Biocatalytic production of 3-hydroxypropionic acid precursors using a regioselective Baeyer-Villiger monooxygenase
Baeyer-Villiger monooxygenases (BVMOs) are versatile biocatalysts that catalyse the oxidation of ketones to esters with high regio- and enantioselectivity, operating under mild reaction conditions while reducing hazardous waste. Some BVMOs can convert cellulose-derived alkyl levulinates to 3-acetoxypropionates (3-APs), which are key intermediates in the production of 3-hydroxypropionic acid (3-HP), a versatile building block chemical. In this study, a BVMO from Acinetobacter radioresistens (Ar-BVMO) was tested as a biocatalyst for the conversion of three marketed alkyl levulinates: methyl, ethyl and butyl levulinate. The enzyme showed 4-fold higher catalytic efficiency (k<sub>cat</sub>/K<sub>M</sub>) and enhanced regioselectivity for the desired 3-AP product (4:1 ratio) when using butyl levulinate as a substrate. Escherichia coli whole-cells over-expressing Ar-BVMO were exploited to increase the product yield, achieving 85% conversion in 9 h. To further improve the sustainability of this biotransformation, butyl levulinate was obtained via microwave-assisted alcoholysis of pulp, a renewable cellulose feedstock, achieving 92.7% selectivity. Despite challenges posed by poor solubility of the resulting mixture in aqueous environment, Ar-BVMO in cell lysates was able to fully convert butyl levulinate within 24 h, efficiently producing 3-HP precursors without additional purification steps. These findings highlight the feasibility of this chemoenzymatic approach to convert cellulose-based raw materials to platform chemicals.
Authors
- Giancarlo Cravotto
- Fabio Bucciol (ORCID: https://orcid.org/0000-0003-0548-9127)
- Carlo Roggero
- Gianfranco Gilardi (ORCID: https://orcid.org/0000-0002-6559-276X)
- Gianluca Catucci (ORCID: https://orcid.org/0000-0002-4593-4507)
- Silvia Tabasso (ORCID: https://orcid.org/0000-0002-1567-8143)
- Danilo Correddu (ORCID: https://orcid.org/0000-0003-4945-8904)
- Sheila J. Sadeghi (ORCID: https://orcid.org/0000-0003-4951-1242)
- Melissa De Angelis
Institutions
- Marconi University (IT)
- Accademia Albertina delle Belle Arti (IT)
- University of Turin (IT)
Publication Details
- Journal
- Scientific Reports
- Published
- 2025-04-22
- DOI
- https://doi.org/10.1038/s41598-025-96783-0
- Citations
- 2
- Primary Topic
- Enzyme Catalysis and Immobilization
- Type
- article
- Field-Weighted Citation Impact
- 1.61