Skip to main content
Log in

Influence of oxygen on sulfate reduction and growth of sulfate-reducing bacteria

  • Original Papers
  • Published:
Archives of Microbiology Aims and scope Submit manuscript

Abstract

The ambivalent relations of sulfate-reducing bacteria to molecular O2 have been studied with ten freshwater and marine strains. Generally, O2 was reduced prior to sulfur compounds and suppressed the reduction of sulfate, sulfite or thiosulfate to sulfide. Three strains slowly formed sulfide at O2 concentrations of below 15 μM (6% air saturation). In homogeneously aerated cultures, two out of seven strains tested, Desulfovibrio desulfuricans and Desulfobacterium autotrophicum, revealed weak growth with O2 as electron acceptor (up to one doubling of protein). However, O2 was concomitantly toxic. Depending on its concentration cell viability and motility decreased with time. In artificial oxygen-sulfide gradients with sulfide-containing agar medium and also in sulfide-free agar medium under an oxygen-containing gas phase, sulfate reducers grew in bands close to the oxic/anoxic interface. The specific O2 tolerance and respiration capacity of different strains led to characteristically stratified gradients. The maximum O2 concentration at the surface of a bacterial band (determined by means of microelectrodes) was 9 μM. The specific rates of O2 uptake per cell were in the same order of magnitude as the sulfate reduction rates in pure cultures. The bacteria stabilized the gradients, which were rapidly oxidized in the absence of cells or after killing the cells by formaldehyde. The motile strain Desulfovibrio desulfuricans CSN slowly migrated in the gradients in response to changing O2 concentrations in the gas phase.

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

  • Abdollahi H, Wimpenny JWT (1990) Effects of oxygen on the growth of Desulfovibrio desulfuricans. J Gen Microbiol 136: 1025–1030

    Google Scholar 

  • Battersby NS, Malcolm SJ, Brown CM, Stanley SO (1985) Sulphate reduction in oxic and suboxic North East Atlantic sediments. FEMS Microbiol Ecol 31: 225–228

    Google Scholar 

  • Bell LC, Ferguson SJ (1991) Nitric and nitrous reductases are active under aerobic conditions in cells of Thiosphaera pantotropha. Biochem J 273: 423–427

    Google Scholar 

  • Canfield DE, DesMarais DJ (1991) Aerobic sulfate reduction. Science 251: 1471–1473

    Google Scholar 

  • Cavalli-Sforza L (1972) Grundzüge biologisch medizinischer Statistik. Gustav Fischer, Stuttgart

    Google Scholar 

  • Cohen Y (1989) Photosynthesis in cyanobacterial mats and its relation to the sulfur cycle: a model for microbial sulfur interactions. In: Cohen Y, Rosenberg E (eds) Microbial mats. Physiological ecology of benthic microbial communities. American Society for Microbiology, Washington, pp 22–36

    Google Scholar 

  • Cypionka H (1986) Sulfide-controlled continuous culture of sulfate-reducing bacteria. J Microbiol Methods 5: 1–9

    Google Scholar 

  • Cypionka H (1989) Characterization of sulfate transport in Desulfovibrio desulfuricans. Arch Microbiol 152: 237–243

    Google Scholar 

  • Cypionka H, Pfennig N (1986) Growth yields of Desulfotomaculum orientis with hydrogen in chemostat culture. Arch Microbiol 143: 396–399

    Google Scholar 

  • Cypionka H, Widdel F, Pfennig N (1985) Survival of sulfate-reducing bacteria after oxygen stress, and growth in sulfate-free oxygen-sulfide gradients. FEMS Microbiol Ecol 31: 39–45

    Google Scholar 

  • Dannenberg S, Kroder M, Dilling W, Cypionka H (1992) Oxidation of H2, organic compounds and inorganic sulfur compounds coupled to reduction of O2 or nitrate by sulfate-reducing bacteria. Arch Microbiol 158: 93–99

    Google Scholar 

  • Dilling W, Cypionka H (1990) Aerobic respiration in sulfate-reducing bacteria. FEMS Microbiol Lett 71: 123–128

    Google Scholar 

  • Ferell RT, Himmelblau DM (1967) Diffusion coefficients of nitrogen and oxygen in water. J Chem Eng Data 12: 111–115

