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Please use this identifier to cite or link to this item: http://dspace.mediu.edu.my:8181/xmlui/handle/10261/3398
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dc.creatorBusch, Andreas-
dc.creatorLacal, Jesús-
dc.creatorMartos, Ariadna-
dc.creatorRamos, Juan L.-
dc.creatorKrell, Tino-
dc.date2008-04-01T09:02:50Z-
dc.date2008-04-01T09:02:50Z-
dc.date2007-08-21-
dc.date.accessioned2017-01-31T01:01:23Z-
dc.date.available2017-01-31T01:01:23Z-
dc.identifierProc Natl Acad Sci U S A. 2007 August 21; 104(34): 13774–13779-
dc.identifier1091-6490-
dc.identifierhttp://hdl.handle.net/10261/3398-
dc.identifier10.1073/pnas.0701547104-
dc.identifier.urihttp://dspace.mediu.edu.my:8181/xmlui/handle/10261/3398-
dc.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-
dc.descriptionThe 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.-
dc.descriptionThis work was supported by Ministry of Science and Education (Spain) Grant BIO-2006-05668, European Union Grant Sysmo GEN-2006- 27750-CS-5B, and Junta de Andalucía Grant CVI-344-
dc.descriptionPeer reviewed-
dc.format374472 bytes-
dc.format67926 bytes-
dc.format33285 bytes-
dc.format30069 bytes-
dc.format80039 bytes-
dc.format42385 bytes-
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dc.languageeng-
dc.publisherNational Academy of Sciences (U.S.)-
dc.rightsclosedAccess-
dc.subjectHistidine kinases-
dc.subjectIsothermal titration calorimetry-
dc.subjectPseudomonas-
dc.subjectTwo-component systems-
dc.subjectAromatic hydrocarbons-
dc.titleBacterial sensor kinase TodS interacts with agonistic and antagonistic signals-
dc.typeArtículo-
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