Replication of the broad host range plasmid RSF1010 in cell-free extracts of Escherichia coli and Pseudomonas aeruginosa

Research output: Contribution to journalArticlepeer-review

28 Scopus citations

Abstract

Replication of exogenous RSF1010 DNA can be carried out by soluble enzyme systems from Escherichia coli and Pseudomonas aeruginosa. It requires the function of RSF1010-encoded replication protein(s), which is not expressed in extracts from plasmid-free bacteria. In contrast to previously described in vitro systems for plasmid replication, initiation of RSF1010 DNA synthesis is independent of transcription catalyzed by host RNA polymerase. This is indicated by the insensitivity of RSF1010 replication to rifampicin as well as to RNA polymerase antibodies. It is proposed that a host RNA polymerase transcription-independent initiation mechanism might be a general property of broad host range plasmids.

Original languageEnglish
Pages (from-to)4687-4702
Number of pages16
JournalNucleic Acids Research
Volume10
Issue number15
DOIs
StatePublished - 11 Aug 1982
Externally publishedYes

Fingerprint

Dive into the research topics of 'Replication of the broad host range plasmid RSF1010 in cell-free extracts of Escherichia coli and Pseudomonas aeruginosa'. Together they form a unique fingerprint.

Cite this