Abstract

Probably one of the most controversial questions about the cell division of rod-shaped bacteria concerns the mechanism that ensures the correct placement of the division septum—mid-cell during vegetative growth but closer to one end during sporulation. In general, bacteria multiply by binary fission in which the division septum forms almost exactly at the cell center. How the division machinery achieves such accuracy is a question of continuing interest. Cell division in Escherichia coli and Bacillus subtilis are the most thoroughly studied cell division mechanisms. The earliest visible event in cell division is the formation of a Z ring by FtsZ, a tubulin like protein, at the future septum site. The Z-ring appears to be an accurate marker for the position of the division site and is furthermore recognized by set of cell division proteins—the divisome. At least two distinct mechanisms contribute to the placement of the division machinery: nucleoid occlusion and the Min system. The mechanism of Min system action is fundamentally different in both model organisms [reviewed in Barak and Wilkinson (2007)].

Highlights

  • Escherichia coli Min SYSTEM DURING VEGETATIVE GROWTH Clearly, the best understood Min system is the three protein MinCDE system from E. coli

  • The introduction of this oscillating Min system into B. subtilis inhibits the formation of asymmetric septation during sporulation

  • Bacillus subtilis Min SYSTEM DURING SPORULATION It is possible that the two different Min systems evolved because of the different life cycles of B. subtilis, which, in addition to vegetative growth, can undergo sporulation, a simple differentiation process

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Summary

Introduction

Escherichia coli Min SYSTEM DURING VEGETATIVE GROWTH Clearly, the best understood Min system is the three protein MinCDE system from E. coli. MinC is a cell division inhibitor which directly binds to FtsZ and is activated by MinD, a membrane-associated ATPase (de Boer et al, 1991).

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