Skip to main content
Log in

Chlorate and nitrate reduction in the phototrophic bacteriaRhodobacter capsulatus andRhodobacter sphaeroides

  • Published:
Current Microbiology Aims and scope Submit manuscript

Abstract

Chlorate or trimethylamine-N-oxide (TMAO) added to phototrophic cultures ofRhodobacter sphaeroides DSM 158 increased both the growth rate and the growth yield although this stimulation was not observed in the presence of tungstate. This strain, exhibited basal activities of nitrate, chlorate, and TMAO reductases independently of the presence of these substrates in the culture medium, and nitrate reductase (NR) activity was competitively inhibited by chlorate. Phototrophic growth ofRhodobacter capsulatus B10, a strain devoid of NR activity, was inhibited only by 100 mM chlorate. However, growth of the nitrate-assimilatingR. capsulatus strains E1F1 and AD2 was sensitive to 10mm chlorate, and their NR activities were not inhibited by chlorate. Both NR and chlorate reductase (CR) activities of strain E1F1 were induced in the presence of nitrate or chlorate respectively, whereas strain AD2 showed basal levels of these activities in the absence of the substrates. A basal TMAO reductase (TR) activity was also observed when these strains ofR. capsulatus were cultured in the absence of this electron acceptor. These results suggest that chlorate and TMAO can be used as ancillary oxidants byRhodobacter strains and that a single enzyme could be responsible for nitrate and chlorate reduction inR. sphaeroides DSM 158, whereas these reactions are catalyzed by two different enzymes inR. capsulatus E1F1 and AD2.

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

Literature Cited

  1. Alef K (1987) The interaction between dimethylsulfoxide and nitrate reducing pathways inRhodobacter capsulatus. FEMS Microbiol Lett 48:11–14

    Google Scholar 

  2. Bisen PS, Shanthy S (1992) Physiological and biochemical characterization of chlorate-resistant mutants ofAnabaena doliolum. Curr Microbiol 25:353–357

    Google Scholar 

  3. Byrne MD, Nicholas DJD (1987) A membrane-bound dissimilatory nitrate reductase fromRhodobacter sphaeroides f.sp.denitrificans. Biochim biophys Acta 915:120–124

    Google Scholar 

  4. Castillo F, Caballero FJ, Cárdenas J (1981) Nitrate photoassimilation by the phototrophic bacteriumRhodopseudomonas capsulata E1F1. Z Naturforsch 36:1025–1029

    Google Scholar 

  5. Cawse PA (1967) The determination of nitrate in soil solution by ultraviolet spectrophotometry. Analyst 92:311–315

    Google Scholar 

  6. Deane-Drummond CE (1984) Nitrate transport intoCharacorallina cells using36ClO3 as an analogue for nitrate. I. Interaction between36ClO3 and NO3 , and characterization of36ClO3 /NO3 -influx. J Exp Bot 35:1289–1298

    Google Scholar 

  7. De Groot GN, Stouthamer AH (1969) Regulation of reductase formation inProteus mirabilis. I. Formation of reductases and enzymes of the formic hydrogenlyase complex in the wild type and in chlorate resistant mutants. Arch Microbiol 66:220–233

    Google Scholar 

  8. Doddema H, Telkamp GP (1979) Uptake of nitrate by mutants ofArabidopsis thaliana disturbed in uptake or reduction of nitrate. Physiol Plant 45:332–338

    Google Scholar 

  9. Ferguson SJ, Jackson JB, McEwan AG (1987) Anaerobic respiration in theRhodospirillaceae characterisation of pathways and evaluation of roles in redox balancing during photosynthesis. FEMS Microbiol Rev 46:117–143

    Google Scholar 

  10. Kelly DJ, Richardson DJ, Ferguson SJ, Jackson JB (1988) Isolation of transposon Tn5 insertion, mutants ofRhodobacter capsulatus unable to reduce trimethylamine-N-oxide and dimethylsulphoxide. Arch Microbiol 150:138–144

