Affiliation:
1. Department of Biochemistry, Osmania University, Hyderabad, India
2. Université de Lyon, Université Lyon 1, INSA de Lyon, CNRS, UMR5240, Microbiologie Adaptation et Pathogénie, Villeurbanne F-69621, France
Abstract
ABSTRACT
We report here the identification and characterization of
mrdH
, a novel chromosomal metal resistance determinant, located in the genomic island 55 of
Pseudomonas putida
KT2440. It encodes for MrdH, a predicted protein of ∼40 kDa with a chimeric domain organization derived from the RcnA and RND (for resistance-nodulation-cell division) metal efflux proteins. The metal resistance function of
mrdH
was identified by the ability to confer nickel resistance upon its complementation into
rcnA
mutant (a nickel- and cobalt-sensitive mutant) of
Escherichia coli
. However, the disruption of
mrdH
in
P. putida
resulted in an increased sensitivity to cadmium and zinc apart from nickel. Expression studies using quantitative reverse transcription-PCR showed the induction of
mrdH
by cadmium, nickel, zinc, and cobalt. In association with
mrdH
, we also identified a conserved hypothetical gene
mreA
whose encoded protein showed significant homology to NreA and NreA-like proteins. Expression of the
mreA
gene in
rcnA
mutant of
E. coli
enhanced its cadmium and nickel resistance. Transcriptional studies showed that both
mrdH
and
mreA
underwent parallel changes in gene expression. The mobile genetic elements Tn
4652
and IS
1246
, flanking
mrdH
and
mreA
were found to be induced by cadmium, nickel, and zinc, but not by cobalt. This study is the first report of a single-component metal efflux transporter,
mrdH
, showing chimeric domain organization, a broad substrate spectrum, and a location amid metal-inducible mobile genetic elements.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
31 articles.
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