Literature DB >> 4970228

Chromosomes in Bacillus subtilis spores and their segregation during germination.

H Yoshikawa.   

Abstract

Spores of a thymine-requiring mutant of Bacillus subtilis 168 leucine(-), indole(-), thymine(-)) were uniformly labeled with (3)H-thymidine. These were seeded on thinlayer agar plates where they germinated into long-chained microcolonies. Autoradiograms were used to measure the distribution of labeled deoxyribonucleic acid in the chains of cells, which ranged in length from 2 to 32 cells. Four major grain clusters appeared in most chains. These clusters were homogeneous in size; their grain numbers were distributed symmetrically from 9 to 15 with an average of 12.0. When three or fewer major clusters appeared in short chains, some of them were composed of two subclusters. However, there were always four clusters per chain when these subclusters were counted as individuals. Groupings containing two to eight grains appeared, as well as the four major clusters in longer chains. These minor groups were fragments of the major clusters. In contrast to the symmetrical distribution of major clusters, fragmented clusters were distributed at random, indicating random fragmentation. The total number of major and minor clusters increased at a constant exponential rate when measured against total cell number per chain, i.e., number of generations. It was calculated from the rate that a detectable fragmentation, at least 16% of a conserved unit (defined as a single strand of the complete chromosome), occurred every 6.0 generations. These results led us to conclude that each B. subtilis spore contained four conserved units or two completed chromosomes. Segregation of the four units into progeny cells was almost random. The one notable exception was a conserved unit which frequently appeared in a terminal cell to which an empty spore coat was attached. The presence of two chromosomes in the spore is consistent with our proposed structure of the completed chromosome, in which two sister chromosomes are covalently linked at the initiation region. This double chromosome may be incorporated into the spore without further structural change.

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Year:  1968        PMID: 4970228      PMCID: PMC315164          DOI: 10.1128/jb.95.6.2282-2292.1968

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


  14 in total

1.  SEQUENTIAL REPLICATION OF THE BACILLUS SUBTILIS CHROMOSOME. 3. REGULATION OF INITIATION.

Authors:  H YOSHIKAWA; A O'SULLIVAN; N SUEOKA
Journal:  Proc Natl Acad Sci U S A       Date:  1964-10       Impact factor: 11.205

2.  The organization and replication of deoxyribonucleic acid in thymine-deficient strains of Escherichia coli.

Authors:  F FORRO; S A WERTHEIMER
Journal:  Biochim Biophys Acta       Date:  1960-05-06

3.  Mutations Resulting from the Transformation of BACILLUS SUBTILIS.

Authors:  H Yoshikawa
Journal:  Genetics       Date:  1966-11       Impact factor: 4.562

4.  The initiation of DNA replication in Bacillus subtilis.

Authors:  H Yoshikawa
Journal:  Proc Natl Acad Sci U S A       Date:  1967-07       Impact factor: 11.205

5.  Sequential replication of the Bacillus subtilis chromosome. IV. Genetic mapping by density transfer experiment.

Authors:  A O'Sullivan; N Sueoka
Journal:  J Mol Biol       Date:  1967-07-28       Impact factor: 5.469

6.  [Segregation of the nuclei during growth and germination of B. subtilis].

Authors:  A Ryter; F Jacob
Journal:  C R Acad Hebd Seances Acad Sci D       Date:  1967-05-03

7.  Chromosome replication in Bacillus subtilis cultures growing at different rates.

Authors:  H Eberle; K G Lark
Journal:  Proc Natl Acad Sci U S A       Date:  1967-01       Impact factor: 11.205

8.  Autoradiography of the Bacillus subtilis chromosome.

Authors:  E S Dennis; R G Wake
Journal:  J Mol Biol       Date:  1966-02       Impact factor: 5.469

Review 9.  Regulation of chromosome replication and segregation in bacteria.

Authors:  K G Lark
Journal:  Bacteriol Rev       Date:  1966-03

10.  Autoradiographic studies of bacterial chromosome replication in amino-acid deficient Escherichia coli 15T-.

Authors:  F Forro
Journal:  Biophys J       Date:  1965-09       Impact factor: 4.033

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  10 in total

1.  Completed Bacillus subtilis nucleoid as a doublet structure.

Authors:  T McGinness; R G Wake
Journal:  J Bacteriol       Date:  1979-11       Impact factor: 3.490

2.  DNA Comparisons among Barley, Oats, Rye, and Wheat.

Authors:  A J Bendich; B J McCarthy
Journal:  Genetics       Date:  1970-08       Impact factor: 4.562

3.  Unintegrated ribosomal genes in diploid and polytene tissues of Drosophila melanogaster.

Authors:  C I Zuchowski; A G Harford
Journal:  Chromosoma       Date:  1976-11-19       Impact factor: 4.316

4.  Cosegregation of cell wall and DNA in Bacillus subtilis.

Authors:  J M Schlaeppi; D Karamata
Journal:  J Bacteriol       Date:  1982-12       Impact factor: 3.490

5.  Ultraviolet sensitivity of Bacillus subtilis spores upon germination and outgrowth.

Authors:  N Munakata
Journal:  J Bacteriol       Date:  1974-10       Impact factor: 3.490

6.  Velocity of chromosome replication in thymine-requiring and independent strains of Bacillus subtilis.

Authors:  E Ephrati-Elizur; S Borenstein
Journal:  J Bacteriol       Date:  1971-04       Impact factor: 3.490

7.  Segregation of Bacillus subtilis chromosomes radioactively labeled during the first round of replication after germination of spores.

Authors:  R G Wake
Journal:  J Bacteriol       Date:  1976-07       Impact factor: 3.490

8.  Initiation of deoxyribonucleic acid replication in germinating spores of Bacillus subtilis 168 carrying the dnaB (Ts)134 mutation.

Authors:  H Callister; S Le Mesurier; R G Wake
Journal:  J Bacteriol       Date:  1977-06       Impact factor: 3.490

9.  Defective bacteriophage PBSH in Bacillus subtilis. II. Intracellular development of the induced prophage.

Authors:  M Haas; H Yoshikawa
Journal:  J Virol       Date:  1969-02       Impact factor: 5.103

10.  Cell wall and DNA cosegregation in Bacillus subtilis studied by electron microscope autoradiography.

Authors:  J M Schlaeppi; O Schaefer; D Karamata
Journal:  J Bacteriol       Date:  1985-10       Impact factor: 3.490

  10 in total

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