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dc.contributor.authorShepherd, Tyson R
dc.contributor.authorDu, Rebecca R
dc.contributor.authorHuang, Hellen
dc.contributor.authorWamhoff, Eike-Christian
dc.contributor.authorBathe, Mark
dc.date.accessioned2021-10-27T20:11:10Z
dc.date.available2021-10-27T20:11:10Z
dc.date.issued2019
dc.identifier.urihttps://hdl.handle.net/1721.1/135186
dc.description.abstract© 2019, The Author(s). Scalable production of kilobase single-stranded DNA (ssDNA) with sequence control has applications in therapeutics, gene synthesis and sequencing, scaffolded DNA origami, and archival DNA memory storage. Biological production of circular ssDNA (cssDNA) using M13 addresses these needs at low cost. However, one unmet goal is to minimize the essential protein coding regions of the exported DNA while maintaining its infectivity and production purity to produce sequences less than 3,000 nt in length, relevant to therapeutic and materials science applications. Toward this end, synthetic miniphage with inserts of custom sequence and size offers scalable, low-cost synthesis of cssDNA at milligram and higher scales. Here, we optimize growth conditions using an E. coli helper strain combined with a miniphage genome carrying only an f1 origin and a β-lactamase-encoding (bla) antibiotic resistance gene, enabling isolation of pure cssDNA with a minimum sequence genomic length of 1,676 nt, without requiring additional purification from contaminating DNA. Low-cost scalability of isogenic, custom-length cssDNA is demonstrated for a sequence of 2,520 nt using a bioreactor, purified with low endotoxin levels (<5 E.U./ml). We apply these exonuclease-resistant cssDNAs to the self-assembly of wireframe DNA origami objects and to encode digital information on the miniphage genome for biological amplification.
dc.language.isoen
dc.publisherSpringer Science and Business Media LLC
dc.relation.isversionof10.1038/s41598-019-42665-1
dc.rightsCreative Commons Attribution 4.0 International license
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScientific Reports
dc.titleBioproduction of pure, kilobase-scale single-stranded DNA
dc.typeArticle
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.relation.journalScientific Reports
dc.eprint.versionFinal published version
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2019-07-19T16:38:56Z
dspace.orderedauthorsShepherd, TR; Du, RR; Huang, H; Wamhoff, E-C; Bathe, M
dspace.date.submission2019-07-19T16:38:58Z
mit.journal.volume9
mit.journal.issue1
mit.metadata.statusAuthority Work and Publication Information Needed


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