Acetate Metabolism and the Inhibition of Bacterial Growth by Acetate

High concentrations of organic acids such as acetate inhibit growth of Escherichia coli and other bacteria. This phenomenon is of interest for understanding bacterial physiology but is also of practical relevance. Growth inhibition by organic acids underlies food preservation and causes problems during high-density fermentation in biotechnology. What causes this phenomenon? Classical explanations invoke the uncoupling effect of acetate and the establishment of an anion imbalance. Here, we propose and investigate an alternative hypothesis: the perturbation of acetate metabolism due to the inflow of excess acetate. We find that this perturbation accounts for 20% of the growth-inhibitory effect through a modification of the acetyl phosphate concentration. Moreover, we argue that our observations are not expected based on uncoupling alone. ABSTRACT During aerobic growth on glucose, Escherichia coli excretes acetate, a mechanism called “overflow metabolism.” At high concentrations, the secreted acetate inhibits growth. Several mechanisms have been proposed for explaining this phenomenon, but a thorough analysis is hampered by the diversity of experimental conditions and strains used in these studies. Here, we describe the construction of a set of isogenic strains that remove different parts of the metabolic network involved in acetate metabolism. Analysis of these strains reveals that (i) high concentrations of acetate in the medium inhibit growth without significantly perturbing central metabolism; (ii) growth inhibition persists even when acetate assimilation is completely blocked; and (iii) regulatory interactions mediated by acetyl-phosphate play a small but significant role in growth inhibition by acetate. The major contribution to growth inhibition by acetate may originate in systemic effects like the uncoupling effect of organic acids or the perturbation of the anion composition of the cell, as previously proposed. Our data suggest, however, that under the conditions considered here, the uncoupling effect plays only a limited role. IMPORTANCE High concentrations of organic acids such as acetate inhibit growth of Escherichia coli and other bacteria. This phenomenon is of interest for understanding bacterial physiology but is also of practical relevance. Growth inhibition by organic acids underlies food preservation and causes problems during high-density fermentation in biotechnology. What causes this phenomenon? Classical explanations invoke the uncoupling effect of acetate and the establishment of an anion imbalance. Here, we propose and investigate an alternative hypothesis: the perturbation of acetate metabolism due to the inflow of excess acetate. We find that this perturbation accounts for 20% of the growth-inhibitory effect through a modification of the acetyl phosphate concentration. Moreover, we argue that our observations are not expected based on uncoupling alone.

[1]  A. Wolfe,et al.  Effects of mutations in acetate metabolism on high-cell-density growth of Escherichia coli , 2000, Journal of Industrial Microbiology and Biotechnology.

[2]  Wim Soetaert,et al.  Minimizing acetate formation in E. coli fermentations , 2007, Journal of Industrial Microbiology & Biotechnology.

[3]  Anne Richelle,et al.  Creation and analysis of biochemical constraint-based models using the COBRA Toolbox v.3.0 , 2019, Nature Protocols.

[4]  M. Eiteman,et al.  Overcoming acetate in Escherichia coli recombinant protein fermentations. , 2006, Trends in biotechnology.

[5]  C W Jones,et al.  The energetics of Escherichia coli during aerobic growth in continuous culture. , 1976, European journal of biochemistry.

[6]  J. Bailey,et al.  Transport of lactate and acetate through the energized cytoplasmic membrane of Escherichia coli , 1995, Biotechnology and bioengineering.

[7]  P. Good Permutation, Parametric, and Bootstrap Tests of Hypotheses , 2005 .

[8]  Chunaram Choudhary,et al.  Acetyl-phosphate is a critical determinant of lysine acetylation in E. coli. , 2013, Molecular cell.

[9]  W. Holms,et al.  Control of carbon flux to acetate excretion during growth of Escherichia coli in batch and continuous cultures. , 1989, Journal of general microbiology.

[10]  D. Annis Permutation, Parametric, and Bootstrap Tests of Hypotheses , 2005 .

[11]  J. Shiloach,et al.  Acetate accumulation through alternative metabolic pathways in ackA−pta−poxB− triple mutant in E. coli B (BL21) , 2010, Biotechnology Letters.

[12]  S. Roseman,et al.  Phosphate transfer between acetate kinase and enzyme I of the bacterial phosphotransferase system. , 1986, The Journal of biological chemistry.

[13]  Brice Enjalbert,et al.  Acetate fluxes in Escherichia coli are determined by the thermodynamic control of the Pta-AckA pathway , 2017, Scientific Reports.

