Skip to main content
Log in

Characterization of a new platelet-forming purple sulfur bacterium, Amoebobacter pedioformis sp. nov.

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

Abstract

The dominant purple sulfur bacterium of a reddish-colored waste water pond near Taichung, Taiwan, was isolated in pure culture, strain CML2. Individual cells were nearly spherical, nonmotile, and contained in their peripheral parts was vacuoles that appeared like elongated, curved tubes. Four to sixteen cells formed platelet-like aggregates reminiscent of Thiopedia rosea. The intracellular photosynthetic membrane system of the cells was of vesicular type; the photosynthetic pigments consisted of bacteriochlorophyll a and spirilloxanthin as the major carotenoid. The color of cell suspensions was pink to rosered. Under anaerobic conditions photolithoautotrophic growth occurred with sulfide, elemental sulfur or thiosulfate; sulfur globules were stored as an intermediary oxidation product. In the presence of sulfide, acetate, lactate and pyruvate were photoassimilated; strain CML2 lacked assimilatory sulfate reduction. Fastest photoautotrophic growth (11 h doubling time) was obtained at pH 7.5, 35°C and a light intensity of about 1000 lux (tungsten lamp). Chemolithoautotrophic growth in the dark was possible under reduced oxygen partial pressure with reduced sulfur compounds as respiratory substrates. The DNA base composition of strain CML2 was 65.5 mol% G+C. Strain CML2 is described as type strain of a new species, Amoebobacter pedioformis sp. nov., in the family Chromatiaceae.

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

  • Bavendamm W (1924) Die farblosen und roten Schwefelbakterien des Süß-und Salzwassers. In: Kolkowitz R (ed) Pflanzenforschung, Heft 2. Fischer, Jena, pp 1–157

    Google Scholar 

  • Caumette P, Schmidt K, Biebl H, Pfennig N (1985) Characterization of a Thiocapsa strain containing okenone as major carotenoid. Syst Appl Microbiol 6:132–136

    Google Scholar 

  • Caumette P, Schmidt K, Biebl H Pfennig N (1985) Characterization of a Thiocapsa strain containing okenone as major carotenoid. Syst Appl Microbiol 6:132–136

    Google Scholar 

  • Clayton RK (1963) Towards the isolation of a photochemical reaction center in Rhodopseudomonas spheroides. Biochim Biophys Acta 75:312–317

    Google Scholar 

  • Cohen-Bazire G, Sistrom WR, Stanier RY (1957) Kinetic studies of pigment synthesis by nonsulfur purple bacteria. J Cell Comp Physiol 49:25–68

    Google Scholar 

  • Czeczuga B (1968) Primary production of the purple sulphuric bacteria, Thiopedia rosea Winogr. (Thiorhodaceae). Photosynthetica 2:161–166

    Google Scholar 

  • DeLey J (1970) Reexamination of the association between melting point, buoyant density and the chemical base composition of deoxyribonucleic acid. J Bacteriol 101:738–754

    Google Scholar 

  • Echlin P (1965) The fine structure of unicellular blue green algae from the genus Merismopedia. Reports of the Proceedings of the Society for General Microbiology J Gen Microbiol 39:429–435

    Google Scholar 

  • Fowler VJ, Pfennig N, Schubert W, Stackebrandt E (1984) Towards a phylogeny of phototrophic purple sulfur bacteria—16Sr RNA oligonucleotide cataloguing of 11 species of Chromatiaceae. Arch Microbiol 139:382–387

    Google Scholar 

  • Goa J (1953) A microbiuret method for protein determination: determination of total protein in cerebrospinal fluid. Scand J Clin Lab Invest 5:218–220

    Google Scholar 

  • Gorlenko VM, Krasilnikova EN, Kikina OG, Tatarinova NJ (1979) The new motile purple sulphur bacteria Lamprobacter modestolophilus nov. gen., nov. sp. with gas vacuoles. Izv Akad Nauk SSSR, Ser Biol 5:755–767

    Google Scholar 

  • Kämpf C, Pfennig N (1980) Capacity of Chromatiaceae for chemotrophic growth. Specific respiration rates of Thiocystis violacea and Chromatium vinosum. Arch Microbiol 127:125–135

