Literature DB >> 1943994

Genetic competence in Bacillus subtilis.

D Dubnau1.   

Abstract

Genetic competence may be defined as a physiological state enabling a bacterial culture to bind and take up high-molecular-weight exogenous DNA (transformation). In Bacillus subtilis, competence develops postexponentially and only in certain media. In addition, only a minority of the cells in a competent culture become competent, and these are physiologically distinct. Thus, competence is subject to three regulatory modalities: growth stage specific, nutritionally responsive, and cell type specific. This review summarizes the present state of knowledge concerning competence in B. subtilis. The study of genes required for transformability has permitted their classification into two broad categories. Late competence genes are expressed under competence control and specify products required for the binding, uptake, and processing of transforming DNA. Regulatory genes specify products that are needed for the expression of the late genes. Several of the late competence gene products have been shown to be membrane localized, and others are predicted to be membrane associated on the basis of amino acid sequence data. Several of these predicted protein sequences show a striking resemblance to gene products that are involved in the export and/or assembly of extracellular proteins and structures in gram-negative organisms. This observation is consistent with the idea that the late products are directly involved in transport of DNA and is equally consistent with the notion that they play a morphogenetic role in the assembly of a transport apparatus. The competence regulatory apparatus constitutes an elaborate signal transduction system that senses and interprets environmental information and passes this information to the competence-specific transcriptional machinery. Many of the regulatory gene products have been identified and partially characterized, and their interactions have been studied genetically and in some cases biochemically as well. These include several histidine kinase and response regulator members of the bacterial two-component signal transduction machinery, as well as a number of known transcriptionally active proteins. Results of genetic studies are consistent with the notion that the regulatory proteins interact in a hierarchical way to make up a regulatory pathway, and it is possible to propose a provisional scheme for the organization of this pathway. It is remarkable that almost all of the regulatory gene products appear to play roles in the control of various forms of postexponential expression in addition to competence, e.g., sporulation, degradative-enzyme production, motility, and antibiotic production. This has led to the notion of a signal transduction network which transduces environmental information to determine the levels and timing of expression of the ultimate products characteristic of each of these systems.

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Year:  1991        PMID: 1943994      PMCID: PMC372826          DOI: 10.1128/mr.55.3.395-424.1991

Source DB:  PubMed          Journal:  Microbiol Rev        ISSN: 0146-0749


  201 in total

1.  Single-strand breakage on binding of DNA to cells in the genetic transformation of Diplococcus pneumoniae.

Authors:  S Lacks; B Greenberg
Journal:  J Mol Biol       Date:  1976-02-25       Impact factor: 5.469

2.  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

3.  The oligopeptide transport system of Bacillus subtilis plays a role in the initiation of sporulation.

Authors:  M Perego; C F Higgins; S R Pearce; M P Gallagher; J A Hoch
Journal:  Mol Microbiol       Date:  1991-01       Impact factor: 3.501

4.  Structure of deoxyribonucleic acid on the cell surface during uptake by pneumococcus.

Authors:  D A Morrison; W R Guild
Journal:  J Bacteriol       Date:  1973-09       Impact factor: 3.490

5.  Gene encoding the 37,000-dalton minor sigma factor of Bacillus subtilis RNA polymerase: isolation, nucleotide sequence, chromosomal locus, and cryptic function.

Authors:  M L Duncan; S S Kalman; S M Thomas; C W Price
Journal:  J Bacteriol       Date:  1987-02       Impact factor: 3.490

6.  Sequence and transcription mapping of Bacillus subtilis competence genes comB and comA, one of which is related to a family of bacterial regulatory determinants.

