Genomic Library Screens for Genes Involved in n-Butanol Tolerance in Escherichia coli

Background n-Butanol is a promising emerging biofuel, and recent metabolic engineering efforts have demonstrated the use of several microbial hosts for its production. However, most organisms have very low tolerance to n-butanol (up to 2% (v/v)), limiting the economic viability of this biofuel. The rational engineering of more robust n-butanol production hosts relies upon understanding the mechanisms involved in tolerance. However, the existing knowledge of genes involved in n-butanol tolerance is limited. The goal of this study is therefore to identify E. coli genes that are involved in n-butanol tolerance. Methodology/Principal Findings Using a genomic library enrichment strategy, we identified approximately 270 genes that were enriched or depleted in n-butanol challenge. The effects of these candidate genes on n-butanol tolerance were experimentally determined using overexpression or deletion libraries. Among the 55 enriched genes tested, 11 were experimentally shown to confer enhanced tolerance to n-butanol when overexpressed compared to the wild-type. Among the 84 depleted genes tested, three conferred increased n-butanol resistance when deleted. The overexpressed genes that conferred the largest increase in n-butanol tolerance were related to iron transport and metabolism, entC and feoA, which increased the n-butanol tolerance by 32.8±4.0% and 49.1±3.3%, respectively. The deleted gene that resulted in the largest increase in resistance to n-butanol was astE, which enhanced n-butanol tolerance by 48.7±6.3%. Conclusions/Significance We identified and experimentally verified 14 genes that decreased the inhibitory effect of n-butanol tolerance on E. coli. From the data, we were able to expand the current knowledge on the genes involved in n-butanol tolerance; the results suggest that an increased iron transport and metabolism and decreased acid resistance may enhance n-butanol tolerance. The genes and mechanisms identified in this study will be helpful in the rational engineering of more robust biofuel producers.

[1]  Katy C. Kao,et al.  Transcriptional Analysis of Lactobacillus brevis to N-Butanol and Ferulic Acid Stress Responses , 2011, PloS one.

[2]  V. Zverlov,et al.  Reconstructing the clostridial n-butanol metabolic pathway in Lactobacillus brevis , 2010, Applied Microbiology and Biotechnology.

[3]  Xilin Zhao,et al.  Escherichia coli genes that reduce the lethal effects of stress , 2010, BMC Microbiology.

[4]  Jay D. Keasling,et al.  Functional Genomic Study of Exogenous n-Butanol Stress in Escherichia coli , 2010, Applied and Environmental Microbiology.

[5]  T. Wood,et al.  Identification of stress‐related proteins in Escherichia coli using the pollutant cis‐dichloroethylene , 2009, Journal of applied microbiology.

[6]  J. Liao,et al.  An integrated network approach identifies the isobutanol response network of Escherichia coli , 2009, Molecular systems biology.

[7]  L. Blank,et al.  Selected Pseudomonas putida Strains Able To Grow in the Presence of High Butanol Concentrations , 2009, Applied and Environmental Microbiology.

[8]  K. Prather,et al.  Engineering alternative butanol production platforms in heterologous bacteria. , 2009, Metabolic engineering.

[9]  Joon-Hee Lee,et al.  SoxRS-Mediated Lipopolysaccharide Modification Enhances Resistance against Multiple Drugs in Escherichia coli , 2009, Journal of bacteriology.

[10]  Alyssa M. Redding,et al.  Metabolic engineering of Saccharomyces cerevisiae for the production of n-butanol , 2008, Microbial cell factories.

[11]  Kevin M. Smith,et al.  Metabolic engineering of Escherichia coli for 1-butanol production. , 2008, Metabolic engineering.

[12]  Qi Zheng,et al.  GOEAST: a web-based software toolkit for Gene Ontology enrichment analysis , 2008, Nucleic Acids Res..

[13]  G. Booker,et al.  Escherichia coli biotin protein ligase: characterization and development of a high-throughput assay. , 2008, Analytical biochemistry.

[14]  J. Kormanec,et al.  Small outer-membrane lipoprotein, SmpA, is regulated by sigmaE and has a role in cell envelope integrity and virulence of Salmonella enterica serovar Typhimurium. , 2008, Microbiology.

