Saccharomyces cerevisiae expressing bacteriophage endolysins reduce Lactobacillus contamination during fermentation

BackgroundOne of the challenges facing the fuel ethanol industry is the management of bacterial contamination during fermentation. Lactobacillus species are the predominant contaminants that decrease the profitability of biofuel production by reducing ethanol yields and causing “stuck” fermentations, which incur additional economic losses via expensive antibiotic treatments and disinfection costs. The current use of antibiotic treatments has led to the emergence of drug-resistant bacterial strains, and antibiotic residues in distillers dried grains with solubles (DDGS) are a concern for the feed and food industries. This underscores the need for new, non-antibiotic, eco-friendly mitigation strategies for bacterial contamination. The specific objectives of this work were to (1) express genes encoding bacteriophage lytic enzymes (endolysins) in Saccharomyces cerevisiae, (2) assess the lytic activity of the yeast-expressed enzymes against different species of Lactobacillus that commonly contaminate fuel ethanol fermentations, and (3) test the ability of yeast expressing lytic enzymes to reduce Lactobacillus fermentum during fermentation. Implementing antibiotic-free strategies to reduce fermentation contaminants will enable more cost-effective fuel ethanol production and will impact both producers and consumers in the farm-to-fork continuum.ResultsTwo genes encoding the lytic enzymes LysA and LysA2 were individually expressed in S. cerevisiae on multi-copy plasmids under the control of a galactose-inducible promoter. The enzymes purified from yeast were lytic against Lactobacillus isolates collected from fermentors at a commercial dry grind ethanol facility including Lactobacillus fermentum, Lactobacillus brevis, and Lactobacillus mucosae. Reductions of L. fermentum in experimentally infected fermentations with yeast expressing LysA or LysA2 ranged from 0.5 log10 colony-forming units per mL (CFU/mL) to 1.8 log10 (CFU/mL) over 72 h and fermentations treated with transformed yeast lysate showed reductions that ranged from 0.9 log10 (CFU/mL) to 3.3 log10 (CFU/mL). Likewise, lactic acid and acetic acid levels were reduced in all experimentally infected fermentations containing transformed yeast (harboring endolysin expressing plasmids) relative to the corresponding fermentations with untransformed yeast.ConclusionsThis study demonstrates the feasibility of using yeast expressing bacteriophage endolysins to reduce L. fermentum contamination during fuel ethanol fermentations.

[1]  R. Dorr Clinical properties of yeast-derived versus Escherichia coli-derived granulocyte-macrophage colony-stimulating factor. , 1993, Clinical therapeutics.

[2]  J. Boeke,et al.  Designer deletion strains derived from Saccharomyces cerevisiae S288C: A useful set of strains and plasmids for PCR‐mediated gene disruption and other applications , 1998, Yeast.

[3]  Alya Limayem,et al.  Antimicrobial strategies for limiting bacterial contaminants in fuel bioethanol fermentations , 2011 .

[4]  Dorr Rt Clinical properties of yeast-derived versus Escherichia coli-derived granulocyte-macrophage colony-stimulating factor , 1993 .

[5]  W. M. Ingledew,et al.  Inhibition of yeast by lactic acid bacteria in continuous culture: nutrient depletion and/or acid toxicity? , 2004, Journal of Industrial Microbiology and Biotechnology.

[6]  Caye M. Drapcho,et al.  Biofuels Engineering Process Technology , 2007 .

[7]  D. Makanjuola,et al.  Some effects of lactic acid bacteria on laboratory-scale yeast fermentations , 1992 .

[8]  M. Sami,et al.  A Review of Hop Resistance in Beer Spoilage Lactic Acid Bacteria , 2006 .

[9]  A. Margolles,et al.  Hop Resistance in the Beer Spoilage Bacterium Lactobacillus brevis Is Mediated by the ATP-Binding Cassette Multidrug Transporter HorA , 2001, Journal of bacteriology.

[10]  I. S. Pretorius,et al.  Tailoring wine yeast for the new millennium: novel approaches to the ancient art of winemaking , 2000, Yeast.

[11]  W. M. Ingledew,et al.  Effects of acetic acid and lactic acid on the growth of Saccharomyces cerevisiae in a minimal medium , 2001, Journal of Industrial Microbiology and Biotechnology.

