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dc.contributor.authorHoff, Bård Helge
dc.contributor.authorSundby, Eirik
dc.date.accessioned2017-11-10T14:54:49Z
dc.date.available2017-11-10T14:54:49Z
dc.date.created2017-09-13T19:06:54Z
dc.date.issued2017
dc.identifier.citationBioorganic chemistry (Print). 2017, 74 260-271.nb_NO
dc.identifier.issn0045-2068
dc.identifier.urihttp://hdl.handle.net/11250/2465614
dc.description.abstractThe use of literature data to identify catalysts for a novel transformation is a commonly used approach. Herein, we have evaluated if this is a viable strategy in enzyme catalysis, using asymmetric reduction of 1-aryl-2-alkanoates as a model system. The study, which includes data from 24 ketone substrates and 108 enzymes, clearly identifies pitfalls with this approach, but anyhow shows that literature data is highly useful for identification of enantioselective catalysts. By combining data for selectivity and rate useful catalyst for converting different substrates to their corresponding (R)- and (S)-enantiomers are highlighted.nb_NO
dc.language.isoengnb_NO
dc.publisherElseviernb_NO
dc.titleIs literature data useful for identifying enzyme catalysts for new substrates? A case study on reduction of 1-aryl-2-alkanoatesnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionsubmittedVersionnb_NO
dc.source.pagenumber260-271nb_NO
dc.source.volume74nb_NO
dc.source.journalBioorganic chemistry (Print)nb_NO
dc.identifier.doi10.1016/j.bioorg.2017.08.005
dc.identifier.cristin1493486
dc.description.localcodeThis is a submitted manuscript of an article published by Elsevier Ltd in Bioorganic Chemistry, 31 August 2017.nb_NO
cristin.unitcode194,66,25,0
cristin.unitnameInstitutt for kjemi
cristin.ispublishedtrue
cristin.fulltextpreprint
cristin.qualitycode1


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