Skip to main content
Log in

Recruiting alternative glucose utilization pathways for improving succinate production

  • Applied Genetics and Molecular Biotechnology
  • Published:
Applied Microbiology and Biotechnology Aims and scope Submit manuscript

Abstract

The phosphoenolpyruvate (PEP): carbohydrate phosphotransferase system (PTS) of Escherichia coli was usually inactivated to increase PEP supply for succinate production. However, cell growth and glucose utilization rate decreased significantly with PTS inactivation. In this work, two glucose transport proteins and two glucokinases (Glk) from E. coli and Zymomonas mobilis were recruited in PTS strains, and their impacts on glucose utilization and succinate production were compared. All PTS strains recruiting Z. mobilis glucose facilitator Glf had higher glucose utilization rates than PTS strains using E. coli galactose permease (GalP), which was suggested to be caused by higher glucose transport velocity and lower energetic cost of Glf. The highest rate obtained by combinatorial modulation of glf and glk E. coli (2.13 g/L•h) was 81 % higher than the wild-type E. coli and 30 % higher than the highest rate obtained by combinatorial modulation of galP and glk E. coli . On the other hand, although glucokinase activities increased after replacing E. coli Glk with isoenzyme of Z. mobilis, glucose utilization rate decreased to 0.58 g/L•h, which was assumed due to tight regulation of Z. mobilis Glk by energy status of the cells. For succinate production, using GalP led to a 20 % increase in succinate productivity, while recruiting Glf led to a 41 % increase. These efficient alternative glucose utilization pathways obtained in this work can also be used for production of many other PEP-derived chemicals, such as malate, fumarate, and aromatic compounds.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  • Cherepanov PP, Wackernagel W (1995) Gene disruption in Escherichia coli: TcR and KmR cassettes with the option of Flp-catalyzed excision of the antibiotic-resistance determinant. Gene 158:9–14

    Article  CAS  Google Scholar 

  • Dimarco AA, Romano AH (1985) D-glucose transport system of Zymomonas mobilis. Appl Environ Microbiol 49:151–157

    CAS  Google Scholar 

  • Doelle HW (1982) Kinetic characteristics and regulatory mechanisms of glucokinase and fructokinase from Zymomonas mobilis. Eur J Appl Microbiol Biotechnol 14:241–246

    Article  CAS  Google Scholar 

  • Escalante A, Salinas Cervantes A, Gosset G, Bolivar F (2012) Current knowledge of the Escherichia coli phosphoenolpyruvate-carbohydrate phosphotransferase system: peculiarities of regulation and impact on growth and product formation. Appl Microbiol Biotechnol 94:1483–1494

    Article  CAS  Google Scholar 

  • Flores N, Xiao J, Berry A, Bolivar F, Valle F (1996) Pathway engineering for the production of aromatic compounds in Escherichia coli. Nat Biotechnol 14:620–623

    Article  CAS  Google Scholar 

  • Fraenkel DG, Horecker BL (1964) Pathways of D-glucose metabolism in Salmonella typhimurium. J Biol Chem 239:2765–2771

    CAS  Google Scholar 

  • Glassner D, Datta R (1992) Process for the production and purification of succinic acid. US patent 5143834

  • Gosset G (2005) Improvement of Escherichia coli production strains by modification of the phosphoenolpyruvate:sugar phosphotransferase system. Microb Cell Fact 4:14

    Article  Google Scholar 

  • Guettler M, Jain M, Soni B (1996) Process for making succinic acid, microorganisms for use in the process and methods of obtaining the microorganisms. US patent 5504004

  • Hernandez-Montalvo V, Martinez A, Hernandez-Chavez G, Bolivar F, Valle F, Gosset G (2003) Expression of galP and glk in a Escherichia coli PTS mutant restores glucose transport and increases glycolytic flux to fermentation products. Biotechnol Bioeng 83:687–694

    Article  CAS  Google Scholar 

  • Jantama K, Zhang X, Moore JC, Shanmugam KT, Svoronos SA, Ingram LO (2008) Eliminating side products and increasing succinate yields in engineered strains of Escherichia coli C. Biotechnol Bioeng 101:881–893

