Abstracts - faqs.org

Abstracts

Biological sciences

Search abstracts:
Abstracts » Biological sciences

Direct binding of FtsZ to ZipA, an essential component of the septal ring structure that mediates cell division in E. coli

Article Abstract:

FtsZ is a soluble, tubulin-like GTPase that produces a membrane-associated ring at the division site of bacterial cells. FtsZ was found to bind directly to a unique integral inner-membrane protein in Escherichia coli which is designated as ZipA. Genetic and morphological evidence show that this interaction is needed for cells division. Also, a fluorescent ZipA-Gfp fusion protein is situated in a ring structure at the division site. Therefore, ZipA is a crucial component of the division mechanism and may be directly involved in the assembly and/or function of the FtsZ ring.

Author: Boer, Piet A.J. de, Hale, Cynthia A.
Publisher: Elsevier B.V.
Publication Name: Cell
Subject: Biological sciences
ISSN: 0092-8674
Year: 1997
Cell division, Guanosine triphosphatase

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Survival of hunger and stress: the role of rpoS in early stationary phase genen regulation in E. coli

Article Abstract:

The rpoS is a stationary-phase induced gene acting as regulator that is essential to gene expression during feast-to-famine transition in Escherichia coli. This regulator is strongly homologous to the vegetative sigma factor, indicating that it acts as an alternative sigma subunit of RNA polymerase. Several rpoS-dependent genes and their corresponding cellular functions have also been identified. In addition, related studies implicate the rpoS gene as an osmoregulatory gene.

Author: Hengge-Aronis, Regine
Publisher: Elsevier B.V.
Publication Name: Cell
Subject: Biological sciences
ISSN: 0092-8674
Year: 1993
Cell cycle

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


On-line monitoring of gene expression

Article Abstract:

Research was conducted to determine the gene expression in cultures of Escherichia coli in situ and online via an electrochemical sensor. The transcriptional fusion of lacZ to the RpoS-dependent osmY gene was used to monitor the online progress of E. coli into stationary phase. Results indicate that the method used will be useful in determining the activity of any promoter with a variety of reporter genes.

Author: Ron, Eliora Z., Hengge-Aronis, Regine, Biran, Israel, Klimentiy, Levcov, Rishpon, Judith
Publisher: Society for General Microbiology
Publication Name: Microbiology
Subject: Biological sciences
ISSN: 1350-0872
Year: 1999
Usage, Genetic aspects, Electrochemical apparatus, Electrochemical instruments

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Subjects list: Research, Escherichia coli, Gene expression
Similar abstracts:
  • Abstracts: Induction of ploidy level increments in an asporogenous industrial strain ofthe yeast Saccharomyces cerevisiae by UV irradiation
  • Abstracts: Methods involving light variation for isolation of cyanobacteria: characterization of isolates from central Australia
  • Abstracts: Production of citric and oxalic acids and solubilization of calcium phosphate by Penicillium bilaii. Manganese peroxidase-dependent oxidation of glyoxylic and oxalic acids synthesized by Ceriporiopsis subvermispora produces extracellular hydrogen peroxide
  • Abstracts: Effect of growth temperature on fatty acid composition of ten Thermus strains. Effect of temperature on fatty acid composition of a white Thermus strain
  • Abstracts: Isozyme variation in Californian and Turkish populations of the colonizing species Trifolium hirtum. Segregation distortion at isozyme locus Lap-1 in Schlumbergera (Cactaceae) is caused by linkage with the gametophytic self-incompatibility (S) locus
This website is not affiliated with document authors or copyright owners. This page is provided for informational purposes only. Unintentional errors are possible.
Some parts © 2025 Advameg, Inc.