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Journal of Bacteriology, February 1999, p. 1099-1109, Vol. 181, No. 4
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Pseudomonas aeruginosa fur Overlaps with
a Gene Encoding a Novel Outer Membrane Lipoprotein, OmlA
Urs A.
Ochsner,
Adriana I.
Vasil,
Zaiga
Johnson, and
Michael L.
Vasil*
Department of Microbiology, University of
Colorado Health Sciences Center, Denver, Colorado 80262
Received 8 September 1998/Accepted 9 December 1998
A novel outer membrane lipoprotein in Pseudomonas
aeruginosa is encoded by the omlA gene, which was
identified immediately upstream of the fur (ferric uptake
regulator) gene. The omlA and fur genes were
divergently transcribed and had overlapping promoter regions. The
proximal fur P2 promoter and the omlA promoter
shared a 5-bp DNA motif for their
10 promoter elements. The distal
fur P1 promoter was located within the omlA
coding sequence, and the omlA and fur T1 mRNAs
overlapped by 154 nucleotides. Optimal expression of both
fur and omlA required roughly 200 bp of DNA
upstream of the promoter regions, suggesting the presence of
cis-acting transcriptional activation elements located
within the omlA and fur genes, respectively. The levels of Fur and OmlA proteins had no influence on
omlA or fur expression, excluding any
trans-acting cross-regulation between fur and
omlA. Expression of omlA was constitutive
regardless of growth phase, oxygen tension, iron concentration, pH, and
temperature. OmlA contained a signal sequence typical of bacterial
lipoproteins, with a cysteine as a putative cleavage and lipid
attachment site. Inhibition of signal peptidase II by globomycin
resulted in failure to process OmlA, thus giving strong evidence that
OmlA is a lipoprotein. Cell fractionation followed by Western blot
analysis indicated that all OmlA protein is localized in the outer
membrane. Mature OmlA was an acidic (pI = 4.5) protein of 17.3 kDa
and had close to 40% amino acid sequence identity to SmpA (small
protein A) of Escherichia coli, Vibrio
cholerae, and Haemophilus influenzae, a protein of
unknown function. All P. aeruginosa strains tested as well
as Pseudomonas fluorescens were found to produce OmlA. A
mutant strain with impaired production of OmlA but no change in the
expression of the overlapping fur gene was constructed. The
omlA mutant was hypersusceptible to anionic detergents such as sodium dodecyl sulfate and deoxycholate, and it showed increased susceptibility to various antibiotics, including nalidixic acid, rifampin, novobiocin, and chloramphenicol. A structural role of OmlA in
maintaining the cell envelope integrity is proposed.
*
Corresponding author. Mailing address: University of
Colorado Health Sciences Center, Department of Microbiology, Campus Box B175, 4200 E. Ninth Ave., Denver, CO 80262. Phone: (303) 315-6784. Fax:
(303) 315-6785. E-mail: Mike.Vasil{at}UCHSC.edu.
Journal of Bacteriology, February 1999, p. 1099-1109, Vol. 181, No. 4
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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