| Literature DB >> 29498824 |
Nicolas Krink-Koutsoubelis1,2, Anne C Loechner1,2, Anna Lechner3, Hannes Link1,2, Charles M Denby3,4, Bastian Vögeli1,2, Tobias J Erb1,2, Satoshi Yuzawa3,4, Tadas Jakociunas5, Leonard Katz6, Michael K Jensen5, Victor Sourjik1,2, Jay D Keasling3,4,6,7,5.
Abstract
Short-chain acyl-coenzyme A esters serve as intermediate compounds in fatty acid biosynthesis, and the production of polyketides, biopolymers and other value-added chemicals. S. cerevisiae is a model organism that has been utilized for the biosynthesis of such biologically and economically valuable compounds. However, its limited repertoire of short-chain acyl-CoAs effectively prevents its application as a production host for a plethora of natural products. Therefore, we introduced biosynthetic metabolic pathways to five different acyl-CoA esters into S. cerevisiae. Our engineered strains provide the following acyl-CoAs: propionyl-CoA, methylmalonyl-CoA, n-butyryl-CoA, isovaleryl-CoA and n-hexanoyl-CoA. We established a yeast-specific metabolite extraction protocol to determine the intracellular acyl-CoA concentrations in the engineered strains. Propionyl-CoA was produced at 4-9 μM; methylmalonyl-CoA at 0.5 μM; and isovaleryl-CoA, n-butyryl-CoA, and n-hexanoyl-CoA at 6 μM each. The acyl-CoAs produced in this study are common building blocks of secondary metabolites and will enable the engineered production of a variety of natural products in S. cerevisiae. By providing this toolbox of acyl-CoA producing strains, we have laid the foundation to explore S. cerevisiae as a heterologous production host for novel secondary metabolites.Entities:
Keywords: S. cerevisiae; acyl-coenzyme A; heterologous pathway; metabolic engineering; platform molecules; precursor engineering
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Year: 2018 PMID: 29498824 DOI: 10.1021/acssynbio.7b00466
Source DB: PubMed Journal: ACS Synth Biol ISSN: 2161-5063 Impact factor: 5.110