酿酒酵母
生物过程
异源的
酵母
异源表达
糖苷水解酶
合成生物学
生物
生物化学
酶
生物技术
纤维素
计算生物学
发酵
重组DNA
生化工程
基因
工程类
古生物学
作者
Riaan den Haan,Shaunita H. Rose,Rosemary A. Cripwell,Kim M. Trollope,Marthinus W. Myburgh,Marinda Viljoen‐Bloom,Willem H. van Zyl
标识
DOI:10.1016/j.biotechadv.2021.107859
摘要
Abstract Selected strains of Saccharomyces cerevisiae are used for commercial bioethanol production from cellulose and starch, but the high cost of exogenous enzymes for substrate hydrolysis remains a challenge. This can be addressed through consolidated bioprocessing (CBP) where S. cerevisiae strains are engineered to express recombinant glycoside hydrolases during fermentation. Looking back at numerous strategies undertaken over the past four decades to improve recombinant protein production in S. cerevisiae, it is evident that various steps in the protein production “pipeline” can be manipulated depending on the protein of interest and its anticipated application. In this review, we briefly introduce some of the strategies and highlight lessons learned with regards to improved transcription, translation, post-translational modification and protein secretion of heterologous hydrolases. We examine how host strain selection and modification, as well as enzyme compatibility, are crucial determinants for overall success. Finally, we discuss how lessons from heterologous hydrolase expression can inform modern synthetic biology and genome editing tools to provide process-ready yeast strains in future. However, it is clear that the successful expression of any particular enzyme is still unpredictable and requires a trial-and-error approach.
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