[12]  S. R. Andrietta,et al.  Use of penicillin and monensin to control bacterial contamination of Brazilian alcohol fermentations , 2000 .

[13]  D. Schmale,et al.  Conversion of deoxynivalenol to 3-acetyldeoxynivalenol in barley-derived fuel ethanol co-products with yeast expressing trichothecene 3-O-acetyltransferases , 2011, Biotechnology for biofuels.

[14]  C. Charpentier,et al.  Yeast adapted to wine: Nitrogen compounds released during induced autolysis in a model wine , 2002, Journal of Industrial Microbiology and Biotechnology.

[15]  T. Leathers,et al.  Antimicrobial susceptibility of Lactobacillus species isolated from commercial ethanol plants , 2007, Journal of Industrial Microbiology & Biotechnology.

[16]  C. Bamforth pH in Brewing: An Overview , 2001 .

[17]  J. Klumpp,et al.  Endolysins as antimicrobials. , 2012, Advances in virus research.

[18]  T. Bernhardt,et al.  Breaking free: "protein antibiotics" and phage lysis. , 2002, Research in microbiology.

[19]  D. Thiele,et al.  Copper ion inducible and repressible promoter systems in yeast. , 1999, Methods in enzymology.

[20]  M. Ueda,et al.  Cell surface engineering of yeast: construction of arming yeast with biocatalyst. , 2000, Journal of bioscience and bioengineering.

[21]  V. Kushnirov Rapid and reliable protein extraction from yeast , 2000, Yeast.

[22]  K. Schleifer,et al.  Peptidoglycan types of bacterial cell walls and their taxonomic implications , 1972, Bacteriological reviews.

[23]  S. Dequin,et al.  The potential of genetic engineering for improving brewing, wine-making and baking yeasts , 2001, Applied Microbiology and Biotechnology.

[24]  M. Rinnerthaler,et al.  Senescence and apoptosis in yeast mother cell-specific aging and in higher cells: a short review. , 2008, Biochimica et biophysica acta.

[25]  C. Charpentier,et al.  Alteration of cell wall structure in Saccharomyces cerevisiae and Saccharomyces bayanus during autolysis , 1986, Applied Microbiology and Biotechnology.

[26]  B. Robillard,et al.  Evolution of the Lipid Contents of Champagne Wine During the Second Fermentation ofSaccharomyces cerevisiae , 1989, American Journal of Enology and Viticulture.

[27]  W. M. Ingledew,et al.  Effects of lactobacilli on yeast-catalyzed ethanol fermentations , 1997, Applied and environmental microbiology.

[28]  S. R. Ceccato-Antonini,et al.  Chlorine dioxide against bacteria and yeasts from the alcoholic fermentation , 2008, Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology].

[29]  W. M. Ingledew,et al.  Influence of Medium Buffering Capacity on Inhibition of Saccharomyces cerevisiae Growth by Acetic and Lactic Acids , 2002, Applied and Environmental Microbiology.

[30]  R. E. Lumpkin,et al.  Contaminant occurrence, identification and control in a pilot-scale corn fiber to ethanol conversion process. , 2007, Bioresource technology.

[31]  C. Meester,et al.  Microbial acetylation of M factor of virginiamycin. , 1976, The Journal of antibiotics.

[32]  L. Bergman,et al.  Growth and maintenance of yeast. , 2001, Methods in molecular biology.

[33]  T. Phister,et al.  Microbial contamination of fuel ethanol fermentations , 2011, Letters in applied microbiology.

[34]  T. Sasaki,et al.  Breeding of a Brewer's Yeast Possessing Anticontaminant Properties , 1984 .

[35]  Manuel T. Silva Secondary necrosis: The natural outcome of the complete apoptotic program , 2010, FEBS letters.

[36]  J. Schnürer,et al.  Antifungal lactic acid bacteria as biopreservatives , 2005 .

[37]  Jan Borysowski,et al.  Bacteriophage Endolysins as a Novel Class of Antibacterial Agents , 2006, Experimental biology and medicine.

[38]  W. M. Ingledew,et al.  Control of Lactobacillus contaminants in continuous fuel ethanol fermentations by constant or pulsed addition of penicillin G , 2003, Applied Microbiology and Biotechnology.

