| Literature DB >> 25792511 |
T C Williams1, N J H Averesch2, G Winter2, M R Plan3, C E Vickers1, L K Nielsen1, J O Krömer4.
Abstract
Some of the most productive metabolic engineering strategies involve genetic modifications that cause severe metabolic burden on the host cell. Growth-limiting genetic modifications can be more effective if they are 'switched on' after a population growth phase has been completed. To address this problem we have engineered dynamic regulation using a previously developed synthetic quorum sensing circuit in Saccharomyces cerevisiae. The circuit autonomously triggers gene expression at a high population density, and was linked with an RNA interference module to enable target gene silencing. As a demonstration the circuit was used to control flux through the shikimate pathway for the production of para-hydroxybenzoic acid (PHBA). Dynamic RNA repression allowed gene knock-downs which were identified by elementary flux mode analysis as highly productive but with low biomass formation to be implemented after a population growth phase, resulting in the highest published PHBA titer in yeast (1.1mM).Entities:
Keywords: Cell–cell communication; Dynamic regulation; PHBA; Quorum sensing; RNA interference; Shikimate pathway
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Year: 2015 PMID: 25792511 DOI: 10.1016/j.ymben.2015.03.008
Source DB: PubMed Journal: Metab Eng ISSN: 1096-7176 Impact factor: 9.783