Literature DB >> 7504069

Haemin-binding proteins of Porphyromonas gingivalis W50 grown in a chemostat under haemin-limitation.

J W Smalley1, A J Birss, A S McKee, P D Marsh.   

Abstract

Porphyromonas gingivalis W50 was grown in a chemostat at pH 7.3 under haemin-limitation and haemin-excess at a constant mean doubling time of 6.9 h. Outer membranes (OM) were extracted from whole cells using EDTA and compared by SDS-PAGE. Haemin-limited cells expressed novel outer membrane proteins (OMPs) of mol. mass 115, 113 and 19 kDa when samples were solubilized at 100 degrees C. A 46 kDa OMP was observed in haemin-excess cells but not in those from haemin-limited conditions. Tetramethylbenzidine (TMBZ) staining of gels, after OM solubilization at 20 degrees C, was used to detect haemin-binding proteins (HBPs). HBPs were observed only in OM from haemin-limited cells. The major HBP (mol. mass 32.4 kDa) corresponded to a similar sized Kenacid-blue-stained protein which was not observed in haemin-excess-derived OM. Haemin-limited cells and OM displayed a ladder-like series of Kenacid-blue-stained proteins. Lighter TMBZ-stained proteins of mol. mass 51, 53, 56 and 60 kDa, with mobilities corresponding to those of silver-stained LPS components, were observed in haemin-limited OM. No soluble HBPs were detected extracellularly. The greater number of HBPs expressed by cells grown under haemin-limitation may reflect an additional cell surface receptor system for haemin acquisition under low environmental levels of this essential cofactor.

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Year:  1993        PMID: 7504069     DOI: 10.1099/00221287-139-9-2145

Source DB:  PubMed          Journal:  J Gen Microbiol        ISSN: 0022-1287


  15 in total

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2.  Binding of hemoglobin to the envelope of Porphyromonas gingivalis and isolation of the hemoglobin-binding protein.

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3.  The periodontopathogen Porphyromonas gingivalis binds iron protoporphyrin IX in the mu-oxo dimeric form: an oxidative buffer and possible pathogenic mechanism.

Authors:  J W Smalley; J Silver; P J Marsh; A J Birss
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4.  Porphyrin-mediated cell surface heme capture from hemoglobin by Porphyromonas gingivalis.

Authors:  Mayuri Paramaesvaran; Ky-Anh Nguyen; Elizabeth Caldon; James A McDonald; Sherean Najdi; Graciel Gonzaga; David B Langley; Arthur DeCarlo; Maxwell J Crossley; Neil Hunter; Charles A Collyer
Journal:  J Bacteriol       Date:  2003-04       Impact factor: 3.490

5.  Characterization of a novel outer membrane hemin-binding protein of Porphyromonas gingivalis.

Authors:  S G Dashper; A Hendtlass; N Slakeski; C Jackson; K J Cross; L Brownfield; R Hamilton; I Barr; E C Reynolds
Journal:  J Bacteriol       Date:  2000-11       Impact factor: 3.490

6.  Isolation and characterization of a hemin-regulated gene, hemR, from Porphyromonas gingivalis.

Authors:  T Karunakaran; T Madden; H Kuramitsu
Journal:  J Bacteriol       Date:  1997-03       Impact factor: 3.490

7.  Degradation of host heme proteins by lysine- and arginine-specific cysteine proteinases (gingipains) of Porphyromonas gingivalis.

Authors:  A Sroka; M Sztukowska; J Potempa; J Travis; C A Genco
Journal:  J Bacteriol       Date:  2001-10       Impact factor: 3.490

8.  Binding specificity of the Porphyromonas gingivalis heme and hemoglobin receptor HmuR, gingipain K, and gingipain R1 for heme, porphyrins, and metalloporphyrins.

Authors:  T Olczak; D W Dixon; C A Genco
Journal:  J Bacteriol       Date:  2001-10       Impact factor: 3.490

9.  Characterization and expression of HmuR, a TonB-dependent hemoglobin receptor of Porphyromonas gingivalis.

Authors:  W Simpson; T Olczak; C A Genco
Journal:  J Bacteriol       Date:  2000-10       Impact factor: 3.490

10.  The Tla protein of Porphyromonas gingivalis W50: a homolog of the RI protease precursor (PrpRI) is an outer membrane receptor required for growth on low levels of hemin.

Authors:  J Aduse-Opoku; J M Slaney; M Rangarajan; J Muir; K A Young; M A Curtis
Journal:  J Bacteriol       Date:  1997-08       Impact factor: 3.490

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