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J. Bacteriol., May 1996, 2637-2644, Vol 178, No. 9
S Kruger, S Gertz and M Hecker
In Bacillus subtilis, aryl-beta-glucosides such as salicin and arbutin are
catabolized by the gene products of bglP and bglH, encoding an enzyme II of
the phosphoenolpyruvate sugar-phosphotransferase system and a
phospho-beta-glucosidase, respectively. These two genes are transcribed
from a single promoter. The presence of a transcript of about 4,000
nucleotides detected by Northern (RNA) blot analysis indicates that bglP
and bglH are part of an operon. However, this transcript is only present
when cells are grown in the presence of the inducing substrate, salicin. In
the absence of the inducer, a transcript of about 110 nucleotides can be
detected, suggesting that transcription terminates downstream of the
promoter at a stable termination structure. Initiation of transcription is
abolished in the presence of rapidly metabolized carbon sources. Catabolite
repression of bglPH expression involves the trans-acting factors CcpA and
HPr. In a ccpA mutant, transcription initiation is relieved from glucose
repression. Furthermore, we report a catabolite responsive element-CcpA-
independent form of catabolite repression requiring the ribonucleic
antiterminator-terminator region, which is the target of antitermination,
and the wild-type HPr protein of the phosphotransferase system. Evidence
that the antitermination protein LicT is a crucial element for this type of
regulation is provided.
Copyright © 1996, American Society for Microbiology
Transcriptional analysis of bglPH expression in Bacillus subtilis: evidence for two distinct pathways mediating carbon catabolite repression
Institut fur Mikrobiologie und Molekularbiologie, Ernst-Moritz-Arndt Universitat Greifswald, Germany.
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