Ethionamide Boosters. 2. Combining Bioisosteric Replacement and Structure-Based Drug Design To Solve Pharmacokinetic Issues in a Series of Potent 1,2,4-Oxadiazole EthR Inhibitors

Archive ouverte

Flipo, Marion | Desroses, Matthieu | Lecat-Guillet, Nathalie | Villemagne, Baptiste | Blondiaux, Nicolas | Leroux, Florence | Piveteau, Catherine | Mathys, Vanessa | Flament, Marie-Pierre | Siepmann, Juergen | Villeret, Vincent | Wohlkönig, Alexandre | Wintjens, René | Soror, Sameh | Christophe, Thierry | Jeon, Hee Kyoung | Locht, Camille | Brodin, Priscille | Déprez, Benoit | Baulard, Alain | Willand, Nicolas

Edité par CCSD ; American Chemical Society -

International audience. Summary In many streptococci, competence for natural DNA transformation is regulated by the Rgg ‐type regulator ComR and the pheromone ComS , which is sensed intracellularly. We compared the ComRS systems of four model streptococcal species using in vitro and in silico approaches, to determine the mechanism of the ComRS ‐dependent regulation of competence. In all systems investigated, ComR was shown to be the proximal transcriptional activator of the expression of key competence genes. Efficient binding of ComR to DNA is strictly dependent on the presence of the pheromone ( C ‐terminal ComS octapeptide), in contrast with other streptococcal Rgg ‐type regulators. The 20 bp palindromic ComR ‐box is the minimal genetic requirement for binding of ComR , and its sequence directly determines the expression level of genes under its control. Despite the apparent species‐specific specialization of the ComR – ComS interaction, mutagenesis of ComS residues from S treptococcus thermophilus highlighted an unexpected permissiveness with respect to its biological activity. In agreement, heterologous ComS , and even primary sequence‐unrelated, casein‐derived octapeptides, were able to induce competence development in S . thermophilus . The lack of stringency of ComS sequence suggests that competence of a specific S treptococcus species may be modulated by other streptococci or by non‐specific nutritive oligopeptides present in its environment.

Consulter en ligne

Suggestions

Du même auteur

Ethionamide Boosters: Synthesis, Biological Activity, and Structure−Activity Relationships of a Series of 1,2,4-Oxadiazole EthR Inhibitors

Archive ouverte | Flipo, Marion | CCSD

International audience

Discovery of Novel N -Phenylphenoxyacetamide Derivatives as EthR Inhibitors and Ethionamide Boosters by Combining High-Throughput Screening and Synthesis

Archive ouverte | Flipo, Marion | CCSD

International audience

Ligand Efficiency Driven Design of New Inhibitors of Mycobacterium tuberculosis Transcriptional Repressor EthR Using Fragment Growing, Merging, and Linking Approaches

Archive ouverte | Villemagne, Baptiste | CCSD

International audience. Tuberculosis remains a major cause of mortality and morbidity, killing each year more than one million people. Although the combined use of first line antibiotics (isoniazid, rifampicin, pyra...

Chargement des enrichissements...