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Engineering Biology to Construct Microbial Chassis for the Production of Difficult-to-Express Proteins

机译:工程生物学以构建难以表达的蛋白质生产的微生物底盘

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摘要

A large proportion of the recombinant proteins manufactured today rely on microbe-based expression systems owing to their relatively simple and cost-effective production schemes. However, several issues in microbial protein expression, including formation of insoluble aggregates, low protein yield, and cell death are still highly recursive and tricky to optimize. These obstacles are usually rooted in the metabolic capacity of the expression host, limitation of cellular translational machineries, or genetic instability. To this end, several microbial strains having precisely designed genomes have been suggested as a way around the recurrent problems in recombinant protein expression. Already, a growing number of prokaryotic chassis strains have been genome-streamlined to attain superior cellular fitness, recombinant protein yield, and stability of the exogenous expression pathways. In this review, we outline challenges associated with heterologous protein expression, some examples of microbial chassis engineered for the production of recombinant proteins, and emerging tools to optimize the expression of heterologous proteins. In particular, we discuss the synthetic biology approaches to design and build and test genome-reduced microbial chassis that carry desirable characteristics for heterologous protein expression.
机译:由于它们相对简单且经济高效的生产方案,当今生产的大部分重组蛋白依赖于基于微生物的表达系统。但是,微生物蛋白表达中的几个问题,包括不溶性聚集体的形成,蛋白产量低和细胞死亡,仍然是高度递归的并且难以优化。这些障碍通常源于表达宿主的代谢能力,细胞翻译机制的限制或遗传不稳定。为此,已经提出了几种具有精确设计的基因组的微生物菌株作为解决重组蛋白表达中反复出现的问题的方法。目前,已经有越来越多的原核底盘菌株在基因组上得到简化,以实现卓越的细胞适应性,重组蛋白产量以及外源表达途径的稳定性。在这篇综述中,我们概述了与异源蛋白表达相关的挑战,为重组蛋白生产而工程化的微生物底盘的一些实例,以及优化异源蛋白表达的新兴工具。特别是,我们讨论了设计,构建和测试基因组减少的微生物底盘的合成生物学方法,这些方法具有异源蛋白表达的理想特性。

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