Evidence map›Paper›PMID 42210522›Full record

ArticleMicrobial biotechnology2026

Kineochelins-A New Group of Siderophores From an Antarctic Bacterium.

Stanislava Kralova, Peter Spacek, Johannes Gafriller, Matej Bezdicek, Viktoria Medvedcova, Joana Séneca, Jay Osvatic, Ulrike Grienke, Thomas Rattei, Olga N Sekurova and 3 more

Abstract read
In one paragraph

Article in Microbial 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

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2 · The registry

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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

13 authors.

Stanislava KralovaDivision of Microbial Ecology, Centre for Microbiology and Environmental Systems Science, University of Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0003-3384-5328
Peter SpacekDivision of Microbial Ecology, Centre for Microbiology and Environmental Systems Science, University of Vienna, Vienna, Austria.
Johannes GafrillerDepartment of Pharmaceutical Sciences, University of Vienna, Vienna, Austria.
Matej BezdicekDivision of Clinical Microbiology and Immunology, Department of Laboratory Medicine, University Hospital Brno, Brno, Czech Republic.ORCID https://orcid.org/0000-0002-5833-8325
Viktoria MedvedcovaDepartment of Pharmacology, Faculty of Medicine, Pavol Jozef Šafárik University, Košice, Slovakia.
Joana SénecaDivision of Microbial Ecology, Centre for Microbiology and Environmental Systems Science, University of Vienna, Vienna, Austria.
Jay OsvaticDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Ulrike GrienkeDepartment of Pharmaceutical Sciences, University of Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0003-0305-9270
Thomas RatteiDivision of Computational Systems Biology, Centre for Microbiology and Environmental Systems Science, University of Vienna, Vienna, Austria.
Olga N SekurovaDepartment of Pharmaceutical Sciences, University of Vienna, Vienna, Austria.
Sergey B ZotchevDepartment of Pharmaceutical Sciences, University of Vienna, Vienna, Austria.
Martin ZehlDepartment of Analytical Chemistry, Faculty of Chemistry, University of Vienna, Vienna, Austria.
Alexander LoyDivision of Microbial Ecology, Centre for Microbiology and Environmental Systems Science, University of Vienna, Vienna, Austria.

Funding

Austrian Science Fund 10.55776/COE7Horizon 2020 Framework Programme No.101020356Masarykova Univerzita MUNI/SC/1946/2024Ministerstvo Zdravotnictví Ceské Republiky FNBr,65269705Ministry of Education, Youth and Sports of the CR VAN2025Universität Wien MetaBacVedecká grantová agentúra Ministerstva školstva, výskumu, vývoja a mládeže Slovenskej republiky a Slovenskej akadémie vied VEGA 1/0498/23
6 · The paper itself

Abstract

The global rise of antimicrobial resistance has intensified the search for new microbial metabolites from underexplored environments and taxonomic groups. Extreme and geographically isolated habitats such as Antarctic terrestrial ecosystems represent promising reservoirs of biosynthetic diversity, particularly among rare and difficult-to-cultivate actinomycetes that may produce chemically diverse metabolites with potential biotechnological applications. Here, we report the characterization of kineochelins, a previously undescribed group of siderophores produced by the Antarctic isolate Actinokineospora sp. UV203, representing a difficult-to-cultivate actinomycete lineage. Structural elucidation revealed a set of closely related congeners with a mixed-ligand architecture consistent with metal-chelating activity. Genome mining combined with transcriptomic analysis identified a dedicated nonribosomal peptide synthetase-encoding biosynthetic gene cluster responsible for kineochelin production. Comparative genomic analyses indicated that, although kineochelin biosynthetic genes share limited similarity with known mixed-ligand siderophores, their gene content and organization differ substantially, suggesting a distinct biosynthetic lineage. Functional characterization of the culture supernatant and an enriched pre-purified kineochelin fraction demonstrated strong and selective iron chelation, with high affinity for ferric and ferrous iron. Crude culture extracts inhibited the growth of bacterial strains isolated from the same Antarctic environment, indicating that kineochelins may contribute to iron-mediated microbial competition. In addition, kineochelin-enriched pre-purified fractions showed moderate selective inhibitory activity against the opportunistic yeast pathogen Nakaseomyces glabratus and a clinical isolate of Saccharomyces cerevisiae associated with invasive infection. These findings expand the chemical and biosynthetic diversity known within the genus Actinokineospora and demonstrate that Antarctic rare actinomycetes represent valuable sources of previously unexplored natural products. The discovery of kineochelins highlights the potential of genome-guided exploration of polar microorganisms for identifying bioactive metabolites with relevance for antimicrobial discovery and biotechnology.

Indexed as

ActinobacteriaSiderophoresAntarctic RegionsBiosynthetic PathwaysGenome, BacterialIronMultigene FamilyPeptide SynthasesPhylogenyIronnon-ribosomal peptide synthasePeptide SynthasesSiderophoresActinokineosporaAntarcticaantimicrobial discoverybiosynthetic gene clustergenome miningmicrobial competitionnonribosomal peptide synthetasesiderophores

Identifiers

PMID42210522
PMCPMC13238742

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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.