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Benefits associated with the stalk of Gallionella ferruginea, evaluated by comparison of a stalk-forming and a non-stalk-forming strain and biofilm studies in situ

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Abstract

Factors that regulate and induce stalk formation by the iron-oxidizing and stalk-forming bacterium Gallionella ferruginea were studied in laboratory cultures and in situ. A stalk-forming strain, Sta+, and a non-stalk-forming strain, Sta-, were used for comparative studies of the benefits associated with the stalk. Two different growth media were used: a ferrous sulfide medium (FS-medium), with slow oxidation of iron giving high concentrations of toxic oxygen radicals and a ferrous carbonate medium (FC-medium), with fast iron oxidation giving low concentration of the toxic oxygen radicals. It was found that Sta+ cells grown in the FS-medium survived 3 weeks longer than Sta- cells grown in the FS-medium. When each strain was grown in the FC-medium, the Sta- cells had an advantage and survived 8 weeks longer than the Sta+ cells. No difference in survival was found for Sta+ cells grown in FS-medium compared to growth in FC-medium. In laboratory cultures, the average stalk length per cell values were 7–2.5 times higher (92 h and 150–300 h growth, respectively) in a medium with 620 μm iron than in a medium with 290 μm iron. Gallionella ferruginea Sta+ outcompeted Sta- cells when inoculated as mixed populations in FC-medium. It has previously been suggested that stalk formation in vitro is induced by oxygen. To confirm this observation, biofilm development in natural waters was studied in two wells, one with trace amounts of oxygen (LH) and one without (TH). A dense biofilm developed on surfaces exposed to flowing well LH water, but no biofilm developed in well TH. Stalks were formed in water samples from both wells when allowed to make contact with air. This work demonstrates for the first time that the stalk has a protecting function against the toxic oxygen radicals formed during the chemical iron oxidation. It also shows that it is the oxidation rate of the ferrous iron and not its concentration that is harmful to the cells. The stalk gives G. ferruginea a unique possibility to colonize and survive in habitats with high contents of iron, inaccessible for bacteria without a defense system against the oxidation of iron.

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References

  1. Artymiuk PJ, Bauminger ER, Harrison PM, Lawson DM, Nowik PJ, Treffry A, Yewdall SJ (1991) Ferritin: a model system for iron biomineralization. In: Frankel RB, Blakemore RP (eds) Iron biominerals. Plenum Press, New York, pp 269–294

    Google Scholar 

  2. Balashova VV (1967) A cumulative culture of Gallionella filamenta N. Sp. Microbiologiya 36: 541–544

    Google Scholar 

  3. Balashova VV (1968) Taxonomy of the genus Gallionella. Microbiologiya 37: 715–723

    Google Scholar 

  4. Carritt DE, Carpenter JH (1972) Dissolved oxygen concentration and saturation. In: Carlberg SR (ed) New Baltic manual with methods for sampling and analyses of physical, chemical and biological parameters. International Council for the exploration of the sea, Denmark, pp 24–29

    Google Scholar 

  5. Cholodny N (1924) Zur Morphologie der Eisenbakterien Gallionella und Spirophyllum. Ber Deut Bot Ges 42:35–44

    Google Scholar 

  6. Dougan WK, Wilson AL (1973) Absorptiometric determination of iron with T.P.T.Z. Water Treat Exam 22:100–113

    Google Scholar 

  7. Ehrenberg CG (1836) Vorläufige Mittheilung uber das wirkliche Vorkommen fossiler Infusorien und ihre grosse Verbreitung. Ann Phys 38:213–227

    Google Scholar 

  8. Ehrlich HL (1990) Geomicrobiology. Marcel Dekker, New York

    Google Scholar 

  9. Hallbeck L, Pedersen K (1990) Culture parameters regulating stalk formation and growth rate of Gallionella ferruginea. J Gen Microb 36:1675–1680

