JAC Advance Access originally published online on December 22, 2005
Journal of Antimicrobial Chemotherapy 2006 57(2):245-251; doi:10.1093/jac/dki426
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Novel synthetic molecules targeting the bacterial RNA polymerase assembly


1 CPBS CNRS UMR 5160, Faculté de Pharmacie 15 Avenue Charles Flahault, BP 14491, 34093 Montpellier Cedex 5, France; 2 Selectbiotics, 69 Rue G Besse, Parc scientifique G Besse, 30000 Nîmes, France; 3 INSERM U-431, Faculté de Médecine, Avenue Kennedy, 30900 Nîmes, France; 4 Laboratoire de Bactériologie, CHU de Nîmes, Groupe hospitalo-universitaire de Caremeau, 30029 Nîmes Cedex 9, France
Received 11 March 2005; revised and accepted 28 October 2005
* Corresponding author. Tel: +33-4-67-54-86-07; Fax: +33-4-67-54-86-10; E-mail: jp.leonetti{at}ibph.pharma.univ-montp1.fr
Objectives: Despite extensive functional screening of the bacterial RNA polymerase (RNAP) over the past years, very few novel inhibitors have been reported. We have, therefore, decided to screen with a radically different, non-enzymic, proteinprotein interaction assay. Our target is the highly conserved RNAP
interaction that is essential for transcription.
Methods: Small molecule inhibitors of the RNAP
interaction were tested for their activity on transcription and on bacteria.
Results: These compounds have antibacterial activity against Gram-positive bacteria including multiresistant clinical isolates.
Conclusions: This is, to our knowledge, the first example of a small molecule inhibitor of this interaction.
Keywords: transcription , antibacterial drug screening , antibacterials , antibiotic resistance , anti-infective agents
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