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PMID: 1091928 Published · ppublish English Journal Article

Nature of R-factor replication in the presence of chloramphenicol.

Crosa JH, Luttropp LK, Falkow S

Abstract

Covalently closed circular deoxyribonucleic acid molecules of RSF1030, a nonconjugative R-factor, initiate and complete rounds of semiconservative replication in the absence of protein synthesis long after the bacterial chromosome has ceased its replication. RSF1030 replication under these conditions is sensitive to the inhibitor of ribonucleic acid synthesis, rifampicin. The product of this replication, a covalently closed DNA molecule, shows, in contrast to those molecules produced during the replication in a logarithmically growing culture of Escherichia coli, a transition to the open circular form upon treatment with ribonucleases of alkali. Analysis of the product resulting from alkali treatment indicates that there is a single break in one strand of the original circular duplex. This alkali-sensitive site occurs with equal probability in either of the complementary strands. These results are interpreted as a requirement for an RNA primer for the initiation of RSF1030 DNA synthesis and as showing that its removal from the covalently closed molecule is inhibited in the absence of protein synthesis.

MeSH Terms
Bacterial Proteins/biosynthesis Chloramphenicol/pharmacology DNA Replication DNA, Bacterial/biosynthesis,metabolism DNA, Circular/biosynthesis,metabolism Escherichia coli/metabolism Extrachromosomal Inheritance Ribonucleases/metabolism Rifampin/pharmacology Thymine/metabolism
Chemicals
Bacterial Proteins DNA, Bacterial DNA, Circular Chloramphenicol Ribonucleases Thymine Rifampin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Crosa J H
Luttropp L K
Falkow S
References (31)
31 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1975-02-00
Pages
654-8
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC432373
Subset
IM
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