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J. Bacteriol., 01 1997, 187-193, Vol 179, No. 1
H Yu, M Mudd, JC Boucher, MJ Schurr and V Deretic
Alginate production in mucoid Pseudomonas aeruginosa isolates from cystic
fibrosis patients is under direct control by AlgU, the P. aeruginosa
equivalent of the extreme heat shock sigma factor sigma(E) in gram-negative
bacteria, and AlgR, a response regulator from the superfamily of
two-component signal transduction systems. In this report, we describe the
identification of the algZ gene, located immediately upstream of algR,
which is involved in the control of alginate production. The predicted
product of the algZ gene showed similarity to a subset of sensory
components from the superfamily of signal transduction systems but lacked
several of the highly conserved motifs typical of histidine protein
kinases. Inactivation of algZ in the wild-type standard genetic strain PAO1
did not affect its nonmucoid morphology. However, inactivation of algZ in a
mucoid mutant P. aeruginosa strain, which had AlgU freed from control by
the anti-sigma factor MucA, resulted in increased alginate production under
growth conditions which did not permit expression of mucoidy in the
parental algZ+ strain. The observed effects were abrogated when algR was
inactivated in the algZ::Tc(r) background. These findings indicate that
algZ plays a regulatory role in alginate production, possibly interacting
with AlgR, and that it may have negative effects on expression of the
mucoid phenotype under the conditions tested. The presented results suggest
that elements of negative regulation exist at the levels of both the
alternative sigma factor AlgU and the transcriptional activator AlgR which,
once relieved from that suppression, cooperate to bring about the
expression of the alginate system.
Copyright © 1997, American Society for Microbiology
Identification of the algZ gene upstream of the response regulator algR and its participation in control of alginate production in Pseudomonas aeruginosa
Department of Microbiology and Immunology, The University of Michigan Medical School, Ann Arbor 48109-0620, USA.
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