<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>Oueslati, Saoussen</dc:creator>
  <dc:creator>Nordmann, Patrice</dc:creator>
  <dc:creator>Poirel, Laurent</dc:creator>
  <dc:date>2015-01-04</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Objectives: Carbapenem-hydrolysing class D β-lactamases of the OXA-48 type are  increasingly reported from Enterobacteriaceae. β-Lactamase OXA-48 hydrolyses  penicillins very efficiently, but carbapenems only weakly and spares broad-spectrum  cephalosporins. Recently, diverse OXA-48-like β-lactamases have been identified  worldwide (OXA-162, OXA-181, OXA-163, OXA-204 and OXA-232). They differ by  few amino acid substitutions or by amino acid deletions.Methods: blaOXA-48,  blaOXA-162, blaOXA-163, blaOXA-181, blaOXA-204 and blaOXA-232 were cloned  into the same expression vector and expressed in the same Escherichia coli  background. Kinetic studies were performed with enzymes purified by ion-exchange  chromatography. Determination of hydrolytic activities was performed by UV  spectrophotometry. MICs were determined for all recombinant strains, using as  background either the WT E. coli TOP10 strain or a porin-deficient E. coli  strain.Results: Kinetic studies showed that OXA-162 and OXA-204 shared the same  hydrolytic properties as OXA-48. On the other hand, OXA-181 possessed a higher  ability to hydrolyse carbapenems, while OXA-232 hydrolysed those substrates less  efficiently. In contrast to the other OXA-48-like β-lactamases, OXA-163 hydrolysed  broad-spectrum cephalosporins very efficiently, but did not possess significant  carbapenemase activity. Although several of these OXA-48-like enzymes possess low  activity against carbapenems, MICs of carbapenems were significantly elevated when  determined for strains possessing permeability defects.Conclusions: A detailed  comparative analysis of the kinetic properties of the OXA-48-like β-lactamases is  provided here. It clarifies the respective features of each OXA-48-like variant and their  respective impacts in terms of carbapenem resistance.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/304249</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/304249/files/dku524.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1093/jac/dku524</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Journal of Antimicrobial Chemotherapy. - 2015, vol. 70, no. 4, p. 1059-1063</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">carbapenemases</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">class D lactamases</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">enzymatic activity</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns4="xml" ns4:lang="en">Heterogeneous hydrolytic features for OXA-48-like β-lactamases</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