Authors:  Y Weinrauch; N Guillen; D A Dubnau
Journal:  J Bacteriol       Date:  1989-10       Impact factor: 3.490

7.  Cloning and characterization of DNA damage-inducible promoter regions from Bacillus subtilis.

Authors:  D L Cheo; K W Bayles; R E Yasbin
Journal:  J Bacteriol       Date:  1991-03       Impact factor: 3.490

8.  Poly-beta-hydroxybutyrate membrane structure and its relationship to genetic transformability in Escherichia coli.

Authors:  R N Reusch; T W Hiske; H L Sadoff
Journal:  J Bacteriol       Date:  1986-11       Impact factor: 3.490

9.  Transformation in Bacillus subtilis: purification and partial characterization of a membrane-bound DNA-binding protein.

Authors:  H Smith; K Wiersma; S Bron; G Venema
Journal:  J Bacteriol       Date:  1983-10       Impact factor: 3.490

10.  A membrane protein with similarity to N-methylphenylalanine pilins is essential for DNA binding by competent Bacillus subtilis.

Authors:  R Breitling; D Dubnau
Journal:  J Bacteriol       Date:  1990-03       Impact factor: 3.490

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  124 in total

1.  Transient growth requirement in Bacillus subtilis following the cessation of exponential growth.

Authors:  H M Sung; R E Yasbin
Journal:  Appl Environ Microbiol       Date:  2000-03       Impact factor: 4.792

Review 2.  Homologous genetic recombination as an intrinsic dynamic property of a DNA structure induced by RecA/Rad51-family proteins: a possible advantage of DNA over RNA as genomic material.

Authors:  T Shibata; T Nishinaka; T Mikawa; H Aihara; H Kurumizaka; S Yokoyama; Y Ito
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-17       Impact factor: 11.205

3.  On the evolutionary advantage of fitness-associated recombination.

Authors:  Lilach Hadany; Tuvik Beker
Journal:  Genetics       Date:  2003-12       Impact factor: 4.562

4.  Transcriptional regulation of Bacillus subtilis glucose starvation-inducible genes: control of gsiA by the ComP-ComA signal transduction system.

Authors:  J P Mueller; G Bukusoglu; A L Sonenshein
Journal:  J Bacteriol       Date:  1992-07       Impact factor: 3.490

5.  Differential action and differential expression of DNA polymerase I during Escherichia coli colony development.

Authors:  J A Shapiro
Journal:  J Bacteriol       Date:  1992-11       Impact factor: 3.490

6.  Not so simple, not so subtle: the interspecies competition between Bacillus simplex and Bacillus subtilis and its impact on the evolution of biofilms.

Authors:  Gili Rosenberg; Nitai Steinberg; Yaara Oppenheimer-Shaanan; Tsvia Olender; Shany Doron; Julius Ben-Ari; Alexandra Sirota-Madi; Zohar Bloom-Ackermann; Ilana Kolodkin-Gal
Journal:  NPJ Biofilms Microbiomes       Date:  2016-01-27       Impact factor: 7.290

7.  Characterization of YvcJ, a conserved P-loop-containing protein, and its implication in competence in Bacillus subtilis.

Authors:  Jennifer Luciano; Elodie Foulquier; Jean-Raphael Fantino; Anne Galinier; Frédérique Pompeo
Journal:  J Bacteriol       Date:  2008-12-12       Impact factor: 3.490

8.  Role of pili and the phase-variable PilC protein in natural competence for transformation of Neisseria gonorrhoeae.

Authors:  T Rudel; D Facius; R Barten; I Scheuerpflug; E Nonnenmacher; T F Meyer
Journal:  Proc Natl Acad Sci U S A       Date:  1995-08-15       Impact factor: 11.205

Review 9.  The sigma factors of Bacillus subtilis.

Authors:  W G Haldenwang
Journal:  Microbiol Rev       Date:  1995-03

10.  Inducible cell lysis system for the study of natural transformation and environmental fate of DNA released by cell death.

Authors:  D U Kloos; M Strätz; A Güttler; R J Steffan; K N Timmis
Journal:  J Bacteriol       Date:  1994-12       Impact factor: 3.490

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