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Overexpression of the Lactobacillus plantarum peptidoglycan biosynthesis murA2 gene increases the tolerance of Escherichia coli to alcohols and enhances ethanol production

  • Bioenergy and biofuels
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Abstract

A major challenge in producing chemicals and biofuels is to increase the tolerance of the host organism to toxic products or byproducts. An Escherichia coli strain with superior ethanol and more generally alcohol tolerance was identified by screening a library constructed by randomly integrating Lactobacillus plantarum genomic DNA fragments into the E. coli chromosome via Cre-lox recombination. Sequencing identified the inserted DNA fragment as the murA2 gene and its upstream intergenic 973-bp sequence, both coded on the negative genomic DNA strand. Overexpression of this murA2 gene and its upstream 973-bp sequence significantly enhanced ethanol tolerance in both E. coli EC100 and wild type E. coli MG1655 strains by 4.1-fold and 2.0-fold compared to control strains, respectively. Tolerance to n-butanol and i-butanol in E. coli MG1655 was increased by 1.85-fold and 1.91-fold, respectively. We show that the intergenic 973-bp sequence contains a native promoter for the murA2 gene along with a long 5′ UTR (286 nt) on the negative strand, while a noncoding, small RNA, named MurA2S, is expressed off the positive strand. MurA2S is expressed in E. coli and may interact with murA2, but it does not affect murA2’s ability to enhance alcohol tolerance in E. coli. Overexpression of murA2 with its upstream region in the ethanologenic E. coli KO11 strain significantly improved ethanol production in cultures that simulate the industrial Melle-Boinot fermentation process.

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References

  • Alper H, Moxley J, Nevoigt E, Fink GR, Stephanopoulos G (2006) Engineering yeast transcription machinery for improved ethanol tolerance and production. Science 314:1565–1568. doi:10.1126/science.1131969

    Article  PubMed  CAS  Google Scholar 

  • Block KF, Puerta-Fernandez E, Wallace JG, Breaker RR (2011) Association of OLE RNA with bacterial membranes via an RNA-protein interaction. Mol Microbiol 79:21–34. doi:10.1111/j.1365-2958.2010.07439.x

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Borden JR, Jones SW, Indurthi D, Chen Y, Papoutsakis ET (2010) A genomic-library based discovery of a novel, possibly synthetic, acid-tolerance mechanism in Clostridium acetobutylicum involving non-coding RNAs and ribosomal RNA processing. Metab Eng 12:268–281. doi:10.1016/j.ymben.2009.12.004

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Cho SH, Lei R, Henninger TD, Contreras LM (2014) Discovery of ethanol responsive small RNAs in Zymomonas mobilis. Appl Environ Microbiol. doi:10.1128/aem.00429-14

  • Couto JA, Pina C, Hogg T (1997) Enhancement of apparent resistance to ethanol in Lactobacillus hilgardii. Biotechnol Lett 19:487–490

    Article  CAS  Google Scholar 

  • Datsenko KA, Wanner BL (2000) One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products. Proc Natl Acad Sci U S A 97:6640–6645. doi:10.1073/pnas.120163297

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Du W, Brown JR, Sylvester DR, Huang J, Chalker AF, So CY, Holmes DJ, Payne DJ, Wallis NG (2000) Two active forms of UDP-N-acetylglucosamine enolpyruvyl transferase in gram-positive bacteria. J Bacteriol 182:4146–4152

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Dunlop MJ (2011) Engineering microbes for tolerance to next-generation biofuels. Biotechnol Biofuels 4:32. doi:10.1186/1754-6834-4-32

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Fernandes P, Ferreira BS, Cabral JMS (2003) Solvent tolerance in bacteria: role of efflux pumps and cross-resistance with antibiotics. Int J Antimicrob Agents 22:211–216

    Article  PubMed  CAS  Google Scholar 

  • Gaida SM, Al-Hinai MA, Indurthi DC, Nicolaou SA, Papoutsakis ET (2013) Synthetic tolerance: three noncoding small RNAs, DsrA, ArcZ and RprA, acting supra-additively against acid stress. Nucleic Acids Res 41:8726–8737. doi:10.1093/nar/gkt651

