Literature DB >> 1332942

FtsL, an essential cytoplasmic membrane protein involved in cell division in Escherichia coli.

L M Guzman1, J J Barondess, J Beckwith.   

Abstract

We have identified a gene involved in bacterial cell division, located immediately upstream of the ftsI gene in the min 2 region of the Escherichia coli chromosome. This gene, which we named ftsL, was detected through characterization of TnphoA insertions in a plasmid containing this chromosomal region. TnphoA topological analysis and fractionation of alkaline phosphatase fusion proteins indicated that the ftsL gene product is a 13.6-kDa cytoplasmic membrane protein with a cytoplasmic amino terminus, a single membrane-spanning segment, and a periplasmic carboxy terminus. The ftsL gene is essential for cell growth and division. A null mutation in ftsL resulted in inhibition of cell division, formation of long, nonseptate filaments, ultimate cessation of growth, and lysis. Under certain growth conditions, depletion of FtsL or expression of the largest ftsL-phoA fusion produced a variety of cell morphologies, including Y-shaped bacteria, indicating a possible general weakening of the cell wall. The FtsL protein is estimated to be present at about 20 to 40 copies per cell. The periplasmic domain of the protein displays a sequence with features characteristic of leucine zippers, which are involved in protein dimerization.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1332942      PMCID: PMC207486     

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


  43 in total

1.  Role of eukaryotic-type functional domains found in the prokaryotic enhancer receptor factor sigma 54.

Authors:  S Sasse-Dwight; J D Gralla
Journal:  Cell       Date:  1990-09-07       Impact factor: 41.582

2.  Regulation of cell division in E. coli.

Authors:  J Lutkenhaus
Journal:  Trends Genet       Date:  1990-01       Impact factor: 11.639

3.  Overproduction of FtsZ induces minicell formation in E. coli.

Authors:  J E Ward; J Lutkenhaus
Journal:  Cell       Date:  1985-10       Impact factor: 41.582

4.  Characterization of a conditional mutant with altered envelope showing pH-dependent morphology and temperature-dependent division.

Authors:  G Satta; R Fontana
Journal:  J Gen Microbiol       Date:  1974-01

5.  Cell shape and division in Escherichia coli: experiments with shape and division mutants.

Authors:  K J Begg; W D Donachie
Journal:  J Bacteriol       Date:  1985-08       Impact factor: 3.490

6.  Determinants of membrane protein topology.

Authors:  D Boyd; C Manoil; J Beckwith
Journal:  Proc Natl Acad Sci U S A       Date:  1987-12       Impact factor: 11.205

7.  On the process of cellular division in Escherichia coli: nucleotide sequence of the gene for penicillin-binding protein 3.

Authors:  M Nakamura; I N Maruyama; M Soma; J Kato; H Suzuki; Y Horota
Journal:  Mol Gen Genet       Date:  1983

8.  Cloning vectors that yield high levels of single-stranded DNA for rapid DNA sequencing.

Authors:  R J Zagursky; M L Berman
Journal:  Gene       Date:  1984-02       Impact factor: 3.688

9.  Membrane topology of penicillin-binding protein 3 of Escherichia coli.

Authors:  L D Bowler; B G Spratt
Journal:  Mol Microbiol       Date:  1989-09       Impact factor: 3.501

10.  Identification, cloning, and expression of bolA, an ftsZ-dependent morphogene of Escherichia coli.

Authors:  M Aldea; C Hernández-Chico; A G de la Campa; S R Kushner; M Vicente
Journal:  J Bacteriol       Date:  1988-11       Impact factor: 3.490

View more
  73 in total

1.  The Cpx envelope stress response is controlled by amplification and feedback inhibition.

Authors:  T L Raivio; D L Popkin; T J Silhavy
Journal:  J Bacteriol       Date:  1999-09       Impact factor: 3.490

2.  On the origin of branches in Escherichia coli.

Authors:  B Gullbrand; T Akerlund; K Nordström
Journal:  J Bacteriol       Date:  1999-11       Impact factor: 3.490

3.  Cell division in Escherichia coli: role of FtsL domains in septal localization, function, and oligomerization.

Authors:  J M Ghigo; J Beckwith
Journal:  J Bacteriol       Date:  2000-01       Impact factor: 3.490

4.  Analysis of ftsQ mutant alleles in Escherichia coli: complementation, septal localization, and recruitment of downstream cell division proteins.

Authors:  Joseph C Chen; Michael Minev; Jon Beckwith
Journal:  J Bacteriol       Date:  2002-02       Impact factor: 3.490

5.  Deletion of the min operon results in increased thermosensitivity of an ftsZ84 mutant and abnormal FtsZ ring assembly, placement, and disassembly.

Authors:  X C Yu; W Margolin
Journal:  J Bacteriol       Date:  2000-11       Impact factor: 3.490

6.  The transmembrane domain of the DnaJ-like protein DjlA is a dimerisation domain.

Authors:  C M Toutain; D J Clarke; J A Leeds; J Kuhn; J Beckwith; I B Holland; A Jacq
Journal:  Mol Genet Genomics       Date:  2003-01-31       Impact factor: 3.291

7.  Interactions of glutaredoxins, ribonucleotide reductase, and components of the DNA replication system of Escherichia coli.

Authors:  Ron Ortenberg; Stéphanie Gon; Amir Porat; Jon Beckwith
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-27       Impact factor: 11.205

8.  Vacuolating cytotoxin of Helicobacter pylori induces apoptosis in the human gastric epithelial cell line AGS.

Authors:  D Kuck; B Kolmerer; C Iking-Konert; P H Krammer; W Stremmel; J Rudi
Journal:  Infect Immun       Date:  2001-08       Impact factor: 3.441

9.  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

10.  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

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.