Notice

This is not the latest version of this item. The latest version can be found at:https://dspace.mit.edu/handle/1721.1/133543.2

Show simple item record

dc.contributor.authorCasini, Arturo
dc.contributor.authorChang, Fang-Yuan
dc.contributor.authorEluere, Raissa
dc.contributor.authorKing, Andrew M
dc.contributor.authorYoung, Eric M
dc.contributor.authorDudley, Quentin M
dc.contributor.authorKarim, Ashty
dc.contributor.authorPratt, Katelin
dc.contributor.authorBristol, Cassandra
dc.contributor.authorForget, Anthony
dc.contributor.authorGhodasara, Amar
dc.contributor.authorWarden-Rothman, Robert
dc.contributor.authorGan, Rui
dc.contributor.authorCristofaro, Alexander
dc.contributor.authorBorujeni, Amin Espah
dc.contributor.authorRyu, Min-Hyung
dc.contributor.authorLi, Jian
dc.contributor.authorKwon, Yong-Chan
dc.contributor.authorWang, He
dc.contributor.authorTatsis, Evangelos
dc.contributor.authorRodriguez-Lopez, Carlos
dc.contributor.authorO’Connor, Sarah
dc.contributor.authorMedema, Marnix H
dc.contributor.authorFischbach, Michael A
dc.contributor.authorJewett, Michael C
dc.contributor.authorVoigt, Christopher
dc.contributor.authorGordon, D Benjamin
dc.date.accessioned2021-10-27T19:53:26Z
dc.date.available2021-10-27T19:53:26Z
dc.date.issued2018
dc.identifier.urihttps://hdl.handle.net/1721.1/133543
dc.description.abstract© 2018 American Chemical Society. Centralized facilities for genetic engineering, or "biofoundries", offer the potential to design organisms to address emerging needs in medicine, agriculture, industry, and defense. The field has seen rapid advances in technology, but it is difficult to gauge current capabilities or identify gaps across projects. To this end, our foundry was assessed via a timed "pressure test", in which 3 months were given to build organisms to produce 10 molecules unknown to us in advance. By applying a diversity of new approaches, we produced the desired molecule or a closely related one for six out of 10 targets during the performance period and made advances toward production of the others as well. Specifically, we increased the titers of 1-hexadecanol, pyrrolnitrin, and pacidamycin D, found novel routes to the enediyne warhead underlying powerful antimicrobials, established a cell-free system for monoterpene production, produced an intermediate toward vincristine biosynthesis, and encoded 7802 individually retrievable pathways to 540 bisindoles in a DNA pool. Pathways to tetrahydrofuran and barbamide were designed and constructed, but toxicity or analytical tools inhibited further progress. In sum, we constructed 1.2 Mb DNA, built 215 strains spanning five species (Saccharomyces cerevisiae, Escherichia coli, Streptomyces albidoflavus, Streptomyces coelicolor, and Streptomyces albovinaceus), established two cell-free systems, and performed 690 assays developed in-house for the molecules.
dc.language.isoen
dc.publisherAmerican Chemical Society (ACS)
dc.relation.isversionof10.1021/JACS.7B13292
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
dc.sourceOther repository
dc.titleA pressure test to make 10 molecules in 90 days: External evaluation of methods to engineer biology
dc.typeArticle
dc.relation.journalJournal of the American Chemical Society
dc.eprint.versionAuthor's final manuscript
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2019-09-19T12:24:24Z
dspace.orderedauthorsCasini, A; Chang, F-Y; Eluere, R; King, AM; Young, EM; Dudley, QM; Karim, A; Pratt, K; Bristol, C; Forget, A; Ghodasara, A; Warden-Rothman, R; Gan, R; Cristofaro, A; Borujeni, AE; Ryu, M-H; Li, J; Kwon, Y-C; Wang, H; Tatsis, E; Rodriguez-Lopez, C; O’Connor, S; Medema, MH; Fischbach, MA; Jewett, MC; Voigt, C; Gordon, DB
dspace.date.submission2019-09-19T12:24:30Z
mit.journal.volume140
mit.journal.issue12
mit.metadata.statusAuthority Work and Publication Information Needed


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record

VersionItemDateSummary

*Selected version