Literature DB >> 8878046

Regulation of competence for genetic transformation in Streptococcus pneumoniae by an auto-induced peptide pheromone and a two-component regulatory system.

E V Pestova1, L S Håvarstein, D A Morrison.   

Abstract

The regulation of competence for genetic transformation in Streptococcus pneumoniae depends on a quorum-sensing system, but the only molecular elements of the system whose specific role have been identified are an extracellular peptide signal and an ABC-transporter required for its export. Here we show that transcription of comC, the gene encoding a predicted 41-residue precursor peptide that is thought to be processed and secreted as the 17-residue mature competence activator, increased approximately 40-fold above its basal level of expression in response to exogenous synthetic activator, consistent with earlier experiments indicating that the activator acts autocatalytically. We also describe two new genes, comD and comE, that encode members of histidine protein kinase and response-regulator families and are linked to comC. Disruption of comE abolished both response to synthetic activator peptide and endogenous competence induction.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8878046     DOI: 10.1046/j.1365-2958.1996.501417.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  168 in total

1.  The Cpx envelope stress response is controlled by amplification and feedback inhibition.

Authors:  T L Raivio; D L Popkin; T J Silhavy
Journal:  J Bacteriol       Date:  1999-09       Impact factor: 3.490

2.  Mutational analysis and membrane topology of ComP, a quorum-sensing histidine kinase of Bacillus subtilis controlling competence development.

Authors:  F Piazza; P Tortosa; D Dubnau
Journal:  J Bacteriol       Date:  1999-08       Impact factor: 3.490

3.  Streptococcus gordonii biofilm formation: identification of genes that code for biofilm phenotypes.

Authors:  C Y Loo; D A Corliss; N Ganeshkumar
Journal:  J Bacteriol       Date:  2000-03       Impact factor: 3.490

4.  Construction and analysis of a library for random insertional mutagenesis in Streptococcus pneumoniae: use for recovery of mutants defective in genetic transformation and for identification of essential genes.

Authors:  M S Lee; B A Dougherty; A C Madeo; D A Morrison
Journal:  Appl Environ Microbiol       Date:  1999-05       Impact factor: 4.792

5.  Gene expression analysis of the Streptococcus pneumoniae competence regulons by use of DNA microarrays.

Authors:  S Peterson; R T Cline; H Tettelin; V Sharov; D A Morrison
Journal:  J Bacteriol       Date:  2000-11       Impact factor: 3.490

Review 6.  Microbial biofilms: from ecology to molecular genetics.

Authors:  M E Davey; G A O'toole
Journal:  Microbiol Mol Biol Rev       Date:  2000-12       Impact factor: 11.056

7.  Microarray-based identification of a novel Streptococcus pneumoniae regulon controlled by an autoinduced peptide.

Authors:  A de Saizieu; C Gardès; N Flint; C Wagner; M Kamber; T J Mitchell; W Keck; K E Amrein; R Lange
Journal:  J Bacteriol       Date:  2000-09       Impact factor: 3.490

8.  Induction of natural competence in Streptococcus pneumoniae triggers lysis and DNA release from a subfraction of the cell population.

Authors:  Hilde Steinmoen; Eivind Knutsen; Leiv Sigve Håvarstein
Journal:  Proc Natl Acad Sci U S A       Date:  2002-05-28       Impact factor: 11.205

9.  A novel type of conserved DNA-binding domain in the transcriptional regulators of the AlgR/AgrA/LytR family.

Authors:  Anastasia N Nikolskaya; Michael Y Galperin
Journal:  Nucleic Acids Res       Date:  2002-06-01       Impact factor: 16.971

10.  RegR, a global LacI/GalR family regulator, modulates virulence and competence in Streptococcus pneumoniae.

Authors:  Sabine Chapuy-Regaud; A David Ogunniyi; Nicole Diallo; Yvette Huet; Jean-François Desnottes; James C Paton; Sonia Escaich; Marie-Claude Trombe
Journal:  Infect Immun       Date:  2003-05       Impact factor: 3.441

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.