Shuo Yang , Liyun Song , Jing Wang , Jianzhi Zhao , Hongting Tang , Xiaoming Bao
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This review focuses on the strategies that enhance protein production by regulating transcription through promoter engineering, codon optimization, and expression system optimization. Additionally, we describe modifications to the secretory pathway, including engineered protein translocation, protein folding, glycosylation modification, and vesicle trafficking. Furthermore, we discuss global metabolic pathway optimization and other relevant strategies, such as the disruption of protein degradation, cell wall engineering, and random mutagenesis. 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However, meeting industrial and market requirements with the current low microbial production of recombinant proteins can be challenging. To address this issue, numerous efforts have been made to enhance the ability of yeast cell factories to efficiently produce proteins. In this review, we provide an overview of recent advances in <em>S. cerevisiae</em> engineering to improve recombinant protein production. This review focuses on the strategies that enhance protein production by regulating transcription through promoter engineering, codon optimization, and expression system optimization. Additionally, we describe modifications to the secretory pathway, including engineered protein translocation, protein folding, glycosylation modification, and vesicle trafficking. Furthermore, we discuss global metabolic pathway optimization and other relevant strategies, such as the disruption of protein degradation, cell wall engineering, and random mutagenesis. 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引用次数: 0
摘要
酿酒酵母具有生长速度快、坚固耐用、生物安全性高、通过成熟的基因组修饰技术易于操作以及在真核生物中存在保守的翻译后修饰途径等特点,是生产有价值的重组蛋白的绝佳微生物细胞工厂。然而,以目前较低的微生物生产重组蛋白来满足工业和市场需求可能具有挑战性。为了解决这个问题,人们做出了许多努力来提高酵母细胞工厂高效生产蛋白质的能力。在这篇综述中,我们概述了为提高重组蛋白产量而进行的酵母工程学研究的最新进展。本综述重点介绍通过启动子工程、密码子优化和表达系统优化来调节转录,从而提高蛋白质产量的策略。此外,我们还介绍了对分泌途径的改造,包括工程化蛋白质转运、蛋白质折叠、糖基化修饰和囊泡运输。此外,我们还讨论了全局代谢途径优化和其他相关策略,如破坏蛋白质降解、细胞壁工程和随机诱变。最后,我们对这一领域的发展趋势进行了展望,为改进 S. cerevisiae 重组蛋白生产的未来方向提供了见解。
Engineering Saccharomyces cerevisiae for efficient production of recombinant proteins
Saccharomyces cerevisiae is an excellent microbial cell factory for producing valuable recombinant proteins because of its fast growth rate, robustness, biosafety, ease of operability via mature genomic modification technologies, and the presence of a conserved post-translational modification pathway among eukaryotic organisms. However, meeting industrial and market requirements with the current low microbial production of recombinant proteins can be challenging. To address this issue, numerous efforts have been made to enhance the ability of yeast cell factories to efficiently produce proteins. In this review, we provide an overview of recent advances in S. cerevisiae engineering to improve recombinant protein production. This review focuses on the strategies that enhance protein production by regulating transcription through promoter engineering, codon optimization, and expression system optimization. Additionally, we describe modifications to the secretory pathway, including engineered protein translocation, protein folding, glycosylation modification, and vesicle trafficking. Furthermore, we discuss global metabolic pathway optimization and other relevant strategies, such as the disruption of protein degradation, cell wall engineering, and random mutagenesis. Finally, we provide an outlook on the developmental trends in this field, offering insights into future directions for improving recombinant protein production in S. cerevisiae.