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. 1971 Feb;7(2):260-6.
doi: 10.1128/JVI.7.2.260-266.1971.

Properties of bacteriophage T4 mutants defective in gene 30 (deoxyribonucleic acid ligase) and the rII gene

Properties of bacteriophage T4 mutants defective in gene 30 (deoxyribonucleic acid ligase) and the rII gene

J D Karam et al. J Virol. 1971 Feb.

Abstract

In Escherichia coli K-12 strains infected with phage T4 which is defective in gene 30 [deoxyribonucleic acid (DNA) ligase] and in the rII gene (product unknown), near normal levels of DNA and viable phage were produced. Growth of such T4 ligase-rII double mutants was less efficient in E. coli B strains which show the "rapidlysis" phenotype of rII mutations. In pulse-chase experiments coupled with temperature shifts and with inhibition of DNA synthesis, it was observed that DNA synthesized by gene 30-defective phage is more susceptible to breakdown in vivo when the phage is carrying a wild-type rII gene. Breakdown was delayed or inhibited by continued DNA synthesis. Mutations of the rII gene decreased but did not completely abolish the breakdown. T4 ligase-rII double mutants had normal sensitivity to ultraviolet irradiation.

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References

    1. J Mol Biol. 1968 Aug 14;35(3):639-42 - PubMed
    1. Cold Spring Harb Symp Quant Biol. 1968;33:145-50 - PubMed
    1. Proc Natl Acad Sci U S A. 1961 Mar;47(3):403-15 - PubMed
    1. Proc Natl Acad Sci U S A. 1968 Dec;61(4):1328-35 - PubMed
    1. J Mol Biol. 1969 Dec 28;46(3):467-79 - PubMed

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