作者
Eric Abbate,Jennifer Andrion,Amanda Reider Apel,M. S. Biggs,Julie E. Chaves,Ka Chun Cheung,Anthony Ciesla,Alia Clark-ElSayed,Michael R. Clay,Riarose Contridas,Richard J. Fox,G.F. Hein,Dan Held,Andrew A. Horwitz,Stefan Jenkins,K. Kalbarczyk,Nandini Krishnamurthy,Mona Mirsiaghi,Katherine Noon,Michael Rowe,Tyson R. Shepherd,Katia Tarasava,Theodore M. Tarasow,Drew Thacker,Gianluca Villa,Krishna Yerramsetty
摘要
Biomanufacturing could contribute as much as $30 trillion to the global economy by 2030. But 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 four 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 scaleup 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 scaleup of industrial strains.