| Literature DB >> 29976056 |
Steven R Brown1, Marta Staff1, Rob Lee2, John Love1, David A Parker2, Stephen J Aves1, Thomas P Howard3.
Abstract
Multifactorial approaches can quickly and efficiently model complex, interacting natural or engineered biological systems in a way that traditional one-factor-at-a-time experimentation can fail to do. We applied a Design of Experiments (DOE) approach to model ethanol biosynthesis in yeast, which is well-understood and genetically tractable, yet complex. Six alcohol dehydrogenase (ADH) isozymes catalyze ethanol synthesis, differing in their transcriptional and post-translational regulation, subcellular localization, and enzyme kinetics. We generated a combinatorial library of all ADH gene deletions and measured the impact of gene deletion(s) and environmental context on ethanol production of a subset of this library. The data were used to build a statistical model that described known behaviors of ADH isozymes and identified novel interactions. Importantly, the model described features of ADH metabolic behavior without explicit a priori knowledge. The method is therefore highly suited to understanding and optimizing metabolic pathways in less well-understood systems.Entities:
Keywords: Design of Experiments (DOE); Saccharomyces cerevisiae; alcohol dehydrogenase; ethanol biosynthesis; metabolic engineering
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Year: 2018 PMID: 29976056 DOI: 10.1021/acssynbio.8b00112
Source DB: PubMed Journal: ACS Synth Biol ISSN: 2161-5063 Impact factor: 5.110