This Article
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 Tompkins, G. R.
Right arrow Articles by Birchmeier, K. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tompkins, G. R.
Right arrow Articles by Birchmeier, K. R.

 Previous Article  |  Next Article 

J. Bacteriol., Feb 1997, 620-626, Vol 179, No. 3
Copyright © 1997, American Society for Microbiology

Detection and comparison of specific hemin binding by Porphyromonas gingivalis and Prevotella intermedia

GR Tompkins, DP Wood and KR Birchmeier
Department of Oral Biology, School of Dentistry, Medical College of Georgia, Augusta 30912-1126, USA. gtompkin@mail.mcg.edu

A radioligand assay was designed to detect and compare specific hemin binding by the periodontal anaerobic black-pigmenting bacteria (BPB) Porphyromonas gingivalis and Prevotella intermedia. The assay included physiological concentrations of the hemin-binding protein rabbit serum albumin (RSA) to prevent self-aggregation and nonspecific interaction of hemin with cellular components. Under these conditions, heme-starved P. intermedia cells (two strains) expressed a single binding site species (4,100 to 4,600 sites/cell) with a dissociation constant (Kd) of 1.0 x 10(-9) M. Heme-starved P. gingivalis cells (two strains) expressed two binding site species; the higher-affinity site (1,000 to 1,500 sites/cell) displayed a Kd of between 3.6 x 10(-11) and 9.6 x 10(- 11) M, whereas the estimated Kd of the lower-affinity site (1.9 x 10(5) to 6.3 x 10(5) sites/cell) ranged between 2.6 x 10(-7) and 6.5 x 10(-8) M. Specific binding was greatly diminished in heme-replete cells of either BPB species and was not displayed by iron-replete Escherichia coli cells, which bound as much hemin in the absence of RSA as did P. intermedia. Hemin binding by BPB was reduced following treatment with protein-modifying agents (heat, pronase, and N-bromosuccinimide) and was blocked by protoporphyrin IX and hemoglobin but not by Congo red. Hemopexin also inhibited bacterial hemin binding. These findings indicate that both P. gingivalis and P. intermedia express heme- repressible proteinaceous hemin-binding sites with affinities intermediate between those of serum albumin and hemopexin. P. gingivalis exhibited a 10-fold-greater specific binding affinity and greater heme storage capacity than did P. intermedia, suggesting that the former would be ecologically advantaged with respect to heme acquisition.


This article has been cited by other articles:

  • Paramaesvaran, M., Nguyen, K.-A., Caldon, E., McDonald, J. A., Najdi, S., Gonzaga, G., Langley, D. B., DeCarlo, A., Crossley, M. J., Hunter, N., Collyer, C. A. (2003). Porphyrin-Mediated Cell Surface Heme Capture from Hemoglobin by Porphyromonas gingivalis. J. Bacteriol. 185: 2528-2537 [Abstract] [Full Text]  
  • Olczak, T., Dixon, D. W., Genco, C. A. (2001). Binding Specificity of the Porphyromonas gingivalis Heme and Hemoglobin Receptor HmuR, Gingipain K, and Gingipain R1 for Heme, Porphyrins, and Metalloporphyrins. J. Bacteriol. 183: 5599-5608 [Abstract] [Full Text]  
  • Carroll, J. A., Coleman, S. A., Smitherman, L. S., Minnick, M. F. (2000). Hemin-Binding Surface Protein from Bartonella quintana. Infect. Immun. 68: 6750-6757 [Abstract] [Full Text]  
  • Simpson, W., Olczak, T., Genco, C. A. (2000). Characterization and Expression of HmuR, a TonB-Dependent Hemoglobin Receptor of Porphyromonas gingivalis. J. Bacteriol. 182: 5737-5748 [Abstract] [Full Text]  
  • Cook, G. M., Poole, R. K. (2000). Oxidase and periplasmic cytochrome assembly in Escherichia coli K-12: CydDC and CcmAB are not required for haem-membrane association. Microbiology 146: 527-536 [Abstract] [Full Text]  
  • DeCarlo, A. A., Paramaesvaran, M., Yun, P. L. W., Collyer, C., Hunter, N. (1999). Porphyrin-Mediated Binding to Hemoglobin by the HA2 Domain of Cysteine Proteinases (Gingipains) and Hemagglutinins from the Periodontal Pathogen Porphyromonas gingivalis. J. Bacteriol. 181: 3784-3791 [Abstract] [Full Text]