Scope and Synthetic Applications of the Aryl-Alcohol Oxidase from <i>Streptomyces hiroshimensis</i> ( <i>Sh</i> AAO)

The sustainable production of carbonyl compounds is of growing interest due to their broad academic and industrial interest. Herein, we explored the aryl-alcohol oxidase from <i>Streptomyces hiroshimensis</i> (<i>Sh</i>AAO), mapping its activity across diverse alcohols, revealing a distinct profile from other natural AAOs. Integrated into tandem organocatalytic processes, <i>Sh</i>AAO enabled the synthesis of various chiral compounds, including an intermediate for paroxetine. Gram-scale reactions delivered high yields and turnover numbers exceeding 65000. Immobilization further enhanced stability, highlighting <i>Sh</i>AAO as an efficient and industrially relevant biocatalyst.

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Publication Details

Journal
Organic Letters
Published
2025-10-22
DOI
https://doi.org/10.1021/acs.orglett.5c03814
Primary Topic
Enzyme Catalysis and Immobilization
Type
article
Field-Weighted Citation Impact
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article

Scope and Synthetic Applications of the Aryl-Alcohol Oxidase from Streptomyces hiroshimensis ( Sh AAO)

Raquel P. Herrera, Juan Mangas‐Sánchez, Sebastian C. Cosgrove, Christian Ascaso‐Alegre et al.
Organic Letters
Enzyme Catalysis and Immobilization
article

Scope and Synthetic Applications of the Aryl-Alcohol Oxidase from Streptomyces hiroshimensis ( Sh AAO)

Raquel P. Herrera, Juan Mangas‐Sánchez, Sebastian C. Cosgrove, Christian Ascaso‐Alegre, Patrícia Ferreira, Paula Cinca-Fernando, Tom L. Roberts, Pablo López-Fernández
article en

Abstract

The sustainable production of carbonyl compounds is of growing interest due to their broad academic and industrial interest. Herein, we explored the aryl-alcohol oxidase from <i>Streptomyces hiroshimensis</i> (<i>Sh</i>AAO), mapping its activity across diverse alcohols, revealing a distinct profile from other natural AAOs. Integrated into tandem organocatalytic processes, <i>Sh</i>AAO enabled the synthesis of various chiral compounds, including an intermediate for paroxetine. Gram-scale reactions delivered high yields and turnover numbers exceeding 65000. Immobilization further enhanced stability, highlighting <i>Sh</i>AAO as an efficient and industrially relevant biocatalyst.

Organic LettersVol. 27(43)
Universidad de Oviedo (ES), Universidad de Zaragoza (ES), Instituto de Síntesis Química y Catálisis Homogénea (ES), Keele University (GB)
Keele University, Universidad de Oviedo, Universidad de Zaragoza, Gobierno de Aragón, Consejo Superior de Investigaciones Científicas, Agencia Estatal de Investigación, European Social Fund
Openalex Percentile: Top 73%
Enzyme Catalysis and Immobilization
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