Klein-Marcuschamer Daniel, Santos Christine Nicole S, Yu Huimin, Stephanopoulos Gregory
Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Appl Environ Microbiol. 2009 May;75(9):2705-11. doi: 10.1128/AEM.01888-08. Epub 2009 Feb 27.
Combinatorial or random methods for strain engineering have been extensively used for the improvement of multigenic phenotypes and other traits for which the underlying mechanism is not fully understood. Although the preferred method has traditionally been mutagenesis and selection, our laboratory has successfully used mutant transcription factors, which direct the RNA polymerase (RNAP) during transcription, to engineer complex phenotypes in microbial cells. Here, we show that it is also possible to impart new phenotypes by altering the RNAP core enzyme itself, in particular through mutagenesis of the alpha subunit of the bacterial polymerase. We present the use of this tool for improving tolerance of Escherichia coli to butanol and other solvents and for increasing the titers of two commercially relevant products, L-tyrosine and hyaluronic acid. In addition, we explore the underlying physiological changes that give rise to the solvent-tolerant mutant.
组合或随机的菌株工程方法已被广泛用于改善多基因表型以及其他潜在机制尚未完全了解的性状。尽管传统上首选的方法是诱变和筛选,但我们实验室已成功使用突变转录因子(其在转录过程中指导RNA聚合酶(RNAP))来改造微生物细胞中的复杂表型。在这里,我们表明通过改变RNAP核心酶本身,特别是通过诱变细菌聚合酶的α亚基,也有可能赋予新的表型。我们展示了使用该工具提高大肠杆菌对丁醇和其他溶剂的耐受性,以及提高两种商业相关产品L-酪氨酸和透明质酸的产量。此外,我们探索了导致耐溶剂突变体产生的潜在生理变化。