Literature DB >> 29498824

Engineered Production of Short-Chain Acyl-Coenzyme A Esters in Saccharomyces cerevisiae.

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

Mesh:

Substances:

Year:  2018        PMID: 29498824     DOI: 10.1021/acssynbio.7b00466

Source DB:  PubMed          Journal:  ACS Synth Biol        ISSN: 2161-5063            Impact factor:   5.110


  4 in total

1.  CLN3 is required for the clearance of glycerophosphodiesters from lysosomes.

Authors:  David M Sabatini; Monther Abu-Remaileh; Nouf N Laqtom; Wentao Dong; Uche N Medoh; Andrew L Cangelosi; Vimisha Dharamdasani; Sze Ham Chan; Tenzin Kunchok; Caroline A Lewis; Ivonne Heinze; Rachel Tang; Christian Grimm; An N Dang Do; Forbes D Porter; Alessandro Ori
Journal:  Nature       Date:  2022-09-21       Impact factor: 69.504

Review 2.  Saccharomyces cerevisiae as host for the recombinant production of polyketides and nonribosomal peptides.

Authors:  Anna Tippelt; Markus Nett
Journal:  Microb Cell Fact       Date:  2021-08-19       Impact factor: 5.328

3.  Biosynthesis of angelyl-CoA in Saccharomyces cerevisiae.

Authors:  Roberta Callari; David Fischer; Harald Heider; Nora Weber
Journal:  Microb Cell Fact       Date:  2018-05-12       Impact factor: 5.328

4.  High-throughput mapping of CoA metabolites by SAMDI-MS to optimize the cell-free biosynthesis of HMG-CoA.

Authors:  Patrick T O'Kane; Quentin M Dudley; Aislinn K McMillan; Michael C Jewett; Milan Mrksich
Journal:  Sci Adv       Date:  2019-06-05       Impact factor: 14.136

  4 in total

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