Baumschlager Armin, Aoki Stephanie K, Khammash Mustafa
Department of Biosystems Science and Engineering (D-BSSE), ETH-Zürich , Mattenstrasse 26, 4058 Basel, Switzerland.
ACS Synth Biol. 2017 Nov 17;6(11):2157-2167. doi: 10.1021/acssynbio.7b00169. Epub 2017 Oct 18.
Light has emerged as a control input for biological systems due to its precise spatiotemporal resolution. The limited toolset for light control in bacteria motivated us to develop a light-inducible transcription system that is independent from cellular regulation through the use of an orthogonal RNA polymerase. Here, we present our engineered blue light-responsive T7 RNA polymerases (Opto-T7RNAPs) that show properties such as low leakiness of gene expression in the dark state, high expression strength when induced with blue light, and an inducible range of more than 300-fold. Following optimization of the system to reduce expression variability, we created a variant that returns to the inactive dark state within minutes once the blue light is turned off. This allows for precise dynamic control of gene expression, which is a key aspect for most applications using optogenetic regulation. The regulators, which only require blue light from ordinary light-emitting diodes for induction, were developed and tested in the bacterium Escherichia coli, which is a crucial cell factory for biotechnology due to its fast and inexpensive cultivation and well understood physiology and genetics. Opto-T7RNAP, with minor alterations, should be extendable to other bacterial species as well as eukaryotes such as mammalian cells and yeast in which the T7 RNA polymerase and the light-inducible Vivid regulator have been shown to be functional. We anticipate that our approach will expand the applicability of using light as an inducer for gene expression independent from cellular regulation and allow for a more reliable dynamic control of synthetic and natural gene networks.
由于具有精确的时空分辨率,光已成为生物系统的一种控制输入方式。细菌中用于光控的工具集有限,这促使我们开发一种光诱导转录系统,该系统通过使用正交RNA聚合酶独立于细胞调控。在此,我们展示了我们设计的蓝光响应型T7 RNA聚合酶(Opto-T7RNAPs),其具有诸如在黑暗状态下基因表达泄漏率低、蓝光诱导时表达强度高以及诱导范围超过300倍等特性。在对系统进行优化以降低表达变异性后,我们创建了一个变体,一旦蓝光关闭,该变体在几分钟内就会回到无活性的黑暗状态。这允许对基因表达进行精确的动态控制,这是大多数使用光遗传学调控的应用的关键方面。这些调控因子仅需要来自普通发光二极管的蓝光进行诱导,已在大肠杆菌中开发和测试,大肠杆菌因其快速且廉价的培养以及对其生理学和遗传学的深入了解,是生物技术领域至关重要的细胞工厂。经过微小改动,Opto-T7RNAP应该也可扩展到其他细菌物种以及真核生物,如哺乳动物细胞和酵母,在这些细胞中T7 RNA聚合酶和光诱导的Vivid调控因子已被证明具有功能。我们预计,我们的方法将扩大使用光作为独立于细胞调控的基因表达诱导剂的适用性,并允许对合成和天然基因网络进行更可靠的动态控制。