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J. Bacteriol., Feb 1997, 620-626, Vol 179, No. 3
GR Tompkins, DP Wood and KR Birchmeier
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.
Copyright © 1997, American Society for Microbiology
Detection and comparison of specific hemin binding by Porphyromonas gingivalis and Prevotella intermedia
Department of Oral Biology, School of Dentistry, Medical College of Georgia, Augusta 30912-1126, USA. gtompkin@mail.mcg.edu
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