Genetic switchboard for synthetic biology applications

被引:125
|
作者
Callura, Jarred M. [1 ,2 ,3 ]
Cantor, Charles R. [1 ]
Collins, James J. [1 ,2 ,3 ,4 ]
机构
[1] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
[2] Boston Univ, Howard Hughes Med Inst, Boston, MA 02215 USA
[3] Boston Univ, Ctr BioDynam, Boston, MA 02215 USA
[4] Harvard Univ, Wyss Inst Biol Inspired Engn, Boston, MA 02215 USA
基金
美国国家卫生研究院;
关键词
ESCHERICHIA-COLI; PHOSPHOGLUCOSE ISOMERASE; PROTEIN EXPRESSION; RIBOREGULATORS; METABOLISM; BACTERIA;
D O I
10.1073/pnas.1203808109
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A key next step in synthetic biology is to combine simple circuits into higher-order systems. In this work, we expanded our synthetic riboregulation platform into a genetic switchboard that independently controls the expression of multiple genes in parallel. First, we designed and characterized riboregulator variants to complete the foundation of the genetic switchboard; then we constructed the switchboard sensor, a testing platform that reported on quorum-signaling molecules, DNA damage, iron starvation, and extracellular magnesium concentration in single cells. As a demonstration of the biotechnological potential of our synthetic device, we built a metabolism switchboard that regulated four metabolic genes, pgi, zwf, edd, and gnd, to control carbon flow through three Escherichia coli glucose-utilization pathways: the Embden-Meyerhof, Entner-Doudoroff, and pentose phosphate pathways. We provide direct evidence for switchboard-mediated shunting of metabolic flux by measuring mRNA levels of the riboregulated genes, shifts in the activities of the relevant enzymes and pathways, and targeted changes to the E. coli metabolome. The design, testing, and implementation of the genetic switchboard illustrate the successful construction of a higher-order systemthat can be used for a broad range of practical applications in synthetic biology and biotechnology.
引用
收藏
页码:5850 / 5855
页数:6
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