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • G-Alegria E, Lopez I, Ruiz JI, Saenz J, Fernandez E, Zarazaga M, Dizy M, Torres C, Ruiz-Larrea F (2004) High tolerance of wild Lactobacillus plantarum and Oenococcus oeni strains to lyophilisation and stress environmental conditions of acid pH and ethanol. FEMS Microbiol Lett 230:53–61

    Article  PubMed  CAS  Google Scholar 

  • Gautam A, Rishi P, Tewari R (2011) UDP-N-acetylglucosamine enolpyruvyl transferase as a potential target for antibacterial chemotherapy: recent developments. Appl Microbiol Biotechnol 92:211–225. doi:10.1007/s00253-011-3512-z

    Article  PubMed  CAS  Google Scholar 

  • Gold RS, Meagher MM, Hutkins R, Conway T (1992) Ethanol tolerance and carbohydrate-metabolism in Lactobacilli. J Ind Microbiol 10:45–54

    Article  CAS  Google Scholar 

  • Goodarzi H, Bennett BD, Amini S, Reaves ML, Hottes AK, Rabinowitz JD, Tavazoie S (2010) Regulatory and metabolic rewiring during laboratory evolution of ethanol tolerance in E. coli. Mol Syst Biol 6:378

    Article  PubMed  PubMed Central  Google Scholar 

  • Gupta A, Singh R, Khare SK, Gupta MN (2006) A solvent tolerant isolate of Enterobacter aerogenes. Bioresour Technol 97:99–103

    Article  PubMed  CAS  Google Scholar 

  • Hosokawa K, Park NH, Inaoka T, Itoh Y, Ochi K (2002) Streptomycin-resistant (rpsL) or rifampicin-resistant (rpoB) mutation in Pseudomonas putida KH146-2 confers enhanced tolerance to organic chemicals. Environ Microbiol 4:703–712

  • Kameyama Y, Kawabe Y, Ito A, Kamihira M (2010) An accumulative site-specific gene integration system using cre recombinase-mediated cassette exchange. Biotechnol Bioeng 105:1106–1114. doi:10.1002/bit.22619

    PubMed  CAS  Google Scholar 

  • Kleerebezem M, Boekhorst J, van Kranenburg R, Molenaar D, Kuipers OP, Leer R, Tarchini R, Peters SA, Sandbrink HM, Fiers MWEJ, Stiekema W, Lankhorst RMK, Bron PA, Hoffer SM, Groot MNN, Kerkhoven R, de Vries M, Ursing B, de Vos WM, Siezen RJ (2003) Complete genome sequence of Lactobacillus plantarum WCFS1. Proc NatI Acad Sci U S A 100:1990–1995

    Article  CAS  Google Scholar 

  • Knoshaug EP, Zhang M (2009) Butanol tolerance in a selection of microorganisms. Appl Biochem Biotechnol 153:13–20

    Article  PubMed  CAS  Google Scholar 

  • Marquardt JL, Siegele DA, Kolter R, Walsh CT (1992) Cloning and sequencing of Escherichia coli murZ and purification of its product, a UDP-N-acetylglucosamine enolpyruvyl transferase. J Bacteriol 174:5748–5752

    PubMed  CAS  PubMed Central  Google Scholar 

  • Nicolaou SA, Gaida SM, Papoutsakis ET (2010) A comparative view of metabolite and substrate stress and tolerance in microbial bioprocessing: from biofuels and chemicals, to biocatalysis and bioremediation. Metab Eng 12:307–331. doi:10.1016/j.ymben.2010.03.004

    Article  PubMed  CAS  Google Scholar 

  • Nicolaou SA, Gaida SM, Papoutsakis ET (2011) Coexisting/Coexpressing Genomic Libraries (CoGeL) identify interactions among distantly located genetic loci for developing complex microbial phenotypes. Nucleic Acids Res 39:e152. doi:10.1093/nar/gkr817

    Article  PubMed  PubMed Central  Google Scholar 

  • Nicolaou SA, Gaida SM, Papoutsakis ET (2012) Exploring the combinatorial genomic space in Escherichia coli for ethanol tolerance. Biotechnol J 7:1337–1345. doi:10.1002/biot.201200227

