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J. Bacteriol., 07 1997, 4616-4619, Vol 179, No. 14
S Pichoff, B Vollrath and JP Bouche
We report that MinE, the topological specificity factor of cell division in
Escherichia coli, inhibits septation when fused to the C terminus of the
maltose-binding protein MalE. This contrasts with overexpression of MinE
alone, which affects growth but has no effect on division. Inhibition by
MalE-MinE was minCD independent and depended on MinE segments involved in
dimerization and prevention of MinCD division inhibition. The SOS and the
heat shock responses were not involved, suggesting that the inhibition
comes from a direct interaction of MalE- MinE with the septation apparatus.
MalE-MinE lethality was suppressed by overexpression of ftsZ, as well as by
overexpression of ftsN, a suppressor of temperature-sensitive mutations in
genes ftsQ, ftsA, and ftsI. We also report that high-level synthesis of
MalE disturbs nucleoid partitioning.
Copyright © 1997, American Society for Microbiology
MinCD-independent inhibition of cell division by a protein that fuses MalE to the topological specificity factor MinE
Laboratoire de Microbiologie et de Genetique Moleculaire du CNRS, Toulouse, France.
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