[15]  J. Liao,et al.  Non-fermentative pathways for synthesis of branched-chain higher alcohols as biofuels , 2008, Nature.

[16]  M. Inui,et al.  Expression of Clostridium acetobutylicum butanol synthetic genes in Escherichia coli , 2008, Applied Microbiology and Biotechnology.

[17]  N. Ogasawara,et al.  Involvement of the YneS/YgiH and PlsX proteins in phospholipid biosynthesis in both Bacillus subtilis and Escherichia coli , 2007, BMC Microbiology.

[18]  J. Pagés,et al.  An Early Response to Environmental Stress Involves Regulation of OmpX and OmpF, Two Enterobacterial Outer Membrane Pore-Forming Proteins , 2007, Antimicrobial Agents and Chemotherapy.

[19]  E. Papoutsakis,et al.  Dynamics of Genomic-Library Enrichment and Identification of Solvent Tolerance Genes for Clostridium acetobutylicum , 2007, Applied and Environmental Microbiology.

[20]  H. Mori,et al.  Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection , 2006, Molecular systems biology.

[21]  H. Mori,et al.  Complete set of ORF clones of Escherichia coli ASKA library (a complete set of E. coli K-12 ORF archive): unique resources for biological research. , 2006, DNA research : an international journal for rapid publication of reports on genes and genomes.

[22]  T. Bagnyukova,et al.  Involvement of soxRS Regulon in Response of Escherichia coli to Oxidative Stress Induced by Hydrogen Peroxide , 2005, Biochemistry (Moscow).

[23]  R. Drijber,et al.  Survey of Extreme Solvent Tolerance in Gram-Positive Cocci: Membrane Fatty Acid Changes in Staphylococcus haemolyticus Grown in Toluene , 2005, Applied and Environmental Microbiology.

[24]  C. Tomas,et al.  Metabolic Engineering of Solventogenic Clostridia , 2005 .

[25]  C. Tomas,et al.  Transcriptional Analysis of Butanol Stress and Tolerance in Clostridium acetobutylicum , 2004, Journal of bacteriology.

[26]  A. Walmsley,et al.  Structure and function of efflux pumps that confer resistance to drugs. , 2003, The Biochemical journal.

[27]  Terry Speed,et al.  Normalization of cDNA microarray data. , 2003, Methods.

[28]  Lee Ann McCue,et al.  Identification of co-regulated genes through Bayesian clustering of predicted regulatory binding sites , 2003, Nature Biotechnology.

[29]  A I Saeed,et al.  TM4: a free, open-source system for microarray data management and analysis. , 2003, BioTechniques.

[30]  John W. Foster,et al.  Collaborative Regulation of Escherichia coli Glutamate-Dependent Acid Resistance by Two AraC-Like Regulators, GadX and GadW (YhiW) , 2002, Journal of bacteriology.

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

[32]  A. Yamaguchi,et al.  The Putative Response Regulator BaeR Stimulates Multidrug Resistance of Escherichia coli via a Novel Multidrug Exporter System, MdtABC , 2002, Journal of bacteriology.

[33]  M. Galbe,et al.  A review of the production of ethanol from softwood , 2002, Applied Microbiology and Biotechnology.

[34]  S. Bhosle,et al.  Tolerance of bacteria to organic solvents. , 2002, Research in microbiology.

[35]  Hajime Tokuda,et al.  Overexpression of yccL (gnsA) andydfY (gnsB) Increases Levels of Unsaturated Fatty Acids and Suppresses both the Temperature-SensitivefabA6 Mutation and Cold-SensitivesecG Null Mutation of Escherichia coli , 2001, Journal of bacteriology.

[36]  Michael L. Bittner,et al.  Microarrays: Optical Technologies and Informatics , 2001 .

[37]  Terence P. Speed,et al.  Normalization for cDNA microarry data , 2001, SPIE BiOS.

[38]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[39]  R. Aono,et al.  Entry into and Release of Solvents byEscherichia coli in an Organic-Aqueous Two-Liquid-Phase System and Substrate Specificity of the AcrAB-TolC Solvent-Extruding Pump , 2000, Journal of bacteriology.

