Improving carotenoids production in yeast via adaptive laboratory evolution.

Adaptive laboratory evolution is an important tool for the engineering of strains for industrially relevant phenotypes. Traditionally, adaptive laboratory evolution has been implemented to improve robustness of industrial strains under diverse operational conditions; however due to the required coupling between growth and survival, its application for increased production of secondary metabolites generally results in decreased production due to the metabolic burden imposed by, or toxicity of, the produced compound. In this study, adaptive laboratory evolution was successfully applied to improve carotenoids production in an engineered Saccharomyces cerevisiae producer strain by exploiting the antioxidant properties of carotenoids. Short-term evolution experiment using periodic hydrogen peroxide shocking schemes resulted in a 3-fold increase in carotenoids production (from 6 mg/g dry cell weight to up to 18 mg/g dry cell weight). Subsequent transcriptome analysis was used to elucidate the molecular mechanisms for increased carotenoids production. Upregulation of genes related with lipid biosynthesis and mevalonate biosynthesis pathways were commonly observed in the carotenoids hyper-producers analyzed.

[1]  G. Britton,et al.  Biosynthesis and metabolism , 1998 .

[2]  Edith D. Wong,et al.  Saccharomyces Genome Database: the genomics resource of budding yeast , 2011, Nucleic Acids Res..

[3]  Gerhard Sandmann,et al.  Metabolic Engineering of the Carotenoid Biosynthetic Pathway in the Yeast Xanthophyllomyces dendrorhous (Phaffia rhodozyma) , 2003, Applied and Environmental Microbiology.

[4]  C. Duan,et al.  Important Role of Catalase in the Production of β-carotene by Recombinant Saccharomyces cerevisiae under H2O2 Stress , 2011, Current Microbiology.

[5]  J. Mano,et al.  Importance of glucose-6-phosphate dehydrogenase in the adaptive response to hydrogen peroxide in Saccharomyces cerevisiae. , 1998, The Biochemical journal.

[6]  Mitsuhiro Itaya,et al.  Metabolic Engineering of Carotenoid Biosynthesis in Escherichia coli by Ordered Gene Assembly in Bacillus subtilis , 2006, Applied and Environmental Microbiology.

[7]  R. Utsumi,et al.  Efficient synthesis of functional isoprenoids from acetoacetate through metabolic pathway-engineered Escherichia coli , 2009, Applied Microbiology and Biotechnology.

[8]  T. G. Truscott,et al.  The carotenoids as anti-oxidants--a review. , 1997, Journal of photochemistry and photobiology. B, Biology.

[9]  J. Hearst,et al.  Genetics and molecular biology of carotenoid pigment biosynthesis , 1996, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[10]  P. Philippsen,et al.  Heterologous modules for efficient and versatile PCR‐based gene targeting in Schizosaccharomyces pombe , 1998, Yeast.

[11]  Jing Wang,et al.  High-Level Production of Beta-Carotene in Saccharomyces cerevisiae by Successive Transformation with Carotenogenic Genes from Xanthophyllomyces dendrorhous , 2007, Applied and Environmental Microbiology.

[12]  Jay D. Keasling,et al.  Identification and microbial production of a terpene-based advanced biofuel , 2011, Nature communications.

[13]  Alexander Vainstein,et al.  Harnessing yeast subcellular compartments for the production of plant terpenoids. , 2011, Metabolic engineering.

[14]  Seung-Pyo Hong,et al.  Production of omega-3 eicosapentaenoic acid by metabolic engineering of Yarrowia lipolytica , 2013, Nature Biotechnology.

[15]  Gavin Sherlock,et al.  Molecular Characterization of Clonal Interference during Adaptive Evolution in Asexual Populations of Saccharomyces cerevisiae , 2008, Nature Genetics.

[16]  W. R. Farmer,et al.  Precursor Balancing for Metabolic Engineering of Lycopene Production in Escherichia coli , 2001, Biotechnology progress.

[17]  W. Liang,et al.  9) TM4 Microarray Software Suite , 2006 .

