Alper Hal, Stephanopoulos Gregory
Department of Chemical Engineering, Massachusetts Institute of Technology, Room 56-469, Cambridge, MA 02139, USA.
Metab Eng. 2007 May;9(3):258-67. doi: 10.1016/j.ymben.2006.12.002. Epub 2007 Jan 8.
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, sigma(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.
现在人们普遍认为,大多数细胞表型受许多基因影响。因此,通过同时进行多个基因修饰,将极大地促进所需表型的构建,然而引入这种修饰的能力非常有限。在这里,我们证明,全局细胞转录机制的组件(具体来说,σ因子(70))可以进行改造,以实现转录组的全局扰动,这有助于揭示复杂的表型。我们给出了三种不同表型(乙醇耐受性、代谢物过量生产和多种表型)的结果作为概念验证。在每种情况下,全局转录机制工程(gTME)工具通过快速且更有效地优化表型,其表现优于传统方法。