Unveiling the photoelectrocatalytic inactivation mechanism of Escherichia coli: Convincing evidence from responses of parent and anti-oxidation single gene knockout mutants

Water Research

Volumn 88, Issue , 2016, Pages 135-143

  Sun, Hongwei ^a,d   Li, Guiying ^a   An, Taicheng ^a   Zhao, Huijun ^b   Wong, Po Keung ^c  

^a GUANGZHOU INSTITUTE OF GEOCHEMISTRY   (China)

^b GRIFFITH UNIVERSITY   (Australia)

^c CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

^d UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

Catalase; Hydrogen peroxide; Oxidative stress; Photocatalytic disinfection; Superoxide dismutase

Indexed keywords

ABLATION; BACTERIA; ENZYMES; HYDROGEN PEROXIDE; MANGANESE; OXIDATIVE STRESS; OXYGEN;

CATALASE; ESCHERICHIA COLI (E. COLI); INACTIVATION EFFICIENCY; INACTIVATION MECHANISMS; OXIDATIVE STRESS RESPONSE; PHOTOCATALYTIC DISINFECTIONS; REACTIVE OXYGEN SPECIES; SUPER OXIDE DISMUTASE;

ESCHERICHIA COLI;

BACTERIAL PROTEIN; BACTERICIDE; CATALASE; DNA BINDING PROTEIN; HYDROGEN PEROXIDE; KATG PROTEIN; REACTIVE OXYGEN METABOLITE; SODA PROTEIN; SUPEROXIDE DISMUTASE; UNCLASSIFIED DRUG;

ANTIOXIDANT; CATALYSIS; CELLS AND CELL COMPONENTS; COLIFORM BACTERIUM; CONCENTRATION (COMPOSITION); DAMAGE; DISINFECTION; ENZYME ACTIVITY; GENETIC ANALYSIS; HYDROGEN PEROXIDE; MUTATION; OXIDATION; PHOTODEGRADATION;

ANTIBIOTIC RESISTANCE; ARTICLE; BACTERIAL CELL; BACTERIAL GROWTH; BACTERIAL MEMBRANE; CATALYST; CELL DENSITY; CELL MEMBRANE; CELL STRUCTURE; CONTROLLED STUDY; DISINFECTION; ENERGY METABOLISM; ENZYME ACTIVITY; ENZYME SYNTHESIS; ESCHERICHIA COLI; GENE FUNCTION; GENE INACTIVATION; KINETIC PARAMETERS; MEMBRANE DAMAGE; MEMBRANE PERMEABILITY; MEMBRANE POTENTIAL; NONHUMAN; OUTER MEMBRANE; OXIDATIVE STRESS; PRIORITY JOURNAL; ULTRAVIOLET IRRADIATION; CATALYSIS; ELECTRICITY; ENZYMOLOGY; GENETICS; LIGHT; METABOLISM; MICROBIOLOGY; MUTATION; OXIDATION REDUCTION REACTION; PHOTOCHEMISTRY; PROCEDURES; RADIATION RESPONSE;

BACTERIA (MICROORGANISMS); ESCHERICHIA COLI;

CATALASE; CATALYSIS; DISINFECTION; ELECTRICITY; ESCHERICHIA COLI; GENE KNOCKOUT TECHNIQUES; HYDROGEN PEROXIDE; LIGHT; MUTATION; OXIDATION-REDUCTION; OXIDATIVE STRESS; PHOTOCHEMICAL PROCESSES; REACTIVE OXYGEN SPECIES; SUPEROXIDE DISMUTASE; WATER MICROBIOLOGY;

EID: 84944810460     PISSN: 00431354     EISSN: 18792448     Source Type: Journal    
DOI: 10.1016/j.watres.2015.10.003     Document Type: Article

References (40)

