生物
质粒
大肠杆菌
基因组DNA
计算生物学
基因
基因组不稳定性
表情盒
基因组
遗传学
DNA
基因表达
DNA损伤
重组DNA
载体(分子生物学)
作者
Anke Goormans,Nico Snoeck,Hannes Decadt,K. Vermeulen,Gert Peters,Pieter Coussement,Dries Van Herpe,Joeri Beauprez,Sofie De Maeseneire,Wim Soetaert
标识
DOI:10.1016/j.ymben.2020.07.007
摘要
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.
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