» Articles » PMID: 23279213

Quorum-sensing Regulation of a Capsular Polysaccharide Receptor for the Rhodobacter Capsulatus Gene Transfer Agent (RcGTA)

Overview
Journal Mol Microbiol
Date 2013 Jan 3
PMID 23279213
Citations 38
Authors
Affiliations
Soon will be listed here.
Abstract

The gene transfer agent produced by Rhodobacter capsulatus (RcGTA) resembles a small tailed bacteriophage that packages almost random genomic DNA segments that may be transferred to other R. capsulatus cells. Gene transfer agents are produced by a number of prokaryotes; however, no receptors have been identified. We investigated the RcGTA recipient capability of wild-type R. capsulatus cells at different culture growth phases, and found that the frequency of RcGTA-dependent acquisition of an allele increases as cultures enter the stationary phase. We also found that RcGTA adsorption to cells follows a similar trend. RcGTA recipient capability and adsorption were found to be dependent on the GtaR/I quorum-sensing (QS) system. Production of an extracellular polysaccharide was found to be regulated by GtaR/I QS, as was production of the cell capsule. A number of QS-regulated putative polysaccharide biosynthesis genes were identified, and mutagenesis of two of these genes, rcc01081 and rcc01932, yielded strains that lack a capsule. Furthermore, these mutants were impaired in RcGTA recipient capability and adsorption, as was a non-encapsulated wild-type isolate of R. capsulatus. Overall, our results indicate that capsular polysaccharide is a receptor for the gene transfer agent of R. capsulatus, RcGTA.

Citing Articles

Gene transfer agents: The ambiguous role of selfless viruses in genetic exchange and bacterial evolution.

Fogg P Mol Microbiol. 2024; 123(2):124-131.

PMID: 38511257 PMC: 11841831. DOI: 10.1111/mmi.15251.


Bacterial capsules: Occurrence, mechanism, and function.

Gao S, Jin W, Quan Y, Li Y, Shen Y, Yuan S NPJ Biofilms Microbiomes. 2024; 10(1):21.

PMID: 38480745 PMC: 10937973. DOI: 10.1038/s41522-024-00497-6.


Co-evolution of gene transfer agents and their alphaproteobacterial hosts.

Kogay R, Zhaxybayeva O J Bacteriol. 2024; 206(2):e0039823.

PMID: 38240570 PMC: 10883770. DOI: 10.1128/jb.00398-23.


Structural insights into the iron nitrogenase complex.

Schmidt F, Schulz L, Zarzycki J, Prinz S, Oehlmann N, Erb T Nat Struct Mol Biol. 2023; 31(1):150-158.

PMID: 38062208 PMC: 10803253. DOI: 10.1038/s41594-023-01124-2.


Diversity and conservation of the genome architecture of phages infecting the Alphaproteobacteria.

Hyde J, Armond T, Herring J, Hope S, Grose J, Breakwell D Microbiol Spectr. 2023; 12(1):e0282723.

PMID: 37991376 PMC: 10783043. DOI: 10.1128/spectrum.02827-23.


References
1.
Lang A, Zhaxybayeva O, Beatty J . Gene transfer agents: phage-like elements of genetic exchange. Nat Rev Microbiol. 2012; 10(7):472-82. PMC: 3626599. DOI: 10.1038/nrmicro2802. View

2.
Peterson G . Determination of total protein. Methods Enzymol. 1983; 91:95-119. DOI: 10.1016/s0076-6879(83)91014-5. View

3.
Bottomley M, Muraglia E, Bazzo R, Carfi A . Molecular insights into quorum sensing in the human pathogen Pseudomonas aeruginosa from the structure of the virulence regulator LasR bound to its autoinducer. J Biol Chem. 2007; 282(18):13592-600. DOI: 10.1074/jbc.M700556200. View

4.
Weckesser J, Drews G, FROMME I . Chemical analysis of and degradation studies on the cell wall lipopolysaccharide of Rhodopseudomonas capsulata. J Bacteriol. 1972; 109(3):1106-13. PMC: 247331. DOI: 10.1128/jb.109.3.1106-1113.1972. View

5.
Davies D, Parsek M, Pearson J, Iglewski B, Costerton J, Greenberg E . The involvement of cell-to-cell signals in the development of a bacterial biofilm. Science. 1998; 280(5361):295-8. DOI: 10.1126/science.280.5361.295. View