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J Biol Chem


Title:Membrane anchoring of the AgrD N-terminal amphipathic region is required for its processing to produce a quorum-sensing pheromone in Staphylococcus aureus
Author(s):Zhang L; Lin J; Ji G;
Address:"Department of Microbiology and Immunology, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD 20814, USA"
Journal Title:J Biol Chem
Year:2004
Volume:20040303
Issue:19
Page Number:19448 - 19456
DOI: 10.1074/jbc.M311349200
ISSN/ISBN:0021-9258 (Print) 0021-9258 (Linking)
Abstract:"Quorum-sensing pheromones are signal molecules that are secreted from Gram-positive bacteria and utilized by these bacteria to communicate among individual cells to regulate their activities as a group through a cell density-sensing mechanism. Typically, these pheromones are processed from precursor polypeptides. The mechanisms of trafficking, processing, and modification of the precursor to generate a mature pheromone are unclear. In Staphylococcus aureus, AgrD is the propeptide for an autoinducing peptide (AIP) pheromone that triggers the Agr cell density-sensing system upon reaching a threshold and subsequently regulates expression of virulence factor genes. The transmembrane protein AgrB, encoded in the agr locus, is necessary for the processing of AgrD to produce mature AIP; however, it is not clear how AgrD interacts with AgrB and how this interaction results in the generation of mature AIP. In this study, we found that the AgrD propeptide was integrated into the cytoplasmic membrane by a conserved alpha-helical amphipathic motif in its N-terminal region. We demonstrated that membrane targeting of AgrD by this motif was required for the stabilization of AgrD and the production of mature AIP, although this region was not specifically involved in the interaction with AgrB. An artificial amphipathic peptide replacing the N-terminal amphipathic motif of AgrD directed the protein to the cytoplasmic membrane and enabled the production of AIP. Analysis of Bacillus ComX precursor protein sequences suggested that the amphipathic membrane-targeting motif might also exist in pheromone precursors of other Gram-positive bacteria"
Keywords:"Amino Acid Motifs Amino Acid Sequence Bacterial Proteins/biosynthesis/metabolism/*physiology Blotting, Western Cell Membrane/*metabolism Cytoplasm/metabolism Electrophoresis, Polyacrylamide Gel Escherichia coli/metabolism Gene Deletion Models, Biological;"
Notes:"MedlineZhang, Linsheng Lin, Jianqun Ji, Guangyong eng R01 AI 46445/AI/NIAID NIH HHS/ Research Support, U.S. Gov't, P.H.S. 2004/03/06 J Biol Chem. 2004 May 7; 279(19):19448-56. doi: 10.1074/jbc.M311349200. Epub 2004 Mar 3"

 
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Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
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