| Literature DB >> 27936603 |
Matthew J Maurer1,2, Lawrence Sutardja1,2, Dominic Pinel1,2, Stefan Bauer1,2, Amanda L Muehlbauer1,2, Tyler D Ames1,2, Jeffrey M Skerker1,2, Adam P Arkin1,2.
Abstract
Engineering complex phenotypes for industrial and synthetic biology applications is difficult and often confounds rational design. Bioethanol production from lignocellulosic feedstocks is a complex trait that requires multiple host systems to utilize, detoxify, and metabolize a mixture of sugars and inhibitors present in plant hydrolysates. Here, we demonstrate an integrated approach to discovering and optimizing host factors that impact fitness of Saccharomyces cerevisiae during fermentation of a Miscanthus x giganteus plant hydrolysate. We first used high-resolution Quantitative Trait Loci (QTL) mapping and systematic bulk Reciprocal Hemizygosity Analysis (bRHA) to discover 17 loci that differentiate hydrolysate tolerance between an industrially related (JAY291) and a laboratory (S288C) strain. We then used this data to identify a subset of favorable allelic loci that were most amenable for strain engineering. Guided by this "genetic blueprint", and using a dual-guide Cas9-based method to efficiently perform multikilobase locus replacements, we engineered an S288C-derived strain with superior hydrolysate tolerance than JAY291. Our methods should be generalizable to engineering any complex trait in S. cerevisiae, as well as other organisms.Entities:
Keywords: CRISPR-Cas9; biofuel; genetic engineering; hydrolysate; quantitative trait loci; strain development
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Year: 2016 PMID: 27936603 DOI: 10.1021/acssynbio.6b00264
Source DB: PubMed Journal: ACS Synth Biol ISSN: 2161-5063 Impact factor: 5.110