Iterative optimization of xylose catabolism in Saccharomyces cerevisiae using combinatorial expression tuning

A common challenge in metabolic engineering is rapidly identifying rate‐controlling enzymes in heterologous pathways for subsequent production improvement. We demonstrate a workflow to address this challenge and apply it to improving xylose utilization in Saccharomyces cerevisiae. For eight reactions required for conversion of xylose to ethanol, we screened enzymes for functional expression in S. cerevisiae, followed by a combinatorial expression analysis to achieve pathway flux balancing and identification of limiting enzymatic activities. In the next round of strain engineering, we increased the copy number of these limiting enzymes and again tested the eight‐enzyme combinatorial expression library in this new background. This workflow yielded a strain that has a ∼70% increase in biomass yield and ∼240% increase in xylose utilization. Finally, we chromosomally integrated the expression library. This library enriched for strains with multiple integrations of the pathway, which likely were the result of tandem integrations mediated by promoter homology. Biotechnol. Bioeng. 2017;114: 1301–1309. © 2017 Wiley Periodicals, Inc.

[1]  M. Koffas,et al.  Microbial production of natural and non-natural flavonoids: Pathway engineering, directed evolution and systems/synthetic biology. , 2016, Biotechnology advances.

[2]  S. Henikoff,et al.  Corrigendum: ChEC-seq kinetics discriminates transcription factor binding sites by DNA sequence and shape in vivo , 2015, Nature Communications.

[3]  William C. Deloache,et al.  A Highly Characterized Yeast Toolkit for Modular, Multipart Assembly. , 2015, ACS synthetic biology.

[4]  Dennis Eichmann,et al.  Metabolic Engineering Principles And Methodologies , 2016 .

[5]  G. Dubin,et al.  A systematic investigation of the stability of green fluorescent protein fusion proteins. , 2015, Acta biochimica Polonica.

[6]  C. Smolke,et al.  Engineering strategies for the fermentative production of plant alkaloids in yeast. , 2015, Metabolic engineering.

[7]  Jamie H. D. Cate,et al.  Selection of chromosomal DNA libraries using a multiplex CRISPR system , 2014, eLife.

[8]  Brian Kuhlman,et al.  Engineering a protein–protein interface using a computationally designed library , 2010, Proceedings of the National Academy of Sciences.

[9]  Luke N. Latimer,et al.  Employing a combinatorial expression approach to characterize xylose utilization in Saccharomyces cerevisiae. , 2014, Metabolic engineering.

[10]  S. Sawayama,et al.  Ethanol production from xylose in engineered Saccharomyces cerevisiae strains: current state and perspectives , 2009, Applied Microbiology and Biotechnology.

[11]  Christopher A. Voigt,et al.  Protein building blocks preserved by recombination , 2002, Nature Structural Biology.

[12]  Manish Kushwaha,et al.  A portable expression resource for engineering cross-species genetic circuits and pathways , 2015, Nature Communications.

[13]  James J. Collins,et al.  Comparative Analysis of Cas9 Activators Across Multiple Species , 2016, Nature Methods.

[14]  Andreas Krause,et al.  Navigating the protein fitness landscape with Gaussian processes , 2012, Proceedings of the National Academy of Sciences.

[15]  Daniel Kaganovich,et al.  Misfolded proteins partition between two distinct quality control compartments , 2008, Nature.

[16]  J. Keasling,et al.  Targeted proteomics for metabolic pathway optimization: application to terpene production. , 2011, Metabolic engineering.

[17]  G. Stephanopoulos,et al.  Improvement of Xylose Uptake and Ethanol Production in Recombinant Saccharomyces cerevisiae through an Inverse Metabolic Engineering Approach , 2005, Applied and Environmental Microbiology.

[18]  Irene M. Brockman,et al.  Dynamic metabolic engineering: New strategies for developing responsive cell factories , 2015, Biotechnology journal.

[19]  Kelly M. Thayer,et al.  Combining metabolic and protein engineering of a terpenoid biosynthetic pathway for overproduction and selectivity control , 2010, Proceedings of the National Academy of Sciences.

