posted on 2013-07-03, 00:00authored byYe-Jin Eun, Maoquan Zhou, Daniela Kiekebusch, Susan Schlimpert, Rishi
R. Trivedi, Somenath Bakshi, Zhou Zhong, Taylor A. Wahlig, Martin Thanbichler, Douglas B. Weibel
Bacterial cell division involves
the dynamic assembly of division
proteins and coordinated constriction of the cell envelope. A wide
range of factors regulates cell divisionincluding growth and
environmental stressesand the targeting of the division machinery
has been a widely discussed approach for antimicrobial therapies.
This paper introduces divin, a small molecule inhibitor of bacterial
cell division that may facilitate mechanistic studies of this process.
Divin disrupts the assembly of late division proteins, reduces peptidoglycan
remodeling at the division site, and blocks compartmentalization of
the cytoplasm. In contrast to other division inhibitors, divin does
not interact with the tubulin homologue FtsZ, affect chromosome segregation,
or activate regulatory mechanisms that inhibit cell division indirectly.
Our studies of bacterial cell division using divin as a probe suggest
that dividing bacteria proceed through several morphological stages
of the cell envelope, and FtsZ is required but not sufficient to compartmentalize
the cytoplasmic membrane at the division site. Divin is only moderately
toxic to mammalian cells at concentrations that inhibit the growth
of clinical pathogens. These characteristics make divin a useful probe
for studying bacterial cell division and a starting point for the
development of new classes of therapeutic agents.