Literature DB >> 9922245

Analysis of FtsZ assembly by light scattering and determination of the role of divalent metal cations.

A Mukherjee1, J Lutkenhaus.   

Abstract

FtsZ is an ancestral homologue of tubulin that polymerizes in a GTP-dependent manner. In this study, we used 90 degrees angle light scattering to investigate FtsZ polymerization. The critical concentration for polymerization obtained by this method is similar to that obtained by centrifugation, confirming that the light scattering is proportional to polymer mass. Furthermore, the dynamics of FtsZ polymerization could be readily monitored by light scattering. Polymerization was very rapid, reaching steady state within 30 s. The length of the steady-state phase was proportional to the GTP concentration and was followed by a rapid decrease in light scattering. This decrease indicated net depolymerization that always occurred as the GTP in the reaction was consumed. FtsZ polymerization was observed over the pH range 6.5 to 7.9. Importantly, Mg2+ was not required for polymerization although it was required for the dynamic behavior of the polymers. It was reported that 7 to 25 mM Ca2+ mediated dynamic assembly of FtsZ (X. -C. Yu and W. Margolin, EMBO J. 16:5455-5463, 1997). However, we found that Ca2+ was not required for FtsZ assembly and that this concentration of Ca2+ reduced the dynamic behavior of FtsZ assembly.

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Year:  1999        PMID: 9922245      PMCID: PMC93448     

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  30 in total

1.  The essential bacterial cell-division protein FtsZ is a GTPase.

Authors:  P de Boer; R Crossley; L Rothfield
Journal:  Nature       Date:  1992-09-17       Impact factor: 49.962

2.  FtsZ ring structure associated with division in Escherichia coli.

Authors:  E F Bi; J Lutkenhaus
Journal:  Nature       Date:  1991-11-14       Impact factor: 49.962

3.  Ionic and nucleotide requirements for microtubule polymerization in vitro.

Authors:  J B Olmsted; G G Borisy
Journal:  Biochemistry       Date:  1975-07       Impact factor: 3.162

4.  Maintenance of intracellular calcium in Escherichia coli.

Authors:  P Gangola; B P Rosen
Journal:  J Biol Chem       Date:  1987-09-15       Impact factor: 5.157

5.  Turbidimetric studies of the in vitro assembly and disassembly of porcine neurotubules.

Authors:  F Gaskin; C R Cantor; M L Shelanski
Journal:  J Mol Biol       Date:  1974-11-15       Impact factor: 5.469

6.  GTP-dependent polymerization of Escherichia coli FtsZ protein to form tubules.

Authors:  D Bramhill; C M Thompson
Journal:  Proc Natl Acad Sci U S A       Date:  1994-06-21       Impact factor: 11.205

Review 7.  Actin polymerization and its regulation by proteins from nonmuscle cells.

Authors:  E D Korn
Journal:  Physiol Rev       Date:  1982-04       Impact factor: 37.312

8.  Escherichia coli cell-division gene ftsZ encodes a novel GTP-binding protein.

Authors:  D RayChaudhuri; J T Park
Journal:  Nature       Date:  1992-09-17       Impact factor: 49.962

9.  Guanine nucleotide-dependent assembly of FtsZ into filaments.

Authors:  A Mukherjee; J Lutkenhaus
Journal:  J Bacteriol       Date:  1994-05       Impact factor: 3.490

10.  Purification and biochemical characterization of tubulin from the budding yeast Saccharomyces cerevisiae.

Authors:  A Davis; C R Sage; L Wilson; K W Farrell
Journal:  Biochemistry       Date:  1993-08-31       Impact factor: 3.162

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  90 in total

1.  Straight and curved conformations of FtsZ are regulated by GTP hydrolysis.

Authors:  C Lu; M Reedy; H P Erickson
Journal:  J Bacteriol       Date:  2000-01       Impact factor: 3.490

2.  The MinC component of the division site selection system in Escherichia coli interacts with FtsZ to prevent polymerization.

Authors:  Z Hu; A Mukherjee; S Pichoff; J Lutkenhaus
Journal:  Proc Natl Acad Sci U S A       Date:  1999-12-21       Impact factor: 11.205

3.  Direct observation of the enhancement of noncooperative protein self-assembly by macromolecular crowding: indefinite linear self-association of bacterial cell division protein FtsZ.

Authors:  G Rivas; J A Fernández; A P Minton
Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-13       Impact factor: 11.205

4.  Assembly of an FtsZ mutant deficient in GTPase activity has implications for FtsZ assembly and the role of the Z ring in cell division.

Authors:  A Mukherjee; C Saez; J Lutkenhaus
Journal:  J Bacteriol       Date:  2001-12       Impact factor: 3.490

5.  Plastid division is driven by a complex mechanism that involves differential transition of the bacterial and eukaryotic division rings.

Authors:  M Takahara; T Mori; H Kuroiwa; T Higashiyama; T Kuroiwa
Journal:  Plant Cell       Date:  2001-10       Impact factor: 11.277

6.  ZipA-induced bundling of FtsZ polymers mediated by an interaction between C-terminal domains.

Authors:  C A Hale; A C Rhee; P A de Boer
Journal:  J Bacteriol       Date:  2000-09       Impact factor: 3.490

7.  A widely conserved bacterial cell division protein that promotes assembly of the tubulin-like protein FtsZ.

Authors:  Frederico J Gueiros-Filho; Richard Losick
Journal:  Genes Dev       Date:  2002-10-01       Impact factor: 11.361

8.  EzrA prevents aberrant cell division by modulating assembly of the cytoskeletal protein FtsZ.

Authors:  Daniel P Haeusser; Rachel L Schwartz; Alison M Smith; Michelle Erin Oates; Petra Anne Levin
Journal:  Mol Microbiol       Date:  2004-05       Impact factor: 3.501

Review 9.  Physics of bacterial morphogenesis.

Authors:  Sean X Sun; Hongyuan Jiang
Journal:  Microbiol Mol Biol Rev       Date:  2011-12       Impact factor: 11.056

10.  Nucleotide-dependent conformations of FtsZ dimers and force generation observed through molecular dynamics simulations.

Authors:  Jen Hsin; Ajay Gopinathan; Kerwyn C Huang
Journal:  Proc Natl Acad Sci U S A       Date:  2012-05-30       Impact factor: 11.205

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