Literature DB >> 4985117

The messenger ribonucleic acid content of Bacillus subtilis 168.

J E Midgley.   

Abstract

Bacillus subtilis 168 messenger RNA was determined by DNA-RNA hybridization techniques, with denatured DNA immobilized upon cellulose nitrate membrane filters. The following results were obtained. (1) Cultures of B. subtilis, growing exponentially in enriched glucose-salts medium at 37 degrees , incorporated [5-(3)H]uracil into both ribosomal and messenger RNA fractions without the kinetic delay expected from the presence of the intracellular nucleotide pools. (2) However short the time of labelling with exogenous labelled uracil (down to 7sec.), 32-36% of the rapidly labelled RNA was messenger RNA and 68-64% was an RNA with the hybridization characteristics of ribosomal RNA. Analysis of the apparent nucleotide base composition of total (32)P-labelled rapidly labelled RNA and the two RNA fractions separated by hybridization at a DNA/RNA ratio 5:1 confirmed this finding. Of the rapidly labelled RNA, 31% readily hybridized with DNA at low DNA/RNA ratios and had an apparent base composition like that of the DNA, whereas 69% was hybridized only at low efficiency at low DNA/RNA ratios and had a composition identical with that of ribosomal RNA. (3) In cultures dividing every 48min. at 37 degrees , kinetic analysis of RNA labelled over a 20min. period showed that the average life-time of messenger RNA was 2.7-3.0min. and that its amount was 3.0% of the total RNA. (4) The hybridization of (3)H-labelled randomly labelled RNA with DNA at a DNA/RNA ratio 5:1 showed that 2.9% of the randomly labelled RNA had the characteristics of messenger RNA. (5) Experiments carried out as described by Pigott & Midgley (1968) indicated that hybridization at low DNA/RNA ratios (5:1) effectively accounted for all the messenger RNA in a given specimen. The efficiency coefficient of RNA hybridization lay within the range of 90-95% input, if an excess of DNA sites was offered for RNA binding. (6) These measurements are compared with other results obtained by different methods, and reasons for any major disagreement are suggested.

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Year:  1969        PMID: 4985117      PMCID: PMC1185087          DOI: 10.1042/bj1150171

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  29 in total

1.  The pattern of flow and sequential stages in bacterial nucleic acid synthesis.

Authors:  R BRITTEN
Journal:  Ann N Y Acad Sci       Date:  1963-05-10       Impact factor: 5.691

2.  INTERACTION OF COMPLEMENTARY RNA AND DNA.

Authors:  B J MCCARTHY; E T BOLTON
Journal:  J Mol Biol       Date:  1964-02       Impact factor: 5.469

3.  FRACTIONATION OF COMPLEMENTARY RNA.

Authors:  E T BOLTON; B J MCCARTHY
Journal:  J Mol Biol       Date:  1964-02       Impact factor: 5.469

4.  Studies on the breakdown of messenger RNA.

Authors:  C WOESE; S NAONO; R SOFFER; F GROS
Journal:  Biochem Biophys Res Commun       Date:  1963-06-20       Impact factor: 3.575

5.  A general method for the isolation of RNA complementary to DNA.

Authors:  E T BOLTON; B J McCARTHY
Journal:  Proc Natl Acad Sci U S A       Date:  1962-08       Impact factor: 11.205

6.  The Synthesis of Ribosomes in E. coli: III. Synthesis of Ribosomal RNA.

Authors:  B J McCarthy; R J Britten; R B Roberts
Journal:  Biophys J       Date:  1962-01       Impact factor: 4.033

7.  Titration of the gene sites on DNA by DNA-RNA hybridization. I. Problem of measurement.

Authors:  D Kennell; A Kotoulas
Journal:  J Mol Biol       Date:  1968-05-28       Impact factor: 5.469

8.  Mechanism of beta-galactosidase induction in Escherichia coli.

Authors:  R O Kaempfer; B Magasanik
Journal:  J Mol Biol       Date:  1967-08-14       Impact factor: 5.469

9.  RNA chain growth-rate in Escherichia coli.

Authors:  H Bremer; D Yuan
Journal:  J Mol Biol       Date:  1968-12-14       Impact factor: 5.469

10.  Characterization of rapidly labelled ribonucleic acid in Escherichia coli by deoxyribonucleic acid-ribonucleic acid hybridization.

Authors:  G H Pigott; J E Midgley
Journal:  Biochem J       Date:  1968-11       Impact factor: 3.857

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  8 in total

1.  Macromolecular synthesis accompanying the transition from spores to vegetative forms of Streptomyces granaticolor.

Authors:  K Mikulík; I Janda; H Masková; J Stastná; A Jiránová
Journal:  Folia Microbiol (Praha)       Date:  1977       Impact factor: 2.099

Review 2.  Extracellular enzyme synthesis in the genus Bacillus.

Authors:  F G Priest
Journal:  Bacteriol Rev       Date:  1977-09

3.  Synthesis of ribosomal ribonucleic acid during sporulation of Bacillus subtilis.

Authors:  C Bonamy; L Hirschbein; J Szulmajster
Journal:  J Bacteriol       Date:  1973-03       Impact factor: 3.490

4.  Synthesis of ribonucleic acid in purine-deficient Escherichia coli and a comparison with the effects of amino acid starvation.

Authors:  N F Varney; G A Thomas; K Burton
Journal:  Biochem J       Date:  1970-11       Impact factor: 3.857

5.  Ribosomal ribonucleic acid synthesis in Bacillus subtilis.

Authors:  R J Avery; J E Midgley
Journal:  Biochem J       Date:  1971-04       Impact factor: 3.857

6.  The control of ribonucleic acid synthesis in bacteria. Steady-state content of messenger ribonucleic acid in Escherichia coli M.R.E. 600.

Authors:  W J Gray; J E Midgley
Journal:  Biochem J       Date:  1970-11       Impact factor: 3.857

7.  Levels and Characteristics of mRNAs in Spores of Firmicute Species.

Authors:  Brandon Byrd; Emily Camilleri; George Korza; D Levi Craft; Joshua Green; Maria Rocha Granados; Wendy W K Mok; Melissa J Caimano; Peter Setlow
Journal:  J Bacteriol       Date:  2021-06-22       Impact factor: 3.490

Review 8.  Bacterial Spore mRNA - What's Up With That?

Authors:  Peter Setlow; Graham Christie
Journal:  Front Microbiol       Date:  2020-10-26       Impact factor: 5.640

  8 in total

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