[40]  B. Wanner,et al.  One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[41]  Zohar Yakhini,et al.  Clustering gene expression patterns , 1999, J. Comput. Biol..

[42]  M. Surette,et al.  Quorum sensing in Escherichia coli, Salmonella typhimurium, and Vibrio harveyi: a new family of genes responsible for autoinducer production. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[43]  T. Humphrey,et al.  Properties of an L‐glutamate‐induced acid tolerance response which involves the functioning of extracellular induction components , 1999, Journal of applied microbiology.

[44]  Rajeev Misra,et al.  Biochemistry and Regulation of a NovelEscherichia coli K-12 Porin Protein, OmpG, Which Produces Unusually Large Channels , 1998, Journal of bacteriology.

[45]  J. D. de Bont,et al.  Bacteria tolerant to organic solvents , 1998, Extremophiles.

[46]  Gerben J. Zylstra,et al.  Identification and Molecular Characterization of an Efflux Pump Involved in Pseudomonas putida S12 Solvent Tolerance* , 1998, The Journal of Biological Chemistry.

[47]  S. Levy,et al.  Role of the acrAB locus in organic solvent tolerance mediated by expression of marA, soxS, or robA in Escherichia coli , 1997, Journal of bacteriology.

[48]  J. Ramos,et al.  Mechanisms for Solvent Tolerance in Bacteria* , 1997, The Journal of Biological Chemistry.

[49]  F J Weber,et al.  Adaptation mechanisms of microorganisms to the toxic effects of organic solvents on membranes. , 1996, Biochimica et biophysica acta.

[50]  D. White,et al.  Cell Envelope Changes in Solvent-Tolerant and Solvent-Sensitive Pseudomonas putida Strains following Exposure to o-Xylene , 1996, Applied and environmental microbiology.

[51]  Yan Xu,et al.  Evidence for distinct ligand-bound conformational states of the multifunctional Escherichia coli repressor of biotin biosynthesis. , 1995, Biochemistry.

[52]  P. Babbitt,et al.  A Novel Activity of OmpT. , 1995, The Journal of Biological Chemistry.

[53]  H. Heipieper,et al.  Mechanisms of resistance of whole cells to toxic organic solvents , 1994 .

[54]  G. Sawers,et al.  Isolation and characterization of hypophosphite‐resistant mutants of Escherichia coli: identification of the FocA protein, encoded by the pfl operon, as a putative formate transporter , 1994, Molecular microbiology.

[55]  K. Burton Adenine transport in Escherichia coli , 1994, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[56]  D. Biran,et al.  Adaptation of Escherichia coli to elevated temperatures: The metA gene product is a heat shock protein , 1990, Antonie van Leeuwenhoek.

[57]  L. K. Bowles,et al.  Effects of butanol on Clostridium acetobutylicum , 1985, Applied and environmental microbiology.

[58]  Hans P. Blaschek,et al.  Butanol Production by a Butanol-Tolerant Strain of Clostridium acetobutylicum in Extruded Corn Broth , 1983, Applied and environmental microbiology.

[59]  K. Burton Transport of adenine, hypoxanthine and uracil into Escherichia coli. , 1977, The Biochemical journal.

[60]  W. Umbreit,et al.  EFFECT OF BIOTIN ON FATTY ACID DISTRIBUTION IN ESCHERICHIA COLI. , 1965, Journal of bacteriology.

[61]  S. Beesch Acetone-butanol fermentation of starches. , 1953, Applied microbiology.

[62]  S. Beesch Acetone-Butanol Fermentation of Sugars , 1952 .

[63]  Min Zhang,et al.  Butanol Tolerance in a Selection of Microorganisms , 2009, Applied biochemistry and biotechnology.

[64]  H. Honda,et al.  Time-course data analysis of gene expression profiles reveals purR regulon concerns in organic solvent tolerance in Escherichia coli. , 2005, Journal of bioscience and bioengineering.

[65]  B. Demple,et al.  Redox signaling and gene control in the Escherichia coli soxRS oxidative stress regulon--a review. , 1996, Gene.