The traE gene of plasmid RP4 encodes a homologue of Escherichia coli DNA topoisomerase III Journal Article


Authors: Li, Z.; Hiasa, H.; Kumar, U.; DiGate, R. J.
Article Title: The traE gene of plasmid RP4 encodes a homologue of Escherichia coli DNA topoisomerase III
Abstract: The polypeptide encoded by the plasmid RP4 traE gene shows extensive protein sequence similarity to Escherichia coli topB, the gene encoding DNA topoisomerase III (Topo III). The traE gene product has been cloned into a bacteriophage T7-based transient expression system, and the polypeptide has been expressed and purified. The TraE protein exhibits topoisomerase activity similar to that of Topo III. Relaxation is stimulated by high temperature and low concentrations of Mg2+. In addition, similar to E. coli Topo III, the TraE protein is a potent decatenase and can substitute for Topo III activity in vivo. The biochemical properties of the TraE protein in vitro suggest that the protein may be involved in the resolution of plasmid DNA replication intermediates either during vegetative replication or in conjugative DNA transfer. Putative homologues of Topo III have been found to be encoded by other broad host range, conjugative plasmids isolated from both Gram-negative and Gram-positive organisms, suggesting that Topo III-like polypeptides may have an essential role in the propagation of many promiscuous plasmids.
Keywords: unclassified drug; dna replication; enzyme activity; structure activity relation; amino acid sequence; molecular sequence data; enzyme analysis; protein purification; escherichia coli; plasmid; plasmids; sequence homology; dna topoisomerase (atp hydrolysing); dna topoisomerases, type i; magnesium; dna, superhelical; peptide analysis; bacteriophage; posibacteria; negibacteria; priority journal; article; decatanase
Journal Title: Journal of Biological Chemistry
Volume: 272
Issue: 31
ISSN: 0021-9258
Publisher: American Society for Biochemistry and Molecular Biology  
Date Published: 1997-08-01
Start Page: 19582
End Page: 19587
Language: English
DOI: 10.1074/jbc.272.31.19582
PUBMED: 9235964
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 17 March 2017 -- Source: Scopus
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  1. Hiroshi   Hiasa
    21 Hiasa