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One-Pot Bioconversion of l-Arabinose to l-Ribulose in an Enzymatic Cascade.
Chuaboon, Litavadee; Wongnate, Thanyaporn; Punthong, Pangrum; Kiattisewee, Cholpisit; Lawan, Narin; Hsu, Chia-Yi; Lin, Chun-Hung; Bornscheuer, Uwe T; Chaiyen, Pimchai.
Afiliação
  • Chuaboon L; Department of Biochemistry and Center for Excellence in Protein and Enzyme Technology, Faculty of Science, Mahidol University, Bangkok, 10400, Thailand.
  • Wongnate T; School of Biomolecular Science & Engineering, Vidyasirimedhi Institute of Science and Technology (VISTEC), Wangchan Valley, Rayong, 21210, Thailand.
  • Punthong P; School of Biomolecular Science & Engineering, Vidyasirimedhi Institute of Science and Technology (VISTEC), Wangchan Valley, Rayong, 21210, Thailand.
  • Kiattisewee C; School of Biomolecular Science & Engineering, Vidyasirimedhi Institute of Science and Technology (VISTEC), Wangchan Valley, Rayong, 21210, Thailand.
  • Lawan N; Department of Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai, 50200, Thailand.
  • Hsu CY; Institute of Biological Chemistry, Academia Sinica, Taipei, 11529, Taiwan.
  • Lin CH; Institute of Biological Chemistry, Academia Sinica, Taipei, 11529, Taiwan.
  • Bornscheuer UT; Institute of Biochemistry, Department of Biotechnology and Enzyme Catalysis, Greifswald University, Felix-Hausdorff-Strasse 4, Greifswald, Germany.
  • Chaiyen P; Department of Biochemistry and Center for Excellence in Protein and Enzyme Technology, Faculty of Science, Mahidol University, Bangkok, 10400, Thailand.
Angew Chem Int Ed Engl ; 58(8): 2428-2432, 2019 02 18.
Article em En | MEDLINE | ID: mdl-30605256
ABSTRACT
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pentoses / Arabinose / Desidrogenases de Carboidrato / Catalase / Aldeído Redutase / Formiato Desidrogenases Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Tailândia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pentoses / Arabinose / Desidrogenases de Carboidrato / Catalase / Aldeído Redutase / Formiato Desidrogenases Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Tailândia