1887

Abstract

We tested the hypothesis that during metabolism of naphthalene and other substrates by sp. strain As1 oxidative stress arises and can be reduced by antioxidant enzymes. Our approach was to prepare plasmid constructs that conferred expression of two single antioxidant enzymes [Fpr (ferredoxin-NADP reductase) and SOD (superoxide dismutase)] and the pair of enzymes SOD plus AhpC (alkyl hydroperoxide reductase). The , and genes were placed under the transcriptional control of both the constitutive promoter and their respective native promoters. Both HPLC and growth-rate analyses showed that naphthalene metabolism was enhanced in the recombinant strains. All antioxidant-overexpressing recombinant strains, with the exception of one with an upregulated gene due to the promoter [strain As1(sodA)], exhibited resistance to the superoxide generating agent paraquat (PQ). The growth of strain As1(sodA) was inhibited by PQ, but this growth defect was rapidly overcome by the simultaneous overproduction of AhpC, which is a known hydrogen peroxide scavenger. After PQ-induced oxidative damage of the [Fe–S] enzyme aconitase, recovery of enzyme activity was enhanced in the recombinant strains. Reporter strains to monitor oxidative stress in strain As1 were prepared by fusing (encoding green fluorescent protein, GFP) to the promoter. Growth on salicylate and naphthalene boosted the GFP fluorescent signal 21- and 14-fold, respectively. Using these same oxidative stress reporters, overexpression of and was found to considerably reduce PQ-induced stress. Taken together, these data demonstrate that the overproduction of Fpr or SodA contributes to oxidative tolerance during naphthalene degradation; however, elevated SOD activity may trigger the generation of excess hydrogen peroxide, resulting in cell death.

Loading

Article metrics loading...

/content/journal/micro/10.1099/mic.0.2007/008896-0
2007-10-01
2024-04-20
Loading full text...

Full text loading...

/deliver/fulltext/micro/153/10/3246.html?itemId=/content/journal/micro/10.1099/mic.0.2007/008896-0&mimeType=html&fmt=ahah

