Escherichia coli multiple [Ni-Fe]-hydrogenases are sensitive to osmotic stress during glycerol fermentation but at different pHs

FEBS Letters

Volumn 587, Issue 21, 2013, Pages 3562-3566

  Trchounian, Karen ^a   Trchounian, Armen ^a  

^a YEREVAN STATE UNIVERSITY   (Armenia)

Author keywords

Ni Fe hydrogenases; Escherichia coli; FhlA; Glycerol fermentation; H2 production; Osmotic stress; pH

Indexed keywords

DICYCLOHEXYLCARBODIIMIDE; GLYCEROL; HYDROGEN; NICKEL IRON HYDROGENASE; NICKEL IRON HYDROGENASE 3; NICKEL IRON HYDROGENASE 4; UNCLASSIFIED DRUG;

ARTICLE; BACTERIAL GENE; BACTERIAL GROWTH; BACTERIAL HYDROGEN GAS PRODUCTION; BACTERIAL METABOLISM; BACTERIAL STRAIN; BACTERIUM MUTANT; CELLULAR STRESS RESPONSE; ESCHERICHIA COLI; FERMENTATION; FHLA GENE; GLYCEROL FERMENTATION; HYPEROSMOTIC STRESS; HYPOOSMOTIC STRESS; NONHUMAN; OSMOREGULATION; PH; PRIORITY JOURNAL; STRAIN DIFFERENCE; TRANSCRIPTION INITIATION; WILD TYPE;

[NI-FE]-HYDROGENASES; ESCHERICHIA COLI; FHLA; GLYCEROL FERMENTATION; H(2) PRODUCTION; OSMOTIC STRESS; PH;

ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; FERMENTATION; GLYCEROL; HYDROGEN; HYDROGEN-ION CONCENTRATION; HYDROGENASE; OSMOREGULATION; OSMOTIC PRESSURE; TRANS-ACTIVATORS;

ESCHERICHIA COLI;

EID: 84886308686     PISSN: 00145793     EISSN: 18733468     Source Type: Journal    
DOI: 10.1016/j.febslet.2013.09.016     Document Type: Article

References (41)

