Mishra Shivangi, Perkovich Paul M, Mitchell Wayne P, Venkataraman Maya, Pfleger Brian F
Department of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, WI 53706, USA.
LanzaTech, Skokie, IL 60077, USA.
J Ind Microbiol Biotechnol. 2024 Jan 9;51. doi: 10.1093/jimb/kuae008.
The Gram-negative betaproteobacterium Cupriavidus necator is a chemolithotroph that can convert carbon dioxide into biomass. Cupriavidus necator has been engineered to produce a variety of high-value chemicals in the past. However, there is still a lack of a well-characterized toolbox for gene expression and genome engineering. Development and optimization of biosynthetic pathways in metabolically engineered microorganisms necessitates control of gene expression via functional genetic elements such as promoters, ribosome binding sites (RBSs), and codon optimization. In this work, a set of inducible and constitutive promoters were validated and characterized in C. necator, and a library of RBSs was designed and tested to show a 50-fold range of expression for green fluorescent protein (gfp). The effect of codon optimization on gene expression in C. necator was studied by expressing gfp and mCherry genes with varied codon-adaptation indices and was validated by expressing codon-optimized variants of a C12-specific fatty acid thioesterase to produce dodecanoic acid. We discuss further hurdles that will need to be overcome for C. necator to be widely used for biosynthetic processes.
革兰氏阴性β-变形菌食铜菌(Cupriavidus necator)是一种化能自养菌,能够将二氧化碳转化为生物质。过去,人们对食铜菌进行了工程改造,使其能够生产多种高价值化学品。然而,目前仍然缺乏一个经过充分表征的用于基因表达和基因组工程的工具箱。在代谢工程改造的微生物中开发和优化生物合成途径需要通过启动子、核糖体结合位点(RBS)和密码子优化等功能遗传元件来控制基因表达。在这项工作中,一组诱导型和组成型启动子在食铜菌中得到了验证和表征,并且设计并测试了一个RBS文库,该文库显示绿色荧光蛋白(gfp)的表达范围可达50倍。通过表达具有不同密码子适应指数的gfp和mCherry基因,研究了密码子优化对食铜菌中基因表达的影响,并通过表达C12特异性脂肪酸硫酯酶的密码子优化变体来生产十二烷酸进行了验证。我们讨论了食铜菌要广泛用于生物合成过程还需要克服的其他障碍。