    Article  CAS  Google Scholar 

  • Lee PC, Lee SY, Hong SH, Chang HN (2002) Isolation and characterization of a new succinic acid-producing bacterium, Mannheimia succiniciproducens MBEL55E, from bovine rumen. Appl Microbiol Biotechnol 58:663–668

    Article  CAS  Google Scholar 

  • Lee SJ, Lee DY, Kim TY, Kim BH, Lee J, Lee SY (2005) Metabolic engineering of Escherichia coli for enhanced production of succinic acid, based on genome comparison and in silico gene knockout simulation. Appl Environ Microbiol 71:7880–7887

    Article  CAS  Google Scholar 

  • Lin H, Bennett GN, San KY (2005) Fed-batch culture of a metabolically engineered Escherichia coli strain designed for high-level succinate production and yield under aerobic conditions. Biotechnol Bioeng 90:775–779

    Article  CAS  Google Scholar 

  • Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method. Methods 25:402–408

    Article  CAS  Google Scholar 

  • Lu J, Tang J, Liu Y, Zhu X, Zhang T, Zhang X (2012) Combinatorial modulation of galP and glk gene expression for improved alternative glucose utilization. Appl Microbiol Biotechnol 93:2455–2426

    Article  CAS  Google Scholar 

  • Martinez A, Grabar TB, Shanmugam KT, Yomano LP, York SW, Ingram LO (2007) Low salt medium for lactate and ethanol production by recombinant Escherichia coli B. Biotechnol Lett 29:397–404

    Article  CAS  Google Scholar 

  • McDonald TP, Walmsley AR, Henderson PJ (1997) Asparagine 394 in putative helix 11 of the galactose-H+ symport protein (GalP) from Escherichia coli is associated with the internal binding site for cytochalasin B and sugar. J Biol Chem 272:15189–15199

    Article  CAS  Google Scholar 

  • McKinlay JB, Vieille C, Zeikus JG (2007) Prospects for a bio-based succinate industry. Appl Microbiol Biotechnol 76:727–740

    Article  CAS  Google Scholar 

  • Meyer D, Schneider-Fresenius C, Horlacher R, Peist R, Boos W (1997) Molecular characterization of glucokinase from Escherichia coli K-12. J Bacteriol 179:1298–1306

    CAS  Google Scholar 

  • Parker C, Barnell WO, Snoep JL, Ingram LO, Conway T (1995) Characterization of the Zymomonas mobilis glucose facilitator gene product (glf) in recombinant Escherichia coli: examination of transport mechanism, kinetics and the role of glucokinase in glucose transport. Mol Microbiol 15:795–802

    Article  CAS  Google Scholar 

  • Postma P, Lengeler J, Jacobson G (1996). Phosphoenolpyruvate: carbohydrate phosphotransferase systems. In: Neidhardt FC et al (ed) Escherichia coli and Salmonella: cellular and molecular biology, 2nd edn. Washington, DC, pp 1149–1174

  • Saier MH Jr, Crasnier M (1996) Inducer exclusion and the regulation of sugar transport. Res Microbiol 147:482–489

    Article  CAS  Google Scholar 

  • Sauer M, Porro D, Mattanovich D, Branduardi P (2008) Microbial production of organic acids: expanding the markets. Trends Biotechnol 26:100–108

    Article  CAS  Google Scholar 

  • Scholten E, Renz T, Thomas J (2009) Continuous cultivation approach for fermentative succinic acid production from crude glycerol by Basfia succiniciproducens DD1. Biotechnol Lett 31:1947–1951

    Article  CAS  Google Scholar 

  • Siedler S, Bringer S, Blank LM, Bott M (2012) Engineering yield and rate of reductive biotransformation in Escherichia coli by partial cyclization of the pentose phosphate pathway and PTS independent glucose transport. Appl Microbiol Biotechnol 93:1459–1467

