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Publicação:
Targeting riboswitches with synthetic small RNAs for metabolic engineering

dc.contributor.authorLins, Milca Rachel da Costa Ribeiro [UNESP]
dc.contributor.authorAmorim, Laura Araujo da Silva [UNESP]
dc.contributor.authorCorrêa, Graciely Gomes [UNESP]
dc.contributor.authorPicão, Bruno Willian [UNESP]
dc.contributor.authorMack, Matthias
dc.contributor.authorCerri, Marcel Otávio [UNESP]
dc.contributor.authorPedrolli, Danielle Biscaro [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionInstitute for Technical Microbiology
dc.date.accessioned2022-04-28T19:44:22Z
dc.date.available2022-04-28T19:44:22Z
dc.date.issued2021-11-01
dc.description.abstractOur growing knowledge of the diversity of non-coding RNAs in natural systems and our deepening knowledge of RNA folding and function have fomented the rational design of RNA regulators. Based on that knowledge, we designed and implemented a small RNA tool to target bacterial riboswitches and activate gene expression (rtRNA). The synthetic rtRNA is suitable for regulation of gene expression both in cell-free and in cellular systems. It targets riboswitches to promote the antitermination folding regardless the cognate metabolite concentration. Therefore, it prevents transcription termination increasing gene expression up to 103-fold. We successfully used small RNA arrays for multiplex targeting of riboswitches. Finally, we used the synthetic rtRNAs to engineer an improved riboflavin producer strain. The easiness to design and construct, and the fact that the rtRNA works as a single genome copy, make it an attractive tool for engineering industrial metabolite-producing strains.en
dc.description.affiliationUniversidade Estadual Paulista (UNESP) School of Pharmaceutical Sciences Department of Bioprocess Engineering and Biotechnology, Rodovia Araraquara-Jau Km1
dc.description.affiliationMannheim University of Applied Sciences Institute for Technical Microbiology, Paul-Wittsack-Str. 10
dc.description.affiliationUnespUniversidade Estadual Paulista (UNESP) School of Pharmaceutical Sciences Department of Bioprocess Engineering and Biotechnology, Rodovia Araraquara-Jau Km1
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdFAPESP: 2014/17564-7
dc.description.sponsorshipIdFAPESP: 2020/08699-7
dc.description.sponsorshipIdCNPq: 290110/2017-3
dc.format.extent59-67
dc.identifierhttp://dx.doi.org/10.1016/j.ymben.2021.09.003
dc.identifier.citationMetabolic Engineering, v. 68, p. 59-67.
dc.identifier.doi10.1016/j.ymben.2021.09.003
dc.identifier.issn1096-7184
dc.identifier.issn1096-7176
dc.identifier.scopus2-s2.0-85114819948
dc.identifier.urihttp://hdl.handle.net/11449/222399
dc.language.isoeng
dc.relation.ispartofMetabolic Engineering
dc.sourceScopus
dc.subjectBacillus subtilis
dc.subjectNon-coding RNA
dc.subjectRiboflavin
dc.subjectRiboswitch
dc.subjectSmall RNA
dc.subjectSynthetic biology
dc.titleTargeting riboswitches with synthetic small RNAs for metabolic engineeringen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.orcid0000-0001-7402-6826[4]
unesp.author.orcid0000-0002-7753-2422[5]
unesp.author.orcid0000-0001-6874-1313[6]
unesp.author.orcid0000-0002-3034-6497[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt

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