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J. Biol. Chem., Vol. 268, Issue 34, 25402-25408, 12, 1993
A Puyet, AM Ibanez and M Espinosa
The gene encoding a transcriptional repressor of the maltosaccharide
utilization operons of the Gram-positive bacterium Streptococcus pneumoniae
(malR) has been cloned and sequenced. The genetic structure of the locus
reveals the presence of an upstream gene necessary for growth on
maltotetraose medium (malA). The phenotype of malR- and malA- mutants
obtained by interruption of the coding regions suggests that both genes
could belong to the same transcription unit. Two copies of a DNA motif
consisting of three conserved regions of 59, 42, and 49 nucleotides were
found located upstream and downstream of the malA-malR putative operon.
These DNA structures are almost identical to the reported Box sequences
associated with several genes of S. pneumoniae. The protein encoded by malR
was visualized and partially purified after selective expression in
Escherichia coli, whereas the product of malA was identified in vitro. The
amino acid sequence of MalR displays similarities with the Lac and Gal
family of repressors. The highest similarities were found when comparing
MalR with the E. coli MalI repressor, which is related with an indirect
induction pathway of the maltose regulon. The significance of these
similarities is discussed in terms of the possible evolutionary pathways
followed by structural and regulatory genes of sugar utilization systems in
bacteria.
Characterization of the Streptococcus pneumoniae maltosaccharide regulator MalR, a member of the LacI-GalR family of repressors displaying distinctive genetic features
Centro de Investigaciones Biologicas, Consejo Superior de Investigaciones Cientificas, Madrid, Spain.
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