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. 1976 Mar;17(3):859–864. doi: 10.1128/jvi.17.3.859-864.1976

Escherichia coli capsule bacteriophages. VIII. Fragments of bacteriophage 28-1.

D Rieger, E Freund-Mölbert, S Stirm
PMCID: PMC515486  PMID: 3668

Abstract

As described previously, a host capsule depolymerase activity is associated with the particles of Escherichia coli capsule bacteriophage 28-1. This is a large virus with a long, contractile tail terminating in a base plate with spikes. In the present work, isolated virions were exposed to a variety of dissociative reagents and conditions. They were then tested for residual infectivity and depolymerase activity, as well as inspected under an electron microscope. Very mild acid treatment (10 to 15 min at pH 4.0 and 37 C) was found to cause a specific detachment of some phage spikes, together with a moderate drop in both infectivity and depolymerase activity. Large batches of viruses were fragmented in this manner, and the detached spikes were isolated. The host capsule depolymerase activity was found to be associated with these organelles. In negatively stained preparations, the spikes exhibited a length of approximately 18 nm and a thickness of about 5 nm. By sodium dodecyl sulfate-polyacrylamide gel electrophoresis, they were found to contain polypeptides with molecular weights of 80,000 and 145, 000.

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Selected References

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  1. ADAMS M. H., PARK B. H. An enzyme produced by a phage-host cell system. II. The properties of the polysaccharide depolymerase. Virology. 1956 Dec;2(6):719–736. doi: 10.1016/0042-6822(56)90054-x. [DOI] [PubMed] [Google Scholar]
  2. Ackermann H. W. Bactériophages: propriétés et premièes étapes d'une classification. Pathol Biol (Paris) 1969 Nov;17(21):1003–1024. [PubMed] [Google Scholar]
  3. Ackermann H. W., Berthiaume L., Kasatiya S. S. Ultrastructure of Vi phages I to VII of Salmonella typhi. Can J Microbiol. 1970 Jun;16(6):411–413. doi: 10.1139/m70-070. [DOI] [PubMed] [Google Scholar]
  4. Bessler W., Freund-Mölbert E., Knüfermann H., Rduolph C., Thurow H., Stirm S. A bacteriophage-induced depolymerase active on Klebsiella K11 capsular polysaccharide. Virology. 1973 Nov;56(1):134–151. doi: 10.1016/0042-6822(73)90293-6. [DOI] [PubMed] [Google Scholar]
  5. Bradley D. E. Ultrastructure of bacteriophage and bacteriocins. Bacteriol Rev. 1967 Dec;31(4):230–314. doi: 10.1128/br.31.4.230-314.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Carrascosa J. L., Camacho A., Viñuela E., Salas M. A precursor of the neck appendage protein of B. subtilis phage phi 29. FEBS Lett. 1974 Aug 30;44(3):317–321. [PubMed] [Google Scholar]
  7. Iwashita S., Kanegasaki S. Smooth specific phage adsorption: endorhamnosidase activity of tail parts of P22. Biochem Biophys Res Commun. 1973 Nov 16;55(2):403–409. doi: 10.1016/0006-291x(73)91101-7. [DOI] [PubMed] [Google Scholar]
  8. Krzywy T., Przondo-Hessek A., Slopek S. Morphology of bacteriophages used for typing Klebsiella scleromatis. Arch Immunol Ther Exp (Warsz) 1971;19(1):1–14. [PubMed] [Google Scholar]
  9. Kwiatkowski B., Taylor A. Two-step attachment of Vi-phage I to the bacterial surface. Acta Microbiol Pol A. 1970;2(1):13–20. [PubMed] [Google Scholar]
  10. Nelson E. T., Buller C. S. Phospholipase activity in bacteriophage-infected Escherichia coli. I. Demonstration of a T4 bacteriophage-associated phospholipase. J Virol. 1974 Sep;14(3):479–484. doi: 10.1128/jvi.14.3.479-484.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Rieger D., Freund-Mölbert E., Stirm S. Escherichia coli capsule bacteriophages. III. Fragments of bacteriophage 29. J Virol. 1975 Apr;15(4):964–975. doi: 10.1128/jvi.15.4.964-975.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Rudolph C., Freund-Mölbert E., Stirm S. Fragments of Klebsiella bacteriophage no. 11. Virology. 1975 Mar;64(1):236–246. doi: 10.1016/0042-6822(75)90095-1. [DOI] [PubMed] [Google Scholar]
  13. Stirm S., Bessler W., Fehmel F., Freund-Mölbert E. Bacteriophage particles with endo-glycosidase activity. J Virol. 1971 Sep;8(3):343–346. doi: 10.1128/jvi.8.3.343-346.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Stirm S., Bessler W., Fehmel F., Freund-Mölbert E., Thurow H. Uber eine Bakteriophagen-induzierte Colansäure-Depolymerase. Zentralbl Bakteriol Orig A. 1974 Feb;226(1):26–35. [PubMed] [Google Scholar]
  15. Stirm S., Freund-Mölbert E. Escherichia coli capsule bacteriophages. II. Morphology. J Virol. 1971 Sep;8(3):330–342. doi: 10.1128/jvi.8.3.330-342.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Taylor K. Enzymatic deacetylation of Vi-polysaccharide by Vi-phage. II. Biochem Biophys Res Commun. 1965 Sep 22;20(6):752–756. doi: 10.1016/0006-291x(65)90081-1. [DOI] [PubMed] [Google Scholar]
  17. Thurow H., Niemann H., Rudolph C., Stirm S. Host capsule depolymerase activity of bacteriophage particles active on Klebsiella K20 and K24 strains. Virology. 1974 Mar;58(1):306–309. doi: 10.1016/0042-6822(74)90166-4. [DOI] [PubMed] [Google Scholar]
  18. Yurewicz E. C., Ghalambor M. A., Duckworth D. H., Heath E. C. Catalytic and molecular properties of a phage-induced capsular polysaccharide depolymerase. J Biol Chem. 1971 Sep 25;246(18):5607–5616. [PubMed] [Google Scholar]

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