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. 1971 Jan;7(1):168–175. doi: 10.1128/jvi.7.1.168-175.1971

Isolation and Characterization of a New Generalized Transducing Bacteriophage Different from Pl in Escherichia coli

Katsutoshi Mise 1
PMCID: PMC356090  PMID: 5543429

Abstract

A new generalized transducing bacteriophage in the Escherichia coli system was isolated and characterized. This phage, designated D108, makes clear plaques on E. coli K-10, K-12, K-12(P1kc), K-12(D6), B/r, C, and 15 T, and Shigella dysenteriae. The plaque of phage D108 is larger in size than that of phage P1kc. Electron-microscopic observation revealed that phages D108 and P1kc are morphologically different from each other, suggesting that phage D108 belongs to a phage group different from phage P1. The fact that all of the 10 markers tested were transduced by phage D108 indicates that this phage is a generalized transducing phage in the E. coli system. The transduction frequency by phage D108 of chromosomal markers and of a drug resistance factor (R factor) ranged from 2 × 10−6 to 3 × 10−8 and 3 × 10−9 to 6 × 10−10 per phage, respectively. The cotransduction frequency of the thr and leu markers was 2.8% for phage P1kc and 1.5% for phage D108. The CM and TC markers (chloramphenicol-resistant and tetracycline-resistant markers, respectively) of the R factor were not cotransduced by phage D108, but the markers were generally cotransduced by phage P1kc. The results suggest that the transducing particle of phage D108 contains a smaller amount of host deoxyribonucleic acid than does phage P1kc.

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Selected References

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  1. Appleyard R K. Segregation of New Lysogenic Types during Growth of a Doubly Lysogenic Strain Derived from Escherichia Coli K12. Genetics. 1954 Jul;39(4):440–452. doi: 10.1093/genetics/39.4.440. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. CLOWES R. C., ROWLEY D. Some observations on linkage effects in genetic recombination in Escherichia coli K-12. J Gen Microbiol. 1954 Oct;11(2):250–260. doi: 10.1099/00221287-11-2-250. [DOI] [PubMed] [Google Scholar]
  3. Drexler H. Transduction by bacteriophage T1. Proc Natl Acad Sci U S A. 1970 Aug;66(4):1083–1088. doi: 10.1073/pnas.66.4.1083. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Ikeda H., Tomizawa J. I. Transducing fragments in generalized transduction by phage P1. I. Molecular origin of the fragments. J Mol Biol. 1965 Nov;14(1):85–109. doi: 10.1016/s0022-2836(65)80232-7. [DOI] [PubMed] [Google Scholar]
  5. JACOB F. Transduction of lysogeny in Escherichia coli. Virology. 1955 Jul;1(2):207–220. doi: 10.1016/0042-6822(55)90017-9. [DOI] [PubMed] [Google Scholar]
  6. LENNOX E. S. Transduction of linked genetic characters of the host by bacteriophage P1. Virology. 1955 Jul;1(2):190–206. doi: 10.1016/0042-6822(55)90016-7. [DOI] [PubMed] [Google Scholar]
  7. Mise K., Suzuki K. New generalized transducing bacteriopahge in Echerichia coli. J Virol. 1970 Aug;6(2):253–255. doi: 10.1128/jvi.6.2.253-255.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. NAKAYA R., NAKAMURA A., MURATA Y. Resistance transfer agents in Shigella. Biochem Biophys Res Commun. 1960 Dec;3:654–659. doi: 10.1016/0006-291x(60)90081-4. [DOI] [PubMed] [Google Scholar]
  9. Okamoto S., Suzuki Y. Chloramphenicol-, dihydrostreptomycin-, and kanamycin-inactivating enzymes from multiple drug-resistant Escherichia coli carrying episome 'R'. Nature. 1965 Dec 25;208(5017):1301–1303. doi: 10.1038/2081301a0. [DOI] [PubMed] [Google Scholar]
  10. Rownd R., Nakaya R., Nakamura A. Molecular nature of the drug-resistance factors of the Enterobacteriaceae. J Mol Biol. 1966 Jun;17(2):376–393. doi: 10.1016/s0022-2836(66)80149-3. [DOI] [PubMed] [Google Scholar]
  11. SUGINO Y., HIROTA Y. Conjugal fertility associated with resistance factor R in Escherichia coli. J Bacteriol. 1962 Nov;84:902–910. doi: 10.1128/jb.84.5.902-910.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Skaar P. D., Garen A. THE ORIENTATION AND EXTENT OF GENE TRANSFER IN ESCHERICHIA COLI. Proc Natl Acad Sci U S A. 1956 Sep;42(9):619–624. doi: 10.1073/pnas.42.9.619. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. WATANABE T., FUKASAWA T. Episome-mediated transfer of drug resistance in Enterobacteriaceae. III. Transduotion of resistance factors. J Bacteriol. 1961 Aug;82:202–209. doi: 10.1128/jb.82.2.202-209.1961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. ZINDER N. D., LEDERBERG J. Genetic exchange in Salmonella. J Bacteriol. 1952 Nov;64(5):679–699. doi: 10.1128/jb.64.5.679-699.1952. [DOI] [PMC free article] [PubMed] [Google Scholar]

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