Skip to main content
Log in

Hydrogenase activity and proton-motive force generation by Escherichia coli during glycerol fermentation

  • Published:
Journal of Bioenergetics and Biomembranes Aims and scope Submit manuscript

Abstract

Proton motive force (Δp) generation by Escherichia coli wild type cells during glycerol fermentation was first studied. Its two components, electrical—the membrane potential (∆φ) and chemical—the pH transmembrane gradient (ΔpH), were established and the effects of external pH (pHex) were determined. Intracellular pH was 7.0 and 6.0 and lower than pHex at pH 7.5 and 6.5, respectively; and it was higher than pHex at pH 5.5. At high pHex, the increase of ∆φ (−130 mV) was only partially compensated by a reversed ΔpH, resulting in a low Δp. At low pHex ∆φ and consequently Δp were decreased. The generation of Δp during glycerol fermentation was compared with glucose fermentation, and the difference in Δp might be due to distinguished mechanisms for H+ transport through the membrane, especially to hydrogenase (Hyd) enzymes besides the F0F1-ATPase. H+ efflux was determined to depend on pHex; overall and N,N’-dicyclohexylcarbodiimide (DCCD)-inhibitory H+ efflux was maximal at pH 6.5. Moreover, ΔpH was changed at pH 6.5 and Δp was different at pH 6.5 and 5.5 with the hypF mutant lacking all Hyd enzymes. DCCD-inhibited ATPase activity of membrane vesicles was maximal at pH 7.5 and decreased with the hypF mutant. Thus, Δp generation by E. coli during glycerol fermentation is different than that during glucose fermentation. Δp is dependent on pHex, and a role of Hyd enzymes in its generation is suggested.

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.

Similar content being viewed by others

References

  • Andrews SC, Berks BC, Mcclay J, Ambler A, Quail MA, Golby P, Guest JR (1997) A 12-cistron Escherichia coli operon (hyf) encoding a putative proton-translocating formate hydrogenlyase system. Microbiology 143(11):3633–3647

    Article  CAS  Google Scholar 

  • Bagramyan K, Mnatsakanyan N, Poladian A, Vassilian A, Trchounian A (2002) The roles of hydrogenases 3 and 4, and the F0F1-ATPase, in H2 production by Escherichia coli at alkaline and acidic pH. FEBS Lett 516(1–3):172–178

    Article  CAS  Google Scholar 

  • Blbulyan S, Avagyan A, Poladyan A, Trchounian A (2011) Role of Escherichia coli different hydrogenases in H+ efflux and the FOF1-ATPase activity during glycerol fermentation at different pH. Biosci Rep 31(3):179–184

    Article  CAS  Google Scholar 

  • Bond DR, Russell JB (2000) Protonmotive force regulates the membrane conductance of Streptococcus bovis in a non-ohmic fashion. Microbiology 146(3):687–694

    CAS  Google Scholar 

  • Cintolesi A, Comburg JM, Rigou V, Zygourakis K, Gonzalez R (2011) Quantitative analysis of the fermentative metabolism of glycerol in Escherichia coli. Biotechnol Bioeng 109(1):187–198

    Article  Google Scholar 

  • Dharmadi Y, Murarka A, Gonzalez R (2006) Anaerobic fermentation of glycerol by Escherichia coli: a new platform for metabolic engineering. Biotechnol Bioeng 94(5):821–829

    Article  CAS  Google Scholar 

  • Eltsova ZA, Vasilieva LG, Tsygankov AA (2010) Hydrogen production by recombinant strains of Rhodobacter sphaeroides using a modified photosynthetic apparatus. Appl Biochem Microbiol 46(5):487–491

    Article  CAS  Google Scholar 

  • Hakobyan M, Sargsyan H, Bagramyan K (2005) Proton translocation coupled to formate oxidation in anaerobically grown fermenting Escherichia coli. Biophys Chem 115(1):55–61

    Article  CAS  Google Scholar 

  • Hakobyan L, Gabrielyan L, Trchounian A (2011) Proton motive force in Rhodobacter sphaeroides under anaerobic conditions in the dark. Curr Microbiol 62(2):415–419

    Article  CAS  Google Scholar 

  • Hakobyan L, Gabrielyan L, Trchounian A (2012) Relationship of proton motive force and the F0F1-ATPase with bio-hydrogen production activity of Rhodobacter sphaeroides: effects of diphenylene iodonium, hydrogenase inhibitor, and its solvent dimethylsulphoxide. J Bioenerg Biomembr 44(4):495–502

