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dc.contributor.authorSolomon, Kevin V
dc.contributor.authorSanders, Tarielle M
dc.contributor.authorPrather, Kristala LJ
dc.date.accessioned2021-10-27T19:57:11Z
dc.date.available2021-10-27T19:57:11Z
dc.date.issued2012
dc.identifier.urihttps://hdl.handle.net/1721.1/133908
dc.description.abstractSuccessful redirection of endogenous resources into heterologous pathways is a central tenet in the creation of efficient microbial cell factories. This redirection, however, may come at a price of poor biomass accumulation, reduced cofactor regeneration and low recombinant enzyme expression. In this study, we propose a metabolite valve to mitigate these issues by dynamically tuning endogenous processes to balance the demands of cell health and pathway efficiency. A control node of glucose utilization, glucokinase (Glk), was exogenously manipulated through either engineered antisense RNA or an inverting gene circuit. Using these techniques, we were able to directly control glycolytic flux, reducing the specific growth rate of engineered Escherichia coli by up to 50% without altering final biomass accumulation. This modulation was accompanied by successful redirection of glucose into a model pathway leading to an increase in the pathway yield and reduced carbon waste to acetate. This work represents one of the first examples of the dynamic redirection of glucose away from central carbon metabolism and enables the creation of novel, efficient intracellular pathways with glucose used directly as a substrate. © 2012 Elsevier Inc.
dc.language.isoen
dc.publisherElsevier BV
dc.relation.isversionof10.1016/j.ymben.2012.08.006
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs License
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceProf. Prather
dc.titleA dynamic metabolite valve for the control of central carbon metabolism
dc.typeArticle
dc.identifier.citationSolomon, K. V., T. M. Sanders, and K. L. J. Prather. "A Dynamic Metabolite Valve for the Control of Central Carbon Metabolism." Metabolic Engineering 14 6 (2012): 661-71.
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineering
dc.contributor.departmentMIT Synthetic Biology Engineering Research Center
dc.relation.journalMetabolic Engineering
dc.eprint.versionAuthor's final manuscript
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2019-07-22T14:02:58Z
dspace.orderedauthorsSolomon, KV; Sanders, TM; Prather, KLJ
dspace.date.submission2019-07-22T14:02:59Z
mit.journal.volume14
mit.journal.issue6
mit.metadata.statusAuthority Work and Publication Information Needed


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