    Google Scholar 

  10. Hallbeck L, Pedersen K (1991) Autotrophic and mixotrophic growth of Gallionella ferruginea. J Gen Microbiol 137:2657–2661

    Google Scholar 

  11. Hallbeck L, Ståhl F, Pedersen K (1993) Phylogeny and phenotypic characterization of the stalk-forming and iron-oxidizing bacterium Gallionella ferruginea. J Gen Microbiol 136:1675–1680

    Google Scholar 

  12. Halliwell B, Gutteridge JMC (1984) Oxygen toxicity, oxygen radicals, transition metals and disease. Biochem J 219:1–14

    Google Scholar 

  13. Hanert HH (1981) The genus Gallionella. In: Starr MP, Truper HG, Balows A, Schlegel HG (eds) The procaryotes. A handbook in habitats, isolation and identification of bacteria. Springer, Berlin, pp 509–515

    Google Scholar 

  14. Hanert HH (1989) Budding and/or appendeged bacteria. In: Staley MP, Bryant MP, Pfennig N, Holt JG (eds) Bergey's manual of systematic bacteriology. Williams & Wilkins, Baltimore, pp 1974–1979

    Google Scholar 

  15. Hanert H (1968) Untersuchungen zur Isolierung, Stoffwechselphysiologie und Morphologie von Gallionella ferruginea Ehrenberg. Arch Mikrob 60:348–376

    Google Scholar 

  16. Hobbie JE, Daley RJ, Jasper S (1977) Use of nuclepore filter for counting bacteria by fluorescense microscopy. Appl Environ Microb 33:1225–1228

    CAS  PubMed  Google Scholar 

  17. Kucera S, Wolfe RS (1957) A selective enrichment method for Gallionella ferruginea. J Bacteriol 74:344–349

    Google Scholar 

  18. Lutters S, Hanert H (1989) The ultrastructure of chemolitotrophic Gallionella ferruginea and Thiobacillus ferrooxidans as revealed by chemical fixation and freeze-etching. Arch Microbiol 151:245–251

    Google Scholar 

  19. Niedhardt FC, Ingraham JL, Schaechter M (1990) Physiology of the bacterial cell. Sinauer Associates, Massachusetts

    Google Scholar 

  20. Niemelä S (1983) Statistical evaluation of results from quantitative microbiological examinations. Nordic Committee on Food Analysis Report No. 1, 2nd ed. Uppsala, Sweden.

  21. Pedersen K, Holmström C, Olsson A-K, Pedersen A (1986) Statistic evaluation of the influence of species variation, culture conditions and fluid shear on attached and biofilm development of marine bacteria. Arch Microbiol 145:1–8

    Google Scholar 

  22. Stookey LL (1970) Ferrozine—a new spectrophotometric reagent for iron. Anal Chem 42:779–781

    CAS  Google Scholar 

  23. Stumm W Lee GF (1960) The chemistry of aqueous iron. J Hydrol 22:295–319

    Google Scholar 

  24. Van Iterson W (1958) Gallionella ferruginea Ehrenberg in a different light. Academisch Proefschrift, University of Amsterdam. N.V. Nodd-Hollandsche Uitgevers Maatschappij, Amsterdam, pp 1–121

    Google Scholar 

  25. Vatter AE, Wolfe RS (1955) Observations on the growth and morphology of Gallionella ferruginea. Bacteriol Proc 35: 35

    Google Scholar 

  26. Woese CR (1987) Bacterial evolution. Microbiol Rev 51:221–271

    CAS  PubMed  Google Scholar 

Download references

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Correspondence to: L. Hallbeck

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Hallbeck, L., Pedersen, K. Benefits associated with the stalk of Gallionella ferruginea, evaluated by comparison of a stalk-forming and a non-stalk-forming strain and biofilm studies in situ. Microb Ecol 30, 257–268 (1995). https://doi.org/10.1007/BF00171933

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  • DOI: https://doi.org/10.1007/BF00171933

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