Literature DB >> 8478341

Cell division and transcription of ftsZ.

R W Smith1, M Masters, W D Donachie.   

Abstract

For normal cell division, the ftsZ gene must be transcribed from a number of promoters that are located within the proximal upstream genes (ddlB, ftsQ, and ftsA). We show that the main promoters have identical responses to changes in growth rate, i.e., under all conditions, the frequency of transcription per septum formed is approximately constant and independent of cell size or growth rate per se. We also show that transcription from these promoters is independent of stationary-phase transcription factor sigma s.

Mesh:

Substances:

Year:  1993        PMID: 8478341      PMCID: PMC204587          DOI: 10.1128/jb.175.9.2788-2791.1993

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


  28 in total

1.  Dependency on medium and temperature of cell size and chemical composition during balanced grown of Salmonella typhimurium.

Authors:  M SCHAECHTER; O MAALOE; N O KJELDGAARD
Journal:  J Gen Microbiol       Date:  1958-12

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

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

3.  Structure and expression of the cell division genes ftsQ, ftsA and ftsZ.

Authors:  Q M Yi; S Rockenbach; J E Ward; J Lutkenhaus
Journal:  J Mol Biol       Date:  1985-08-05       Impact factor: 5.469

4.  Chromosome replication and the division cycle of Escherichia coli B/r.

Authors:  S Cooper; C E Helmstetter
Journal:  J Mol Biol       Date:  1968-02-14       Impact factor: 5.469

5.  Further evidence for overlapping transcriptional units in an Escherichia coli cell envelope-cell division gene cluster: DNA sequence and transcriptional organization of the ddl ftsQ region.

Authors:  A C Robinson; D J Kenan; J Sweeney; W D Donachie
Journal:  J Bacteriol       Date:  1986-09       Impact factor: 3.490

6.  Improved single and multicopy lac-based cloning vectors for protein and operon fusions.

Authors:  R W Simons; F Houman; N Kleckner
Journal:  Gene       Date:  1987       Impact factor: 3.688

7.  Transcriptional organization within an Escherichia coli cell division gene cluster: direction of transcription of the cell separation gene envA.

Authors:  N F Sullivan; W D Donachie
Journal:  J Bacteriol       Date:  1984-11       Impact factor: 3.490

8.  DNA sequence and transcriptional organization of essential cell division genes ftsQ and ftsA of Escherichia coli: evidence for overlapping transcriptional units.

Authors:  A C Robinson; D J Kenan; G F Hatfull; N F Sullivan; R Spiegelberg; W D Donachie
Journal:  J Bacteriol       Date:  1984-11       Impact factor: 3.490

9.  Determination of transcriptional units and gene products from the ftsA region of Escherichia coli.

Authors:  J F Lutkenhaus; H C Wu
Journal:  J Bacteriol       Date:  1980-09       Impact factor: 3.490

10.  Analysis of cell division gene ftsZ (sulB) from gram-negative and gram-positive bacteria.

Authors:  J C Corton; J E Ward; J Lutkenhaus
Journal:  J Bacteriol       Date:  1987-01       Impact factor: 3.490

View more
  4 in total

1.  Epitope mapping of Escherichia coli cell division protein FtsZ with monoclonal antibodies.

Authors:  J L Voskuil; C A Westerbeek; C Wu; A H Kolk; N Nanninga
Journal:  J Bacteriol       Date:  1994-04       Impact factor: 3.490

Review 2.  Metabolic alarms and cell division in Escherichia coli.

Authors:  D Joseleau-Petit; D Vinella; R D'Ari
Journal:  J Bacteriol       Date:  1999-01       Impact factor: 3.490

Review 3.  Fundamental principles in bacterial physiology-history, recent progress, and the future with focus on cell size control: a review.

Authors:  Suckjoon Jun; Fangwei Si; Rami Pugatch; Matthew Scott
Journal:  Rep Prog Phys       Date:  2018-01-09

4.  The Q gene of Rhodobacter sphaeroides: its role in puf operon expression and spectral complex assembly.

Authors:  L Gong; J K Lee; S Kaplan
Journal:  J Bacteriol       Date:  1994-05       Impact factor: 3.490

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.