English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/13053
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar a otros formatos:


Crystal structures of multidrug binding protein TtgR in complex with antibiotics and plant antimicrobials

AuthorsAlguel, Yilmaz; Meng, Cuixiang; Terán, Wilson; Krell, Tino; Ramos, Juan L.; Gallegos, María Trinidad ; Zhang, Xiaodong
KeywordsCrystal structure
Multidrug binding
Antibiotic resistance
Protein–ligand interaction
Issue Date30-Mar-2007
CitationJournal of Molecular Biology 369(3): 829-840 (2007)
AbstractAntibiotic resistance is a widely spread phenomenon. One major mechanism that underlies antibiotic resistance in bacteria is the active extrusion of toxic compounds through the membrane-bound efflux pumps that are often regulated at the transcriptional level. TtgR represses the transcription of TtgABC, a key efflux pump in Pseudomonas putida, which is highly resistant to antibiotics, solvents and toxic plant secondary products. Previously we showed that TtgR is the only reported repressor that binds to different classes of natural antimicrobial compounds, which are also extruded by the efflux pump. We report here five high-resolution crystal structures of TtgR from the solvent-tolerant strain DOT-T1E, including TtgR in complex with common antibiotics and plant secondary metabolites. We provide structural basis for the unique ligand binding properties of TtgR. We identify two distinct and overlapping ligand binding sites; the first one is broader and consists of mainly hydrophobic residues, whereas the second one is deeper and contains more polar residues including Arg176, a unique residue present in the DOT-T1E strain but not in other Pseudomonas strains. Phloretin, a plant antimicrobial, can bind to both binding sites with distinct binding affinities and stoichiometries. Results on ligand binding properties of native and mutant TtgR proteins using isothermal titration calorimetry confirm the binding affinities and stoichiometries, and suggest a potential positive cooperativity between the two binding sites. The importance of Arg176 in phloretin binding was further confirmed by the reduced ability of phloretin in releasing the mutant TtgR from bound DNA compared to the native protein. The results presented here highlight the importance and versatility of regulatory systems in bacterial antibiotic resistance and open up new avenues for novel antimicrobial development.
Description12 pages, 5 figures, 2 tables.-- PMID: 17466326 [PubMed].-- Printed version published Jun 8, 2007.
Supporting information (Suppl. figures S1-S2) available at Appendix A: http://dx.doi.org/10.1016/j.jmb.2007.03.062
All the structural data have been deposited to the RCSB Protein Data Bank through European Bioinformatics Institute and are available under accession codes 2UXP, 2UXO, 2UXI, 2UXU, 2UXH.
Publisher version (URL)http://dx.doi.org/10.1016/j.jmb.2007.03.062
Appears in Collections:(EEZ) Artículos
Files in This Item:
There are no files associated with this item.
Show full item record
Review this work

Related articles:

WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.