    Google Scholar 

  11. Kerber NL, Cárdenas J (1982) Nitrate reductase fromRhodopseudomonas sphaeroides. J Bacteriol 150:1091–1097

    PubMed  Google Scholar 

  12. Lowry OH, Rosebrough MJ, Farr AL, Randall RJ (1951) Protein measurement with the Folin-phenol reagent. J Biol Chem 193:265–275

    PubMed  Google Scholar 

  13. Malmqvist A, Welander T, Gunnarsson L (1991) Anaerobic growth of microorganisms with chlorate as an electron acceptor. Appl Environ Microbiol 57:2229–2232

    Google Scholar 

  14. Martínez-Luque M, Dobao MM, Castillo F (1991) Characterization of the assimilatory and dissimilatory nitrate-reducing systems inRhodobacter: a comparative study. FEMS Microbiol Lett 83:329–334

    Google Scholar 

  15. McEwan AG, Cotton NPJ, Ferguson SJ, Jackson JB (1985) The role of auxiliary oxidants in the maintenance of a balanced redox poise for photosynthesis in bacteria. Biochim Biophys Acta 810:140–147

    Google Scholar 

  16. McEwan AG, Wetzstein HG, Meyer O, Jackson JB, Ferguson SJ (1987) The periplasmic nitrate reductase ofRhodobacter capsulatus: purification, characterisation and distinction from a single reductase for trimethylamine-N-oxide, dimethylsulphoxide and chlorate. Arch Microbiol 147:340–345

    Google Scholar 

  17. Moreno-Vivián C, Cárdenas J, Castillo F (1986)In vivo short-term inhibition of nitrogenase by nitrate inRhodopseudomonas capsulata E1F1. FEMS Microbiol Lett 34:105–109

    Google Scholar 

  18. Nakagawa H, Yamashita N (1986) Chlorate reducing activity of spinach nitrate reductase. Agric Biol Chem 50:1893–1894

    Google Scholar 

  19. Pichinoty F (1966) Propriétés, régulation et fonctions physiologiques des nitrate-réductase bacteriennes A et B Bull Soc Fran Physiol Vég 12:97–104

    Google Scholar 

  20. Pino-Pérez F, Pérez-Bendito D (1983) Análisis des los elementos-traza por espectrofotometría de absorción molecular UV-visible. Córdoba: Universidad de Sevilla y Monte de Piedad y Caja de Ahorros de Córdoba, pp 421–423

    Google Scholar 

  21. Prieto R, Fernández E (1993) Toxicity of and mutagenesis by chlorate are independent of nitrate reductase activity inChlamydomonas reinhardtii. Mol Gen Genet 237:429–438

    PubMed  Google Scholar 

  22. Snell FD, Snell CT (1949) Colorimetric methods of analysis, 3rd ed, vol 2., Princeton, N.J.: D. van Nostrand Reinhold, pp 804–805

    Google Scholar 

  23. Solomonson LP, Vennesland B (1972) Nitrate reductase and chlorate toxicity inChlorella vulgaris Beijerinck. Plant Physiol 50:421–424

    Google Scholar 

  24. Weaver PF, Wall JD, Gest H (1975) Characterization ofRhodopseudomonas capsulata. Arch Microbiol 105:207–216

    PubMed  Google Scholar 

  25. Willison JC (1990) Derivative ofRhdobacter capsulatus strain AD2 cured of their endogenous plasmid are unable to utilize nitrate. FEMS Microbiol Lett 66:23–28

    Google Scholar 

  26. Witt A, Klemme JH (1991) No correlation between plasmid content and ability to reduce nitrate in wild-type strains ofRhodobacter capsulatus. Z Naturforsch 46:703–705

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Roldán, M.D., Reyes, F., Moreno-Vivián, C. et al. Chlorate and nitrate reduction in the phototrophic bacteriaRhodobacter capsulatus andRhodobacter sphaeroides . Current Microbiology 29, 241–245 (1994). https://doi.org/10.1007/BF01570161

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01570161

Keywords

Navigation