Journal of Bacteriology, July 2001, p. 4323-4329, Vol. 183, No. 14
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.14.4323-4329.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Department of Biological Sciences, Faculty of Chemistry and Biology, University of Santiago,1 and Institute of Biomedical Sciences, Faculty of Medicine, University of Chile,3 Santiago, Chile, and Laboratory of Chemical Biology, CNRS, Marseille, France2
Received 6 September 2000/Accepted 20 April 2001
A 1.3-kb insertion sequence, termed ISAfe1 (U66426), from
Acidithiobacillus ferrooxidans ATCC 19859 is described.
ISAfe1 exhibits the features of a typical bacterial insertion sequence. It has 26-bp, imperfectly matched, terminal inverted repeats and an
open reading frame (ORF) that potentially encodes a transposase (TPase)
of 404 amino acids (AAB07489) with significant similarity to members of
the ISL3 family of insertion sequences. A potential ribosome-binding
site and potential
10 and
35 promoter sites for the TPase ORF were
identified, and a +1 transcriptional start site was detected
experimentally. A potential outwardly directed
35 site was identified
in the right inverted repeat of ISAfe1. A second ORF (ORF B), of
unknown function, was found on the complementary strand with
significant similarity to ORF 2 of ISAe1 from Ralstonia eutropha. Southern blot analyses demonstrated that ISAfe1-like elements can be found in multiple copies in a variety of A. ferrooxidans strains and that they exhibit transposition. A codon
adaptation index (CAI) analysis of the TPase of ISAfe1 indicates that
is has a CAI of 0.726 and can be considered well adapted to its host, suggesting that ISAfe1 might be an ancient resident of A. ferrooxidans. Analysis of six of its target sites of insertion in
the genome of A. ferrooxidans ATCC 19859 indicates a
preference for 8-bp pseudopalindromic sequences, one of which resembles
the termini of its inverted repeats. Evidence is presented here that is
consistent with the possibility that ISAfe1 can promote both plasmid
cointegrate formation and resolution in E. coli.
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