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    <title>Verhoef, G.G.</title>
    <link>http://repub.eur.nl/res/aut/5422/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>Differential protein expression in phenotypic variants of Streptococcus pneumoniae (Article)</title>
      <link>http://repub.eur.nl/res/pub/9425/</link>
      <pubDate>2000-01-01T00:00:00Z</pubDate>
      <description>Streptococcus pneumoniae undergoes spontaneous phase variation resulting
          in opaque and transparent colony forms. Differences in colony opacity
          correlate with differences in virulence: the transparent variants are more
          capable of colonizing the nasopharynx, whereas the opaque variants show
          increased virulence during systemic infections. To gain insight into the
          pathogenesis of pneumococcal disease at the molecular level, protein
          expression patterns of the phenotypic variants of two pneumococcal strains
          were compared by high-resolution two-dimensional protein electrophoresis.
          In comparison with transparent variants, the opaque variants reduced the
          expression of two proteins and overexpressed one protein. The proteins
          were identified by mass spectrometric analysis. The protein overexpressed
          in the opaque phenotype revealed significant homology to elongation factor
          Ts of Helicobacter pylori. One of the two proteins that were
          underexpressed in the opaque variants revealed significant homology to the
          proteinase maturation protein PrtM of Lactocobacillus paracasei, a member
          of the family of peptidyl-prolyl cis/trans isomerases. A consensus
          lipoprotein signal sequence suggests that the putative proteinase
          maturation protein A, designated PpmA, is located at the surface of the
          pneumococcus and may play a role in the maturation of surface or secreted
          proteins. The second underexpressed protein was identified as pyruvate
          oxidase, SpxB. The lower SpxB expression in opaque variants most probably
          explains the reduced production of hydrogen peroxide, a reaction product
          of SpxB, in this variant. Since a spxB-defective pneumococcal mutant has
          decreased ability to colonize the nasopharynx (B. Spellerberg, D. R.
          Cundell, J. Sandros, B. J. Pearce, I. Idanpaan-Heikkila, C. Rosenow, and
          H. R. Masure, 1996. Mol. Microbiol. 19:803-813, 1996), our data suggest
          that SpxB plays an important role in enhancing the ability of transparent
          variants to efficiently colonize the nasopharynx.</description>
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