Castillo-Hair Sebastian M, Fujita Masaya, Igoshin Oleg A, Tabor Jeffrey J
Department of Bioengineering , Rice University , 6100 Main Street , Houston , Texas 77005 , United States.
Department of Biology and Biochemistry , University of Houston , 4800 Calhoun Road , Houston , Texas 77004 , United States.
ACS Synth Biol. 2019 Jul 19;8(7):1673-1678. doi: 10.1021/acssynbio.8b00469. Epub 2019 Jun 28.
is the leading model Gram-positive bacterium, and a widely used chassis for industrial protein production. However, research is limited by a lack of inducible promoter systems with low leakiness and high dynamic range. Here, we engineer an inducible promoter system based on the T7 RNA Polymerase (T7 RNAP), the lactose repressor LacI, and the chimeric promoter P, integrated as a single copy in the genome. In the absence of IPTG, LacI strongly represses T7 RNAP and P and minimizes leakiness. Addition of IPTG derepresses P and simultaneously induces expression of T7RNAP, which results in very high output expression. Using green fluorescent and β-galactosidase reporter proteins, we estimate that this LacI-T7 system can regulate expression with a dynamic range of over 10 000, by far the largest reported for an inducible promoter system. Furthermore, LacI-T7 responds to similar IPTG concentrations and with similar kinetics as the widely used P IPTG-inducible system, which we show has a dynamic range of at most 300 in a similar genetic context. Due to its superior performance, our LacI-T7 system should have broad applications in fundamental biology studies and biotechnology.
是革兰氏阳性菌的主要模型,也是工业蛋白质生产中广泛使用的底盘。然而,研究受到缺乏低渗漏率和高动态范围的诱导型启动子系统的限制。在这里,我们构建了一种基于T7 RNA聚合酶(T7 RNAP)、乳糖阻遏物LacI和嵌合启动子P的诱导型启动子系统,该系统作为单拷贝整合到基因组中。在没有异丙基-β-D-硫代半乳糖苷(IPTG)的情况下,LacI强烈抑制T7 RNAP和P,并将渗漏率降至最低。添加IPTG可解除对P的抑制,并同时诱导T7RNAP的表达,从而导致非常高的输出表达。使用绿色荧光蛋白和β-半乳糖苷酶报告蛋白,我们估计这个LacI-T7系统可以在超过10000的动态范围内调节表达,这是迄今为止报道的诱导型启动子系统中最大的动态范围。此外,LacI-T7对IPTG浓度的响应和动力学与广泛使用的P IPTG诱导系统相似,我们发现在相似的遗传背景下,该系统的动态范围最多为300。由于其卓越的性能,我们的LacI-T7系统应该在基础生物学研究和生物技术中有广泛的应用。