Literature DB >> 15165235

A complex of the Escherichia coli cell division proteins FtsL, FtsB and FtsQ forms independently of its localization to the septal region.

Nienke Buddelmeijer1, Jon Beckwith.   

Abstract

Three membrane proteins required for cell division in Escherichia coli, FtsQ, FtsL and FtsB, localize to the cell septum. FtsL and FtsB, which each contain a leucine zipper-like sequence, are dependent on each other for this localization, and each of them is dependent on FtsQ. However, FtsQ is found at the cell division site in the absence of FtsL and FtsB. FtsQ, in turn, requires FtsK for its localization. Here, we show that FtsL, FtsB and FtsQ form a complex in vivo. Strikingly, this complex forms in the absence of FtsK, which is required for the localization of all three proteins to the mid-cell. These findings indicate that the FtsL, FtsB, FtsQ interactions can take place in cells before movement to the mid-cell and that migration to this position might occur only after the formation of the complex. Evidence indicating the regions of the three proteins involved in complex formation is presented. These findings provide the first example of preassembly of a subcomplex of cell division proteins before their localization to the septal region.

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Year:  2004        PMID: 15165235     DOI: 10.1111/j.1365-2958.2004.04044.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  81 in total

1.  DivIC stabilizes FtsL against RasP cleavage.

Authors:  Inga Wadenpohl; Marc Bramkamp
Journal:  J Bacteriol       Date:  2010-07-19       Impact factor: 3.490

Review 2.  Essential biological processes of an emerging pathogen: DNA replication, transcription, and cell division in Acinetobacter spp.

Authors:  Andrew Robinson; Anthony J Brzoska; Kylie M Turner; Ryan Withers; Elizabeth J Harry; Peter J Lewis; Nicholas E Dixon
Journal:  Microbiol Mol Biol Rev       Date:  2010-06       Impact factor: 11.056

3.  Evidence from artificial septal targeting and site-directed mutagenesis that residues in the extracytoplasmic β domain of DivIB mediate its interaction with the divisomal transpeptidase PBP 2B.

Authors:  Susan L Rowland; Kimberly D Wadsworth; Scott A Robson; Carine Robichon; Jon Beckwith; Glenn F King
Journal:  J Bacteriol       Date:  2010-09-24       Impact factor: 3.490

Review 4.  The bacterial divisome: ready for its close-up.

Authors:  Veronica W Rowlett; William Margolin
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2015-10-05       Impact factor: 6.237

5.  Functional analysis of the cell division protein FtsW of Escherichia coli.

Authors:  Soumya Pastoret; Claudine Fraipont; Tanneke den Blaauwen; Benoît Wolf; Mirjam E G Aarsman; André Piette; Annick Thomas; Robert Brasseur; Martine Nguyen-Distèche
Journal:  J Bacteriol       Date:  2004-12       Impact factor: 3.490

6.  Premature targeting of a cell division protein to midcell allows dissection of divisome assembly in Escherichia coli.

Authors:  Nathan W Goehring; Frederico Gueiros-Filho; Jon Beckwith
Journal:  Genes Dev       Date:  2005-01-01       Impact factor: 11.361

7.  Roles for both FtsA and the FtsBLQ subcomplex in FtsN-stimulated cell constriction in Escherichia coli.

Authors:  Bing Liu; Logan Persons; Lynda Lee; Piet A J de Boer
Journal:  Mol Microbiol       Date:  2015-01-24       Impact factor: 3.501

8.  A role for the FtsQLB complex in cytokinetic ring activation revealed by an ftsL allele that accelerates division.

Authors:  Mary-Jane Tsang; Thomas G Bernhardt
Journal:  Mol Microbiol       Date:  2015-01-24       Impact factor: 3.501

9.  The bypass of ZipA by overexpression of FtsN requires a previously unknown conserved FtsN motif essential for FtsA-FtsN interaction supporting a model in which FtsA monomers recruit late cell division proteins to the Z ring.

Authors:  Sebastien Pichoff; Shishen Du; Joe Lutkenhaus
Journal:  Mol Microbiol       Date:  2015-02-04       Impact factor: 3.501

10.  Role for the nonessential N terminus of FtsN in divisome assembly.

Authors:  Nathan W Goehring; Carine Robichon; Jon Beckwith
Journal:  J Bacteriol       Date:  2006-10-27       Impact factor: 3.490

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