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Title

Bacterial sensor kinase TodS interacts with agonistic and antagonistic signals

AuthorsBusch, Andreas; Lacal, Jesús ORCID; Martos, Ariadna CSIC; Ramos, Juan L.; Krell, Tino
KeywordsHistidine kinases
Isothermal titration calorimetry
Pseudomonas
Two-component systems
Aromatic hydrocarbons
Issue Date21-Aug-2007
PublisherNational Academy of Sciences (U.S.)
CitationProc Natl Acad Sci U S A. 2007 August 21; 104(34): 13774–13779
AbstractThe TodS/TodT two-component system controls expression of the toluene dioxygenase (TOD) pathway for the metabolism of toluene in Pseudomonas putida DOT-T1E. TodS is a sensor kinase that ultimately controls tod gene expression through its cognate response regulator, TodT. We used isothermal titration calorimetry to study the binding of different compounds to TodS and related these findings to their capacity to induce gene expression in vivo. Agonistic compounds bound to TodS and induced gene expression in vivo. Toluene was a powerful agonist, but ortho-substitutions of toluene reduced or abolished in vivo responses, although TodS recognized o-xylene with high affinity. These compounds were called antagonists. We show that agonists and antagonists compete for binding to TodS both in vitro and in vivo. The failure of antagonists to induce gene expression in vivo correlated with their inability to stimulate TodS autophosphorylation in vitro. We propose intramolecular TodS signal transmission, not molecular recognition of compounds by TodS, to be the phenomenon that determines whether a given compound will lead to activation of expression of the tod genes. Molecular modeling identified residues F46, I74, F79, and I114 as being potentially involved in the binding of effector molecules. Alanine substitution mutants of these residues reduced affinities (2- to 345-fold) for both agonistic and antagonistic compounds. Our data indicate that determining the inhibitory activity of antagonists is a potentially fruitful alternative to design specific two-component system inhibitors for the development of new drugs to inhibit processes regulated by two-component systems.
DescriptionCopyright © by National Academy of Sciences. Final full-text version of the paper available at: http://www.pnas.org/cgi/content/abstract/104/34/13774
URIhttp://hdl.handle.net/10261/3398
DOI10.1073/pnas.0701547104
ISSN1091-6490
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