    Google Scholar 

  • Mandel M, Leadbetter ER, Pfennig N, Trüper HG (1971) Deoxyribonucleic acid base compositions of phototrophic bacteria. Int J Syst Bacteriol 21:222–230

    Google Scholar 

  • Marmur J (1961) A procedure for the isolation of deoxyribonucleic acid from microorganisms. J Mol Biol 3:208–218

    Google Scholar 

  • Pfennig N (1973) Culture and ecology of Thiopedia rosea. Symposium on prokaryotic photosynthetic organisms, Freiburg 1973, pp 75/76 Abstract

  • Pfennig N, Trüper HG (1971) New nomenclatural combinations in the phototrophic sulfur bacteria. Int J Syst Bacteriol 21:11–14

    Google Scholar 

  • Pfennig N, Trüper HG (1974) The phototrophic bacteria. In: Buchanan RE, Gibbons NE (eds) Bergey's manual of determinative bacteriology, 8th edn. Williams & Wilkins, Baltimore, pp 24–60

    Google Scholar 

  • Pfennig N, Trüper HG (1981) Isolation of members of the families Chromatiaceae and Chlorobiaceae. In: Starr MP, Stolp H, Trüper HG, Balows A, Schlegel HG (eds) The prokaryotes, vol 1. Springer, Berlin Heidelberg New York, pp 279–289

    Google Scholar 

  • Pfennig N, Markham MC, Liaaen Jensen S (1968) Carotenoids of Thiorhodaceae. 8. Isolation and characterization of a Thiothece, Lamprocystis and Thiodictyon strain and their carotenoid pigments. Arch Microbiol 62:178–191

    Google Scholar 

  • Pringsheim EG (1932) Neues über Purpurbakterien. Naturwissenschaften 20:479–483

    Google Scholar 

  • Pringsheim EG (1955) Lampropedia hyalina Schroeter 1886 and Vannielia aggregata n.g., n.sp., with remarks on natural and on organized colonies in bacteria. J Gen Microbiol 13:285–291

    Google Scholar 

  • Schmidt K, Pfennig N, Liaaen-Jensen S (1965) Carotenoids of Thiorhodaceae. IV. The carotenoid composition of 25 pure isolates. Arch Mikrobiol 52:132–146

    Google Scholar 

  • Schroeter J (1886) Die Pilze Schlesiens. In: Cohn F (ed) Kryptogamen-Flora von Schlesien, Dritter Band, Erste Hälfte. JU Kern's Verlag, Breslau, pp 129–256

    Google Scholar 

  • Thiele HH (1968) Die Verwertung einfacher organischer Substrate durch Thiorhodaceae. Arch Mikrobiol 60:124–138

    Google Scholar 

  • Trüper HG, Pfennig N (1981) Characterization and identification of the anoxygenic phototrophic bacteria. In: Starr MP, Stolp H, Trüper HG, Balows A, Schlegel HG (eds) The Prokaryotes, Vol 1, Springer, Berlin Heidelberg New York, pp 299–312

    Google Scholar 

  • Utermöhl H (1924) Phaeobacterien. Biol Zentralbl 43:605–610

    Google Scholar 

  • Widdel F, Kohring GW, Mayer F (1983) Studies on dissimilatory sulfate-reducing bacteria that decompose fatty acids. III. Characterization of the filamentous gliding Desulfonema limicola gen. nov. sp. nov., and Desulfonema magnum sp. nov. Arch Mikrobiol 134:286–294

    Google Scholar 

  • Winogradsky S (1888) Zur Morphologie und Physiologie der Schwefelbakterien. In: Beiträge zur Morphologie und Physiologie der Bakterien, Heft 1. Felix, Leipzig

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Eichler, B., Pfennig, N. Characterization of a new platelet-forming purple sulfur bacterium, Amoebobacter pedioformis sp. nov.. Arch. Microbiol. 146, 295–300 (1986). https://doi.org/10.1007/BF00403233

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00403233

Key words

Navigation