[18]  W. Liang,et al.  TM4 microarray software suite. , 2006, Methods in enzymology.

[19]  L. W. Parks,et al.  Biochemical and physiological effects of sterol alterations in yeast—A review , 1995, Lipids.

[20]  J. Daran,et al.  Heterologous carotenoid production in Saccharomyces cerevisiae induces the pleiotropic drug resistance stress response , 2010, Yeast.

[21]  Jay D Keasling,et al.  Carotenoid-based phenotypic screen of the yeast deletion collection reveals new genes with roles in isoprenoid production. , 2013, Metabolic engineering.

[22]  Stefan Hohmann,et al.  The Yeast Glycerol 3-Phosphatases Gpp1p and Gpp2p Are Required for Glycerol Biosynthesis and Differentially Involved in the Cellular Responses to Osmotic, Anaerobic, and Oxidative Stress* , 2001, The Journal of Biological Chemistry.

[23]  R. Schiestl,et al.  Improved method for high efficiency transformation of intact yeast cells. , 1992, Nucleic acids research.

[24]  Brad T. Sherman,et al.  Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists , 2008, Nucleic acids research.

[25]  Xueli Zhang,et al.  Engineering central metabolic modules of Escherichia coli for improving β-carotene production. , 2013, Metabolic engineering.

[26]  M. Bard,et al.  Disruption of the Candida albicans CYB5 Gene Results in Increased Azole Sensitivity , 2004, Antimicrobial Agents and Chemotherapy.

[27]  H. Takagi,et al.  Metabolic Engineering of Saccharomyces cerevisiae for Astaxanthin Production and Oxidative Stress Tolerance , 2009, Applied and Environmental Microbiology.

[28]  Sabrina Schübbe,et al.  Genetic analysis of coenzyme A biosynthesis in the yeast Saccharomyces cerevisiae: identification of a conditional mutation in the pantothenate kinase gene CAB1 , 2009, Current Genetics.

[29]  C. Duan,et al.  Enhancement of β-Carotene Production by Over-Expression of HMG-CoA Reductase Coupled with Addition of Ergosterol Biosynthesis Inhibitors in Recombinant Saccharomyces cerevisiae , 2011, Current Microbiology.

[30]  K. Patil,et al.  Enhancing sesquiterpene production in Saccharomyces cerevisiae through in silico driven metabolic engineering. , 2009, Metabolic engineering.

[31]  Markus J. Tamás,et al.  The Saccharomyces cerevisiae Sko1p transcription factor mediates HOG pathway‐dependent osmotic regulation of a set of genes encoding enzymes implicated in protection from oxidative damage , 2001, Molecular microbiology.

[32]  J. Rosen,et al.  INSIG: a broadly conserved transmembrane chaperone for sterol‐sensing domain proteins , 2005, The EMBO journal.

[33]  D. Kelly,et al.  Biodiversity of the P450 catalytic cycle: yeast cytochrome b 5/NADH cytochrome b 5 reductase complex efficiently drives the entire sterol 14‐demethylation (CYP51) reaction , 1999, FEBS letters.

[34]  R. Russell,et al.  Beta-carotene and other carotenoids as antioxidants. , 1999, Journal of the American College of Nutrition.

[35]  P. Lazarow,et al.  Peroxisome biogenesis. , 2001, Annual review of cell and developmental biology.

[36]  P. Bernstein,et al.  Microbial carotenoids. , 2012, Methods in molecular biology.

[37]  G. Sandmann,et al.  Metabolic engineering of tomato for high-yield production of astaxanthin. , 2013, Metabolic engineering.

[38]  C. Schmidt-Dannert,et al.  Investigation of factors influencing production of the monocyclic carotenoid torulene in metabolically engineered Escherichia coli , 2004, Applied Microbiology and Biotechnology.

[39]  John Quackenbush Microarray data normalization and transformation , 2002, Nature Genetics.

[40]  R. Russell,et al.  β-Carotene and Other Carotenoids as Antioxidants , 1999 .

[41]  Brad T. Sherman,et al.  Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources , 2008, Nature Protocols.