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dc.contributor.authorRoehner, Nicholas
dc.contributor.authorMikkelsen, Tarjei S.
dc.contributor.authorDensmore, Douglas
dc.contributor.authorWoodruff, Lauren B
dc.contributor.authorGordon, David B
dc.contributor.authorVoigt, Christopher A.
dc.contributor.authorGorochowski, Thomas Edward
dc.contributor.authorNicol, Robert
dc.date.accessioned2017-04-13T18:17:50Z
dc.date.available2017-04-13T18:17:50Z
dc.date.issued2016-12
dc.date.submitted2016-11
dc.identifier.issn0305-1048
dc.identifier.issn1362-4962
dc.identifier.urihttp://hdl.handle.net/1721.1/108126
dc.description.abstractGenetic designs can consist of dozens of genes and hundreds of genetic parts. After evaluating a design, it is desirable to implement changes without the cost and burden of starting the construction process from scratch. Here, we report a two-step process where a large design space is divided into deep pools of composite parts, from which individuals are retrieved and assembled to build a final construct. The pools are built via multiplexed assembly and sequenced using next-generation sequencing. Each pool consists of ∼20 Mb of up to 5000 unique and sequence-verified composite parts that are barcoded for retrieval by PCR. This approach is applied to a 16-gene nitrogen fixation pathway, which is broken into pools containing a total of 55 848 composite parts (71.0 Mb). The pools encompass an enormous design space (1043 possible 23 kb constructs), from which an algorithm-guided 192-member 4.5 Mb library is built. Next, all 1030 possible genetic circuits based on 10 repressors (NOR/NOT gates) are encoded in pools where each repressor is fused to all permutations of input promoters. These demonstrate that multiplexing can be applied to encompass entire design spaces from which individuals can be accessed and evaluated.en_US
dc.description.sponsorshipInstitute for Collaborative Biotechnologies (W911NF-09-0001)en_US
dc.description.sponsorshipUnited States. Office of Naval Research. Multidisciplinary University Research Initiative (N00014-13-1-0074)en_US
dc.description.sponsorshipUnited States. Defense Advanced Research Projects Agency. Living Foundries Program (Awards HR0011-12-C-0067, HR0011- 13-1-0001, HR0011-15-C-0084 and HR0011-15-C-0084)en_US
dc.language.isoen_US
dc.publisherOxford University Pressen_US
dc.relation.isversionofhttp://dx.doi.org/10.1093/nar/gkw1226en_US
dc.rightsCreative Commons Attribution-NonCommercial 4.0 Internationalen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/en_US
dc.sourceOxford University Pressen_US
dc.titleRegistry in a tube: multiplexed pools of retrievable parts for genetic design space explorationen_US
dc.typeArticleen_US
dc.identifier.citationWoodruff, Lauren B. A. et al. “Registry in a Tube: Multiplexed Pools of Retrievable Parts for Genetic Design Space Exploration.” Nucleic Acids Research (2016): gkw1226. © 2016 American Chemical Societyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.mitauthorWoodruff, Lauren B
dc.contributor.mitauthorGordon, David B
dc.contributor.mitauthorVoigt, Christopher A.
dc.contributor.mitauthorGorochowski, Thomas Edward
dc.contributor.mitauthorNicol, Robert
dc.relation.journalNucleic Acids Researchen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsWoodruff, Lauren B. A.; Gorochowski, Thomas E.; Roehner, Nicholas; Mikkelsen, Tarjei S.; Densmore, Douglas; Gordon, D. Benjamin; Nicol, Robert; Voigt, Christopher A.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-1627-1430
dc.identifier.orcidhttps://orcid.org/0000-0003-0844-4776
dc.identifier.orcidhttps://orcid.org/0000-0003-1702-786X
mit.licensePUBLISHER_CCen_US


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