1. 2 catalyst via intense anodic bias. Electrochem. Commun. 2007, 9:1684-1688.
2. Bosshard F., Bucheli M., Meur Y., Egli T. The respiratory chain is the cell's Achilles' heel during UVA inactivation in Escherichia coli. Microbiology 2010, 156:2006-2015.
3. Calhoun L.N., Kwon Y.M. Structure, function and regulation of the DNA-binding protein Dps and its role in acid and oxidative stress resistance in Escherichia coli: a review. J. Appl. Microbiol. 2011, 110:375-386.
4. 2 photocatalysis damages lipids and proteins in Escherichia coli. Appl. Environ. Microbiol. 2014, 80:2573-2581.
5. Chiang S.M., Schellhorn H.E. Regulators of oxidative stress response genes in Escherichia coli and their functional conservation in bacteria. Arch. Biochem. Biophys. 2012, 525:161-169.
6. 2 photocatalytic disinfection. Water Res. 2004, 38:1069-1077.
7. Chung H.J., Bang W., Drake M.A. Stress response of Escherichia coli. Compr. Rev. Food Sci. Food Saf. 2006, 5:52-64.
8. Dalle-Donne I., Rossi R., Giustarini D., Milzani A., Colombo R. Protein carbonyl groups as biomarkers of oxidative stress. Clin. Chim. Acta 2003, 329:23-38.
9. Dalrymple O.K., Stefanakos E., Trotz M.A., Goswami D.Y. A review of the mechanisms and modeling of photocatalytic disinfection. Appl. Catal. B Environ. 2010, 98:27-38.
10. Foster H.A., Ditta I.B., Varghese S., Steele A. Photocatalytic disinfection using titanium dioxide: spectrum and mechanism of antimicrobial activity. Appl. Microbiol. Biotechnol. 2011, 90:1847-1868.
11. Gao M.H., An T.C., Li G.Y., Nie X., Yip H.Y., Zhao H., Wong P.K. Genetic studies of the role of fatty acid and coenzyme A in photocatalytic inactivation of Escherichia coli. Water Res. 2012, 46:3951-3957.
12. Gao P., Liu J., Sun D.D., Ng W. Graphene oxide-CdS composite with high photocatalytic degradation and disinfection activities under visible light irradiation. J. Hazard. Mater. 2013, 250:412-420.
13. Geeraerd A.H., Herremans C.H., Van Impe J.F. Structural model requirements to describe microbial inactivation during a mild heat treatment. Int. J. Food Microbiol. 2000, 59:185-209.
14. Geeraerd A.H., Valdramidis V.P., Van Impe J.F. GInaFiT, a freeware tool to assess non-log-linear microbial survivor curves. Int. J. Food Microbiol. 2005, 102:95-105.
15. 2 photocatalysis causes DNA damage via fenton reaction-generated hydroxyl radicals during the recovery period. Appl. Environ. Microbiol. 2007, 73:7740-7743.
16. GonzalezFlecha B., Demple B. Homeostatic regulation of intracellular hydrogen peroxide concentration in aerobically growing Escherichia coli. J. Bacteriol. 1997, 179:382-388.
17. Imlay J.A., Linn S. Bimodal pattern of killing of DNA-repair-defective or anoxically grown Escherichia-coli by hydrogen-peroxide. J. Bacteriol. 1986, 166:519-527.
18. 2 thin films: dynamic view of the active oxygen species responsible for the effect. J. Photochem. Photobiol. A 1997, 106:51-56.
19. Kulkarni P., Chellam S. Disinfection by-product formation following chlorination of drinking water: artificial neural network models and changes in speciation with treatment. Sci. Total Environ. 2010, 408:4202-4210.
20. Leung T.Y., Chan C.Y., Hu C., Yu J.C., Wong P.K. Photocatalytic disinfection of marine bacteria using fluorescent light. Water Res. 2008, 42:4827-4837.
21. Li G.Y., Liu X.L., Zhang H.M., Wong P.K., An T.C., Zhao H.J. Comparative studies of photocatalytic and photoelectrocatalytic inactivation of E. coli in presence of halides. Appl. Catal. B Environ. 2013, 140-141:225-232.