    Article  CAS  Google Scholar 

  • Snoep JL, Arfman N, Yomano LP, Fliege RK, Conway T, Ingram LO (1994) Reconstitution of glucose-uptake and phosphorylation in a glucose-negative mutant of Escherichia coli by using Zymomonas mobilis genes encoding the glucose facilitator protein and glucokinase. J Bacteriol 176:2133–2135

    CAS  Google Scholar 

  • Sprenger G, Siewe H, Sahm M, Karutz M, Sonke T (1998a) Microbial production of substances from aromatic metabolism/I. WO 98/18936

  • Sprenger G, Siewe H, Sahm M, Karutz M, Sonke T (1998b) Microbial preparation of substances from aromatic metabolism/II. WO 98/18937

  • Supple SG, Joachimsthal EL, Dunn NW, Rogers PL (2000) Isolation and preliminary characterization of a Zymomonas mobilis mutant with an altered preference for xylose and glucose utilization. Biotechnol Lett 22:157–164

    Article  CAS  Google Scholar 

  • Vemuri GN, Eiteman MA, Altman E (2002) Effects of growth mode and pyruvate carboxylase on succinic acid production by metabolically engineered strains of Escherichia coli. Appl Environ Microbiol 68:1715–1727

    Article  CAS  Google Scholar 

  • Wang Q, Wu C, Chen T, Chen X, Zhao X (2006) Expression of galactose permease and pyruvate carboxylase in Escherichia coli ptsG mutant increases the growth rate and succinate yield under anaerobic conditions. Biotechnol Lett 28:89–93

    Article  Google Scholar 

  • Weisser P, Kramer R, Sahm H, Sprenger GA (1995) Functional expression of the glucose transporter of Zymomonas mobilis leads to restoration of glucose and fructose uptake in Escherichia coli mutants and provides evidence for its facilitator action. J Bacteriol 177:3351–3354

    CAS  Google Scholar 

  • Yi J, Draths KM, Li K, Frost JW (2003) Altered glucose transport and shikimate pathway product yields in E. coli. Biotechnol Prog 19:1450–1459

    Article  CAS  Google Scholar 

  • Zhang X, Jantama K, Moore JC, Shanmugam KT, Ingram LO (2007) Production of L-alanine by metabolically engineered Escherichia coli. Appl Microbiol Biotechnol 77:355–366

    Article  CAS  Google Scholar 

  • Zhang X, Jantama K, Moore JC, Jarboe LR, Shanmugam KT, Ingram LO (2009a) Metabolic evolution of energy-conserving pathways for succinate production in Escherichia coli. Proc Natl Acad Sci USA 106:20180–20185

    Article  CAS  Google Scholar 

  • Zhang X, Jantama K, Shanmugam KT, Ingram LO (2009b) Reengineering Escherichia coli for succinate production in mineral salts medium. Appl Environ Microbiol 75:7807–7813

    Article  CAS  Google Scholar 

Download references

Acknowledgments

This research was supported by grants from the Knowledge Innovation Project of the Chinese Academy of Sciences (KSCX2-EW-G-2), the National Basic Research Program of China (2011CBA00806), the National High Technology Research and Development Program of China (2011AA02A203), and the Hundred Talent Program of the Chinese Academy of Sciences. The authors thank Dr. Lonnie Ingram in University of Florida for kindly providing E. coli ATCC 8739, Zymomonas mobilis subsp. mobilis ZM4, and plasmid pLOI4162. The authors thank Dr. Chaoguang Tian and Pengli Cai in Tianjin Institute of Industrial Biotechnology for their help with real-time PCR analysis.

Competing interests

The authors declare that they have no competing interests.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Xueli Zhang.

Additional information

Jinlei Tang and Xinna Zhu contributed equally to this work.

Electronic supplementary material

Below is the link to the electronic supplementary material.

ESM 1

(PDF 52 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Tang, J., Zhu, X., Lu, J. et al. Recruiting alternative glucose utilization pathways for improving succinate production. Appl Microbiol Biotechnol 97, 2513–2520 (2013). https://doi.org/10.1007/s00253-012-4344-1

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00253-012-4344-1

Keywords

Navigation