    Article  PubMed  CAS  Google Scholar 

  • Ohta K, Beall DS, Mejia JP, Shanmugam KT, Ingram LO (1991) Genetic improvement of Escherichia coli for ethanol production: chromosomal integration of Zymomonas mobilis genes encoding pyruvate decarboxylase and alcohol dehydrogenase II. Appl Environ Microbiol 57:893–900

    PubMed  CAS  PubMed Central  Google Scholar 

  • Papoutsakis ET, Bi C, Nicolaou S (2011) Engineering complex microbial phenotypes with successive integrations of exogenous DNA (Siedna). USA Patent US2011300553-A1; WO2011153342-A2; WO2011153342-A3,

  • Santos PM, Benndorf D, Sa-Correia I (2004) Insights into Pseudomonas putida KT2440 response to phenol-induced stress by quantitative proteomics. Proteomics 4:2640–2652

    Article  PubMed  CAS  Google Scholar 

  • Venkataramanan KP, Jones SW, McCormick KP, Kunjeti SG, Ralston MT, Meyers BC, Papoutsakis ET (2013) The Clostridium small RNome that responds to stress: the paradigm and importance of toxic metabolite stress in C. acetobutylicum. BMC Genomics. 14 doi:10.1186/1471-2164-14-849

  • Vollmer W, Blanot D, de Pedro MA (2008) Peptidoglycan structure and architecture. FEMS Microbiol Rev 32:149–167. doi:10.1111/j.1574-6976.2007.00094.x

    Article  PubMed  CAS  Google Scholar 

  • Wilkins BM, Pritchard RH (1987) Escherichia coli and Salmonella typhimurium—cellular and molecular biology, Vol 1–2 - Neidhardt, Fc. Nature 330:707–708

  • Woodruff LBA, Pandhal J, Ow SY, Karimpour-Fard A, Weiss SJ, Wright PC, Gill RT (2013) Genome-scale identification and characterization of ethanol tolerance genes in Escherichia coli. Metab Eng 15:124–133. doi:10.1016/j.ymben.2012.10.007

    Article  PubMed  CAS  Google Scholar 

  • Zhou K, Zhou L, Lim Q, Zou R, Stephanopoulos G, Too HP (2011) Novel reference genes for quantifying transcriptional responses of Escherichia coli to protein overexpression by quantitative PCR. BMC Mol Biol 12:18. doi:10.1186/1471-2199-12-18

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Zingaro KA, Papoutsakis ET (2012) Toward a semisynthetic stress response system to engineer microbial solvent tolerance. Mbio 3(5) doi:10.1128/mBio.00308-12

  • Zingaro KA, Papoutsakis ET (2013) GroESL overexpression imparts Escherichia coli tolerance to i-, n-, and 2-butanol, 1,2,4-butanetriol and ethanol with complex and unpredictable patterns. Metab Eng 15:196–205. doi:10.1016/j.ymben.2012.07.009

  • Zingaro KA, Nicolaou SA, Papoutsakis ET (2013) Dissecting the assays to assess microbial tolerance to toxic chemicals in bioprocessing. Trends Biotechnol 31:643–653. doi:10.1016/j.tibtech.2013.08.005

    Article  PubMed  CAS  Google Scholar 

  • Zingaro KA, Nicolaou SA, Yuan Y, Papoutsakis ET (2014) Exploring the heterologous genomic space for building, stepwise, complex, multicomponent tolerance to toxic chemicals. ACS Synth Biol 3:476–486. doi:10.1021/sb400156v

    Article  PubMed  CAS  Google Scholar 

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Acknowledgments

This work was supported by a National Science Foundation Grant, CBET-1033926, and an Office of Naval Research (USA) Grant N000141010161.

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The authors declare that they have no conflict of interest.

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Correspondence to Eleftherios T. Papoutsakis.

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Yuan, Y., Bi, C., Nicolaou, S.A. et al. Overexpression of the Lactobacillus plantarum peptidoglycan biosynthesis murA2 gene increases the tolerance of Escherichia coli to alcohols and enhances ethanol production. Appl Microbiol Biotechnol 98, 8399–8411 (2014). https://doi.org/10.1007/s00253-014-6004-0

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  • DOI: https://doi.org/10.1007/s00253-014-6004-0

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