Scinovex
review Open AccessTop 1% cited

Quorum sensing by peptide pheromones and two‐component signal‐transduction systems in Gram‐positive bacteria

Molecular Microbiology · 1997 · Vol. 24(5) · pp. 895–904
Michiel KleerebezemLuis E. N. QuadriOscar P. KuipersWillem M. de Vos

Abstract

Cell-density-dependent gene expression appears to be widely spread in bacteria. This quorum-sensing phenomenon has been well established in Gram-negative bacteria, where N-acyl homoserine lactones are the diffusible communication molecules that modulate cell-density-dependent phenotypes. Similarly, a variety of processes are known to be regulated in a cell-density- or growth-phase-dependent manner in Gram-positive bacteria. Examples of such quorum-sensing modes in Gram-positive bacteria are the development of genetic competence in Bacillus subtilis and Streptococcus pneumoniae, the virulence response in Staphylococcus aureus, and the production of antimicrobial peptides by several species of Gram-positive bacteria including lactic acid bacteria. Cell-density-dependent regulatory modes in these systems appear to follow a common theme, in which the signal molecule is a post-translationally processed peptide that is secreted by a dedicated ATP-binding-cassette exporter. This secreted peptide pheromone functions as the input signal for a specific sensor component of a two-component signal-transduction system. Moreover, genetic linkage of the common elements involved results in autoregulation of peptide-pheromone production.

Probiotics and Fermented FoodsBiochemical Analysis and Sensing TechniquesAdvanced Chemical Sensor TechnologiesQuorum sensingBiologyBacteriaBacillus subtilisHomoserineTwo-component regulatory systemSignal transductionMicrobiologyGram-negative bacteriaCell signaling

MeSH terms

Amino Acid SequenceAnti-Bacterial AgentsBacterial ProteinsBacteriocinsGram-Positive BacteriaMolecular Sequence DataNisinPeptidesPheromonesVirulenceSignal Transduction
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.