Centre for Industrial Biotechnology and Biocatalysis (InBio.be), Department of Biotechnology, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, 9000, Ghent, Belgium.
Department of Data Analysis and Mathematical Modelling, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, 9000, Ghent, Belgium.
Metab Eng. 2020 Nov;62:10-19. doi: 10.1016/j.ymben.2020.07.007. Epub 2020 Aug 11.
As a biorefinery platform host, Escherichia coli has been used extensively to produce metabolites of commercial interest. Integration of foreign DNA onto the bacterial genome allows for stable expression overcoming the need for plasmid expression and its associated instability. Despite the development of numerous tools and genome editing technologies, the question of where to incorporate a synthetic pathway remains unanswered. To address this issue, we studied the genomic expression in E. coli and linked it not only to 26 rationally selected genomic locations, but also to the gene direction in relation to the DNA replication fork, to the carbon and nitrogen source, to DNA folding and supercoiling, and to metabolic burden. To enable these experiments, we have designed a fluorescent expression cassette to eliminate specific local effects on gene expression. Overall it can be concluded that although the expression range obtained by changing the genomic location of a pathway is small compared to the range typically seen in promoter-RBS libraries, the effect of culture medium, environmental stress and metabolic burden can be substantial. The characterization of multiple effects on genomic expression, and the associated libraries of well-characterized strains, will only stimulate and improve the creation of stable production hosts fit for industrial settings.
作为生物炼制平台宿主,大肠杆菌被广泛用于生产具有商业价值的代谢产物。将外源 DNA 整合到细菌基因组中可以进行稳定表达,克服了质粒表达及其相关不稳定性的需要。尽管已经开发了许多工具和基因组编辑技术,但外源基因整合的位置仍然是一个悬而未决的问题。为了解决这个问题,我们研究了大肠杆菌的基因组表达,并将其不仅与 26 个经过合理选择的基因组位置相关联,还与基因方向相对于 DNA 复制叉、碳源和氮源、DNA 折叠和超螺旋以及代谢负担相关联。为了进行这些实验,我们设计了一个荧光表达盒,以消除基因表达的特定局部影响。总的来说,可以得出结论,尽管与启动子-RBS 文库中通常看到的范围相比,改变途径的基因组位置所获得的表达范围很小,但培养基、环境压力和代谢负担的影响可能很大。对基因组表达的多种影响的特性分析,以及相关的经过良好表征的菌株文库,将只会刺激和改进适合工业环境的稳定生产宿主的创建。