Literature DB >> 40135

Competence for genetic transformation in pneumococcus depends on synthesis of a small set of proteins.

D A Morrison, M F Baker.   

Abstract

In bacterial genetic transformation the uptake of DNA and its integration into the resident chromosome is dependent on a special cellular state, termed competence. In those species where appearance of competence has been studied, specific (but often poorly defined) growth conditions lead to a simultaneous development of competence in a substantial fraction of the cells in a culture. In Bacillus subtilis, and in Haemophilus species, competence appears in the stationary phase of growth or in certain other growth-limiting conditions. Streptococcus pneumoniae (pneumococcus) is perhaps unusual in that virtually all cells of a culture become competent, for a short period at a specific cell density during logarithmic growth, without perturbing the growth rate. The synchronous appearance of competence in pneumococcal cultures results from an autocatalytic effect of a small protein released by the cells that induces competence. The response to competence factor has been shown to require protein synthesis. We report here additional information on the nature of competence in pneumococcus: pulse-labelling studies show that for the brief period of competence protein synthesis is restricted to a few specific polypeptides.

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Year:  1979        PMID: 40135     DOI: 10.1038/282215a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  48 in total

1.  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

2.  Genetic transformation in Streptococcus pneumoniae: molecular cloning and characterization of recP, a gene required for genetic recombination.

Authors:  D K Rhee; D A Morrison
Journal:  J Bacteriol       Date:  1988-02       Impact factor: 3.490

3.  An unstable competence-induced protein, CoiA, promotes processing of donor DNA after uptake during genetic transformation in Streptococcus pneumoniae.

Authors:  Bhushan V Desai; Donald A Morrison
Journal:  J Bacteriol       Date:  2006-07       Impact factor: 3.490

4.  Identification of the major protein component of the pneumococcal eclipse complex.

Authors:  Donald A Morrison; Isabelle Mortier-Barrière; Laetitia Attaiech; Jean-Pierre Claverys
Journal:  J Bacteriol       Date:  2007-06-29       Impact factor: 3.490

5.  The spo0K locus of Bacillus subtilis is homologous to the oligopeptide permease locus and is required for sporulation and competence.

Authors:  D Z Rudner; J R LeDeaux; K Ireton; A D Grossman
Journal:  J Bacteriol       Date:  1991-02       Impact factor: 3.490

6.  Transient association of an alternative sigma factor, ComX, with RNA polymerase during the period of competence for genetic transformation in Streptococcus pneumoniae.

Authors:  Ping Luo; Donald A Morrison
Journal:  J Bacteriol       Date:  2003-01       Impact factor: 3.490

7.  Competence for genetic transformation in Streptococcus pneumoniae: molecular cloning of com, a competence control locus.

Authors:  M S Chandler; D A Morrison
Journal:  J Bacteriol       Date:  1987-05       Impact factor: 3.490

8.  Identification of a Streptococcus pneumoniae gene locus encoding proteins of an ABC phosphate transporter and a two-component regulatory system.

Authors:  R Novak; A Cauwels; E Charpentier; E Tuomanen
Journal:  J Bacteriol       Date:  1999-02       Impact factor: 3.490

9.  Natural genetic transformation in Streptococcus gordonii: comX imparts spontaneous competence on strain wicky.

Authors:  R D Lunsford; J London
Journal:  J Bacteriol       Date:  1996-10       Impact factor: 3.490

10.  Isolation and characterization of three new classes of transformation-deficient mutants of Streptococcus pneumoniae that are defective in DNA transport and genetic recombination.

Authors:  D A Morrison; S A Lacks; W R Guild; J M Hageman
Journal:  J Bacteriol       Date:  1983-10       Impact factor: 3.490

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