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Journal of Bacteriology, April 2001, p. 2646-2653, Vol. 183, No. 8
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.8.2646-2653.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Suppression of Hypersensitivity of
Escherichia coli acrB Mutant to Organic Solvents by
Integrational Activation of the acrEF Operon with the
IS1 or IS2 Element
Kei
Kobayashi,
Norihiko
Tsukagoshi, and
Rikizo
Aono*
Department of Biological Information,
Graduate School of Bioscience and Biotechnology, Tokyo Institute of
Technology, Nagatsuta 4259, Midori-ku, Yokohama 226-8501, Japan
Received 21 August 2000/Accepted 17 January 2001
The AcrAB-TolC efflux pump plays an intrinsic role in resistance to
hydrophobic solvents in Escherichia coli. E. coli OST5500 is hypersensitive to solvents due to inactivation of the
acrB gene by insertion of IS30. Suppressor
mutants showing high solvent resistance were isolated from OST5500.
These mutants produced high levels of AcrE and AcrF proteins, which
were not produced in OST5500, and in each mutant an insertion sequence
(IS1 or IS2) was found integrated upstream of
the acrEF operon, coding for the two proteins. The
suppressor mutants lost solvent resistance on inactivation of the
acrEF operon. The solvent hypersensitivity of
OST5500 was suppressed by introduction of the acrEF
operon with IS1 or IS2 integrated
upstream but not by introduction of the operon lacking the
integrated IS. It was concluded that IS integration activated
acrEF, resulting in functional complementation of the
acrB mutation. The acrB mutation was also
complemented by a plasmid containing acrF or
acrEF under the control of Plac. The wild-type
tolC gene was found to be essential for complementation of
the acrB mutation by acrEF. Thus, it is
concluded that in these cells a combination of the proteins AcrA, AcrF,
and TolC or the proteins AcrE, AcrF, and TolC is functional in solvent
efflux instead of the AcrAB-TolC efflux pump.
*
Corresponding author. Mailing address: Department of
Biological Information, Graduate School of Bioscience and
Biotechnology, Tokyo Institute of Technology, Nagatsuta 4259, Midori-ku, Yokohama 226-8501, Japan. Phone: 81 45-924-5966. Fax: 81 45-924-5819. E-mail: raono{at}bio.titech.ac.jp.

Present address: Marine Biotechnology Institute, Shimizu-shi,
Shizuoka 424-0037,
Japan.
Journal of Bacteriology, April 2001, p. 2646-2653, Vol. 183, No. 8
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.8.2646-2653.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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