[20]  Florian David,et al.  EasyClone: method for iterative chromosomal integration of multiple genes in Saccharomyces cerevisiae , 2013, FEMS yeast research.

[21]  Keith E. J. Tyo,et al.  Isoprenoid Pathway Optimization for Taxol Precursor Overproduction in Escherichia coli , 2010, Science.

[22]  H. Eiberg,et al.  Assignment of dominant inherited nocturnal enuresis (ENUR1) to chromosome 13q , 1995, Nature Genetics.

[23]  R. D. Gietz,et al.  Yeast transformation by the LiAc/SS carrier DNA/PEG method. , 2014, Methods in molecular biology.

[24]  John E Dueber,et al.  A Barcoding Strategy Enabling Higher-Throughput Library Screening by Microscopy. , 2015, ACS synthetic biology.

[25]  Timothy S. Ham,et al.  Production of the antimalarial drug precursor artemisinic acid in engineered yeast , 2006, Nature.

[26]  C. Tomlin,et al.  Expression-level optimization of a multi-enzyme pathway in the absence of a high-throughput assay , 2013, Nucleic acids research.

[27]  Matthew Deaner,et al.  Promoter and Terminator Discovery and Engineering. , 2016, Advances in biochemical engineering/biotechnology.

[28]  N. Barkai,et al.  The Cost of Protein Production , 2015, Cell reports.

[29]  Andrew J. Bannister,et al.  Acetylation of histone H3 at lysine 64 regulates nucleosome dynamics and facilitates transcription , 2014, eLife.

[30]  Kelly M. Wetmore,et al.  Rapid Quantification of Mutant Fitness in Diverse Bacteria by Sequencing Randomly Bar-Coded Transposons , 2015, mBio.

[31]  Le Cong,et al.  Multiplex Genome Engineering Using CRISPR/Cas Systems , 2013, Science.

[32]  Sylvestre Marillonnet,et al.  Golden Gate cloning. , 2014, Methods in molecular biology.

[33]  Hung Lee,et al.  Genetic improvement of Saccharomyces cerevisiae for xylose fermentation. , 2007, Biotechnology advances.

[34]  Thomas Jeffries,et al.  Shuffling of Promoters for Multiple Genes To Optimize Xylose Fermentation in an Engineered Saccharomyces cerevisiae Strain , 2007, Applied and Environmental Microbiology.

[35]  P. K. Ajikumar,et al.  The future of metabolic engineering and synthetic biology: towards a systematic practice. , 2012, Metabolic engineering.

[36]  V. Marx Targeted proteomics , 2013, Nature Methods.

[37]  Gregory Stephanopoulos,et al.  Combinatorial engineering of microbes for optimizing cellular phenotype. , 2008, Current opinion in chemical biology.

[38]  M. Katze,et al.  Toll-Like Receptor 3 Signaling via TRIF Contributes to a Protective Innate Immune Response to Severe Acute Respiratory Syndrome Coronavirus Infection , 2015, mBio.

[39]  Drew Endy,et al.  Precise and reliable gene expression via standard transcription and translation initiation elements , 2013, Nature Methods.

[40]  Virginia W Cornish,et al.  Reiterative Recombination for the in vivo assembly of libraries of multigene pathways , 2011, Proceedings of the National Academy of Sciences.

[41]  Ying-Ta Wu,et al.  Engineering transaldolase in Pichia stipitis to improve bioethanol production. , 2012, ACS chemical biology.

[42]  Joseph Heijnen,et al.  Metabolic Control Analysis , 2009 .

[43]  D. Fell,et al.  Metabolic control analysis. The effects of high enzyme concentrations. , 1990, European journal of biochemistry.

[44]  Marjan De Mey,et al.  Multivariate modular metabolic engineering for pathway and strain optimization. , 2014, Current opinion in biotechnology.

[45]  Tae Seok Moon,et al.  Programmable genetic circuits for pathway engineering. , 2015, Current opinion in biotechnology.

[46]  Mingzi M. Zhang,et al.  A highly efficient single-step, markerless strategy for multi-copy chromosomal integration of large biochemical pathways in Saccharomyces cerevisiae. , 2016, Metabolic engineering.