Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/5196
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dc.contributor.authorAtanasković, Ivaen_US
dc.contributor.authorBencherif, Amel Caméliaen_US
dc.contributor.authorDeyell, Matthewen_US
dc.contributor.authorJaramillo-Riveri, Sebastiánen_US
dc.contributor.authorBenony, Margueriteen_US
dc.contributor.authorBernheim, Aude G.en_US
dc.contributor.authorLibis, Vincent K.en_US
dc.contributor.authorKoutsoubelis, Nicolasen_US
dc.contributor.authorZegman, Yonatanen_US
dc.contributor.authorLöchner, Anne C.en_US
dc.contributor.authorBasier, Clovisen_US
dc.contributor.authorAghoghogbe, Idonnyaen_US
dc.contributor.authorMarinković, Zoran S.en_US
dc.contributor.authorZahra, Sarahen_US
dc.contributor.authorToulouze, Matthiasen_US
dc.contributor.authorLindner, Ariel B.en_US
dc.contributor.authorWintermute, Edwin H.en_US
dc.date.accessioned2022-11-23T12:04:47Z-
dc.date.available2022-11-23T12:04:47Z-
dc.date.issued2014-12-19-
dc.identifier.citationEngineering a genome-reduced bacterium to eliminate Staphylococcus aureus biofilms in vivo. Garrido V, Piñero-Lambea C, Rodriguez-Arce I, Paetzold B, Ferrar T, Weber M, Garcia-Ramallo E, Gallo C, Collantes M, Peñuelas I, Serrano L, Grilló MJ, Lluch-Senar M. Mol Syst Biol. 2021 Oct;17(10):e10145. doi: 10.15252/msb.202010145. PMID: 34612607 Free PMC article. Engineering microbes for targeted strikes against human pathogens. Hwang IY, Lee HL, Huang JG, Lim YY, Yew WS, Lee YS, Chang MW. Cell Mol Life Sci. 2018 Aug;75(15):2719-2733. doi: 10.1007/s00018-018-2827-7. Epub 2018 May 7. PMID: 29736607 Review.en_US
dc.identifier.issn2161-5063-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/5196-
dc.description.abstractThe emergence of extremely drug resistant Mycobacterium tuberculosis necessitates new strategies to combat the pathogen. Engineered bacteria may serve as vectors to deliver proteins to human cells, including mycobacteria-infected macrophages. In this work, we target Mycobacterium smegmatis, a nonpathogenic tuberculosis model, with E. coli modified to express trehalose dimycolate hydrolase (TDMH), a membrane-lysing serine esterase. We show that TDMH-expressing E. coli are capable of lysing mycobacteria in vitro and at low pH. Vectorized E. coli producing TDMH were found suppress the proliferation of mycobacteria in infected macrophages.en_US
dc.language.isoenen_US
dc.publisherNational Library of Medicineen_US
dc.relation.ispartofACS Synthetic Biologyen_US
dc.subjectLLOen_US
dc.subjectTDMHen_US
dc.subjectMacrophagesen_US
dc.subjectMycobacteriaen_US
dc.subjectProtein vectorsen_US
dc.subjectTuberculosisen_US
dc.titleIn situ characterization of mycobacterial growth inhibition by lytic enzymes expressed in vectorized E. coli.en_US
dc.typeArticleen_US
dc.identifier.doi10.1021/sb500039z-
dc.description.rankM21en_US
dc.description.impact4,978en_US
dc.description.startpage932en_US
dc.description.endpage934en_US
dc.description.volume3en_US
dc.description.issue12en_US
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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