Genomic analysis for the identification of bioactive compounds in Xenorhabdus stockiae strain RT25.5

dc.contributor.authorMeesil W.
dc.contributor.authorBode H.B.
dc.contributor.authorRückert-Reed C.
dc.contributor.authorShi Y.M.
dc.contributor.authorPidot S.J.
dc.contributor.authorMuangpat P.
dc.contributor.authorRattanarojpong T.
dc.contributor.authorChantratita N.
dc.contributor.authorSitthisak S.
dc.contributor.authorVitta A.
dc.contributor.authorThanwisai A.
dc.contributor.correspondenceMeesil W.
dc.contributor.otherMahidol University
dc.date.accessioned2025-07-17T18:12:00Z
dc.date.available2025-07-17T18:12:00Z
dc.date.issued2025-12-01
dc.description.abstractElucidating microorganism genomes holds great promise for the discovery of novel bioactive compounds with diverse applications. In this study, we investigated the complete genome of Xenorhabdus stockiae strain RT25.5, which is recognized for its symbiotic association with entomopathogenic nematodes (EPNs) and its biosynthesis of secondary metabolites relevant to the pharmaceutical industry, agriculture, and ecology. Through high-throughput genome sequencing, assembly, and annotation, followed by advanced bioinformatics analyses, we elucidated the genetic basis of its antimicrobial potential. Our analysis revealed 21 putative biosynthetic gene clusters (BGCs) associated with bioactive compound production. Notably, LC‒MS/MS analysis of the bacterial cultures confirmed the presence of diverse secondary metabolites, which aligned with the in silico predictions. Furthermore, the crude extract of X. stockiae strain RT25.5 exhibited antibacterial activity against 10 pathogenic bacterial isolates, highlighting its potential as a source of novel antimicrobial agents. This study highlights the importance of X. stockiae as a promising candidate for natural product discovery. The integration of genome mining, LC‒MS/MS, and bioassays not only advances our understanding of its biosynthetic capabilities but also paves the way for the development of novel antimicrobial agents. Future research should focus on the isolation and structural characterization of key metabolites, as well as evaluations of their mechanisms of action against multidrug-resistant pathogens.
dc.identifier.citationScientific Reports Vol.15 No.1 (2025)
dc.identifier.doi10.1038/s41598-025-08454-9
dc.identifier.eissn20452322
dc.identifier.scopus2-s2.0-105010130295
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/111246
dc.rights.holderSCOPUS
dc.subjectMultidisciplinary
dc.titleGenomic analysis for the identification of bioactive compounds in Xenorhabdus stockiae strain RT25.5
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105010130295&origin=inward
oaire.citation.issue1
oaire.citation.titleScientific Reports
oaire.citation.volume15
oairecerif.author.affiliationGoethe-Universität Frankfurt am Main
oairecerif.author.affiliationPhilipps-Universität Marburg
oairecerif.author.affiliationUniversität Bielefeld
oairecerif.author.affiliationShenzhen Institute of Advanced Technology
oairecerif.author.affiliationKing Mongkut's University of Technology Thonburi
oairecerif.author.affiliationNaresuan University
oairecerif.author.affiliationFaculty of Tropical Medicine, Mahidol University
oairecerif.author.affiliationThe Peter Doherty Institute for Infection and Immunity
oairecerif.author.affiliationSenckenberg Gesellschaft für Naturforschung
oairecerif.author.affiliationMax Planck Institute for Terrestrial Microbiology

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