[14]  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.

[15]  A. Wolfe Physiologically relevant small phosphodonors link metabolism to signal transduction. , 2010, Current opinion in microbiology.

[16]  Uwe Sauer,et al.  Protein acetylation affects acetate metabolism, motility and acid stress response in Escherichia coli , 2014, Molecular systems biology.

[17]  Joseph A. Wolkan Introduction to Probability and Statistics (2nd ed.) , 1992 .

[18]  Regulation of acetate metabolism in Escherichia coli BL21 by protein Nε-lysine acetylation , 2015, Applied Microbiology and Biotechnology.

[19]  Neil Swainston,et al.  Improving metabolic flux predictions using absolute gene expression data , 2012, BMC Systems Biology.

[20]  Hidde de Jong,et al.  Experimental and computational validation of models of fluorescent and luminescent reporter genes in bacteria , 2010, BMC Systems Biology.

[21]  Adam M. Feist,et al.  A genome-scale metabolic reconstruction for Escherichia coli K-12 MG1655 that accounts for 1260 ORFs and thermodynamic information , 2007, Molecular systems biology.

[22]  Joan L. Slonczewski,et al.  pH of the Cytoplasm and Periplasm of Escherichia coli: Rapid Measurement by Green Fluorescent Protein Fluorimetry , 2007, Journal of bacteriology.

[23]  D. Ropers,et al.  The post‐transcriptional regulatory system CSR controls the balance of metabolic pools in upper glycolysis of Escherichia coli , 2016, Molecular microbiology.

[24]  William Mendenhall,et al.  Introduction to Probability and Statistics , 1961, The Mathematical Gazette.

[25]  Jae-Gu Pan,et al.  Evolved Cobalamin-Independent Methionine Synthase (MetE) Improves the Acetate and Thermal Tolerance of Escherichia coli , 2013, Applied and Environmental Microbiology.

[26]  Margarida Casal,et al.  SATP (YaaH), a succinate-acetate transporter protein in Escherichia coli. , 2013, The Biochemical journal.

[27]  Kaspar Valgepea,et al.  Systems biology approach reveals that overflow metabolism of acetate in Escherichia coli is triggered by carbon catabolite repression of acetyl-CoA synthetase , 2010, BMC Systems Biology.

[28]  A. Wolfe The Acetate Switch , 2005, Microbiology and Molecular Biology Reviews.

[29]  B. Palsson,et al.  Stoichiometric interpretation of Escherichia coli glucose catabolism under various oxygenation rates , 1993, Applied and environmental microbiology.

[30]  E. Ziegel Permutation, Parametric, and Bootstrap Tests of Hypotheses (3rd ed.) , 2005 .

[31]  J. Bailey,et al.  Effect of alteration of the acetic acid synthesis pathway on the fermentation pattern of escherichia coli , 1991, Biotechnology and bioengineering.

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

[33]  T. Hwa,et al.  Overflow metabolism in E. coli results from efficient proteome allocation , 2015, Nature.

[34]  John M. A. Grime,et al.  Quantitative visualization of passive transport across bilayer lipid membranes , 2008, Proceedings of the National Academy of Sciences.

[35]  Jesús Picó,et al.  Validation of a constraint-based model of Pichia pastoris metabolism under data scarcity , 2010, BMC Systems Biology.

[36]  Dylan J. Sorensen,et al.  Structural, Kinetic and Proteomic Characterization of Acetyl Phosphate-Dependent Bacterial Protein Acetylation , 2014, PloS one.

[37]  J. Russell,et al.  The effects of fermentation acids on bacterial growth. , 1998, Advances in microbial physiology.

[38]  Johannes Geiselmann,et al.  A synthetic growth switch based on controlled expression of RNA polymerase , 2015, Molecular systems biology.

[39]  D. Court,et al.  Recombineering: a homologous recombination-based method of genetic engineering , 2009, Nature Protocols.

[40]  Manuel Cánovas,et al.  An insight into the role of phosphotransacetylase (pta) and the acetate/acetyl-CoA node in Escherichia coli , 2009, Microbial cell factories.

[41]  B. Palsson,et al.  Uniform sampling of steady-state flux spaces: means to design experiments and to interpret enzymopathies. , 2004, Biophysical journal.

[42]  A. Wolfe,et al.  The Intracellular Concentration of Acetyl Phosphate in Escherichia coli Is Sufficient for Direct Phosphorylation of Two-Component Response Regulators , 2007, Journal of bacteriology.

