Please use this identifier to cite or link to this item:
https://biore.bio.bg.ac.rs/handle/123456789/5196
DC Field | Value | Language |
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dc.contributor.author | Atanasković, Iva | en_US |
dc.contributor.author | Bencherif, Amel Camélia | en_US |
dc.contributor.author | Deyell, Matthew | en_US |
dc.contributor.author | Jaramillo-Riveri, Sebastián | en_US |
dc.contributor.author | Benony, Marguerite | en_US |
dc.contributor.author | Bernheim, Aude G. | en_US |
dc.contributor.author | Libis, Vincent K. | en_US |
dc.contributor.author | Koutsoubelis, Nicolas | en_US |
dc.contributor.author | Zegman, Yonatan | en_US |
dc.contributor.author | Löchner, Anne C. | en_US |
dc.contributor.author | Basier, Clovis | en_US |
dc.contributor.author | Aghoghogbe, Idonnya | en_US |
dc.contributor.author | Marinković, Zoran S. | en_US |
dc.contributor.author | Zahra, Sarah | en_US |
dc.contributor.author | Toulouze, Matthias | en_US |
dc.contributor.author | Lindner, Ariel B. | en_US |
dc.contributor.author | Wintermute, Edwin H. | en_US |
dc.date.accessioned | 2022-11-23T12:04:47Z | - |
dc.date.available | 2022-11-23T12:04:47Z | - |
dc.date.issued | 2014-12-19 | - |
dc.identifier.citation | Engineering 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.issn | 2161-5063 | - |
dc.identifier.uri | https://biore.bio.bg.ac.rs/handle/123456789/5196 | - |
dc.description.abstract | The 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.iso | en | en_US |
dc.publisher | National Library of Medicine | en_US |
dc.relation.ispartof | ACS Synthetic Biology | en_US |
dc.subject | LLO | en_US |
dc.subject | TDMH | en_US |
dc.subject | Macrophages | en_US |
dc.subject | Mycobacteria | en_US |
dc.subject | Protein vectors | en_US |
dc.subject | Tuberculosis | en_US |
dc.title | In situ characterization of mycobacterial growth inhibition by lytic enzymes expressed in vectorized E. coli. | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1021/sb500039z | - |
dc.description.rank | M21 | en_US |
dc.description.impact | 4,978 | en_US |
dc.description.startpage | 932 | en_US |
dc.description.endpage | 934 | en_US |
dc.description.volume | 3 | en_US |
dc.description.issue | 12 | en_US |
item.languageiso639-1 | en | - |
item.cerifentitytype | Publications | - |
item.openairetype | Article | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
Appears in Collections: | Journal Article |
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