Affiliation:
1. Department of Medical Microbiology and Immunology, Texas A&M University, College Station, Texas 77843-11141;
2. Robert Koch-Institut2 and
3. Bundesinstitut für Gesundheitlichen Verbraucherschutz und Veterinärmedizin,3 38843 Wernigerode, Germany; and
4. Department of Molecular Microbiology and Immunology, Oregon Health Sciences University, Portland, Oregon 97201-30984
Abstract
ABSTRACT
Speciation in enterobacteria involved horizontal gene transfer. Therefore, analysis of genes acquired by horizontal transfer that are present in one species but not its close relatives is expected to give insights into how new bacterial species were formed. In this study we characterize
iroN
, a gene located downstream of the
iroBC
operon in the
iroA
locus of
Salmonella enterica
serotype Typhi. Like
iroBC
, the
iroN
gene is present in all phylogenetic lineages of
S. enterica
but is absent from closely related species such as
Salmonella bongori
or
Escherichia coli
. Comparison of the deduced amino acid sequence of
iroN
with other proteins suggested that this gene encodes an outer membrane siderophore receptor protein. Mutational analysis in
S. enterica
and expression in
E. coli
identified a 78-kDa outer membrane protein as the
iroN
gene product. When introduced into an
E. coli fepA cir fiu aroB
mutant on a cosmid,
iroN
mediated utilization of structurally related catecholate siderophores, including
N
-(2,3-dihydroxybenzoyl)-
l
-serine, myxochelin A, benzaldehyde-2,3-dihydroxybenzhydrazone, 2-
N
,6-
N
-bis(2,3-dihydroxybenzoyl)-
l
-lysine, 2-
N
,6-
N
-bis(2,3-dihydroxybenzoyl)-
l
-lysine amide, and enterochelin. These results suggest that the
iroA
locus functions in iron acquisition in
S. enterica.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
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