This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bartosch, S.
Right arrow Articles by Bock, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bartosch, S.
Right arrow Articles by Bock, E.
Agricola
Right arrow Articles by Bartosch, S.
Right arrow Articles by Bock, E.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, September 1999, p. 4126-4133, Vol. 65, No. 9
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Identification of Nitrite-Oxidizing Bacteria with Monoclonal Antibodies Recognizing the Nitrite Oxidoreductase

Sabine Bartosch, Iris Wolgast, Eva Spieck,* and Eberhard Bock

Institut für Allgemeine Botanik, Universität Hamburg, D-22609 Hamburg, Germany

Received 29 January 1999/Accepted 20 May 1999

Immunoblot analyses performed with three monoclonal antibodies (MAbs) that recognized the nitrite oxidoreductase (NOR) of the genus Nitrobacter were used for taxonomic investigations of nitrite oxidizers. We found that these MAbs were able to detect the nitrite-oxidizing systems (NOS) of the genera Nitrospira, Nitrococcus, and Nitrospina. The MAb designated Hyb 153-2, which recognized the alpha  subunit of the NOR (alpha -NOR), was specific for species belonging to the genus Nitrobacter. In contrast, Hyb 153-3, which recognized the beta -NOR, reacted with nitrite oxidizers of the four genera. Hyb 153-1, which also recognized the beta -NOR, bound to members of the genera Nitrobacter and Nitrococcus. The molecular masses of the beta -NOR of the genus Nitrobacter and the beta  subunit of the NOS (beta -NOS) of the genus Nitrococcus were identical (65 kDa). In contrast, the molecular masses of the beta -NOS of the genera Nitrospina and Nitrospira were different (48 and 46 kDa). When the genus-specific reactions of the MAbs were correlated with 16S rRNA sequences, they reflected the phylogenetic relationships among the nitrite oxidizers. The specific reactions of the MAbs allowed us to classify novel isolates and nitrite oxidizers in enrichment cultures at the genus level. In ecological studies the immunoblot analyses demonstrated that Nitrobacter or Nitrospira cells could be enriched from activated sludge by using various substrate concentrations. Fluorescence in situ hybridization and electron microscopic analyses confirmed these results. Permeated cells of pure cultures of members of the four genera were suitable for immunofluorescence labeling; these cells exhibited fluorescence signals that were consistent with the location of the NOS.


* Corresponding author. Mailing address: Institut für Allgemeine Botanik, Ohnhorststr. 18, D-22609 Hamburg, Germany. Phone: 49 40 42816 426. Fax: 49 40 42816 400. E-mail: Spieck{at}mikrobiologie.uni-hamburg.de.


Applied and Environmental Microbiology, September 1999, p. 4126-4133, Vol. 65, No. 9
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Lebedeva, E. V., Alawi, M., Maixner, F., Jozsa, P.-G., Daims, H., Spieck, E. (2008). Physiological and phylogenetic characterization of a novel lithoautotrophic nitrite-oxidizing bacterium, 'Candidatus Nitrospira bockiana'. Int. J. Syst. Evol. Microbiol. 58: 242-250 [Abstract] [Full Text]  
  • Pinck, C., Coeur, C., Potier, P., Bock, E. (2001). Polyclonal Antibodies Recognizing the AmoB Protein of Ammonia Oxidizers of the {beta}-Subclass of the Class Proteobacteria. Appl. Environ. Microbiol. 67: 118-124 [Abstract] [Full Text]