Literature DB >> 11807057

Characterization of Streptococcus suis genes encoding proteins homologous to sortase of gram-positive bacteria.

Makoto Osaki1, Daisuke Takamatsu, Yoshihiro Shimoji, Tsutomu Sekizaki.   

Abstract

Many surface proteins which are covalently linked to the cell wall of gram-positive bacteria have a consensus C-terminal motif, Leu-Pro-X-Thr-Gly (LPXTG). This sequence is cleaved, and the processed protein is attached to an amino group of a cross-bridge in the peptidoglycan by a specific enzyme called sortase. Using the type strain of Streptococcus suis, NCTC 10234, we found five genes encoding proteins that were homologous to sortases of other bacteria and determined the nucleotide sequences of the genetic regions. One gene, designated srtA, was linked to gyrA, as were the sortase and sortase-like genes of other streptococci. Three genes, designated srtB, srtC, and srtD, were tandemly clustered in a different location, where there were three segments of directly repeated sequences of approximately 110 bp in close vicinity. The remaining gene, designated srtE, was located separately on the chromosome with a pseudogene which may encode a transposase. The deduced amino acid sequences of the five Srt proteins showed 18 to 31% identity with the sortases of Streptococcus gordonii and Staphylococcus aureus, except that SrtA of S. suis had 65% identity with that of S. gordonii. Isogenic mutants deficient for srtA, srtBCD, or srtE were generated by allelic exchanges. The protein fraction which was released from partially purified cell walls by digestion with N-acetylmuramidase was profiled by two-dimensional gel electrophoresis. More than 15 of the protein spots were missing in the profile of the srtA mutant compared with that of the parent strain, and this phenotype was completely complemented by srtA cloned from S. suis. Four genes encoding proteins corresponding to such spots were identified and sequenced. The deduced translational products of the four genes possessed the LPXTG motif in their C-terminal regions. On the other hand, the protein spots that were missing in the srtA mutant appeared in the profiles of the srtBCD and srtE mutants. These results provide evidence that the cell wall sorting system involving srtA is also present in S. suis.

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Year:  2002        PMID: 11807057      PMCID: PMC134807          DOI: 10.1128/jb.184.4.971-982.2002

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  63 in total

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  37 in total

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Review 3.  Sortases and the art of anchoring proteins to the envelopes of gram-positive bacteria.

Authors:  Luciano A Marraffini; Andrea C Dedent; Olaf Schneewind
Journal:  Microbiol Mol Biol Rev       Date:  2006-03       Impact factor: 11.056

4.  Molecular architecture of Streptococcus pneumoniae TIGR4 pili.

Authors:  Markus Hilleringmann; Philippe Ringler; Shirley A Müller; Gabriella De Angelis; Rino Rappuoli; Ilaria Ferlenghi; Andreas Engel
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5.  Evidence for lateral transfer of the Suilysin gene region of Streptococcus suis.

Authors:  Daisuke Takamatsu; Makoto Osaki; Tsutomu Sekizaki
Journal:  J Bacteriol       Date:  2002-04       Impact factor: 3.490

6.  Different foreign genes incidentally integrated into the same locus of the Streptococcus suis genome.

Authors:  Tsutomu Sekizaki; Daisuke Takamatsu; Makoto Osaki; Yoshihiro Shimoji
Journal:  J Bacteriol       Date:  2005-02       Impact factor: 3.490

Review 7.  Surface Proteins on Gram-Positive Bacteria.

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Journal:  Microbiol Spectr       Date:  2019-07

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10.  Mutations in the gene encoding the ancillary pilin subunit of the Streptococcus suis srtF cluster result in pili formed by the major subunit only.

Authors:  Nahuel Fittipaldi; Daisuke Takamatsu; María de la Cruz Domínguez-Punaro; Marie-Pier Lecours; Diane Montpetit; Makoto Osaki; Tsutomu Sekizaki; Marcelo Gottschalk
Journal:  PLoS One       Date:  2010-01-05       Impact factor: 3.240

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