| Literature DB >> 33017684 |
Matthew Rienzo1, Shaina J Jackson1, Lawrence K Chao1, Timothy Leaf1, Thomas J Schmidt1, Adam H Navidi1, Dana C Nadler1, Maud Ohler1, Michael D Leavell2.
Abstract
Systems metabolic engineering faces the formidable task of rewiring microbial metabolism to cost-effectively generate high-value molecules from a variety of inexpensive feedstocks for many different applications. Because these cellular systems are still too complex to model accurately, vast collections of engineered organism variants must be systematically created and evaluated through an enormous trial-and-error process in order to identify a manufacturing-ready strain. The high-throughput screening of strains to optimize their scalable manufacturing potential requires execution of many carefully controlled, parallel, miniature fermentations, followed by high-precision analysis of the resulting complex mixtures. This review discusses strategies for the design of high-throughput, small-scale fermentation models to predict improved strain performance at large commercial scale. Established and promising approaches from industrial and academic groups are presented for both cell culture and analysis, with primary focus on microplate- and microfluidics-based screening systems.Keywords: Analytical techniques; Automation; Bioprocess development; Bioreactors; Fermentation; High-throughput screening; Metabolomics; Microfluidics
Year: 2020 PMID: 33017684 DOI: 10.1016/j.ymben.2020.09.004
Source DB: PubMed Journal: Metab Eng ISSN: 1096-7176 Impact factor: 9.783