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dc.contributor.authorTucker, Alex C.
dc.contributor.authorVoigt, Christopher A.
dc.contributor.authorLu, Timothy K
dc.contributor.authorMimee, Mark Kyle
dc.date.accessioned2017-03-09T19:52:36Z
dc.date.available2017-03-09T19:52:36Z
dc.date.issued2015-07
dc.date.submitted2015-05
dc.identifier.issn2405-4712
dc.identifier.urihttp://hdl.handle.net/1721.1/107264
dc.description.abstractEngineering commensal organisms for challenging applications, such as modulating the gut ecosystem, is hampered by the lack of genetic parts. Here, we describe promoters, ribosome-binding sites, and inducible systems for use in the commensal bacterium Bacteroides thetaiotaomicron, a prevalent and stable resident of the human gut. We achieve up to 10,000-fold range in constitutive gene expression and 100-fold regulation of gene expression with inducible promoters and use these parts to record DNA-encoded memory in the genome. We use CRISPR interference (CRISPRi) for regulated knockdown of recombinant and endogenous gene expression to alter the metabolic capacity of B. thetaiotaomicron and its resistance to antimicrobial peptides. Finally, we show that inducible CRISPRi and recombinase systems can function in B. thetaiotaomicron colonizing the mouse gut. These results provide a blueprint for engineering new chassis and a resource to engineer Bacteroides for surveillance of or therapeutic delivery to the gut microbiome.en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Grant EEC-0540879)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grants P50GM098792, 1DP2OD008435, 1R01EB017755, and GM095765)en_US
dc.description.sponsorshipUnited States. Defense Advanced Research Projects Agency (Grant CLIO N66001-12-C-4016)en_US
dc.description.sponsorshipUnited States. Defense Threat Reduction Agency (Grant HDTRA1-14-1-0007)en_US
dc.description.sponsorshipUnited States. Office of Naval Research (Grant N00014-13-1-0424)en_US
dc.description.sponsorshipMassachusetts Institute of Technology. Center for Microbiome Informatics and Therapeuticsen_US
dc.description.sponsorshipQUALCOMM Inc. (Innovation Fellowship)en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.cels.2015.06.001en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleProgramming a Human Commensal Bacterium, Bacteroides thetaiotaomicron, to Sense and Respond to Stimuli in the Murine Gut Microbiotaen_US
dc.typeArticleen_US
dc.identifier.citationMimee, Mark et al. “Programming a Human Commensal Bacterium, Bacteroides Thetaiotaomicron, to Sense and Respond to Stimuli in the Murine Gut Microbiota.” Cell Systems 1.1 (2015): 62–71.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.mitauthorMimee, Mark K
dc.contributor.mitauthorTucker, Alex C.
dc.contributor.mitauthorVoigt, Christopher A.
dc.contributor.mitauthorLu, Timothy K
dc.relation.journalCell Systemsen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsMimee, Mark; Tucker, Alex C.; Voigt, Christopher A.; Lu, Timothy K.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-3083-2671
dc.identifier.orcidhttps://orcid.org/0000-0003-0844-4776
dc.identifier.orcidhttps://orcid.org/0000-0002-9999-6690
mit.licensePUBLISHER_CCen_US


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