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Preventing Production Escape Using an Engineered Glucose-Inducible Genetic Circuit

dc.contributor.authorTavares, Leonardo F. [UNESP]
dc.contributor.authorRibeiro, Nathan V. [UNESP]
dc.contributor.authorZocca, Vitória F. B. [UNESP]
dc.contributor.authorCorrêa, Graciely G. [UNESP]
dc.contributor.authorAmorim, Laura A. S. [UNESP]
dc.contributor.authorLins, Milca R. C. R.
dc.contributor.authorPedrolli, Danielle B. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade Federal do ABC (UFABC)
dc.date.accessioned2025-04-29T19:33:15Z
dc.date.issued2023-10-20
dc.description.abstractA proper balance of metabolic pathways is crucial for engineering microbial strains that can efficiently produce biochemicals on an industrial scale while maintaining cell fitness. High production loads can negatively impact cell fitness and hinder industrial-scale production. To address this, fine-tuning gene expression using engineered promoters and genetic circuits can promote control over multiple targets in pathways and reduce the burden. We took advantage of the robust carbon catabolite repression system of Bacillus subtilis to engineer a glucose-inducible genetic circuit that supports growth and production. The circuit is resilient, enabling a quick switch in the production status when exposed to the correct carbon source. By performing serial cultivations for 61 generations under repressive conditions, we preserved the production capacity of the cells, which could be fully accessed by switching to glucose in the next cultivation step. Switching to glucose after 61 generations resulted in 34-fold activation and generated 70% higher production in comparison to standard cultivation in glucose. Conversely, serial cultivation under permanent induction resulted in 62% production loss after 67 generations alongside an increase in the culture growth rate. As a pathway-independent circuit activated by the preferred carbon source, our engineered glucose-inducible genetic circuit is broadly useful and imposes no additional cost to traditional production processes.en
dc.description.affiliationUniversidade Estadual Paulista (UNESP) School of Pharmaceutical Sciences Department of Bioprocess Engineering and Biotechnology
dc.description.affiliationFederal University of ABC (UFABC) Center for Natural and Human Sciences, Campus Santo André
dc.description.affiliationUnespUniversidade Estadual Paulista (UNESP) School of Pharmaceutical Sciences Department of Bioprocess Engineering and Biotechnology
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.format.extent3124-3130
dc.identifierhttp://dx.doi.org/10.1021/acssynbio.3c00134
dc.identifier.citationACS Synthetic Biology, v. 12, n. 10, p. 3124-3130, 2023.
dc.identifier.doi10.1021/acssynbio.3c00134
dc.identifier.issn2161-5063
dc.identifier.scopus2-s2.0-85174641375
dc.identifier.urihttps://hdl.handle.net/11449/303868
dc.language.isoeng
dc.relation.ispartofACS Synthetic Biology
dc.sourceScopus
dc.subjectBacillus subtilis
dc.subjectcarbon catabolic repression
dc.subjectgenetic circuit
dc.subjectglucose induction
dc.subjectlong-term fermentation
dc.subjectproduction escape
dc.titlePreventing Production Escape Using an Engineered Glucose-Inducible Genetic Circuiten
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.orcid0000-0002-3034-6497[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt

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