechnology2026

A survey of Burkholderiales secondary metabolites using library-scale stable isotope labeling reveals selective production of methyl-esterified 3-hydroxybutyrate oligomers.

Liana Zaroubi, Stephanie C Heard, Matthew Sutherland, Alessandra S Eustaquio, Roger G Linington

Abstract read
In one paragraph

Article in Journal of industrial microbiology & biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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.

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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

5 authors.

Liana ZaroubiDepartment of Chemistry, Simon Fraser University, Burnaby, Canada.ORCID 0000-0001-8218-7216
Stephanie C HeardDepartment of Pharmaceutical Sciences, Retzky College of Pharmacy, University of Illinois Chicago, Chicago, United States.ORCID 0000-0003-4312-5105
Matthew SutherlandDepartment of Chemistry, Simon Fraser University, Burnaby, Canada.ORCID 0009-0007-8539-4158
Alessandra S EustaquioDepartment of Pharmaceutical Sciences, Retzky College of Pharmacy, University of Illinois Chicago, Chicago, United States.ORCID 0000-0002-7852-7844
Roger G LiningtonDepartment of Chemistry, Simon Fraser University, Burnaby, Canada.ORCID 0000-0003-1818-4971

Funding

Development of a Bacterial Host for Natural Product Discovery and ProductionR01GM129344 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI EUSTAQUIO, ALESSANDRA S · 2020 to 2023
$1.5M
Natural Sciences and Engineering Research Council of CanadaNIGMS NIH HHS R01 GM129344NIH HHS R01-GM129344
6 · The paper itself

Abstract

Large-scale untargeted bacterial metabolomics studies are often challenging to interpret, particularly for natural product discovery. Complex raw mass spectrometry data contains media components, biotransformation products, workup contaminants, and in-source fragments, making it difficult to resolve true biosynthesized bacterial products from background features. Incorporating stable isotope labels into untargeted workflows enables the selective detection of actively biosynthesized compounds, drastically reducing candidate mass spectrometry features to highlight novel or robustly expressed metabolites. Recently, our lab introduced IsoAnalyst, a parallel stable isotope labeling platform that links secondary metabolites to biosynthetic gene clusters by determining the incorporation rates of a panel of isotopically labeled building blocks. In this study we applied the IsoAnalyst protocol to a library of 114 Burkholderiales strains with the goals of profiling the specialized metabolite chemistry of this bacterial order and connecting detected natural products to their cognate BGCs based on their labeling profiles. While our strain-matching protocol, which evaluates correlations between detected metabolites and BiG-SCAPE-defined gene cluster families, did not yield confident BGC assignments, it successfully highlighted widely distributed metabolites with distinct labeling profiles. We targeted a set of these molecules for isolation, revealing two classes of compounds derived from primary biomolecule metabolism that are implicated in cellular stress responses. The first class of molecules were identified as lysophosphatidyl ethanolamine analogues while the second was characterized via NMR spectroscopy and mass spectrometry as methyl-esterified 3-hydroxybutyrate oligomers (HB6-OMe, HB7-OMe, and HB8-OMe), representing higher-degree polymer units than previously reported. One-sentence summary Large-scale isotope labelling of a panel of 114 Burkholderiales strains reveals the secondary metabolite diversity of this microbial order, leading to the discovery of novel butyric acid polymers.

Indexed as

3-Hydroxybutyric AcidIsotope LabelingSecondary MetabolismMass SpectrometryMetabolomicsMultigene Family3-Hydroxybutyric AcidBurkholderialesgene cluster familylibrary-scalemetabolomicsstable isotope

Identifiers

PMID42720419
PMCPMC13614103

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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.