    Google Scholar 

  • Fründ C, Cohen Y (1992) Diurnal cycles of sulfate reduction under oxic conditions in cyanobacterial mats. Appl Environ Microbiol 58: 70–77

    Google Scholar 

  • Fukui M, Takii S (1990) Survival of sulfate-reducing bacteria in oxic surface sediment of a seawater lake. FEMS Microbiol Ecol 73: 317–322

    Google Scholar 

  • Hardy JA, Hamilton WA (1981) The oxygen tolerance of sulfate-reducing bacteria isolated from North Sea waters. Curr Microbiol 6: 259–262

    Google Scholar 

  • Hatchikian CE, LeGall J, Bell GR (1977) Significance of superoxide dismutase and catalase activities in the strict anaerobes, sulphate-reducing bacteria. In: Michelson AM, McCord JM, Fridovich I (eds) Superoxide and superoxide dismutases. Academic Press, New York, London, pp 159–172

    Google Scholar 

  • Hewitt J, Morris JG (1975) Superoxide dismutase in some obligately anaerobic bacteria. FEBS Lett 50: 315–318

    Google Scholar 

  • Jørgensen BB (1977) Bacterial sulfate reduction within reduced microniches of oxidized marine sediments. Mar Biol 41: 7–17

    Google Scholar 

  • Jørgensen BB (1978) A comparison of methods for the quantitation of bacterial sulfate reduction in coastal marine sediments. III. Estimation from chemical and bacteriological field data. Geomicrobiol J 1: 49–64

    Google Scholar 

  • Jørgensen BB, Bak F (1991) Pathways and microbiology of thiosulfate transformations and sulfate reduction in a marine sediment (Kattegatt, Denmark). Appl Environ Microbiol 57: 847–856

    Google Scholar 

  • Laanbroek HJ, Pfennig N (1981) Oxidation of short-chain fatty acids by sulfate-reducing bactgeria in freshwater and marine sediments. Arch Microbiol 128: 330–335

    Google Scholar 

  • Morris JG (1976) Oxygen and the obligate anaerobes. J Appl Bacteriol 40: 229–244

    Google Scholar 

  • Nelson DC, Jannasch HW (1983) Chemoautotrophic growth of a marine Beggiatoa in sulfide-gradient cultures. Arch Microbiol 136: 262–269

    Google Scholar 

  • Pfennig N, Widdel F, Trüper HG (1981) The dissimilatory sulfate-reducing bacteria. In: Starr MP, Stolp H, Trüper HG, Balows A, Schlegel HG (eds) The prokaryotes. Springer, Berlin Heidelberg New York, pp 926–940

    Google Scholar 

  • Robertson LA, Kuenen JG (1983) Thiosphaera pantotropha gen. nov. sp. nov., a facultatively anaerobic, facultatively autotrophic sulphur bacterium. J Gen Microbiol 129: 2847–2855

    Google Scholar 

  • Schmidt K, Liaaen-Jensen S, Schlegel HG (1963) Die Carotinoide der Thiorhodaceae. I. Okenon als Hauptcarotinoid von Chromatium okenii Perty. Arch Mikrobiol 46: 117–126

    Google Scholar 

  • Seitz HJ, Cypionka H (1986) Chemolithotrophic growth of Desulfovibrio desulfuricans with hydrogen coupled to ammonification of nitrate or nitrite. Arch Microbiol 146: 63–67

    Google Scholar 

  • Widdel F, Pfennig N (1982) Studies on dissimilatory sulfate-reducing bacteria that decompose fatty acids. II. Incomplete oxidation of propionate by Desulfobulbus propionicus gen. nov., sp. nov. Arch Microbiol 131: 360–365

    Google Scholar 

  • Wimpenny JWT, Jones DE (1988) One-dimensional gel-stabilized systems. In: Wimpenny JWT (ed) CRC handbook of laberatory model systems for microbial ecosystems. CRC Press, Boca Raton, Fla., pp 1–30

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Marschall, C., Frenzel, P. & Cypionka, H. Influence of oxygen on sulfate reduction and growth of sulfate-reducing bacteria. Arch. Microbiol. 159, 168–173 (1993). https://doi.org/10.1007/BF00250278

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00250278

Key words

Navigation