Johnson Abayomi Oluwanbe, Gonzalez-Villanueva Miriam, Tee Kang Lan, Wong Tuck Seng
Department of Chemical & Biological Engineering and Advanced Biomanufacturing Centre , University of Sheffield , Sir Robert Hadfield Building, Mappin Street , Sheffield S1 3JD , United Kingdom.
ACS Synth Biol. 2018 Aug 17;7(8):1918-1928. doi: 10.1021/acssynbio.8b00136. Epub 2018 Jul 19.
Well-characterized promoters with variable strength form the foundation of heterologous pathway optimization. It is also a key element that bolsters the success of microbial engineering and facilitates the development of biological tools like biosensors. In comparison to microbial hosts such as Escherichia coli and Saccharomyces cerevisiae, the promoter repertoire of Cupriavidus necator H16 is highly limited. This limited number of characterized promoters poses a significant challenge during the engineering of C. necator H16 for biomanufacturing and biotechnological applications. In this article, we first examined the architecture and genetic elements of the four most widely used constitutive promoters of C. necator H16 (i.e., P , P , P , and P ) and established a narrow 6-fold difference in their promoter activities. Next, using these four promoters as starting points and applying a range of genetic modifications (including point mutation, length alteration, incorporation of regulatory genetic element, promoter hybridization, and configuration alteration), we created a library of 42 constitutive promoters, all of which are functional in C. necator H16. Although these promoters are also functional in E. coli, they show different promoter strength and hierarchical rank of promoter activity. Subsequently, the activity of each promoter was individually characterized, using l-arabinose-inducible P promoter as a benchmark. This study has extended the range of constitutive promoter activities to 137-fold, with some promoter variants exceeding the l-arabinose-inducible range of P promoter. Not only has the work enhanced our flexibility in engineering C. necator H16, it presented novel strategies in adjusting promoter activity in C. necator H16 and highlighted similarities and differences in transcriptional activity between this organism and E. coli.
具有可变强度且特征明确的启动子构成了异源途径优化的基础。它也是推动微生物工程成功并促进生物传感器等生物工具发展的关键要素。与大肠杆菌和酿酒酵母等微生物宿主相比,食酸丛毛单胞菌H16的启动子库非常有限。在对食酸丛毛单胞菌H16进行生物制造和生物技术应用的工程改造过程中,这种数量有限的已表征启动子构成了重大挑战。在本文中,我们首先研究了食酸丛毛单胞菌H16四个最广泛使用的组成型启动子(即P 、P 、P 和P )的结构和遗传元件,并确定了它们的启动子活性存在6倍的微小差异。接下来,以这四个启动子为起点,应用一系列基因改造(包括点突变、长度改变、调控基因元件的掺入、启动子杂交和构型改变),我们创建了一个由42个组成型启动子组成的文库,所有这些启动子在食酸丛毛单胞菌H16中均具有功能。尽管这些启动子在大肠杆菌中也具有功能,但它们表现出不同的启动子强度和启动子活性等级。随后,以L-阿拉伯糖诱导型P 启动子为基准,分别对每个启动子的活性进行了表征。这项研究将组成型启动子活性范围扩展到了137倍,一些启动子变体超过了P 启动子的L-阿拉伯糖诱导范围。这项工作不仅提高了我们对食酸丛毛单胞菌H16进行工程改造的灵活性,还提出了在食酸丛毛单胞菌H16中调节启动子活性的新策略,并突出了该生物体与大肠杆菌之间转录活性的异同。