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Appl. Environ. Microbiol., 06 1997, 2318-2323, Vol 63, No. 6
HT Sojar, N Hamada and RJ Genco
Porphyromonas gingivalis W50 (ATCC 53978) possesses the gene for fimbriae;
however, the surface-expressed fimbriae are sparse and have not been
previously isolated and characterized. We purified fimbriae from strain W50
to homogeneity by ammonium sulfate precipitation and reverse-phase
high-performance liquid chromatography [H. T. Sojar, N. Hamada, and R. J.
Genco, Protein Expr. Purif. 9(1):49-52, 1997]. Negative staining of
purified fimbriae viewed by electron microscopy revealed that the fimbriae
were identical in diameter to fimbriae of other P. gingivalis strains, such
as 2561, but were shorter in length. On sodium dodecyl
sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analysis, the
apparent molecular weight of isolated fimbrillin from strain W50 was found
to be identical to that of the fimbrillin molecule of strain 2561. Unlike
2561 fimbriae, W50 fimbriae, under reducing condition, exhibited a
monomeric structure on SDS-PAGE at room temperature. However, under
nonreduced conditions, even at 100 degrees C, no monomer was observed. In
immunoblot analysis as well as immunogold labeling of isolated fimbriae,
polyclonal antibodies against 2561 fimbriae, as well as antibodies against
peptide I (V-V-M-A-N-T-G-A- M-E-V-G-K-T-L-A-E-V-K-Cys) and peptide J
(A-L-T-T-E-L-T-A-E-N-Q-E-A-A-G- L-I-M-T-A-E-P-Cys), reacted. However,
antifimbrial antibodies against strain 2561 reacted very weakly compared to
anti-peptide I and anti- peptide J. Negative staining of whole W50 cells,
as well as immunogold electron microscopy with anti-peptide I and
anti-peptide J, showed fimbriae shorter in length and very few in number
compared to those of strain 2561. Purified fimbriae showed no
hemagglutinating activity. Amino acid composition was very similar to that
of previously reported fimbriae of the 2561 strain.
Copyright © 1997, American Society for Microbiology
Isolation and characterization of fimbriae from a sparsely fimbriated strain of Porphyromonas gingivalis
Department of Oral Biology, School of Dental Medicine, State University of New York at Buffalo 14214, USA. Hakim_Sojar@sdm.buffalo.edu
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