Skip to main content
Log in

A strictly anaerobic nitrate-reducing bacterium growing with resorcinol and other aromatic compounds

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

Abstract

With resorcinol as sole source of energy and organic carbon, two stains of gram-negative, nitrate-reducing bacteria were isolated under strictly anaerobic conditions. Strain LuBRes1 was facultatively anaerobic and catalase- and superoxide dismutase-positive. This strain was affiliated with Alcaligenes denitrificans on the basis of substrate utilization spectrum and peritrichous flagellation. Strain LuFRes1 could grow only under anaerobic conditions with oxidized nitrogen compounds as electron acceptor. Cells were catalase-negative but superoxide dismutase-positive. Since this strain was apparently an obligate nitrate reducer, it could not be grouped with any existing genus. Resorcinol was completely oxidized to CO2 by both strains. Neither an enzyme activity reducing or hydrolyzing the resorcinol molecule, nor an acyl-CoA-synthetase activating resorcylic acids or benzoate was detected in cell-free extracts of cells grown with resorcinol. In dense cell suspensions, both strains produced a compound which was identified as 5-oxo-2-hexenoic acid by mass spectrometric analysis. This would indicate a direct, hydrolytic cleavage of the resorcinol nucleus without initial reduction.

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

  • Bergmeyer HU (ed) (1983) Methods of enzymatic analysis, Volumes I–III. Verlag Chemie, Weinheim, FRG

    Google Scholar 

  • Blenden DC, Goldberg HS (1965) Silver impregnation stain for Leptospira and flagella. J Bacteriol 89: 899–900

    Google Scholar 

  • Brune A, Schink B (1990) Pyrogallol-to-phloroglucinol conversion and other hydroxyl-transfer reactions catalyzed by cell extracts of Pelobacter acidigallici. J Bacteriol 172: 1070–1076

    Google Scholar 

  • Evans WC, Fuchs G (1988) Anaerobic degradation of aromatic compounds Ann Rev Microbiol 42: 289–317

    Google Scholar 

  • Glöckler R, Tschech A, Fuchs G (1989) Reductive dehydroxylation of 4-hydroxybenzoyl-CoA to benzoyl-CoA in a denitrifying, phenol degrading Pseudomonas species. FEBS Microbiol Lett 251: 237–240

    Google Scholar 

  • Gregersen T (1978) Rapid method for distinction of Gram-negative from Gram-positive bacteria. Eur J Appl Microbiol Biotechnol 5: 123–127

    Google Scholar 

  • Kluge C, Tschech A, Fuchs G (1990) Anaerobic metabolism of resorcylic acids (m-dihydroxybenzoic acids) and resorcinol (1,3-benzenediol) in a fermenting and in a denitrifying bacterium. Arch Microbiol 155: 68–74

    Google Scholar 

  • Krieg NR, Holt JG (eds) (1984) Bergey's manual of systematic bacteriology, vol 1. Williams and Willkins, Baltimore

    Google Scholar 

  • Krumholz LR, Crawford RL, Hemling ME, Bryant MP (1987) Metabolism of gallate and phloroglucinol in Eubacterium oxidoreducens via 3-hydroxy-5-oxohexanoate. J Bacteriol 169: 1886–1890

    Google Scholar 

  • Law FW, Slepecky RA (1962) Assay of poly-β-hydroxybutyric acid. J Bacteriol 82: 33–36

    Google Scholar 

  • Lange B, Vejdelek ZJ (1980) Photometrische Analyse. Verlag Chemie, Weinheim, FRG

    Google Scholar 

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

    Google Scholar 

  • Magee CM, Rodeheaver G, Edgerton MT, Edlich RF (1975) A more reliable Gram staining technic for diagnosis of surgical infections. Am J Surg 130: 341–345

    Google Scholar 

  • Marmur J, Doty P (1962) Determination of the base composition of deoxyribonucleic acid from its thermal denaturation temperature. J Mol Biol 5: 109–118

    Google Scholar 

  • Patel TR, Jure KG, Jones GA (1981) Catabolism of phloroglucinol by the rumen anaerobe Coprococcus. Appl Environ Microbiol 42: 1010–1017

    Google Scholar 

  • Pfennig N (1978) Rhodocyclus purpureus gen. nov. sp. nov., a ring-shaped, vitamin B12-requiring member of the family Rhodospirillaceae. Int J Syst Bacteriol 28: 283–288

    Google Scholar 

  • Procházková L (1959) Bestimmung der Nitrate im Wasser. Z Anal Chem 167: 254–260

    Google Scholar 

  • Rudolphi A, Tschech A, Fuchs G (1991) Anaerobic degradation of cresols by denitrifying bacteria. Arch Microbiol 155: 238–248

    Google Scholar 

  • Schink B, Brune A, Schnell S (1992) Anaerobic degradation of aromatic compounds. In: GWinkelmann (ed) Microbial degradation of natural products. Verlag Chemie, Weinheim, FRG

    Google Scholar 

  • Samain E, Albagnac G, Dubourguier HC (1986) Initial steps of catabolism of trihydroxybenzenes in Pelobacter acidigallict. Arch Microbiol 144: 242–244

    Google Scholar 

  • Schnell S, Schink B (1991) Anaerobic aniline degradation via reductive deamination of 4-aminobenzoyl-CoA in Desulfobacterium anilini. Arch Microbiol 155: 183–190

    Google Scholar 

  • Staley JT, Marvin PB, Pfennig N, Holt JG (1989) Bergey's manual of systematic bacteriology, vol 3. Williams and Wilkins, Baltimore

    Google Scholar 

  • Tschech A (1989) Der anaerobe Abbau von aromatischen Verbindugen. Forum Mikrobiol 12: 251–217

    Google Scholar 

  • Tschech A, Pfennig N (1984) Growth yield increase linked to caffeate reduction in Acetobacterium woodii. Arch Microbiol 137: 163–167

    Google Scholar 

  • Tschech A, Fuchs G (1989) Anaerobic degradation of phenol via carboxylation to 4-hydroxybenzoate: in vitro study of isotope exchange between 14CO2 and 4-hydroxybenzoate. Arch Microbiol 152: 594–599

    Google Scholar 

  • Tschech A, Schink B (1985) Fermentative degradation of resorcinol and resorcylic acids. Arch Microbiol 143: 52–59

    Google Scholar 

  • Widdel F, Pfennig N (1981) Studies on dissimilatory sulfate-reducing bacteria that decompose fatty acids. I. Isolation of new sulfate-reducing bacteria enriched with acetate from saline environments. Description of Desulfobacter postgatei gen. nov. sp. nov. Arch Microbiol 129: 395–400

    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 Microbiol 134: 286–294

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Gorny, N., Wahl, G., Brune, A. et al. A strictly anaerobic nitrate-reducing bacterium growing with resorcinol and other aromatic compounds. Arch. Microbiol. 158, 48–53 (1992). https://doi.org/10.1007/BF00249065

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00249065

Key words

Navigation