Quorum-sensing linked RNA interference for dynamic metabolic pathway control in Saccharomyces cerevisiae

被引:99
作者
Williams, T. C. [1 ]
Averesch, N. J. H. [2 ]
Winter, G. [2 ]
Plan, M. R. [1 ,3 ]
Vickers, C. E. [1 ]
Nielsen, L. K. [1 ]
Kroemer, J. O. [2 ,4 ]
机构
[1] Univ Queensland, AIBN, St Lucia, Qld 4072, Australia
[2] Univ Queensland, Ctr Microbial Electrosynth CEMES, St Lucia, Qld 4072, Australia
[3] Univ Queensland, Metabol Australia Queensland Node, St Lucia, Qld 4072, Australia
[4] Univ Queensland, AWMC, St Lucia, Qld 4072, Australia
基金
澳大利亚研究理事会;
关键词
Quorum sensing; Dynamic regulation; Cell-cell communication; PHBA; Shikimate pathway; RNA interference; P-HYDROXYBENZOIC ACID; 4-HYDROXYBENZOIC ACID; SYNTHETIC BIOLOGY; ESCHERICHIA-COLI; BUDDING YEAST; UBIC GENE; EXPRESSION; PROTEIN; BIOSYNTHESIS; CONSTRUCTION;
D O I
10.1016/j.ymben.2015.03.008
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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 Sacchuromyces 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 (1.1 mM). (C) 2015 International Metabolic Engineering Society. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:124 / 134
页数:11
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