References

  1. Ahn I. S., Ghiorse W. C., Lion L. W., Shuler M. L. 1998; Growth kinetics of Pseudomonas putida G7 on naphthalene and occurrence of naphthalene toxicity during nutrient deprivation. Biotechnol Bioeng 59:587–594
    [Google Scholar]
  2. Amstad P., Peskin A., Shah G., Mirault M.-E., Moret R., Zbinden I., Cerutti P. 1991; The balance between Cu,Zn-superoxide dismutase and catalase affects the sensitivity of mouse epidermal cells to oxidative stress. Biochemistry 30:9305–9313
    [Google Scholar]
  3. Battaglia V., Salvi M., Toninello A. 2005; Oxidative stress is responsible for mitochondrial permeability transition induction by salicylate in liver mitochondria. J Biol Chem 280:33864–33872
    [Google Scholar]
  4. Beauchamp C., Fridovich I. 1971; Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Anal Biochem 44:276–287
    [Google Scholar]
  5. Beers R. F. Jr, Sizer I. W. 1952; A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. J Biol Chem 195:133–140
    [Google Scholar]
  6. Bhattacharya J., GhoshDastidar K., Chatterjee A., Majee M., Majumder A. L. 2004; Synechocystis Fe superoxide dismutase gene confers oxidative tolerance to Escherichia coli . Biochem Biophys Res Commun 316:540–544
    [Google Scholar]
  7. Bianchi V., Haggard-Liungguist E., Pontis E., Reichard P. 1995; Interruption of the ferredoxin (flavodoxin) NADP+ oxidoreductase gene of Escherichia coli does not affect anaerobic growth but increases sensitivity to paraquat. J Bacteriol 177:4528–4531
    [Google Scholar]
  8. Costa V., Reis E., Quintanilha A., Moradas-Ferreira P. 1993; Acquisition of ethanol tolerance in Saccharomyces cerevisiae : the key role of the mitochondrial superoxide dismutase. Arch Biochem Biophys 300:608–614
    [Google Scholar]
  9. Djaman O., Outten F., Imlay J. A. 2004; Repair of oxidized iron–sulfur clusters in Escherichia coli . J Biol Chem 279:44590–44599
    [Google Scholar]
  10. Figurski D. H., Helinski D. R. 1979; Replication of an origin-containing derivative of plasmid RK2 dependent on a plasmid function provided in trans . Proc Natl Acad Sci U S A 76:1648–1652
    [Google Scholar]
  11. Flint D. H., Tuminello J. F., Emptage M. H. 1993; The inactivation of Fe–S cluster containing hydrolyases by superoxide. J Biol Chem 268:22369–22376
    [Google Scholar]
  12. Garcia E. M., Siegert I. G., Suarez P. 1998; Toxicity assay and naphthalene utilization by natural bacteria selected in marine environments. Bull Environ Contam Toxicol 61:370–377
    [Google Scholar]
  13. Giro M., Carrillo N., Krapp A. R. 2006; Glucose-6-phosphate dehydrogenase and ferredoxin-NADP(H) reductase contribute to damage repair during the soxRS response of Escherichia coli . Microbiology 152:1119–1128
    [Google Scholar]
  14. Goulielmos G. N., Arhontaki K., Eliopoulos E., Tserpistali K., Tsakas S., Loukas M. 2003; Drosophila Cu,Zn superoxide dismutase gene confers resistance to paraquat in Escherichia coli . Biochem Biophys Res Commun 308:433–438
    [Google Scholar]
  15. Greene J. F., Zheng J., Grant D. F., Hammock B. D. 2000; Cytotoxicity of 1,2-epoxynaphthalene is correlated with protein binding and in situ glutathione depletion in cytochrome P4501A1 expressing Sf-21 cells. Toxicol Sci 53:352–360
    [Google Scholar]
  16. Halliwell B., Gutteridge J. M. C. 1984; Oxygen toxicity, oxygen radicals, transition metals and disease. Biochem J 219:1–14
    [Google Scholar]
  17. Halliwell B., Gutteridge J. M. C. 1999 Free Radicals in Biology and Medicine , 3rd edn. New York: Oxford University Press;
  18. Hausladen A., Fridovich I. 1994; Superoxide and peroxynitrite inactivate aconitases, but nitric oxide does not. J Biol Chem 269:29405–29408
    [Google Scholar]
  19. Imlay J. A. 2003; Pathways of oxidative damage. Annu Rev Microbiol 57:395–418
    [Google Scholar]
  20. Kang Y.-S., Kim Y. J., Jeon C. O., Park W. 2006; Characterization of naphthalene-degrading Pseudomonas species isolated from pollutant-contaminated sites: oxidative stress during their growth on naphthalene. J Microbiol Biotechnol 16:1819–1825
    [Google Scholar]
  21. Karlsson A., Parales J. V., Parales R. E., Gibson D. T., Eklund H., Ramaswamy S. 2003; Crystal structure of naphthalene dioxygenase: side-on binding of dioxygen to iron. Science 299:1039–1042
    [Google Scholar]
  22. Kim Y. C., Miller C. D., Anderson A. J. 2000; Superoxide dismutase activity in Pseudomonas putida affects utilization of sugars and growth on root surfaces. Appl Environ Microbiol 66:1460–1467
