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J Bacteriol, March 1998, p. 1135-1147, Vol. 180, No. 5
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
An ABC Transporter System of Yersinia pestis Allows
Utilization of Chelated Iron by Escherichia coli
SAB11
Scott W.
Bearden,
Teanna M.
Staggs,
and
Robert D.
Perry*
Department of Microbiology and Immunology,
University of Kentucky, Lexington, Kentucky 40536-0084
Received 6 August 1997/Accepted 19 December 1997
The acquisition of iron is an essential component in the
pathogenesis of Yersinia pestis, the agent of bubonic and
pneumonic plague. A cosmid library derived from the genomic DNA of
Y. pestis KIM6+ was used for transduction of an
Escherichia coli mutant (SAB11) defective in the
biosynthesis of the siderophore enterobactin. Recombinant plasmids
which had a common 13-kb BamHI fragment were isolated from
SAB11 transductants in which growth but not enterobactin synthesis was
restored on media containing the iron chelator EDDA [ethylenediamine-di(o-hydroxyphenyl acetic acid)].
Subcloning and transposon mutagenesis revealed a 5.6-kb region,
designated yfe, essential for SAB11 growth stimulation. In
vitro transcription-translation analysis identified polypeptides of 18, 29.5, 32, and 33 kDa encoded by the yfe locus. Sequence
analysis shows this locus to be comprised of five genes in two separate
operons which have potential Fur-binding sequences in both promoters. A
putative polycistronic operon, yfeABCD, is Fur regulated
and responds to iron and manganese. A functional Fur protein is
required for the observed manganese repression of this operon. This
operon encodes polypeptides which have strong similarity to the
ATP-binding cassette (ABC) family of transporters and include a
periplasmic binding protein (YfeA), an ATP-binding protein (YfeB), and
two integral membrane proteins (YfeC and -D), which likely function in
the acquisition of inorganic iron and possibly other ions. The
~21-kDa protein encoded by the separately transcribed
yfeE gene may be located in the cell envelope, since a
yfeE::TnphoA fusion is
PhoA+. Mutations in this gene abrogate growth of SAB11 on
iron-chelated media.
*
Corresponding author. Mailing address: Department of
Microbiology and Immunology, University of Kentucky, MS415 Med. Ctr., Lexington, KY 40536-0084. Phone: (606) 323-6341. Fax: (606) 257-8994. E-mail: rperry{at}pop.uky.edu.

Present address: Department of Biology, San Antonio College, San
Antonio, TX 78284.
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