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Enantioselective hydrolysis of (R/S)-Naproxen methyl ester with sol-gel encapculated lipase in presence of calix[n]arene derivatives

Sahin, Ozlem; Erdemir, Serkan; Uyanik, Arzu; Yilmaz, Mustafa


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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/39899</identifier>
  <creators>
    <creator>
      <creatorName>Sahin, Ozlem</creatorName>
      <givenName>Ozlem</givenName>
      <familyName>Sahin</familyName>
      <affiliation>Selcuk Univ, Dept Chem, TR-42031 Konya, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Erdemir, Serkan</creatorName>
      <givenName>Serkan</givenName>
      <familyName>Erdemir</familyName>
      <affiliation>Selcuk Univ, Dept Chem, TR-42031 Konya, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Uyanik, Arzu</creatorName>
      <givenName>Arzu</givenName>
      <familyName>Uyanik</familyName>
      <affiliation>Selcuk Univ, Dept Chem, TR-42031 Konya, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Yilmaz, Mustafa</creatorName>
      <givenName>Mustafa</givenName>
      <familyName>Yilmaz</familyName>
      <affiliation>Selcuk Univ, Dept Chem, TR-42031 Konya, Turkey</affiliation>
    </creator>
  </creators>
  <titles>
    <title>Enantioselective Hydrolysis Of (R/S)-Naproxen Methyl Ester With Sol-Gel Encapculated Lipase In Presence Of Calix[N]Arene Derivatives</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>2009</publicationYear>
  <dates>
    <date dateType="Issued">2009-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/39899</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1016/j.apcata.2009.08.030</relatedIdentifier>
  </relatedIdentifiers>
  <rightsList>
    <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights>
    <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
  </rightsList>
  <descriptions>
    <description descriptionType="Abstract">Lipases are enzymes that catalyses a variety of reactions, such esterifications, interesterification and hydrolysis. Several methods have been reported for the immobilization of lipases, such as deposition onto solid supports, covalent binding and encapsulation within a polymer matrix or silica glasses obtained by sol-gel techniques. In this study, the Candido rugosa lipase was encapsulated within a chemically inert sol-gel support prepared by polycondensation by tetraetoxysilane (TEOS)and octyltrietoxysilane(OTES) in the presence and absence of calix[n]arene, calix[n]-NH2 and calix[n]-COOH (n = 4,6,8) compounds as additives. The catalytic activity of the encapsulated lipases was evaluated into model reactions, i.e. the hydrolysis of p-nitrophenylpalmitate (p-NPP), and the enantioselective hydrolysis of rasemic Naproxen methyl ester that was studied in aqueous buffer solution/isooctane reaction system. The results indicated that the particularly calix[4,6]-NH2 and calix[6]-COOH based encapsulated lipases had higher conversion and enantioselectivity compared to the sol-gel free lipase. (C) 2009 Elsevier B.V. All rights reserved.</description>
  </descriptions>
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