    Article  CAS  Google Scholar 

  • Hayes ET, Wilks C, Yohannes E, Tate DP, Radmacher M, BonDurant SS, Slonczewski JL (2006) pH and anaerobiosis co-regulate catabolism, hydrogenases, ion and multidrug transporters, and envelope composition in Escherichia coli K-12. BMC Microbiol 6:89

    Article  Google Scholar 

  • Hong Y, Brown DG (2010) Alteration of bacterial surface electrostatic potential and pH upon adhesion to a solid surface and impacts to cellular bioenergetics. Biotechnol Bioeng 105(5):965–972

    CAS  Google Scholar 

  • Hong S, Pedersen PL (2008) ATP synthase and the actions of inhibitors utilized to study its roles in human health, disease, and other scientific areas. Microbiol Mol Biol Rev 72(4):590–641

    Article  CAS  Google Scholar 

  • Kashket ER (1985) The proton motive force in bacteria: a critical assessment of methods. Annu Rev Microbiol 39(1):219–242

    Article  CAS  Google Scholar 

  • Kirkpatrick C, Maurer LM, Oyelakin NE, Yontcheva Y, Maurer R, Slonczewski JL (2001) Acetate and formate stress: opposite responses in the proteome of Escherichia coli. J Bacteriol 183 (21):6466–6477

    Google Scholar 

  • Lowry OH, Rosebrough NJ, Farr AL, Randall RG (1951) Protein measurement with the Folin phenol reagent. J Biol Chem 193(1):265–275

    CAS  Google Scholar 

  • Nichols DG, Ferguson SJ (2003) Bioenergetics 3. Acad. Press, London, 288 p

    Google Scholar 

  • Noguchi K, Riggins DP, Eldahan KC, Kitko RD, Slonczewski JL (2010) Hydrogenase-3 contributes to anaerobic acid resistance of Escherichia coli. PLoS One 5:e10132

    Article  Google Scholar 

  • Piskarev IM, Ushkanov VA, Aristova NA, Likhachev PP, Myslivets TS (2010) Establishment of the redox potential of water saturated with hydrogen. Biophysics (Moscow) 55(1):13–17

    Article  Google Scholar 

  • Poladyan A, Avagyan A, Vassilian A, Trchounian A (2012) Oxidative and reductive routes of glycerol and glucose fermentation by Escherichia coli batch cultures and their regulation by oxidizing and reducing reagents at different pHs. Curr Microbiol. doi:10.1007/s00284-012-0240-2, Epub 29 Sep

  • Puchkov EO, Bulatov IS, Zimchenko VP (1983) Investigation of intracellular pH in Escherichia coli by 9-aminoacridine fluorescence measurements. FEMS Microbiol Lett 20(1):41–45

    Article  CAS  Google Scholar 

  • Russell JB, Diez-Gonzalez F (1998) The effects of fermentation acids on bacterial growth. Adv Microb Physiol 39(1):205–234

    CAS  Google Scholar 

  • Sarma SJ, Brar SK, Sydney EB, Bihan YL, Buelna G, Soccol CR (2012) Microbial hydrogen production by bioconversion of crude glycerol; a review. Int J Hydrog Energy 37(8):6473–6490

    Article  CAS  Google Scholar 

  • Skulachev VP, Bogachev AV, Kasparinsky FO (2011) Membrane bioenergetics. Moscow State Univ. Press, Moscow, 350 p

    Google Scholar 

  • Slonszewski JL, Fugisawa M, Dopson M, Krulwich TA (2009) Cytoplasmic pH measurements and homeostatis in bacteria and archaea. Adv Microb Physiol 55(1):1–79

    Article  Google Scholar 

  • Ten Brink B, Konings WN (1986) Generation of a proton motive force in anaerobic bacteria by end-product efflux. Methods Enzymol 125(1):492–510

    Article  Google Scholar 

  • Torgomyan H, Hovnanyan K, Trchounian A (2012) Escherichia coli growth changes by the mediated effects after low-intensity electromagnetic irradiation of extremely high frequencies. Cell Biochem Biophys. doi:10.1007/s12013-012-9448-9, Epub 18 Oct

