Transcriptomic and metabolomic profiling of ionic liquid stimuli unveils enhanced secondary metabolism in Aspergillus nidulans

dc.contributor.authorAlves, Paula C.
dc.contributor.authorHartmann, Diego O.
dc.contributor.authorNúñez Burcio, Oscar
dc.contributor.authorMartins, Isabel
dc.contributor.authorGomes, Teresa L.
dc.contributor.authorGarcia, Helga
dc.contributor.authorGalcerán Huguet, M. Teresa
dc.contributor.authorHampson, Richard
dc.contributor.authorBecker, Jörg D.
dc.contributor.authorPereira, Cristina Silvia
dc.date.accessioned2016-04-14T11:22:47Z
dc.date.available2016-04-14T11:22:47Z
dc.date.issued2016-04-12
dc.date.updated2016-04-14T11:22:52Z
dc.description.abstractBackground: The inherent potential of filamentous fungi, especially of Ascomycota, for producing diverse bioactive metabolites remains largely silent under standard laboratory culture conditions. Innumerable strategies have been described to trigger their production, one of the simplest being manipulation of the growth media composition. Supplementing media with ionic liquids surprisingly enhanced the diversity of extracellular metabolites generated by penicillia. This finding led us to evaluate the impact of ionic liquids' stimuli on the fungal metabolism in Aspergillus nidulans and how it reflects on the biosynthesis of secondary metabolites (SMs). Results: Whole transcriptional profiling showed that exposure to 0.7 M cholinium chloride or 1-ethyl-3- methylimidazolium chloride dramatically affected expression of genes encoding both primary and secondary metabolism. Both ionic liquids apparently induced stress responses and detoxification mechanisms but response profiles to each stimulus were unique. Primary metabolism was up-regulated by choline, but down-regulated by 1- ethyl-3-methylimidazolium chloride; both stimulated production of acetyl-CoA (key precursor to numerous SMs) and non proteinogenic amino acids (building blocks of bioactive classes of SMs). In total, twenty one of the sixty six described backbone genes underwent up-regulation. Accordingly, differential analysis of the fungal metabolome showed that supplementing growth media with ionic liquids resulted in ca. 40 differentially accumulated ion masses compared to control conditions. In particular, it stimulated production of monodictyphenone and orsellinic acid, otherwise cryptic. Expression levels of genes encoding corresponding polyketide biosynthetic enzymes (i.e. backbone genes) increased compared to control conditions. The corresponding metabolite extracts showed increased cell polarity modulation potential in an ex vivo whole tissue assay (Thelial Live Targeted Epithelia; theLiTE¿). Conclusions: Ionic liquids, a diverse class of chemicals composed solely of ions, can provide an unexpected means to further resolve the diversity of natural compounds, guiding discovery of fungal metabolites with clinical potential.
dc.format.extent18 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec657890
dc.identifier.issn1471-2164
dc.identifier.pmid27072538
dc.identifier.urihttps://hdl.handle.net/2445/97407
dc.language.isoeng
dc.publisherBioMed Central
dc.relation.isformatofReproducció del document publicat a: http://dx.doi.org/10.1186/s12864-016-2577-6
dc.relation.ispartofBmc Genomics, 2016, vol. 17, p. 284
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/647928/EU//MIMESIS
dc.relation.urihttp://dx.doi.org/10.1186/s12864-016-2577-6
dc.rightscc-by (c) Alves, Paula C. et al., 2016
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Enginyeria Química i Química Analítica)
dc.subject.classificationFongs
dc.subject.classificationMetabolisme secundari
dc.subject.classificationSolucions iòniques
dc.subject.otherFungi
dc.subject.otherSecondary metabolism
dc.subject.otherIonic solutions
dc.titleTranscriptomic and metabolomic profiling of ionic liquid stimuli unveils enhanced secondary metabolism in Aspergillus nidulans
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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