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PMID: 4925772 Published · ppublish English Journal Article

Degradation of Escherichia coli B deoxyribonucleic acid after infection with deoxyribonucleic acid-defective amber mutants of bacteriophage T7.

Journal of virology ·Vol. 6 ·No. 2 ·1970-08-00 ·Pages 149-55

Sadowski PD, Kerr C

Abstract

The degradation of bacterial deoxyribonucleic acid (DNA) was studied after infection of Escherichia coli B with DNA-negative amber mutants of bacteriophage T7. Degradation occurred in three stages. (i) Release of the DNA from a rapidly sedimenting cellular structure occurred between 5 and 6 min after infection. (ii) The DNA was cleaved endonucleolytically to fragments having a molecular weight of about 2 x 10(6) between 6 and 10 min after infection. (iii) These fragments of DNA were reduced to acid-soluble products between 7.5 and 15 min after infection. Stage 1 did not occur in the absence of the gene 1 product (ribonucleic acid polymerase sigma factor), stage 2 did not occur in the absence of the gene 3 product (phage T7-induced endonuclease), and stage 3 did not occur in the absence of the gene 6 product.

MeSH Terms
Carbon Isotopes Centrifugation, Density Gradient Chemical Precipitation Coliphages/enzymology,growth & development DNA, Bacterial/analysis,metabolism Deoxyribonucleases/metabolism Detergents Escherichia coli/analysis,metabolism Genes Genetics, Microbial Mutation RNA Nucleotidyltransferases/metabolism Sodium Chloride Sucrose Thymidine/metabolism Thymine/metabolism Trichloroacetic Acid Tritium
Chemicals
Carbon Isotopes DNA, Bacterial Detergents Tritium Sodium Chloride Sucrose Trichloroacetic Acid RNA Nucleotidyltransferases Deoxyribonucleases Thymine Thymidine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Sadowski P D
Kerr C
References (23)
23 references, click to expand
  1. Mutants of bacteriophage T4 unable to cause breakdown of host DNA.
    Proc Natl Acad Sci U S A. 1966 Mar;55(3):614-21 PMID: 4287490
  2. Degradation of cytosin-containing bacterial and bacteriophage DNA after infection of Escherichia coli B with bacteriophage T4D wild type and with mutants defective in genes 46, 47 and 56.
    J Mol Biol. 1968 Dec;38(3):395-411 PMID: 4305016
  3. Bacteriophage-induced inhibition of host functions. II. Evidence for multiple, sequential bacteriophage-induced deoxyribonucleases responsible for degradation of cellular deoxyribonucleic acid.
    J Virol. 1969 Jun;3(6):549-56 PMID: 4894764
  4. Control of template specificity of E. coli RNA polymerase by a phage-coded protein.
    Nature. 1969 Sep 13;223(5211):1111-3 PMID: 4897557
  5. Enzymatic breakage of deoxyribonucleic acid. I. Purification and properties of endonuclease II from T4 phage-infected Escherichia coli.
    J Biol Chem. 1969 Nov 25;244(22):6182-91 PMID: 4310836
  6. Enzymatic breakage of deoxyribonucleic acid. II. Purification and properties of endonuclease IV from T4 phage-infected Escherichia coli.
    J Biol Chem. 1969 Nov 25;244(22):6192-8 PMID: 4900512
  7. The genetics and physiology of bacteriophage T7.
    Virology. 1969 Nov;39(3):562-74 PMID: 4902069
  8. T7-directed protein synthesis.
    Virology. 1969 Nov;39(3):575-86 PMID: 4902070
  9. Integration of two sets of T7 mutants.
    Virology. 1969 Nov;39(3):587-8 PMID: 5358083
  10. Isolation of a cell membrane-DNA-nascent RNA complex from bacteria.
    J Mol Biol. 1969 Feb 28;40(1):65-76 PMID: 4983147
  11. The structural gene for a T7 endonuclease essential for phage DNA synthesis.
    Proc Natl Acad Sci U S A. 1970 Jan;65(1):242-8 PMID: 5263754
  12. Bacteriophage-induced inhibition of host functions. I. Degradation of Escherichia coli deoxyribonucleic acid after T4 infection.
    J Virol. 1968 Apr;2(4):327-34 PMID: 4911847
  13. Amber mutants of bacteriophages T3 and T7 defective in phage-directed deoxyribonucleic acid synthesis.
    J Virol. 1967 Aug;1(4):779-92 PMID: 4912235
  14. The origin of phosphorus in Escherichia coli bacteriophages.
    J Bacteriol. 1951 Aug;62(2):169-73 PMID: 14861175
  15. Nucleic acid economy in bacteria infected with bacteriophage T2. I. Purine and pyrimidine composition.
    J Gen Physiol. 1953 Jul;36(6):777-89 PMID: 13069681
  16. The origin of phosphorus in the T1, T5, T6, and T7 bacteriophages of Escherichia coli.
    J Bacteriol. 1953 Oct;66(4):429-36 PMID: 13096499
  17. The amino acid composition of T3 bacteriophage.
    J Biol Chem. 1953 Nov;205(1):291-5 PMID: 13117907
  18. Origin and fate of bacteriophage material.
    Cold Spring Harb Symp Quant Biol. 1953;18:209-20 PMID: 13168988
  19. Nucleic acid metabolism in Escherichia coli infected with phage T5.
    Virology. 1959 Apr;7(4):359-74 PMID: 13669308
  20. Studies on the deoxyribonucleases of bacteriophage-infected Escherichia coli.
    Biochem J. 1962 Dec;85:600-6 PMID: 13984375
  21. Sedimentation rate as a measure of molecular weight of DNA.
    Biophys J. 1963 Jul;3:309-21 PMID: 14016998
  22. Chromatin staining of bacteria during bacteriophage infection.
    J Bacteriol. 1950 Apr;59(4):551-60 PMID: 15436430
  23. Electron microscopical studies of phage multiplication. IV. The establishment of the DNA pool of vegetative phage and the maturation of phage particles.
    Virology. 1959 Aug;8:478-98 PMID: 14405215
Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1970-08-00
Pages
149-55
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC376101
Subset
IM
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