[39]  J. Shetty,et al.  Production of ethanol from winter barley by the EDGE (enhanced dry grind enzymatic) process , 2010, Biotechnology for biofuels.

[40]  H. Jungwirth,et al.  Chronological aging leads to apoptosis in yeast , 2004, The Journal of cell biology.

[41]  W. Frommer Heterologous Expression of Genes in Bacterial, Fungal, Animal, and Plant Cells , 1995 .

[42]  W. M. Ingledew,et al.  Acetic Acid and Lactic Acid Inhibition of Growth of Saccharomyces Cerevisiae by Different Mechanisms , 2001 .

[43]  M. Galbe,et al.  Bio-ethanol--the fuel of tomorrow from the residues of today. , 2006, Trends in biotechnology.

[44]  M. Loessner,et al.  Bacteriophage endolysins as novel antimicrobials. , 2012, Future microbiology.

[45]  I. Rayment,et al.  Bioprospecting for Trichothecene 3-O-Acetyltransferases in the Fungal Genus Fusarium Yields Functional Enzymes with Different Abilities To Modify the Mycotoxin Deoxynivalenol , 2010, Applied and Environmental Microbiology.

[46]  H. Blanch,et al.  By‐product inhibition effects on ethanolic fermentation by Saccharomyces cerevisiae , 1983, Biotechnology and bioengineering.

[47]  I. S. Pretorius,et al.  Yeast Stress Response and Fermentation Efficiency: How to Survive the Making of Wine - A Review , 2019, South African Journal of Enology & Viticulture.

[48]  J. Cohen,et al.  Expression of a prokaryotic gene in yeast: isolation and characterization of mutants with increased expression , 2004, Molecular and General Genetics MGG.

[49]  I. S. Pretorius,et al.  The development of bactericidal yeast strains by expressing the Pediococcus acidilactici pediocin gene (pedA) in Saccharomyces cerevisiae , 1999, Yeast.

[50]  E. Díaz,et al.  Chimeric phage-bacterial enzymes: a clue to the modular evolution of genes. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[51]  T. Leathers,et al.  Modeling bacterial contamination of fuel ethanol fermentation , 2009, Biotechnology and bioengineering.

[52]  G. Stewart,et al.  Effects of high-gravity brewing and acid washing on Brewers' yeast , 1998 .

[53]  K. Takegawa,et al.  Engineering of protein secretion in yeast: strategies and impact on protein production , 2010, Applied Microbiology and Biotechnology.

[54]  M. Loureiro-Dias,et al.  Combined effect of acetic acid, pH and ethanol on intracellular pH of fermenting yeast , 1989, Applied Microbiology and Biotechnology.

[55]  V. Fischetti,et al.  Bacteriophage endolysins: a novel anti-infective to control Gram-positive pathogens. , 2010, International journal of medical microbiology : IJMM.

[56]  K. Bettenbrock,et al.  The gal Genes for the Leloir Pathway ofLactobacillus casei 64H , 1998, Applied and Environmental Microbiology.

[57]  N. Borth,et al.  Assessing viability and cell-associated product of recombinant protein producing Pichia pastoris with flow cytometry. , 2003, Journal of biotechnology.

[58]  Megan N. McClean,et al.  Fast-acting and Nearly Gratuitous Induction of Gene Expression and Protein Depletion in Saccharomyces Cerevisiae Graduate Program in Quantitative and Computational Biology, And , 2022 .

[59]  T. Leathers,et al.  Biofilm formation by bacterial contaminants of fuel ethanol production , 2007, Biotechnology Letters.

[60]  Christopher J. Murakami,et al.  A molecular mechanism of chronological aging in yeast , 2009, Cell cycle.

[61]  S. Hughes,et al.  Bacteriophage-encoded lytic enzymes control growth of contaminating Lactobacillus found in fuel ethanol fermentations , 2013, Biotechnology for Biofuels.

[62]  C. Scorer,et al.  Foreign gene expression in yeast: a review , 1992, Yeast.

[63]  T. Leathers,et al.  Bacterial contaminants of fuel ethanol production , 2004, Journal of Industrial Microbiology and Biotechnology.

[64]  R. López,et al.  The lytic enzyme of the pneumococcal phage Dp‐1: a chimeric lysin of intergeneric origin , 1997, Molecular microbiology.