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    <subfield code="a">Velasco-Lozano, S.</subfield>
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    <subfield code="a">Co-immobilization and Colocalization of Multi-Enzyme Systems for the Cell-Free Biosynthesis of Aminoalcohols</subfield>
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    <subfield code="c">2020</subfield>
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    <subfield code="a">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.</subfield>
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    <subfield code="a">Physical and Theoretical Chemistry</subfield>
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    <subfield code="a">Organic Chemistry</subfield>
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    <subfield code="a">Santiago-Arcos, J.</subfield>
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    <subfield code="a">Mayoral, J.A.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
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    <subfield code="a">López-Gallego, F.</subfield>
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    <subfield code="1">2013</subfield>
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    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Química Orgánica</subfield>
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    <subfield code="g">12, 11 (2020), 3030-3041</subfield>
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