    [Google Scholar]
  23. Kim Y. H., Cho K., Yun S. H., Kim J. Y., Kwon K. H., Yoo J. S., Kim S. I. 2006a; Analysis of aromatic catabolic pathways in Pseudomonas putida KT2440 using a combined proteomic approach: 2-DE/MS and cleavable isotope-coded affinity tag analysis. Proteomics 6:1301–1318
    [Google Scholar]
  24. Kim Y. H., Lee Y., Kim S., Yeom J., Yeom S., Kim B. S., Oh S., Park S., Jeon C. O., Park W. 2006b; The role of periplasmic antioxidant enzymes (superoxide dismutase and thiol peroxidase) of the Shiga toxin-producing Escherichia coli O157: H7 in the formation of biofilms. Proteomics 6:6181–6193
    [Google Scholar]
  25. Kovach M. E., Elzer P. H., Hill D. S., Robertson G. T., Farris M. A., Roop R. M. I. I., Peterson K. M. 1995; Four new derivatives of the broad-host-range cloning vector pBBR1MCS, carrying different antibiotic-resistance cassettes. Gene 166:175–176
    [Google Scholar]
  26. Lee K. 1999; Benzene-induced uncoupling of naphthalene dioxygenase activity and enzyme inactivation by production of hydrogen peroxide. J Bacteriol 181:2719–2725
    [Google Scholar]
  27. Lee Y., Ahn E. Y., Park S. S., Madsen E. L., Jeon C. O., Park W. 2006a; Construction of a reporter strain Pseudomonas putida for the detection of oxidative stress caused by environmental pollutants. J Microbiol Biotechnol 16:386–390
    [Google Scholar]
  28. Lee Y., Pena-Llopis S., Kang Y.-S., Shin H. D., Demple B., Madsen E. L., Jeon C. O., Park W. 2006b; Expression analysis of the fpr (ferredoxin-NADP+ reductase) gene in Pseudomonas putida KT2440. Biochem Biophys Res Commun 339:1246–1254
    [Google Scholar]
  29. Li Z., Demple B. 1996; Sequence specificity for DNA binding by Escherichia coli SoxS and Rob proteins. Mol Microbiol 20:937–945
    [Google Scholar]
  30. Murphy J. F., Stone R. W. 1955; The bacterial dissimilation of naphthalene. Can J Microbiol 1:579–588
    [Google Scholar]
  31. Park W., Jeon C. O., Cadillo H., DeRito C., Madsen E. L. 2004; Survival of naphthalene-degrading Pseudomonas putida NCIB 9816-4 in naphthalene-amended soils: toxicity of naphthalene and its metabolites. Appl Microbiol Biotechnol 64:429–435
    [Google Scholar]
  32. Price C. T. D., Lee I. R., Gustafson J. E. 2000; The effects of salicylate on bacteria. Int J Biochem Cell Biol 32:1029–1043
    [Google Scholar]
  33. Pumphrey G. M., Madsen E. L. 2007; Naphthalene metabolism and growth inhibition by naphthalene in Polaromonas naphthalenivorans strain CJ2. Microbiology 153: (in press
    [Google Scholar]
  34. Rodriguez A. M., Carrico P. M., Mazurkiewicz J. E., Melendez J. A. 2000; Mitochondrial or cytosolic catalase reverses the Mn-dependent inhibition of proliferation by enhancing respiratory chain activity, net ATP production, and decreasing the steady state levels of H2O2 . Free Radic Biol Med 29:801–813
    [Google Scholar]
  35. Saxena K., Henry T. R., Solem L. E., Wallace K. B. 1995; Enhanced induction of the mitochondrial permeability transition following acute menadione administration. Arch Biochem Biophys 317:79–84
    [Google Scholar]
  36. Scott M. D., Meshnick S. R., Eaton J. W. 1987; Superoxide dismutase rich bacteria. Paradoxical increase in oxidant toxicity. J Biol Chem 262:3640–3645
    [Google Scholar]
  37. Seaver L. C., Imlay J. A. 2001; Alkyl hydroperoxide reductase is the primary scavenger of endogenous hydrogen peroxide in Escherichia coli . J Bacteriol 183:7173–7181
    [Google Scholar]
  38. Stanier R. Y., Palleroni N. J., Dudorhoff M. 1966; The aerobic pseudomonads: a taxonomic study. J Gen Microbiol 43:159–271
    [Google Scholar]
  39. Stohs S. J., Ohia S., Bagchi D. 2002; Naphthalene toxicity and antioxidant nutrients. Toxicology 180:97–105
    [Google Scholar]
  40. Wang G., Hong Y., Johnson M. K., Maier R. J. 2006; Lipid peroxidation as a source of oxidative damage in Helicobacter pylori : protective roles of peroxiredoxins. Biochim Biophys Acta 17601596–1603
    [Google Scholar]
  41. Yin S., Fuangthong M., Laratta W. P., Shapleigh J. P. 2003; Use of a green fluorescent protein-based reporter fusion for detection of nitric oxide produced by denitrifiers. Appl Environ Microbiol 69:3938–3944
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/micro/10.1099/mic.0.2007/008896-0
Loading
/content/journal/micro/10.1099/mic.0.2007/008896-0
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error