  • Tran QH, Unden G (1998) Changes in the proton potential and the cellular energetics of Escherichia coli during growth by aerobic and anaerobic respiration or by fermentation. Eur J Biochem 251(1–2):538–543

    Article  CAS  Google Scholar 

  • Trchounian A (2004) Escherichia coli proton-translocating F0F1-ATP synthase and its association with solute secondary transpopters and/or enzymes of anaerobic oxidation-reduction under fermentation. Biochem Biophys Res Commun 315(4):1051–1057

    Article  CAS  Google Scholar 

  • Trchounian K (2012) Trnascriptional control of hydrogen production during mixed carbon fermentation by hydrogenases 4 (hyf) and 3 (hyc) in Escherichia coli. Gene 506(1):156–160

    Article  CAS  Google Scholar 

  • Trchounian A, Kobayashi H (1999) Kup is the major K+ uptake system in Escherichia coli upon hyper-osmotic stress at low pH. FEBS Lett 447(2–3):144–148

    Article  CAS  Google Scholar 

  • Trchounian K, Trchounian A (2009) Hydrogenase 2 is most and hydrogenase 1 is less responsible for hydrogen production by Escherichia coli under glycerol fermentation at neutral and slightly alkaline pH. Int J Hydrog Energy 34(21):8839–8845

    Article  CAS  Google Scholar 

  • Trchounian AA, Vassilian AV (1994) Relationship between the F0F1-ATPase and the K+-transport system within the membrane of anaerobically grown Escherichia coli. N, N'-dicyclohexylcarbodiimide-sensitive ATPase activity in mutants with defects in K+-transport. J Bioenerg Biomembr 26(5):563–571

    Article  CAS  Google Scholar 

  • Trchounian A, Bagramyan K, Ogandjanian E, Vassilian A, Zakharyan E (1996) An electrochemical study of energy-dependent potassium accumulation in E. coli. 14. Comparison of K+ uptake characteristics in anaerobically grown cells performing fermentation and nitrate/nitrite respiration: role of the respiratory chain. Bioelectrochem Bioenerg 39(1):13–19

    Article  CAS  Google Scholar 

  • Trchounian K, Pinske C, Sawers G, Trchounian A (2011a) Dependence on the FOF1-ATP synthase for the activities of the hydrogen-oxidizing hydrogenases 1 and 2 during glucose and glycerol fermentation at high and low pH in Escherichia coli. J Bioenerg Biomembr 43(6):645–650

    Article  CAS  Google Scholar 

  • Trchounian K, Sanchez-Torres V, Wood KT, Trchounian A (2011b) Escherichia coli hydrogenase activity and H2 production under glycerol fermentation at a low pH. Int J Hydrog Energy 36(7):4323–4331

    Article  CAS  Google Scholar 

  • Trchounian K, Pinske C, Sawers G, Trchounian A (2012a) Characterization of Escherichia coli [NiFe]-hydrogenase distribution during fermentative growth at different pHs. Cell Biochem Biophys 62(3):433–440

    Article  CAS  Google Scholar 

  • Trchounian K, Poladyan A, Vassilian A, Trchounian A (2012b) Multiple and reversible hydrogenases for hydrogen production by Escherichia coli: dependence on fermentation substrate, pH and F0F1-ATPase. Crit Rev Biochem Mol Biol 47(3):236–249

    Article  CAS  Google Scholar 

  • Trchounian K, Soboh B, Sawers RG, Trchounian A (2012c) Contribution of hydrogenase 2 to stationary phase H2 production by Escherichia coli during fermentation of glycerol. Cell Biochem Biophys. doi:10.1007/s12013-012-9458-7, E-pub 23 Oct

  • Tseng CP, Tsau JL, Montville TJ (1991) Bioenergetic consequences of catabolic shifts by Lactobacillus plantarum in response to shifts in environmental oxygen and pH in chemostat cultures. J Bacteriol 173(14):4411–4416

    CAS  Google Scholar 

  • Zakharyan E, Trchounian A (2001) K+ influx in Escherichia coli is accompanied by a decrease in H+ efflux. FEMS Microbiol Lett 204(1):61–64

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Armen Trchounian.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Trchounian, K., Blbulyan, S. & Trchounian, A. Hydrogenase activity and proton-motive force generation by Escherichia coli during glycerol fermentation. J Bioenerg Biomembr 45, 253–260 (2013). https://doi.org/10.1007/s10863-012-9498-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10863-012-9498-0

Keywords

Navigation