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dc.contributor.authorLitavadee Chuaboonen_US
dc.contributor.authorThanyaporn Wongnateen_US
dc.contributor.authorPangrum Punthongen_US
dc.contributor.authorCholpisit Kiattiseweeen_US
dc.contributor.authorNarin Lawanen_US
dc.contributor.authorChia Yi Hsuen_US
dc.contributor.authorChun Hung Linen_US
dc.contributor.authorUwe T. Bornscheueren_US
dc.contributor.authorPimchai Chaiyenen_US
dc.date.accessioned2019-03-18T02:21:37Z-
dc.date.available2019-03-18T02:21:37Z-
dc.date.issued2019-02-18en_US
dc.identifier.issn15213773en_US
dc.identifier.issn14337851en_US
dc.identifier.other2-s2.0-85060784297en_US
dc.identifier.other10.1002/anie.201814219en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85060784297&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/63605-
dc.description.abstract© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim This work reports the one-pot enzymatic cascade that completely converts l-arabinose to l-ribulose using four reactions catalyzed by pyranose 2-oxidase (P2O), xylose reductase, formate dehydrogenase, and catalase. As wild-type P2O is specific for the oxidation of six-carbon sugars, a pool of P2O variants was generated based on rational design to change the specificity of the enzyme towards the oxidation of l-arabinose at the C2-position. The variant T169G was identified as the best candidate, and this had an approximately 40-fold higher rate constant for the flavin reduction (sugar oxidation) step, as compared to the wild-type enzyme. Computational calculations using quantum mechanics/molecular mechanics (QM/MM) molecular dynamics (MD) showed that this improvement is due to a decrease in the steric effects at the axial C4-OH of l-arabinose, which allows a reduction in the distance between the C2-H and flavin N5, facilitating hydride transfer and enabling flavin reduction.en_US
dc.subjectChemical Engineeringen_US
dc.subjectChemistryen_US
dc.titleOne-Pot Bioconversion of l-Arabinose to l-Ribulose in an Enzymatic Cascadeen_US
dc.typeJournalen_US
article.title.sourcetitleAngewandte Chemie - International Editionen_US
article.volume58en_US
article.stream.affiliationsMahidol Universityen_US
article.stream.affiliationsVidyasirimedhi Institute of Science and Technologyen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsAcademia Sinica, Institute of Biological Chemistryen_US
article.stream.affiliationsErnst-Moritz-Arndt-Universität Greifswalden_US
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