Abstract
The addition of chloramphenicol (CM) 5 min after infection of the nonpermissive host Escherichia coli B with the ligase-negative T4 amber, T4 AmH39X, allowed replication of parental deoxyribonucleic acid (DNA) and the production of high-molecular-weight progeny DNA, composed mostly of subunits with a D2/D1 of 0.6. When CM was removed after the accumulation of a large pool of this DNA, most of the infected bacteria were able to produce viable progeny phage, with an average yield of approximately 15 bacteriophage per bacterium. This phenomenon is called CM rescue of the ligase-negative T4 Am. CsCl and sucrose gradient analyses showed both the resulting phage and DNA extracted from them to be similar to the phage and DNA produced on the permissive host. The total transfer of the parental label to progeny phages was as high as 20%. In contrast, in bacteria not treated with CM or in bacteria to which CM was added after phage-coded nucleases had already been synthesized, both parental and progeny (newly synthesized) DNA was composed of very short fragments. Phage which are produced under conditions other than those of CM rescue are dead, light in CsCl, and contain only very short fragments of DNA. Parent-to-progeny transfer in this case is below 1%. When light radio-active parental DNA was used to infect heavy bacteria, DNA replicating in the CM rescue conditions assumed only a hybrid density. After removal of CM and maturation, the parental DNA was incorporated into progeny molecules in fragments constituting approximately 7 to 10% of its mass. This pattern of distribution is essentially what is observed in similar experiments in the permissive host. The role of ligase as an enzyme which compensates for the lethal action of phage-coded nuclease and which is stringently required for the repair of single-stranded nicks is emphasized. The possibility of specific sites for a unique cutting enzyme is discussed in connection with the hypothesis of a circularly permuted assembly of sets.
Full text
PDF













Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- APOSHIAN H. V., KORNBERG A. Enzymatic synthesis of deoxyribonucleic acid. IX. The polymerase formed after T2 bacteriophage infection of Escherichia coli: a new enzyme. J Biol Chem. 1962 Feb;237:519–525. [PubMed] [Google Scholar]
- Fareed G. C., Richardson C. C. Enzymatic breakage and joining of deoxyribonucleic acid. II. The structural gene for polynucleotide ligase in bacteriophage T4. Proc Natl Acad Sci U S A. 1967 Aug;58(2):665–672. doi: 10.1073/pnas.58.2.665. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Frankel F. R. Evidence for long DNA strands in the replicating pool after T4 infection. Proc Natl Acad Sci U S A. 1968 Jan;59(1):131–138. doi: 10.1073/pnas.59.1.131. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hurwitz J., Becker A., Gefter M. L., Gold M. Enzymatic reactions at termini of DNA. J Cell Physiol. 1967 Oct;70(2 Suppl):181–199. doi: 10.1002/jcp.1040700413. [DOI] [PubMed] [Google Scholar]
- KOZINSKI A. W., KOZINSKI P. B. Fragmentary transfer of P32-labeled parental DNA to progeny phage. II. The average size of the transferred parental fragment. Two-cycletransfer. Repair of the polynucleotide chain after fragmentation. Virology. 1963 Jun;20:213–229. doi: 10.1016/0042-6822(63)90109-0. [DOI] [PubMed] [Google Scholar]
- KOZINSKI A. W., SZYBALSKI W. Dispersive transfer of the parental DNA molecule to the progeny of phage phiX-174. Virology. 1959 Oct;9:260–274. doi: 10.1016/0042-6822(59)90119-9. [DOI] [PubMed] [Google Scholar]
- Kozinski A. W., Felgenhauer Z. Z. Molecular recombination in T4 bacteriophage deoxyribonucleic acid. II. Single-strand breaks and exposure of uncomplemented areas as a prerequisite for recombination. J Virol. 1967 Dec;1(6):1193–1202. doi: 10.1128/jvi.1.6.1193-1202.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kozinski A. W., Kozinski P. B. Autonomous replication of short DNA fragments in the ligase negative T4 AM H39X. Biochem Biophys Res Commun. 1968 Nov 25;33(4):670–674. doi: 10.1016/0006-291x(68)90348-3. [DOI] [PubMed] [Google Scholar]
- Kozinski A. W., Kozinski P. B. Covalent repair of molecular recombinants in the ligase-negative amber mutant of T4 bacteriophage. J Virol. 1969 Jan;3(1):85–88. doi: 10.1128/jvi.3.1.85-88.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kozinski A. W., Kozinski P. B., James R. Molecular recombination in T4 bacteriophage deoxyribonucleic acid. I. Tertiary structure of early replicative and recombining deoxyribonucleic acid. J Virol. 1967 Aug;1(4):758–770. doi: 10.1128/jvi.1.4.758-770.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kozinski A. W. Molecular recombination in the ligase negative T4 amber mutant. Cold Spring Harb Symp Quant Biol. 1968;33:375–391. doi: 10.1101/sqb.1968.033.01.044. [DOI] [PubMed] [Google Scholar]
- Kozinski A. W. Unbiased participation of T4 phage DNA strands in replication. Biochem Biophys Res Commun. 1969 Apr 29;35(2):294–299. doi: 10.1016/0006-291x(69)90281-2. [DOI] [PubMed] [Google Scholar]
- Okazaki R., Okazaki T., Sakabe K., Sugimoto K., Sugino A. Mechanism of DNA chain growth. I. Possible discontinuity and unusual secondary structure of newly synthesized chains. Proc Natl Acad Sci U S A. 1968 Feb;59(2):598–605. doi: 10.1073/pnas.59.2.598. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Richardson C. C., Masamune Y., Live T. R., Jacquemin-Sablon A., Weiss B., Fareed G. C. Studies on the joining of DNA by polynucleotide ligase of phage T4. Cold Spring Harb Symp Quant Biol. 1968;33:151–164. doi: 10.1101/sqb.1968.033.01.019. [DOI] [PubMed] [Google Scholar]
- Shahn E., Kozinski A. Fragmentary transfer of P32 labeled parental DNA to progeny phage. 3. Incorporation of a single parental fragment to the progeny molecule. Virology. 1966 Nov;30(3):455–470. doi: 10.1016/0042-6822(66)90122-x. [DOI] [PubMed] [Google Scholar]
- WIBERG J. S., DIRKSEN M. L., EPSTEIN R. H., LURIA S. E., BUCHANAN J. M. Early enzyme synthesis and its control in E. coli infected with some amber mutants of bacteriophage T4. Proc Natl Acad Sci U S A. 1962 Feb;48:293–302. doi: 10.1073/pnas.48.2.293. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wu R., Kaiser A. D. Structure and base sequence in the cohesive ends of bacteriophage lambda DNA. J Mol Biol. 1968 Aug 14;35(3):523–537. doi: 10.1016/s0022-2836(68)80012-9. [DOI] [PubMed] [Google Scholar]
