Resumen: The manufacturing of aminoalcohols is an appealing transformation for industrial biocatalysis due to their high value as building blocks in synthetic chemistry. By co-immobilizing dehydrogenases, ¿-transaminases and oxidases on porous carriers, we fabricated and characterized a multi-functional heterogeneous biocatalyst that was further applied to the cell-free biosynthesis of amines and aminoalcohols from alcohols and diols, respectively. This immobilized cascade integrates both redox cofactor and amine donor recycling systems into the amino alcohol biosynthesis. Spatial co-localization of the multi-enzyme system significantly increases the cofactor recycling efficiency, the system productivity and the product conversion. Using this multi-functional heterogeneous biocatalyst, we achieved 80 % conversion of alcohols into amines and accessed a palette of up to 5 aminoalcohols starting from their corresponding diols in one-pot. The results herein presented contribute to understanding the effects of the confinement of co-immobilized enzymes on the cascade processes. Idioma: Inglés DOI: 10.1002/cctc.201902404 Año: 2020 Publicado en: ChemCatChem 12, 11 (2020), 3030-3041 ISSN: 1867-3880 Factor impacto JCR: 5.686 (2020) Categ. JCR: CHEMISTRY, PHYSICAL rank: 50 / 162 = 0.309 (2020) - Q2 - T1 Factor impacto SCIMAGO: 1.497 - Catalysis (Q1) - Physical and Theoretical Chemistry (Q1) - Organic Chemistry (Q1) - Inorganic Chemistry (Q1)