Key Laboratory of Systems Bioengineering (Ministry of Education), School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, PR China; SynBio Research Platform, Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin University, Tianjin 300072, PR China.
Key Laboratory of Systems Bioengineering (Ministry of Education), School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, PR China; SynBio Research Platform, Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin University, Tianjin 300072, PR China.
Biotechnol Adv. 2017 Dec;35(8):1022-1031. doi: 10.1016/j.biotechadv.2017.09.002. Epub 2017 Sep 6.
Microbial production of monoterpenes is often limited by their cytotoxicity and in vivo conversion. Therefore, alleviating cytotoxicity and reducing conversion by chassis engineering are highly desirable. On the other hand, engineering key enzymes is also critical for improving monoterpenes production through facilitating the biosynthesis process. Here we critically review recent advances in cytotoxicity alleviation, reducing in vivo conversion, selecting geranyl diphosphate synthase and engineering monoterpene synthases. These achievements would lead to the development of superior chassis with improved tolerance to cytotoxicity and rationally tailored metabolites profiles to improve titer, yield and productivity for the production of monoterpenes by microbial cells.
萜类化合物的微生物生产通常受到其细胞毒性和体内转化的限制。因此,通过底盘工程减轻细胞毒性和减少转化是非常理想的。另一方面,通过促进生物合成过程,工程关键酶对于提高萜类化合物的生产也至关重要。在这里,我们批判性地回顾了减轻细胞毒性、减少体内转化、选择香叶基二磷酸合酶和工程单萜合酶的最新进展。这些成就将导致开发出具有更高耐受性的底盘,以及合理调整代谢物谱,以提高萜类化合物的产量、产率和生产力,从而通过微生物细胞生产萜类化合物。