Optimizing the strain engineering process for industrial-scale production of bio-based molecules.

IF 3.2 4区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Eric Abbate, Jennifer Andrion, Amanda Apel, Matthew Biggs, Julie Chaves, Kristi Cheung, Anthony Ciesla, Alia Clark-ElSayed, Michael Clay, Riarose Contridas, Richard Fox, Glenn Hein, Dan Held, Andrew Horwitz, Stefan Jenkins, Karolina Kalbarczyk, Nandini Krishnamurthy, Mona Mirsiaghi, Katherine Noon, Mike Rowe, Tyson Shepherd, Katia Tarasava, Theodore M Tarasow, Drew Thacker, Gladys Villa, Krishna Yerramsetty
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引用次数: 0

Abstract

Biomanufacturing could contribute as much as ${\$}$30 trillion to the global economy by 2030. However, the success of the growing bioeconomy depends on our ability to manufacture high-performing strains in a time- and cost-effective manner. The Design-Build-Test-Learn (DBTL) framework has proven to be an effective strain engineering approach. Significant improvements have been made in genome engineering, genotyping, and phenotyping throughput over the last couple of decades that have greatly accelerated the DBTL cycles. However, to achieve a radical reduction in strain development time and cost, we need to look at the strain engineering process through a lens of optimizing the whole cycle, as opposed to simply increasing throughput at each stage. We propose an approach that integrates all 4 stages of the DBTL cycle and takes advantage of the advances in computational design, high-throughput genome engineering, and phenotyping methods, as well as machine learning tools for making predictions about strain scale-up performance. In this perspective, we discuss the challenges of industrial strain engineering, outline the best approaches to overcoming these challenges, and showcase examples of successful strain engineering projects for production of heterologous proteins, amino acids, and small molecules, as well as improving tolerance, fitness, and de-risking the scale-up of industrial strains.

Abstract Image

Abstract Image

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优化菌株工程工艺,实现生物基分子的工业规模生产。
到2030年,生物制造业可为全球经济贡献多达30万亿美元。然而,不断增长的生物经济的成功取决于我们以时间和成本效益高的方式生产高性能菌株的能力。设计-建造-测试-学习(DBTL)框架已被证明是一种有效的应变工程方法。在过去的几十年里,在基因组工程、基因分型和表型处理方面取得了显著的进步,极大地加速了DBTL周期。然而,为了彻底减少应变开发时间和成本,我们需要从优化整个周期的角度来看待应变工程过程,而不是简单地增加每个阶段的产量。我们提出了一种方法,该方法集成了DBTL循环的所有4个阶段,并利用了计算设计、高通量基因组工程和表型分析方法的进步,以及用于预测菌株放大性能的机器学习工具。从这个角度来看,我们讨论了工业菌株工程的挑战,概述了克服这些挑战的最佳方法,并展示了成功的菌株工程项目的例子,这些项目用于生产异源蛋白质、氨基酸和小分子,以及提高工业菌株的耐受性、适应性和降低扩大规模的风险。
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来源期刊
Journal of Industrial Microbiology & Biotechnology
Journal of Industrial Microbiology & Biotechnology 工程技术-生物工程与应用微生物
CiteScore
7.70
自引率
0.00%
发文量
25
审稿时长
3 months
期刊介绍: The Journal of Industrial Microbiology and Biotechnology is an international journal which publishes papers describing original research, short communications, and critical reviews in the fields of biotechnology, fermentation and cell culture, biocatalysis, environmental microbiology, natural products discovery and biosynthesis, marine natural products, metabolic engineering, genomics, bioinformatics, food microbiology, and other areas of applied microbiology
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