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A combination of both arginine- and lysine-specific gingipain activity of Porphyromonas gingivalis is necessary for the generation of the micro-oxo bishaem-containing pigment from haemoglobin.
- Source :
-
The Biochemical journal [Biochem J] 2004 May 01; Vol. 379 (Pt 3), pp. 833-40. - Publication Year :
- 2004
-
Abstract
- The black pigment of Porphyromonas gingivalis is composed of the mu-oxo bishaem complex of Fe(III) protoporphyrin IX (mu-oxo oligomer, dimeric haem), namely [Fe(III)PPIX]2O. P. gingivalis W50 and Rgp (Arg-gingipain)- and Kgp (Lys-gingipain)-deficient mutants K1A, D7, E8 and W501 [Aduse-Opoku, Davies, Gallagher, Hashim, Evans, Rangarajan, Slaney and Curtis (2000) Microbiology 146, 1933-1940] were grown on horse blood/agar for 14 days and examined for the production of mu-oxo bishaem. Mu-oxo Bishaem was detected by UV-visible, Mössbauer and Raman spectroscopies in wild-type W50 and in the black-pigmented RgpA- and RgpB-deficient mutants (W501 and D7 respectively), whereas no haem species were detected in the straw-coloured colonies of Kgp-deficient strain K1A. The dark brown pigment of the double RgpA/RgpB knockout mutant (E8) was not composed of mu-oxo bishaem, but of a high-spin monomeric Fe(III) protoporphyrin IX species (possibly a haem-albumin complex). In vitro incubation of oxyhaemoglobin with cells of the W50 strain and the RgpA- and RgpB-deficient mutants (W501 and D7) resulted in the formation of mu-oxo bishaem via methaemoglobin as an intermediate. Although the Kgp-deficient strain K1A converted oxyhaemoglobin into methaemoglobin, this was not further degraded into mu-oxo bishaem. The double RgpA/RgpB knockout was also not capable of producing mu-oxo bishaem from oxyhaemoglobin, but instead generated a haemoglobin haemichrome. Inhibition of Arg-X protease activity of W50, W501, D7 and K1A with leupeptin, under conditions where Lys-X protease activity was unaffected, prevented the production of mu-oxo bishaem from oxyhaemoglobin, but resulted in the formation of a haemoglobin haemichrome. These results show that one or both of RgpA and RgpB gingipains, in addition to the lysine-specific gingipain, is necessary for the production of mu-oxo bishaem from haemoglobin by whole cells of P. gingivalis.
- Subjects :
- Adhesins, Bacterial
Agar
Animals
Cysteine Endopeptidases deficiency
Cysteine Endopeptidases genetics
Gingipain Cysteine Endopeptidases
Hemagglutinins genetics
Horses blood
Leupeptins metabolism
Pigments, Biological analysis
Porphyromonas gingivalis chemistry
Porphyromonas gingivalis genetics
Porphyromonas gingivalis growth & development
Protoporphyrins analysis
Protoporphyrins chemistry
Spectrophotometry, Ultraviolet
Spectroscopy, Mossbauer
Spectrum Analysis, Raman
Time Factors
Cysteine Endopeptidases metabolism
Hemagglutinins metabolism
Oxyhemoglobins metabolism
Pigments, Biological chemistry
Pigments, Biological metabolism
Porphyromonas gingivalis enzymology
Protoporphyrins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1470-8728
- Volume :
- 379
- Issue :
- Pt 3
- Database :
- MEDLINE
- Journal :
- The Biochemical journal
- Publication Type :
- Academic Journal
- Accession number :
- 14741050
- Full Text :
- https://doi.org/10.1042/BJ20031221