Affiliation:
1. Department of Biology
2. Department of Chemistry, Indiana University Bloomington, Bloomington, Indiana 47405
Abstract
ABSTRACT
PcsB is a protein of unknown function that plays a critical role in cell division in
Streptococcus pneumoniae
and other ovococcus species of
Streptococcus
. We constructed isogenic sets of mutants expressing different amounts of PcsB in laboratory strain R6 and virulent serotype 2 strain D39 to evaluate its cellular roles. Insertion mutagenesis in parent and
pcsB
+
merodiploid strains indicated that
pcsB
is essential in serotype 2
S. pneumoniae.
Quantitative Western blotting of wild-type and epitope-tagged PcsB showed that all PcsB was processed into cell-associated and secreted forms of the same molecular mass and that cell-associated PcsB was moderately abundant and present at ≈4,900 monomers per cell. Controlled expression and complementation experiments indicated that there was a causative relationship between the severity of defects in cell division and decreasing PcsB amount. These experiments also showed that perturbations of expression of the upstream
mreCD
genes did not contribute to the cell division defects of
pcsB
mutants and that
mreCD
could be deleted. Unexpectedly, capsule influenced the cell shape and chain formation phenotypes of the wild-type D39 strain and mutants underexpressing PcsB or deleted for other genes involved in peptidoglycan biosynthesis, such as
dacA
. Underexpression of PcsB did not result in changes in the amounts or composition of lactoyl-peptides, which were markedly different in the R6 and D39 strains, and there was no correlation between decreased PcsB amount and sensitivity to penicillin. Finally, microarray analyses indicated that underexpression of PcsB may generate a signal that increases expression of the VicRK regulon, which includes
pcsB
.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
75 articles.
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