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J. Bacteriol., Mar 1997, 2065-2067, Vol 179, No. 6
SS Choi, SK Kim, TG Oh and EC Choi
To study the role of mRNA termination in the regulation of ermK, we
introduced mismatches into terminators by in vitro mutagenesis. In wild-
type ermK, only truncated transcription products were detected in the
absence of induction. In contrast, only the full-length transcript was
synthesized in the terminator 1 and terminator 2 double mutants, even in
the absence of erythromycin. These results indicate that the expression of
ermK is primarily regulated by transcriptional attenuation rather than
translational attenuation. We also tested the possible contribution of
translational attenuation control to the regulation of ermK by constructing
a triple mutant (terminator 1 plus terminator 2 plus the methylase
Shine-Dalgarno region). A higher level of beta-galactosidase synthesis was
seen in the triple mutant. Therefore, unlike with previously described
attenuators, it can be concluded that both transcriptional and
translational attenuation contribute to the regulation of ermK, although
transcriptional attenuation plays a larger role.
Copyright © 1997, American Society for Microbiology
Role of mRNA termination in regulation of ermK
College of Pharmacy, Seoul National University, Korea.
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