Abstract
The inactivation of bacteriophage HP1c1 by X rays in a complex medium was found to be exponential, with a D0 (the X-ray exposure necessary to reduce the survival of the phage to 37%) of approximately 90 kR. Analysis of results of sucrose sedimentation of DNA from X-irradiated whole phage showed that the D0 for intactness of single strands was about 105kR, and for intactness of double strands, it was much higher. The D0 for attachment of X-irradiated phage to the host was roughly estimated as about 1,100 kR. Loss of DNA from the phage occurred and was probably due to lysis of the phage by X irradiation, but the significance of the damage is not clear. The production of single-strand breaks approaches the rate of survival loss after X irradiation. However, single-strand breaks produced by UV irradiation, in the presence of H2O2, equivalent to 215 kR of X rays, showed no lethal effect on the phage. Although UV-sensitive mutants of the host cell, Haemophilus influenzae, have been shown to reactivate UV-irradiated phage less than does the wild-type host cell, X-irradiated phage survive equally well on the mutants as on the wild type, a fact suggesting that other repair systems are involved in X-ray repair.
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Selected References
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- Boling M. E., Setlow J. K., Allison D. P. Bacteriophage of Haemophilus influenzae. I. Differences between infection by whole phage, extracted phage DNA and prophage DNA extracted from lysogenic cells. J Mol Biol. 1972 Feb 14;63(3):335–348. doi: 10.1016/0022-2836(72)90431-7. [DOI] [PubMed] [Google Scholar]
- Boyle J. M., Symonds N. Radiation-sensitive mutants of T4D. I. T4y: a new radiation-sensitive mutant; effect of the mutation on radiation survival, growth and recombination. Mutat Res. 1969 Nov-Dec;8(3):431–439. doi: 10.1016/0027-5107(69)90060-8. [DOI] [PubMed] [Google Scholar]
- Carlson K., Lorkiewicz Z. K., Kozinski A. W. Host-mediated repair of discontinuities in DNA from T4 bacteriophage. J Virol. 1973 Aug;12(2):310–319. doi: 10.1128/jvi.12.2.310-319.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Carrier W. L., Setlow R. B. Paper strip method for assaying gradient fractions containing radioactive macromolecules. Anal Biochem. 1971 Oct;43(2):427–432. doi: 10.1016/0003-2697(71)90272-7. [DOI] [PubMed] [Google Scholar]
- Fangman W. L., Russel M. X-irradiation sensitivity in Escherichia coli defective in DNA replication. Mol Gen Genet. 1971;110(4):332–347. doi: 10.1007/BF00438275. [DOI] [PubMed] [Google Scholar]
- Freifelder D. Inactivation of phage alpha by single-strand breakage. Virology. 1966 Nov;30(3):328–332. doi: 10.1016/0042-6822(66)90110-3. [DOI] [PubMed] [Google Scholar]
- Freifelder D. Mechanism of inactivation of coliphage T7 by x-rays. Proc Natl Acad Sci U S A. 1965 Jul;54(1):128–134. doi: 10.1073/pnas.54.1.128. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HARM W., RUPERT C. S. INFECTION OF TRANSFORMABLE CELLS OF HAEMOPHILUS INFLUENZAE BY BACTERIOPHAGE AND BACTERIOPHAGE DNA. Z Vererbungsl. 1963 Dec 30;94:336–348. doi: 10.1007/BF00897593. [DOI] [PubMed] [Google Scholar]
- Kimball R. F., Liu M., Setlow J. K. Effects of posttreatment on single-strand breaks in DNA of Haemophilus influenzae exposed to nitrosoguanidine and methyl methanesulfonate. Mutat Res. 1971 Dec;13(4):289–295. doi: 10.1016/0027-5107(71)90039-x. [DOI] [PubMed] [Google Scholar]
- McAllister W. T., Green D. M. Effects of the decay of incorporated radioactive phosphorus on the transfer of the bacteriophage SP82G genome. J Virol. 1973 Aug;12(2):300–309. doi: 10.1128/jvi.12.2.300-309.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McGrath R. A., Williams R. W. Reconstruction in vivo of irradiated Escherichia coli deoxyribonucleic acid; the rejoining of broken pieces. Nature. 1966 Oct 29;212(5061):534–535. doi: 10.1038/212534a0. [DOI] [PubMed] [Google Scholar]
- Notani N. K., Setlow J. K., Allison D. P. Intracellular events during infection by Haemophilus influenzae phage and transfection by its DNA. J Mol Biol. 1973 Apr 25;75(4):581–599. doi: 10.1016/0022-2836(73)90293-3. [DOI] [PubMed] [Google Scholar]
- Randolph M. L., Setlow J. K. Degradation of DNA in haemophilus influenzae cells after X-ray irradiation I. Experimental results. Biophys J. 2009 Jan 1;15(5):441–453. doi: 10.1016/S0006-3495(75)85829-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rhaese H. J., Freese E. Chemical analysis of DNA alterations. I. Base liberation and backbone breakage of DNA and oligodeoxyadenylic acid induced by hydrogen peroxide and hydroxylamine. Biochim Biophys Acta. 1968 Feb 26;155(2):476–490. [PubMed] [Google Scholar]
- Setlow J. K., Brown D. C., Boling M. E., Mattingly A., Gordon M. P. Repair of deoxyribonucleic acid in Haemophilus influenzae. I. X-ray sensitivity of ultraviolet-sensitive mutants and their behavior as hosts to ultraviolet-irradiated bacteriophage and transforming deoxyribonucleic acid. J Bacteriol. 1968 Feb;95(2):546–558. doi: 10.1128/jb.95.2.546-558.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Setlow J. K., Randolph M. L., Boling M. E., Mattingly A., Price G., Gordon M. P. Repair of DNA in Haemophilus influenzae. II. Excision, repair of single-strand breaks, defects in transformation, and host cell modification in UV-sensitive mutants. Cold Spring Harb Symp Quant Biol. 1968;33:209–218. doi: 10.1101/sqb.1968.033.01.024. [DOI] [PubMed] [Google Scholar]
- Setlow R. B., Setlow J. K. Effects of radiation on polynucleotides. Annu Rev Biophys Bioeng. 1972;1:293–346. doi: 10.1146/annurev.bb.01.060172.001453. [DOI] [PubMed] [Google Scholar]
- Setlow R. B. The photochemistry, photobiology, and repair of polynucleotides. Prog Nucleic Acid Res Mol Biol. 1968;8:257–295. doi: 10.1016/s0079-6603(08)60548-6. [DOI] [PubMed] [Google Scholar]
- TESSMAN I. Some unusual properties of the nucleic acid in bacteriophages S13 and phi X174. Virology. 1959 Mar;7(3):263–275. doi: 10.1016/0042-6822(59)90197-7. [DOI] [PubMed] [Google Scholar]
- Wallace S. S., Melamede R. J. Host- and phage-mediated repair of radiation damage in bacteriophage T4. J Virol. 1972 Dec;10(6):1159–1169. doi: 10.1128/jvi.10.6.1159-1169.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- van der Schans G. P., Bleichrodt J. F., Blok J. Contribution of various types of damage to inactivation of a biologically-active double-stranded circular DNA by gamma-radiation. Int J Radiat Biol Relat Stud Phys Chem Med. 1973 Feb;23(2):133–150. doi: 10.1080/09553007314550151. [DOI] [PubMed] [Google Scholar]
