Literature DB >> 6185466

Formation of competent Bacillus subtilis cells.

Y Sadaie, T Kada.   

Abstract

The process of competent cell formation for transformation has been studied with early-stationary-phase (T1) cells of Bacillus subtilis which had been grown in an enriched Spizizen minimal medium and transferred to a second synthetic medium. Rifampin, chloramphenicol, and tunicamycin were strong inhibitors of competent cell formation, as well as vegetative growth. After formation, competent cells were no longer sensitive to the above agents. Methicillin and an inhibitor of chromosomal replication, hydroxyphenylazouracil, did not inhibit the development of competence. A D-alanine-requiring mutant strain developed competence even in the absence of D-alanine in the second medium. A T1-stage culture showed the activity of extracellular serine protease which is necessary for sporulation. Competent cell formation was completely blocked by 0.7 M ethanol, which is a specific inhibitor of early events during sporulation, including forespore septum formation. Competent cells were formed even in media which supported sporulation. The development of competence was also studied with spo0 mutants at 10 different loci. Most spo0 mutations repressed the development of competence except for spo0C, spo0G, and spo0J. These results suggest that competent cells are formed from early sporulating cells with the synthesis of cell wall materials and by factors whose genes are activated by the supply of nutrients. It is suggested that common steps are involved both in forespore septation and in competent cell formation.

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Year:  1983        PMID: 6185466      PMCID: PMC221700          DOI: 10.1128/jb.153.2.813-821.1983

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  34 in total

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Authors:  C Anagnostopoulos; J Spizizen
Journal:  J Bacteriol       Date:  1961-05       Impact factor: 3.490

2.  Tunicamycin inhibition of bacterial wall polymer synthesis.

Authors:  J B Ward
Journal:  FEBS Lett       Date:  1977       Impact factor: 4.124

Review 3.  Polarity and topology of DNA segregation and septation in cells and sporangia of the bacilli.

Authors:  A D Hitchins
Journal:  Can J Microbiol       Date:  1978-10       Impact factor: 2.419

4.  Transformation in Bacillus subtilis. II. The development and maintenance of the competent state.

Authors:  H O Kammen; R J Wojnar; E S Canellakis
Journal:  Biochim Biophys Acta       Date:  1966-07-20

5.  Repair deficiency, mutator activity, and thermal prophage inducibility in dna-8132 strains of Bacillus subtilis.

Authors:  Y Sadaie; K Narui
Journal:  J Bacteriol       Date:  1976-06       Impact factor: 3.490

6.  Criteria for categorizing early biochemical events occurring during sporulation of Bacillus subtilis.

Authors:  B N Dancer; J Mandelstam
Journal:  J Bacteriol       Date:  1975-02       Impact factor: 3.490

7.  Lipid intermediates in the biosynthesis of the linkage unit between teichoic acids and peptidoglycan.

Authors:  H A McArthur; F M Roberts; I C Hancock; J Baddiley
Journal:  FEBS Lett       Date:  1978-02-15       Impact factor: 4.124

8.  Uptake of DNA by competent bacteria--a possible mechanism.

Authors:  A Akrigg; S R Ayad; J Blamire
Journal:  J Theor Biol       Date:  1969-09       Impact factor: 2.691

9.  Autolytic enzyme-deficient mutants of Bacillus subtilis 168.

Authors:  J E Fein; H J Rogers
Journal:  J Bacteriol       Date:  1976-09       Impact factor: 3.490

10.  Inhibition of a DNA polymerase from Bacillus subtilis by hydroxyphenylazopyrimidines.

Authors:  K B Gass; R L Low; N R Cozzarelli
Journal:  Proc Natl Acad Sci U S A       Date:  1973-01       Impact factor: 11.205

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  31 in total

1.  Enhancement of secretion and extracellular stability of staphylokinase in Bacillus subtilis by wprA gene disruption.

Authors:  S J Lee; D M Kim; K H Bae; S M Byun; J H Chung
Journal:  Appl Environ Microbiol       Date:  2000-02       Impact factor: 4.792

2.  Suppression of early competence mutations in Bacillus subtilis by mec mutations.

Authors:  M Roggiani; J Hahn; D Dubnau
Journal:  J Bacteriol       Date:  1990-07       Impact factor: 3.490

3.  Identification of proteins phosphorylated by ATP during sporulation of Bacillus subtilis.

Authors:  C Mitchell; P W Morris; J C Vary
Journal:  J Bacteriol       Date:  1992-04       Impact factor: 3.490

4.  Sequence and properties of comQ, a new competence regulatory gene of Bacillus subtilis.

Authors:  Y Weinrauch; T Msadek; F Kunst; D Dubnau
Journal:  J Bacteriol       Date:  1991-09       Impact factor: 3.490

5.  Localization of a new promoter, P5, in the sigA operon of Bacillus subtilis and its regulation in some spo mutant strains.

Authors:  F X Qi; X S He; R H Doi
Journal:  J Bacteriol       Date:  1991-11       Impact factor: 3.490

6.  Growth stage signal transduction and the requirements for srfA induction in development of competence.

Authors:  J Hahn; D Dubnau
Journal:  J Bacteriol       Date:  1991-11       Impact factor: 3.490

7.  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

8.  The effect of spo0 mutations on the expression of spo0A- and spo0F-lacZ fusions.

Authors:  S Yamashita; H Yoshikawa; F Kawamura; H Takahashi; T Yamamoto; Y Kobayashi; H Saito
Journal:  Mol Gen Genet       Date:  1986-10

9.  Construction of a Bacillus subtilis double mutant deficient in extracellular alkaline and neutral proteases.

Authors:  F Kawamura; R H Doi
Journal:  J Bacteriol       Date:  1984-10       Impact factor: 3.490

10.  The primary role of comA in establishment of the competent state in Bacillus subtilis is to activate expression of srfA.

Authors:  M M Nakano; P Zuber
Journal:  J Bacteriol       Date:  1991-11       Impact factor: 3.490

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