1. 1-ATPase Crit. Rev. Biochem. Mol. Biol. 47 2012 236 249
2. A. Trchounian Mechanisms for hydrogen production by different bacteria during mixed-acid and photo-fermentation and perspectives of hydrogen production biotechnology Crit. Rev. Biotechnol. 2013 10.3109/07388551.2013.809047
3. Y. Dharmadi, A. Murarka, and R. Gonzalez Anaerobic fermentation of glycerol by Escherichia coli: a new platform for metabolic engineering Biotechnol. Bioeng. 94 2006 821 829
4. 2 production by Escherichia coli under glycerol fermentation at neutral and slightly alkaline pH Int. J. Hydrogen Energy 34 2009 8839 8845
5. R. Gonzalez, A. Murarka, Y. Dharmadi, and S.S. Yasdani A new model for the anaerobic fermentation of glycerol in enteric bacteria: trunk and auxiliary pathways in Escherichia coli Metab. Eng. 10 2008 234 245
6. A. Cintolesi, J.M. Comburg, V. Rigou, K. Zygourakis, and R. Gonzalez Quantitative analysis of the fermentative metabolism of glycerol in Escherichia coli Biotechnol. Bioeng. 109 2011 187 198
7. A. Poladyan, A. Avagyan, A. Vassilian, and A. Trchounian 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. 66 2013 49 55
8. 2 production under glycerol fermentation at a low pH Int. J. Hydrogen Energy 36 2011 4323 4331
9. K. Trchounian, C. Pinske, G. Sawers, and A. Trchounian Characterization of Escherichia coli NiFe-hydrogenase distribution during fermentative growth at different pHs Cell Biochem. Biophys. 62 2011 433 440
10. 2 production by Escherichia coli at alkaline and acidic pH FEBS Lett. 516 2002 172 178
11. N. Mnatsakanyan, K. Bagramyan, and A. Trchounian Hydrogenase 3 but not hydrogenase 4 is major in hydrogen gas production by Escherichia coli formate hydrogenlyase at acidic pH and in the presence of external formate Cell Biochem. Biophys. 41 2004 357 366
12. T. Maeda, V. Sanchez-Torres, and T.K. Wood Escherichia coli hydrogenase 3 is a reversible enzyme possessing hydrogen uptake and synthesis activities Appl. Microbiol. Biotechnol. 76 2007 1036 1042
13. N.K. Menon, J. Robbins, J.C. Wendt, K.T. Shanmugan, and A.E. Przybyla Mutational analysis and characterization of the Escherichia coli hya operon, which encodes [NiFe] hydrogenase 1 J. Bacteriol. 173 1991 4851 4861
14. P.W. King, and A.E. Przybyla Response of hya expression to external pH in Escherichia coli J. Bacteriol. 181 1999 5250 5256
15. D.J. Richard, G. Sawers, F. Sargent, L. McWalter, and D.H. Boxer Transcriptional regulation in response to oxygen and nitrate of the operons encoding the [NiFe] hydrogenases 1 and 2 of Escherichia coli Microbiology 145 1999 2903 2912
16. S.P. Ballantine, and D.H. Boxer Isolation and characterization of a soluble active fragment of hydrogenase isoenzyme 2 from the membranes of anaerobically grown Escherichia coli Eur J. Biochem. 156 1986 277 284
17. M.D. Redwood, I.P. Mikheenko, F. Sargent, and L.E. Macaskie Dissecting the roles of Escherichia coli hydrogenases in biohydrogen production FEMS Microbiol. Lett. 278 2008 48 55
18. M.J. Lukey, A. Parkin, M.M. Roessler, B.J. Murphy, J. Harmer, T. Palmer, F. Sargent, and F.A. Armstrong How Escherichia coli is equipped to oxidize hydrogen under different redox conditions J. Biol. Chem. 285 2010 3928 3938
19. S.C. Andrews, B.C. Berks, J. Mcclay, A. Ambler, M.A. Quail, P. Golby, and J.R. Guest A 12-cistron Escherichia coli operon (hyf) encoding a putative proton-translocating formate hydrogenlyase system Microbiology 143 1997 3633 3647
20. V. Schlensog, S. Lutz, and A. Bock Purification and DNA-binding properties of FhlA, the transcriptional activator of the formate hydrogen lyase system from Escherichia coli J. Biol. Chem. 269 1994 19590 19596
21. 2 in Salmonella enterica serovar typhimurium Appl. Environ. Microbiol. 75 2009 1456 1459
22. 1-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 2011 645 650
23. 2 production during mixed carbon (glucose and glycerol) fermentation at pH 7.5 and pH 5.5 Int. J. Hydrogen Energy 38 2013 3919 3927
24. 1-ATP synthase and its association with solute secondary transpopters and/or enzymes of anaerobic oxidation-reduction under fermentation Biochem. Biophys. Res. Commun. 315 2004 1051 1057
25. O cysteine, bCys21, in the Escherichia coli ATP synthase is involved in regulation of potassium uptake and molecular hydrogen production in anaerobic conditions Biosci. Rep. 22 2002 421 430
26. 1 ATPase activity J. Bacteriol. 179 1997 6736 6740
27. K. Trchounian, S. Blbulyan, and A. Trchounian Hydrogenase activity and proton-motive force generation by Escherichia coli during glycerol fermentation J. Bioenerg. Biomembr. 45 2013 253 260
28. W. Epstein The roles and regulation of potassium in bacteria Prog. Nucleic Acid Res. Mol. Biol. 75 2003 293 320
29. 1 in anaerobically grown Escherichia coli Curr. Microbiol. 29 1994 187 191
30. G. Kirakosyan, K. Bagramyan, and A. Trchounian Intensity of oxidation-reduction processes and molecular hydrogen production by Escherichia coli in hyper-osmotic media Biophysics 46 2001 245 250
31. N. Empadinhas, and M.S. da Costa Osmoadaptation mechanisms in prokaryotes: distribution of compatible solutes Int. Microbiol. 11 2008 151 161
32. D. Labeikute, and J. Sereikate Influence of osmotic shock on Escherichia coli insoluble protein fraction in the presence of exogenous osmolytes J. Mol. Microbiol. Biotechol. 23 2013 219 226
33. 1 ATPase under growth conditions without anaerobic or aerobic respiration Biosci. Rep. 18 1998 143 154
34. K. Trchounian Transcriptional control of hydrogen production during mixed carbon fermentation by hydrogenases 4 (hyf) and 3 (hyc) in Escherichia coli Gene 506 2012 156 160
35. V.M. Fernandez An electrochemical cell for reduction of biochemical: its application to the study of th effect pf pH and redox potential on the activity of hydrogenases Anal. Biochem. 130 1983 54 59
36. I.M. Piskarev, V.A. Ushkanov, N.A. Aristova, P.P. Likhachev, and T.S. Myslivets Establishment of the redox potential of water saturated with hydrogen Biophysics 55 2010 13 17
37. 2 production by Escherichia coli during fermentation of glycerol Cell Biochem. Biophys. 66 2013 103 108
38. V. Sanchez-Torres, M.Y.M. Yusoff, C. Nakano, M. Maeda, H.I. Ogawa, and T.K. Wood Influence of Escherichia coli hydrogenases on hydrogen fermentation from glycerol Int. J. Hydrogen Energy 38 2013 3905 3912
39. A. Dubini, R.L. Pye, R.L. Jack, T. Palmer, and F. Sargent How bacteria get energy from hydrogen: a genetic analysis of periplasmic hydrogen oxidation in Escherichia coli Int. J. Hydrogen Energy 27 2002 1413 1420
40. R.D. Kitko, J.C. Wilks, G.M. Garduque, and J.L. Slonczewski Osmolytes contribute to pH homeostasis of Escherichia coli PLoS One 5 2010 e10078
41. L. Sutherland, J. Cairney, M.J. Elmore, I.R. Booth, and C.F. Higgins Osmotic regulation of transcription: induction of the proU betaine transport gene is dependent on accumulation of intracellular potassium J. Bacteriol. 168 1986 805 812