| Literature DB >> 31577419 |
Raphael Ferreira1,2, Christos Skrekas1,2, Alex Hedin1, Benjamín J Sánchez1,2, Verena Siewers1,2, Jens Nielsen1,2,3, Florian David1,2.
Abstract
Engineering Saccharomyces cerevisiae for industrial-scale production of valuable chemicals involves extensive modulation of its metabolism. Here, we identified novel gene expression fine-tuning set-ups to enhance endogenous metabolic fluxes toward increasing levels of acetyl-CoA and malonyl-CoA. dCas9-based transcriptional regulation was combined together with a malonyl-CoA responsive intracellular biosensor to select for beneficial set-ups. The candidate genes for screening were predicted using a genome-scale metabolic model, and a gRNA library targeting a total of 168 selected genes was designed. After multiple rounds of fluorescence-activated cell sorting and library sequencing, the gRNAs that were functional and increased flux toward malonyl-CoA were assessed for their efficiency to enhance 3-hydroxypropionic acid (3-HP) production. 3-HP production was significantly improved upon fine-tuning genes involved in providing malonyl-CoA precursors, cofactor supply, as well as chromatin remodeling.Entities:
Keywords: CRISPR; biosensor; flux balance analysis; synthetic biology
Year: 2019 PMID: 31577419 DOI: 10.1021/acssynbio.9b00258
Source DB: PubMed Journal: ACS Synth Biol ISSN: 2161-5063 Impact factor: 5.110