Biosynthesis of Peptide Signals in Gram-Positive Bacteria

被引:55
作者
Thoendel, Matthew [1 ]
Horswill, Alexander R. [1 ]
机构
[1] Univ Iowa, Dept Microbiol, Roy J & Lucille A Carver Coll Med, Iowa City, IA 52242 USA
来源
ADVANCES IN APPLIED MICROBIOLOGY, VOL 71 | 2010年 / 71卷
关键词
TO-CELL COMMUNICATION; QUORUM-SENSING SYSTEMS; FAECALIS PLASMID PCF10; STAPHYLOCOCCUS-AUREUS; ENTEROCOCCUS-FAECALIS; SEX-PHEROMONE; CYCLIC PEPTIDE; POSTTRANSLATIONAL MODIFICATION; LACTOBACILLUS-PLANTARUM; LISTERIA-MONOCYTOGENES;
D O I
10.1016/S0065-2164(10)71004-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Gram-positive bacteria coordinate social behavior by sensing the extracellular level of peptide signals. These signals are biosynthesized through divergent pathways and some possess unusual functional chemistry as a result of posttranslational modifications.in this chapter, the biosynthetic pathways of Bacillus intracellular signaling peptides, Enterococcus pheromones, Bacillus subtilis competence pheromones, and cyclic peptide signals from Staphylococcus and other bacteria are covered. With the increasing prevalence of the cyclic peptide signals in diverse Gram-positive bacteria, a focus on this biosynthetic mechanism and variations on the theme are discussed. Due to the importance of peptide systems in pathogenesis, there is emerging interest in quorum-quenching approaches for therapeutic intervention. The quenching strategies that have successfully blocked signal biosynthesis are also covered. As peptide signaling systems continue to be discovered, there is a growing need to understand the details of these communication mechanisms. This information will provide insight on how Gram-positives coordinate cellular events and aid strategies to target these pathways for infection treatments.
引用
收藏
页码:91 / 112
页数:22
相关论文
共 71 条
[1]   THE ACCESSORY GENE REGULATOR (AGR) CONTROLS STAPHYLOCOCCUS-AUREUS VIRULENCE IN A MURINE ARTHRITIS MODEL [J].
ABDELNOUR, A ;
ARVIDSON, S ;
BREMELL, T ;
RYDEN, C ;
TARKOWSKI, A .
INFECTION AND IMMUNITY, 1993, 61 (09) :3879-3885
[2]   Identification and characterization of a determinant (eep) on the Enterococcus faecalis chromosome that is involved in production of the peptide sex pheromone cAD1 [J].
An, FY ;
Sulavik, MC ;
Clewell, DB .
JOURNAL OF BACTERIOLOGY, 1999, 181 (19) :5915-5921
[3]   Identification of the cAD1 sex pheromone precursor in Enterococcus faecalis [J].
An, FY ;
Clewell, DB .
JOURNAL OF BACTERIOLOGY, 2002, 184 (07) :1880-1887
[4]   Specific activation of the Bacillus quorum-sensing systems by isoprenylated pheromone variants [J].
Ansaldi, M ;
Marolt, D ;
Stebe, T ;
Mandic-Mulec, I ;
Dubnau, D .
MOLECULAR MICROBIOLOGY, 2002, 44 (06) :1561-1573
[5]   ccfA, the genetic determinant for the cCF10 peptide pheromone in Enterococcus faecalis OG1RF [J].
Antiporta, MH ;
Dunny, GM .
JOURNAL OF BACTERIOLOGY, 2002, 184 (04) :1155-1162
[6]   Identification of the agr locus of Listeria monocytogenes:: Role in bacterial virulence [J].
Autret, N ;
Raynaud, C ;
Dubail, I ;
Berche, P ;
Charbit, A .
INFECTION AND IMMUNITY, 2003, 71 (08) :4463-4471
[7]   agr-mediated dispersal of Staphylococcus aureus biofilms [J].
Boles, Blaise R. ;
Horswill, Alexander R. .
PLOS PATHOGENS, 2008, 4 (04)
[8]   Molecular basis for group-specific activation of the virulence regulator PlcR by PapR heptapeptides [J].
Bouillaut, L. ;
Perchat, S. ;
Arold, S. ;
Zorrilla, S. ;
Slamti, L. ;
Henry, C. ;
Gohar, M. ;
Declerck, N. ;
Lereclus, D. .
NUCLEIC ACIDS RESEARCH, 2008, 36 (11) :3791-3801
[9]   Comparison of OG1RF and an isogenic fsrB deletion mutant by transcriptional analysis:: the Fsr system of Enterococcus faecalis is more than the activator of gelatinase and serine protease [J].
Bourgogne, A ;
Hilsenbeck, SG ;
Dunny, GM ;
Murray, BE .
JOURNAL OF BACTERIOLOGY, 2006, 188 (08) :2875-2884
[10]   Regulated intramembrane proteolysis: A control mechanism conserved from bacteria to humans [J].
Brown, MS ;
Ye, J ;
Rawson, RB ;
Goldstein, JL .
CELL, 2000, 100 (04) :391-398