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dc.contributor.authorLeonard, Effendi
dc.contributor.authorRunguphan, Weerawat
dc.contributor.authorO'Connor, Sarah Ellen
dc.contributor.authorPrather, Kristala L. Jones
dc.date.accessioned2012-01-30T16:41:27Z
dc.date.available2012-01-30T16:41:27Z
dc.date.issued2009-04
dc.identifier.issn1552-4450
dc.identifier.issn1552-4469
dc.identifier.urihttp://hdl.handle.net/1721.1/68707
dc.description.abstractNumerous drugs and drug precursors in the current pharmacopoeia originate from plant sources. The limited yield of some bioactive compounds in plant tissues, however, presents a significant challenge for large-scale drug development. Metabolic engineering has facilitated the development of plant cell and tissue systems as alternative production platforms that can be scaled up in a controlled environment. Nevertheless, effective metabolic engineering approaches and the predictability of genetic transformations are often obscured due to the myriad cellular complexities. Progress in systems biology has aided the understanding of genome-wide interconnectivities in plant-based systems. In parallel, the bottom-up assembly of plant biosynthetic pathways in microorganisms demonstrated the possibilities of a new means of production. In this Perspective, we discuss the opportunities and challenges of implementing metabolic engineering in various platforms for the synthesis of natural and unnatural plant alkaloids.en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (grant no. 0540879)en_US
dc.description.sponsorshipSynthetic Biology Engineering Research Centeren_US
dc.description.sponsorshipMassachusetts Institute of Technology. Energy Initiative (Grant 6917278)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (GM074820)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (MCB-0719120)en_US
dc.language.isoen_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/nchembio.160en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourceProf. Prather via Erja Kajosaloen_US
dc.titleOpportunities in metabolic engineering to facilitate scalable alkaloid productionen_US
dc.typeArticleen_US
dc.identifier.citationLeonard, Effendi et al. “Opportunities in metabolic engineering to facilitate scalable alkaloid production.” Nature Chemical Biology 5.5 (2009): 292-300.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.approverPrather, Kristala L. Jones
dc.contributor.mitauthorLeonard, Effendi
dc.contributor.mitauthorRunguphan, Weerawat
dc.contributor.mitauthorO'Connor, Sarah Ellen
dc.contributor.mitauthorPrather, Kristala L. Jones
dc.relation.journalNature Chemical Biologyen_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.orderedauthorsLeonard, Effendi; Runguphan, Weerawat; O'Connor, Sarah; Prather, Kristala Jonesen
dc.identifier.orcidhttps://orcid.org/0000-0003-0437-3157
dspace.mitauthor.errortrue
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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