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dc.contributorFacultad de Ciencias Biologicas y Ambientaleses_ES
dc.contributor.authorDel Carratore, Francesco
dc.contributor.authorIorio, Marianna
dc.contributor.authorPérez-Bonilla, Mercedes
dc.contributor.authorSchmidt, Kamila
dc.contributor.authorPérez Redondo, Rosario
dc.contributor.authorSosio, Margherita
dc.contributor.authorMacdonald, Sandy J.
dc.contributor.authorGyulev, Ivan S.
dc.contributor.authorTsigkinopoulou, Areti
dc.contributor.authorThomas, Gavin H.
dc.contributor.authorGenilloud, Olga
dc.contributor.authorRodríguez García, Antonio 
dc.contributor.authorDonadio, Stefano
dc.contributor.authorBreitling, Rainer
dc.contributor.authorTakano, Eriko
dc.contributor.otherMicrobiologiaes_ES
dc.date2021-06-22
dc.date.accessioned2024-02-06T08:54:37Z
dc.date.available2024-02-06T08:54:37Z
dc.identifier.citationDel Carratore, F., Iorio, M., Pérez-Bonilla, M., Schmidt, K., Pérez-Redondo, R., Sosio, M., Macdonald, S. J., Gyulev, I. S., Tsigkinopoulou, A., Thomas, G. H., Genilloud, O., Rodríguez-García, A., Donadio, S., Breitling, R., & Takano, E. (2021). Multi-omics study of planobispora rosea, producer of the thiopeptide antibiotic GE2270A. mSystems, 6(3), Article e341. https://doi.org/10.1128/MSYSTEMS.00341-21es_ES
dc.identifier.otherhttps://journals.asm.org/doi/10.1128/msystems.00341-21es_ES
dc.identifier.urihttps://hdl.handle.net/10612/18086
dc.description.abstract[EN] Planobispora rosea is the natural producer of the potent thiopeptide antibiotic GE2270A. Here, we present the results of a metabolomics and transcriptomics analysis of P. rosea during production of GE2270A. The data generated provides useful insights into the biology of this genetically intractable bacterium. We characterize the details of the shutdown of protein biosynthesis and the respiratory chain associated with the end of the exponential growth phase. We also provide the first description of the phosphate regulon in P. rosea. Based on the transcriptomics data, we show that both phosphate and iron are limiting P. rosea growth in our experimental conditions. Additionally, we identified and validated a new biosynthetic gene cluster associated with the production of the siderophores benarthin and dibenarthin in P. rosea. Together, the metabolomics and transcriptomics data are used to inform and refine the very first genome-scale metabolic model for P. rosea, which will be a valuable framework for the interpretation of future studies of the biology of this interesting but poorly characterized specieses_ES
dc.languageenges_ES
dc.publisherAmerican Society for Microbiologyes_ES
dc.subjectBiologíaes_ES
dc.subjectBiotecnologíaes_ES
dc.subject.otherPlanobispora roseaes_ES
dc.subject.otherAntibiotics biosynthesis regulationes_ES
dc.subject.otherPhosphate regulationes_ES
dc.subject.otherTranscriptomicses_ES
dc.subject.otherMetabolomicses_ES
dc.subject.otherSystems biologyes_ES
dc.subject.otherThiopeptide antibioticses_ES
dc.subject.otherGE2270Aes_ES
dc.subject.otherGenome-scale metabolic modeles_ES
dc.titleMulti-omics Study of Planobispora rosea, Producer of the Thiopeptide Antibiotic GE2270Aes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.identifier.doi10.1128/mSystems.00341-21
dc.description.peerreviewedSIes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/720793/EUes_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn2379-5077
dc.journal.titlemSystemses_ES
dc.volume.number6es_ES
dc.issue.number3es_ES
dc.page.initial341es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.unesco2414.01 Antibióticoses_ES
dc.subject.unesco2414.02 Fisiología Bacterianaes_ES
dc.subject.unesco2415.01 Biología Molecular de Microorganismoses_ES
dc.description.projectF.D.C., M.I., M.P.-B., K.S., R.P.-R., M.S., S.J.M., I.S.G., A.T., G.H.T., O.G., A.R.-G., S.D., R.B., and E.T. were funded by the European Union’s Horizon 2020 Research and Innovation Program under grant agreement 720793 “TOPCAPI: Thoroughly Optimised Production Chassis for Advanced Pharmaceutical Ingredients.” S.J.M., I.S.G., and G.H.T. were also supported from BBSRC IB Catalyst program, DETOX (BB/N01040X/1). We thank the Manchester Synthetic Biology Research Centre SYNBIOCHEM team, especially Katherine Hollywood, for their support and use of the QExactive for the untargeted metabolomics analysis. We thank all the TOPCAPI consortium partners for their support. F.D.C. performed the data processing of the metabolomics data, performed the statistical analysis of the transcriptomics and metabolomics data, and wrote the first draft of the manuscript. M.I. and M.S. prepared the samples for the transcriptomics and metabolomics analysis and performed the supplementation experiment. M.P.-B. and K.S. performed the metabolomics analysis and the data processing. R.P.-R. performed the RNA extraction and quality control. S.M. and I.G. processed and analyzed data included in MORF. F.D.C. and A.T. built the genome-scale metabolic model. F.D.C., A.T., and A.R.-G. performed RNAseq analyses. G.H.T., O.G., A.R.-G., S.D., R.B., and E.T. conceived the experiments, analyzed the data, and coordinated the activities. F.D.C., M.P.-B., K.S., G.H.T., A.R.-G., S.D., R.B., and E.T. contributed to writing the manuscript. All the authors edited and approved the final version.es_ES


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