22. 2 photoanode: a case study of nucleotide bases. Catal. Today 2015, 242:363-371.
23. Li G.Y., Liu X.L., Zhang H.M., An T.C., Zhang S.Q., Carroll A.R., Zhao H.J. In situ photoelectrocatalytic generation of bactericide for instant inactivation and rapid decomposition of Gram-negative bacteria. J. Catal. 2011, 277:88-94.
24. Luo W., Abbas M.E., Zhu L.H., Deng K.J., Tang H.Q. Rapid quantitative determination of hydrogen peroxide by oxidation decolorization of methyl orange using a Fenton reaction system. Anal. Chim. Acta 2008, 629:1-5.
25. Mukhopadhyay S., Schellhorn H.E. Induction of Escherichia-coli hydroperoxidase-I by acetate and other weak acids. J. Bacteriol. 1994, 176:2300-2307.
26. Nachin L., Nannmark U., Nystrom T. Differential roles of the universal stress proteins of Escherichia coli in oxidative stress resistance, adhesion, and motility. J. Bacteriol. 2005, 187:6265-6272.
27. 2 nanotube photoanode and its application in photoelectrocatalytic degradation of model environmental pharmaceuticals. J. Chem. Technol. Biotechnol. 2013, 88:1488-1497.
28. 2 nanotubes as a photoanode. Appl. Catal. B Environ. 2014, 147:562-570.
29. 2 solar-light-assisted inactivation of E-coli at field scale - implications in solar disinfection at low temperature of large quantities of water. Catal. Today 2007, 122:128-136.
30. Robertson P.K.J., Robertson J.M.C., Bahnemann D.W. Removal of microorganisms and their chemical metabolites from water using semiconductor photocatalysis. J. Hazard. Mater. 2012, 211:161-171.
31. Rohnstock A., Lehmann L. Evaluation of the probe dihydrocalcein acetoxymethylester as an indicator of reactive oxygen species formation and comparison with oxidative DNA base modification determined by modified alkaline elution technique. Toxicol. Vitro 2007, 21:1552-1562.
32. 2 in cultured endothelial-cells. Arch. Biochem. Biophys. 1993, 302:348-355.
33. 2 in the visible-light-driven photocatalytic inactivation of E. coli using natural sphalerite: a genetic study. J. Phys. Chem. B 2015, 119:3104-3111.
34. Shi H.X., Li G.Y., Sun H.W., An T.C., Zhao H.J., Wong P.K. Visible-light-driven photocatalytic inactivation of E. coli by Ag/AgX-CNTs (X = Cl, Br, I) plasmonic photocatalysts: bacterial performance and deactivation mechanism. Appl. Catal. B Environ. 2014, 158-159:301-307.
35. Stone J.R., Yang S.P. Hydrogen peroxide: a signaling messenger. Antioxid. Redox Sign. 2006, 8:243-270.
36. Storz G., Tartaglia L.A., Farr S.B., Ames B.N. Bacterial defenses against oxidative stress. Trends Genet. 1990, 6:363-368.
37. Sun H.W., Li G.Y., Nie X., Shi H.X., Wong P.K., Zhao H.J., An T.C. Systematic approach to in-depth understanding of photoelectrocatalytic bacterial inactivation mechanisms by tracking the decomposed building blocks. Environ. Sci. Technol. 2014, 48:9412-9419.
38. Wang H.Y.L., O'Doherty G.A. Modulators of Na/K-ATPase: a patent review. Expert Opin. Ther. Pat. 2012, 22:587-605.
39. 2 microspheres: the role of different reactive species. Appl. Catal. B Environ. 2011, 108-109:108-116.
40. Wang W.J., Yu Y., An T.C., Li G.Y., Yip H.Y., Yu J.C., Wong P.K. Visible-light-driven photocatalytic inactivation of E. coli K-12 by bismuth vanadate nanotubes: bactericidal performance and mechanism. Environ. Sci. Technol. 2012, 46:4599-4606.