Native metabolomics for mass spectrometry-based siderophore discovery.

Direct infusion Metallophore discovery Native mass spectrometry Native metabolomics Natural product discovery Siderophore discovery

Journal

Methods in enzymology
ISSN: 1557-7988
Titre abrégé: Methods Enzymol
Pays: United States
ID NLM: 0212271

Informations de publication

Date de publication:
2024
Historique:
medline: 19 8 2024
pubmed: 19 8 2024
entrez: 18 8 2024
Statut: ppublish

Résumé

Microorganisms, plants, and animals alike have specialized acquisition pathways for obtaining metals, with microorganisms and plants biosynthesizing and secreting small molecule natural products called siderophores and metallophores with high affinities and specificities for iron or other non-iron metals, respectively. This chapter details a novel approach to discovering metal-binding molecules, including siderophores and metallophores, from complex samples ranging from microbial supernatants to biological tissue to environmental samples. This approach, called Native Metabolomics, is a mass spectrometry method in which pH adjustment and metal infusion post-liquid chromatography are interfaced with ion identity molecular networking (IIMN). This rule-based data analysis workflow that enables the identification of metal-binding species based on defined mass (m/z) offsets with the same chromatographic profiles and retention times. Ion identity molecular networking connects compounds that are structurally similar by their fragmentation pattern and species that are ion adducts of the same compound by chromatographic shape correlations. This approach has previously revealed new insights into metal binding metabolites, including that yersiniabactin can act as a biological zincophore (in addition to its known role as a siderophore), that the recently elucidated lepotchelin natural products are cyanobacterial metallophores, and that antioxidants in traditional medicine bind iron. Native metabolomics can be conducted on any liquid chromatography-mass spectrometry system to explore the binding of any metal or multiple metals simultaneously, underscoring the potential for this method to become an essential strategy for elucidating biological metal-binding molecules.

Identifiants

pubmed: 39155117
pii: S0076-6879(24)00327-6
doi: 10.1016/bs.mie.2024.07.001
pii:
doi:

Substances chimiques

Siderophores 0
Iron E1UOL152H7

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

317-352

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Auteurs

Marquis T Yazzie (MT)

Department of Chemistry and Biochemistry, University of Denver, Denver, CO, United States.

Zachary L Reitz (ZL)

Department of Ecology, Evolution and Marine Biology, University of California, Santa Barbara, CA, United States.

Robin Schmid (R)

Institute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czechia.

Daniel Petras (D)

Department of Biochemistry, University of California Riverside, Riverside, CA, United States; Interfaculty of Microbiology and Infection Medicine, University of Tübingen, Tübingen, Germany.

Allegra T Aron (AT)

Department of Chemistry and Biochemistry, University of Denver, Denver, CO, United States. Electronic address: allegra.aron@du.edu.

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Classifications MeSH