Li Songyuan, Jendresen Christian Bille, Grünberger Alexander, Ronda Carlotta, Jensen Sheila Ingemann, Noack Stephan, Nielsen Alex Toftgaard
The Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Building 220, Kemitorvet, 2800 Kgs. Lyngby, Denmark.
Forschungszentrum Jülich GmbH, IBG-1: Biotechnology, 52425, Jülich, Germany.
Metab Eng. 2016 Nov;38:274-284. doi: 10.1016/j.ymben.2016.09.003. Epub 2016 Sep 16.
Production of proteins and biochemicals in microbial cell factories is often limited by carbon and energy spent on excess biomass formation. To address this issue, we developed several genetic growth switches based on CRISPR interference technology. We demonstrate that growth of Escherichia coli can be controlled by repressing the DNA replication machinery, by targeting dnaA and oriC, or by blocking nucleotide synthesis through pyrF or thyA. This way, total GFP-protein production could be increased by up to 2.2-fold. Single-cell dynamic tracking in microfluidic systems was used to confirm functionality of the growth switches. Decoupling of growth from production of biochemicals was demonstrated for mevalonate, a precursor for isoprenoid compounds. Mass yield of mevalonate was increased by 41%, and production was maintained for more than 45h after activation of the pyrF-based growth switch. The developed methods represent a promising approach for increasing production yield and titer for proteins and biochemicals.
微生物细胞工厂中蛋白质和生物化学物质的生产常常受到用于过量生物质形成的碳和能量的限制。为了解决这个问题,我们基于CRISPR干扰技术开发了几种基因生长开关。我们证明,通过靶向dnaA和oriC抑制DNA复制机制,或通过pyrF或thyA阻断核苷酸合成,可以控制大肠杆菌的生长。通过这种方式,总绿色荧光蛋白(GFP)产量可提高至2.2倍。利用微流控系统中的单细胞动态跟踪来确认生长开关的功能。对于类异戊二烯化合物的前体甲羟戊酸,证明了生长与生物化学物质生产的解耦。基于pyrF的生长开关激活后,甲羟戊酸的质量产率提高了41%,并且生产维持了超过45小时。所开发的方法是提高蛋白质和生物化学物质产量和滴度的一种有前景的方法。