Division accuracy in a stochastic model of Min oscillations in Escherichia coli.

Accurate cell division in Escherichia coli requires the Min proteins MinC, MinD, and MinE as well as the presence of nucleoids. MinD and MinE exhibit spatial oscillations, moving from pole to pole of the bacterium, resulting in an average MinD concentration that is low at the center of the cell and high at the poles. This concentration minimum is thought to signal the site of cell division. Deterministic models of the Min oscillations reproduce many observed features of the system, including the concentration minimum of MinD. However, there are only a few thousand Min proteins in a bacterium, so stochastic effects are likely to play an important role. Here, we show that Monte Carlo simulations with a large number of proteins agree well with the results from a deterministic treatment of the equations. The location of minimum local MinD concentration is too variable to account for cell division accuracy in wild-type, but is consistent with the accuracy of cell division in cells without nucleoids. This finding confirms the need to include additional mechanisms, such as reciprocal interactions with the cell division ring or positioning of the nucleoids, to explain wild-type accuracy.

[1]  H T van der Voort,et al.  Confocal scanning light microscopy of the Escherichia coli nucleoid: comparison with phase-contrast and electron microscope images , 1985, Journal of bacteriology.

[2]  S. Eykyn Microbiology , 1950, The Lancet.

[3]  J. Lutkenhaus FtsZ ring in bacterial cytokinesis , 1993, Molecular microbiology.

[4]  P. D. de Boer,et al.  Proper placement of the Escherichia coli division site requires two functions that are associated with different domains of the MinE protein. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[5]  W. Margolin,et al.  Assembly of the FtsZ ring at the central division site in the absence of the chromosome , 1998, Molecular microbiology.

[6]  P. D. de Boer,et al.  MinDE-Dependent Pole-to-Pole Oscillation of Division Inhibitor MinC in Escherichia coli , 1999, Journal of bacteriology.

[7]  P A de Boer,et al.  Rapid pole-to-pole oscillation of a protein required for directing division to the middle of Escherichia coli. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[8]  W. Margolin,et al.  FtsZ ring clusters in min and partition mutants: role of both the Min system and the nucleoid in regulating FtsZ ring localization , 1999, Molecular microbiology.

[9]  J. Lutkenhaus,et al.  Topological regulation of cell division in Escherichia coli involves rapid pole to pole oscillation of the division inhibitor MinC under the control of MinD and MinE , 1999, Molecular microbiology.

[10]  H. Meinhardt,et al.  Pattern formation in Escherichia coli: A model for the pole-to-pole oscillations of Min proteins and the localization of the division site , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[11]  M. Howard,et al.  Dynamic compartmentalization of bacteria: accurate division in E. coli. , 2001, Physical review letters.

[12]  P A de Boer,et al.  Dynamic localization cycle of the cell division regulator MinE in Escherichia coli , 2001, The EMBO journal.

[13]  W. Margolin,et al.  Bacterial cell division: A moving MinE sweeper boggles the MinD , 2001, Current Biology.

[14]  Andrew D. Rutenberg,et al.  Dynamic Compartmentalization of Bacteria , 2001 .

[15]  Karsten Kruse,et al.  A dynamic model for determining the middle of Escherichia coli. , 2002, Biophysical journal.

[16]  Yu-Ling Shih,et al.  Division site placement in E.coli: mutations that prevent formation of the MinE ring lead to loss of the normal midcell arrest of growth of polar MinD membrane domains , 2002, The EMBO journal.

[17]  R. Valluzzi,et al.  Dynamic assembly of MinD into filament bundles modulated by ATP, phospholipids, and MinE , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[18]  J. Lutkenhaus,et al.  Dynamic proteins in bacteria. , 2002, Current opinion in microbiology.

[19]  T. Åkerlund,et al.  Effects of the Min system on nucleoid segregation in Escherichia coli. , 2002, Microbiology.

[20]  Yu-Ling Shih,et al.  Division site selection in Escherichia coli involves dynamic redistribution of Min proteins within coiled structures that extend between the two cell poles , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[21]  Andrew D Rutenberg,et al.  Pattern formation inside bacteria: fluctuations due to the low copy number of proteins. , 2003, Physical review letters.

[22]  N. Wingreen,et al.  Dynamic structures in Escherichia coli: Spontaneous formation of MinE rings and MinD polar zones , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[23]  Martina Sterneck,et al.  Living donor liver transplantation. , 2003, Journal of hepatology.

[24]  S. Zimmerman Underlying regularity in the shapes of nucleoids of Escherichia coli: implications for nucleoid organization and partition. , 2003, Journal of structural biology.

[25]  Frederico J. Gueiros-Filho,et al.  Assembly Dynamics of FtsZ Rings in Bacillus subtilis and Escherichia coli and Effects of FtsZ-Regulating Proteins , 2004, Journal of bacteriology.

[26]  N. Wingreen,et al.  Pattern formation within Escherichia coli: diffusion, membrane attachment, and self-interaction of MinD molecules. , 2004, Physical review letters.

[27]  Maryann E Martone,et al.  Evidence for Ectopic Neurotransmission at a Neuronal Synapse , 2005, Science.

[28]  H. Erickson,et al.  Rapid in Vitro Assembly Dynamics and Subunit Turnover of FtsZ Demonstrated by Fluorescence Resonance Energy Transfer* , 2005, Journal of Biological Chemistry.

[29]  Donald A. Drew,et al.  A polymerization-depolymerization model that accurately generates the self-sustained oscillatory system involved in bacterial division site placement , 2005, Proceedings of the National Academy of Sciences of the United States of America.