Global transcription machinery engineering: A new approach for improving cellular phenotype

被引:321
作者
Alper, Hal [1 ]
Stephanopoulos, Gregory [1 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
关键词
sigma factor engineering; ethanol tolerance; metabolic engineering; directed evolution; lycopene production;
D O I
10.1016/j.ymben.2006.12.002
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
It is now generally accepted that most cellular phenotypes are affected by many genes. As a result, engineering a desired phenotype would be facilitated enormously by simultaneous multiple gene modification, yet the capacity to introduce such modifications is very limited. Here, we demonstrate that the components of global cellular transcription machinery (specifically, a 70) can be engineered to allow for global perturbations of the transcriptome, which can help unlock complex phenotypes. Results from three distinct phenotypes (ethanol tolerance, metabolite overproduction, and multiple phenotypes) are provided as proof- of-concept. In each case, the tool of global transcription machinery engineering (gTME) outperformed traditional approaches by quickly and more effectively optimizing phenotypes. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:258 / 267
页数:10
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