<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Pozzi, Cecilia</dc:creator>
  <dc:creator>Luca, Filomena De</dc:creator>
  <dc:creator>Benvenuti, Manuela</dc:creator>
  <dc:creator>Poirel, Laurent</dc:creator>
  <dc:creator>Nordmann, Patrice</dc:creator>
  <dc:creator>Rossolini, Gian Maria</dc:creator>
  <dc:creator>Mangani, Stefano</dc:creator>
  <dc:creator>Docquier, Jean-Denis</dc:creator>
  <dc:date>2016-01-12</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">BEL-1 is an acquired class A extended-spectrum β-lactamase (ESBL) found in  Pseudomonas aeruginosa clinical isolates from Belgium which is divergent from other  ESBLs (maximum identity of 54% with GES-type enzymes). This enzyme is efficiently  inhibited by clavulanate, imipenem, and moxalactam. Crystals of BEL-1 were obtained  at pH 5.6, and the structure of native BEL-1 was determined from orthorhombic and  monoclinic crystal forms at 1.60-Å and 1.48-Å resolution, respectively. By soaking  native BEL-1 crystals, complexes with imipenem (monoclinic form, 1.79-Å resolution)  and moxalactam (orthorhombic form, 1.85-Å resolution) were also obtained. In the  acyl-enzyme complexes, imipenem and moxalactam differ by the position of the α- substituent and of the carbonyl oxygen (in or out of the oxyanion hole). More  surprisingly, the Ω-loop, which includes the catalytically relevant residue Glu166, was  found in different conformations in the various subunits, resulting in the Glu166 side  chain being rotated out of the active site or even in displacement of its Cα atom up to  approximately 10 Å. A BEL-1 variant showing the single Leu162Phe substitution (BEL- 2) confers a higher level of resistance to CAZ, CTX, and FEP and shows significantly  lower Km values than BEL-1, especially with oxyiminocephalosporins. BEL-1 Leu162 is  located at the beginning of the Ω-loop and is surrounded by Phe72, Leu139, and  Leu148 (contact distances, 3.5 to 3.9 Å). This small hydrophobic cavity could not  reasonably accommodate the bulkier Phe162 found in BEL-2 without altering  neighboring residues or the Ω-loop itself, thus likely causing an important alteration of  the enzyme kinetic properties.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/305464</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/305464/files/nor_csp.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1128/AAC.00936-16</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Antimicrobial Agents and Chemotherapy. - 2016, vol. 60, no. 12, p. 7189–7199</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Crystal structure of the Pseudomonas aeruginosa BEL-1 extended-spectrum β-lactamase and its complexes with moxalactam and imipenem</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