[43]  B. Snedecor,et al.  Growth inhibition of Clostridium thermocellum by carboxylic acids: A mechanism based on uncoupling by weak acids , 1985, Applied Microbiology and Biotechnology.

[44]  G. Bennett,et al.  Effect of inactivation of nuo and ackA-pta on redistribution of metabolic fluxes in Escherichia coli. , 1999, Biotechnology and bioengineering.

[45]  G. Bennett,et al.  Redistribution of Metabolic Fluxes in the Central Aerobic Metabolic Pathway of E. coli Mutant Strains with Deletion of the ackA‐pta and poxB Pathways for the Synthesis of Isoamyl Acetate , 2008, Biotechnology progress.

[46]  Brice Enjalbert,et al.  Physiological and Molecular Timing of the Glucose to Acetate Transition in Escherichia coli , 2013, Metabolites.

[47]  Rongrong Jiang,et al.  Improving Acetate Tolerance of Escherichia coli by Rewiring Its Global Regulator cAMP Receptor Protein (CRP) , 2013, PloS one.

[48]  M. Antoniewicz Methods and advances in metabolic flux analysis: a mini-review , 2015, Journal of Industrial Microbiology & Biotechnology.

[49]  C. V. Rao,et al.  Extracellular Acidic pH Inhibits Acetate Consumption by Decreasing Gene Transcription of the Tricarboxylic Acid Cycle and the Glyoxylate Shunt , 2018, Journal of bacteriology.

[50]  Frank Buchholz,et al.  A new logic for DNA engineering using recombination in Escherichia coli , 1998, Nature Genetics.

[51]  Rongrong Jiang,et al.  Improving Ethanol Tolerance of Escherichia coli by Rewiring Its Global Regulator cAMP Receptor Protein (CRP) , 2013, PloS one.

[52]  I. Booth,et al.  Inhibition of Escherichia coli growth by acetic acid: a problem with methionine biosynthesis and homocysteine toxicity. , 2002, Microbiology.

[53]  Eugenio Cinquemani,et al.  Inference of Quantitative Models of Bacterial Promoters from Time-Series Reporter Gene Data , 2015, PLoS Comput. Biol..

[54]  R. Gill,et al.  Organic acid toxicity, tolerance, and production in Escherichia coli biorefining applications , 2005, Microbial cell factories.

[55]  G W Luli,et al.  Comparison of growth, acetate production, and acetate inhibition of Escherichia coli strains in batch and fed-batch fermentations , 1990, Applied and environmental microbiology.

[56]  Matthias Heinemann,et al.  Phenotypic bistability in Escherichia coli's central carbon metabolism , 2014, Molecular systems biology.

[57]  J. Russell,et al.  Effects of carbonylcyanide-m-chlorophenylhydrazone (CCCP) and acetate on Escherichia coli O157:H7 and K-12: uncoupling versus anion accumulation. , 1997, FEMS microbiology letters.

[58]  W. J. DeCoursey,et al.  Introduction: Probability and Statistics , 2003 .

[59]  Santosh S. Vempala,et al.  CHRR: coordinate hit-and-run with rounding for uniform sampling of constraint-based models , 2017, Bioinform..

[60]  W. R. Farmer,et al.  Reduction of aerobic acetate production by Escherichia coli , 1997, Applied and environmental microbiology.

[61]  J. Geiselmann,et al.  A genome-wide screen for identifying all regulators of a target gene , 2013, Nucleic acids research.

[62]  J. Broadbent,et al.  External concentration of organic acid anions and pH: key independent variables for studying how organic acids inhibit growth of bacteria in mildly acidic foods. , 2009, Journal of food science.

[63]  N. Costantino,et al.  E. coli genome manipulation by P1 transduction. , 2007, Current protocols in molecular biology.

[64]  J. Russell,et al.  Another explanation for the toxicity of fermentation acids at low pH: anion accumulation versus uncoupling , 1992 .

[65]  H. Holms,et al.  Flux analysis and control of the central metabolic pathways in Escherichia coli. , 1996, FEMS microbiology reviews.

[66]  Ian R. Booth,et al.  Perturbation of Anion Balance during Inhibition of Growth of Escherichia coli by Weak Acids , 1998, Journal of bacteriology.

[67]  Maria Papagianni,et al.  Recent advances in engineering the central carbon metabolism of industrially important bacteria , 2012, Microbial Cell Factories.