Literature DB >> 4962301

Development of competence in the Bacillus subtilis transformation system.

K F Bott, G A Wilson.   

Abstract

Competence in Bacillus subtilis, assayed by the ability of cells to be transformed with bacterial deoxyribonucleic acid (DNA) or transfected by phage DNA, has been shown to occur in a single semisynthetic medium with peak activity occurring 3 hr after the cessation of logarithmic growth. No step-down conditions or culture manipulations were necessary for routine transfection of 1% of the population. The results demonstrate that bacteriophage DNA is a valid assay for studying the development of competence in B. subtilis. Predictions of workers using transforming bacterial DNA, who have suggested that competence in B. subtilis is associated with a specific phase of growth, are substantiated. The peak of competence is not affected by marked differences in the rate of growth during the logarithmic phase. The effect on development of competence by this procedure of some components (including casein hydrolysate, tryptophan, and histidine) which were routinely included in the transformation medium by other investigators has been determined by use of infectious phage DNA as an assay. We have demonstrated that tryptophan, as well as histidine, increases the transformation frequency-even in strains which do not have auxotrophic demands for these components. Glutamic acid and alanine depress optimal levels of transfection.

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Year:  1967        PMID: 4962301      PMCID: PMC251923          DOI: 10.1128/jb.94.3.562-570.1967

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


  18 in total

1.  Physiological and genetic factors affecting transformation of Bacillus subtilis.

Authors:  F E YOUNG; J SPIZIZEN
Journal:  J Bacteriol       Date:  1961-05       Impact factor: 3.490

2.  Genetic activity of deoxyribonucleic acid in the reconstitution of biosynthetic pathways.

Authors:  J SPIZIZEN
Journal:  Fed Proc       Date:  1959-12

3.  REQUIREMENTS FOR TRANSFORMATION IN BACILLUS SUBTILIS.

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

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.  Impaired transformability of Bacillus subtilis mutant sensitive to mitomycin C and ultraviolet radiation.

Authors:  S Okubo; W R Romig
Journal:  J Mol Biol       Date:  1966-02       Impact factor: 5.469

6.  Variation in the chemical composition of the cell walls of Bacillus subtilis during growth in different media.

Authors:  F E Young
Journal:  Nature       Date:  1965-07-03       Impact factor: 49.962

7.  Autolytic enzyme associated with cell walls of Bacillus subtilis.

Authors:  F E Young
Journal:  J Biol Chem       Date:  1966-08-10       Impact factor: 5.157

8.  Structure of Bacillus subtilis bacteriophage phi 29 and the length of phi 29 deoxyribonucleic acid.

Authors:  D L Anderson; D D Hickman; B E Reilly
Journal:  J Bacteriol       Date:  1966-05       Impact factor: 3.490

9.  BACTERIOPHAGE DEOXYRIBONUCLEATE INFECTION OF COMPETENT BACILLUS SUBTILIS.

Authors:  B E REILLY; J SPIZIZEN
Journal:  J Bacteriol       Date:  1965-03       Impact factor: 3.490

10.  INCORPORATION OF DEOXYRIBONUCLEIC ACID IN THE BACILLUS SUBTILIS TRANSFORMATION SYSTEM.

Authors:  F E YOUNG; J SPIZIZEN
Journal:  J Bacteriol       Date:  1963-09       Impact factor: 3.490

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  85 in total

1.  Bacillus subtilis mutants dependent on streptomycin.

Authors:  G R Quan; K M Campbell; G H Chambliss
Journal:  Mol Gen Genet       Date:  1979-09

2.  Membrane enrichment of genetic markers close to the origin and terminus during the deoxyribonucleic acid replication cycle in Bacillus subtilis.

Authors:  J Beeson; N Sueoka
Journal:  J Bacteriol       Date:  1979-09       Impact factor: 3.490

3.  Tracing the domestication of a biofilm-forming bacterium.

Authors:  Anna L McLoon; Sarah B Guttenplan; Daniel B Kearns; Roberto Kolter; Richard Losick
Journal:  J Bacteriol       Date:  2011-01-28       Impact factor: 3.490

4.  Cloning and expression in Escherichia coli of chromosomal mercury resistance genes from a Bacillus sp.

Authors:  Y Wang; I Mahler; H S Levinson; H O Halvorson
Journal:  J Bacteriol       Date:  1987-10       Impact factor: 3.490

5.  Production and Regeneration of Lactobacillus casei Protoplasts.

Authors:  L J Lee-Wickner; B M Chassy
Journal:  Appl Environ Microbiol       Date:  1984-11       Impact factor: 4.792

6.  Cloning and expression of a Bacillus subtilis division initiation gene for which a homolog has not been identified in another organism.

Authors:  E J Harry; R G Wake
Journal:  J Bacteriol       Date:  1989-12       Impact factor: 3.490

7.  Genetic mapping of a mutation causing an alteration in Bacillus subtilis ribosomal protein S4.

Authors:  T M Henkin; G H Chambliss
Journal:  Mol Gen Genet       Date:  1984

8.  Selective expression of a plasmid cat gene at a late stage of Bacillus subtilis sporulation.

Authors:  S Mongkolsuk; P S Lovett
Journal:  Proc Natl Acad Sci U S A       Date:  1984-06       Impact factor: 11.205

9.  Genetic and biochemical characterization of mutants of Bacillus subtilis defective in succinate dehydrogenase.

Authors:  M Ohné; B Rutberg; J A Hoch
Journal:  J Bacteriol       Date:  1973-09       Impact factor: 3.490

10.  Bacillus pumilus plasmid pPL10: properties and insertion into Bacillus subtilis 168 by transformation.

Authors:  P S Lovett; E J Duvall; K M Keggins
Journal:  J Bacteriol       Date:  1976-08       Impact factor: 3.490

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