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

被引:102
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
相关论文
共 50 条
[1]   Dynamic metabolic engineering for increasing bioprocess productivity [J].
Anesiadis, Nikolaos ;
Cluett, William R. ;
Mahadevan, Radhakrishnan .
METABOLIC ENGINEERING, 2008, 10 (05) :255-266
[2]  
Averesch Nils J H, 2014, Metab Eng Commun, V1, P19, DOI 10.1016/j.meteno.2014.09.001
[3]   A walk-through of the yeast mating pheromone response pathway (vol 25, pg 1465, 2004) [J].
Bardwell, L .
PEPTIDES, 2005, 26 (02) :337-+
[4]   Microbial synthesis of p-hydroxybenzoic acid from glucose [J].
Barker, JL ;
Frost, JW .
BIOTECHNOLOGY AND BIOENGINEERING, 2001, 76 (04) :376-390
[5]   PLASMID-ENCODED PROTEIN - THE PRINCIPAL FACTOR IN THE METABOLIC BURDEN ASSOCIATED WITH RECOMBINANT BACTERIA [J].
BENTLEY, WE ;
MIRJALILI, N ;
ANDERSEN, DC ;
DAVIS, RH ;
KOMPALA, DS .
BIOTECHNOLOGY AND BIOENGINEERING, 1990, 35 (07) :668-681
[6]   Construction of synthetic regulatory networks in yeast [J].
Blount, Benjamin A. ;
Weenink, Tim ;
Ellis, Tom .
FEBS LETTERS, 2012, 586 (15) :2112-2121
[7]   Characterization of a glucose-repressed pyruvate kinase (Pyk2p) in Saccharomyces cerevisiae that is catalytically insensitive to fructose-1,6-bisphosphate [J].
Boles, E ;
Schulte, F ;
Miosga, T ;
Freidel, K ;
Schluter, E ;
Zimmermann, FK ;
Hollenberg, CP ;
Heinisch, JJ .
JOURNAL OF BACTERIOLOGY, 1997, 179 (09) :2987-2993
[8]   Applications of quorum sensing in biotechnology [J].
Choudhary, Swati ;
Schmidt-Dannert, Claudia .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2010, 86 (05) :1267-1279
[9]   Optimization of a Yeast RNA Interference System for Controlling Gene Expression and Enabling Rapid Metabolic Engineering [J].
Crook, Nathan C. ;
Schmitz, Alexander C. ;
Alper, Hal S. .
ACS SYNTHETIC BIOLOGY, 2014, 3 (05) :307-313
[10]   Metabolic engineering of muconic acid production in Saccharomyces cerevisiae [J].
Curran, Kathleen A. ;
Leavitt, Johnm. ;
Karim, AshtyS. ;
Alper, Hal S. .
METABOLIC ENGINEERING, 2013, 15 :55-66