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Synthesis of a precursor of D-fagomine by immobilized fructose-6-phosphate aldolase.
Masdeu, Gerard; Vázquez, Luis Miguel; López-Santín, Josep; Caminal, Gloria; Kralj, Slavko; Makovec, Darko; Álvaro, Gregorio; Guillén, Marina.
Afiliação
  • Masdeu G; Department of Chemical, Biological and Environmental Engineering, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.
  • Vázquez LM; Department of Chemical, Biological and Environmental Engineering, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.
  • López-Santín J; Department of Chemical, Biological and Environmental Engineering, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.
  • Caminal G; Institute of Advanced Chemistry of Catalonia, IAQC-CSIC, Barcelona, Spain.
  • Kralj S; Department for Materials Synthesis, Jozef Stefan Institute, Ljubljana, Slovenia.
  • Makovec D; Department for Materials Synthesis, Jozef Stefan Institute, Ljubljana, Slovenia.
  • Álvaro G; Department of Chemical, Biological and Environmental Engineering, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.
  • Guillén M; Department of Chemical, Biological and Environmental Engineering, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.
PLoS One ; 16(4): e0250513, 2021.
Article em En | MEDLINE | ID: mdl-33886681
Fructose-6-phosphate aldolase (FSA) is an important enzyme for the C-C bond-forming reactions in organic synthesis. The present work is focused on the synthesis of a precursor of D-fagomine catalyzed by a mutant FSA. The biocatalyst has been immobilized onto several supports: magnetic nanoparticle clusters (mNC), cobalt-chelated agarose (Co-IDA), amino-functionalized agarose (MANA-agarose) and glyoxal-agarose, obtaining a 29.0%, 93.8%, 89.7% and 53.9% of retained activity, respectively. Glyoxal-agarose FSA derivative stood up as the best option for the synthesis of the precursor of D-fagomine due to the high reaction rate, conversion, yield and operational stability achieved. FSA immobilized in glyoxal-agarose could be reused up to 6 reaction cycles reaching a 4-fold improvement in biocatalyst yield compared to the non-immobilized enzyme.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aldeído Liases / Enzimas Imobilizadas / Imino Piranoses / Nanopartículas de Magnetita Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aldeído Liases / Enzimas Imobilizadas / Imino Piranoses / Nanopartículas de Magnetita Idioma: En Ano de publicação: 2021 Tipo de documento: Article