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Scalable bioreactor production of an O2‐protected [FeFe]‐hydrogenase enables simple aerobic handling for clean chemical synthesis

Cleary, Sarah Elizabeth; Hall, Stephen J; Galan-Bataller, Regina; Lurshay, Tara C.; Hancox, Charlotte; Williamson, James J; Heap, John T.; Reeve, Holly A.; Morra, Simone

Scalable bioreactor production of an O2‐protected [FeFe]‐hydrogenase enables simple aerobic handling for clean chemical synthesis Thumbnail


Authors

Sarah Elizabeth Cleary

Stephen J Hall

Regina Galan-Bataller

Tara C. Lurshay

Charlotte Hancox

Profile image of JOHN HEAP

JOHN HEAP JOHN.HEAP@NOTTINGHAM.AC.UK
Associate Professor

Holly A. Reeve

Profile image of SIMONE MORRA

SIMONE MORRA SIMONE.MORRA@NOTTINGHAM.AC.UK
Assistant Professor in Chemical &environmental Engineering



Abstract

The enzyme CbA5H, a [FeFe]-hydrogenase from Clostridium beijerinckii, has previously been shown to survive exposure to oxygen, making it a promising candidate for biotechnological applications. Thus far [NiFe]-hydrogenases are typically considered for such applications, due to the superior O2-tolerance and therefore simplified enzyme handling. However, methods for production of [FeFe]-hydrogenases are generally more successful than for other classes of hydrogenases, therefore in this work we focus on demonstrating scalable CbA5H production, and report results with active enzyme prepared in bioreactors (up to 10 L) with >20-fold improvement in purified enzyme yield. We then go on to confirm excellent H2/H+-cycling activity of the air-purified protein, highlighting that CbA5H can be prepared and isolated without the need for complex and expensive infrastructure. Next, we demonstrate good stability of the air-purified CbA5H both in solution assays, and as a heterogenous catalyst system when immobilized on a carbon support. Finally, we successfully implement this enzyme within previously demonstrated biotechnologies for flavin and NADH recycling, highlighting its relevance in chemical synthesis, and we demonstrate production of an important API precursor, 3-quinuclidinol at >0.4 g scale in standard benchtop hydrogenation infrastructure, with >100,000 CbA5H turnovers over 18 operational hours.

Citation

Cleary, S. E., Hall, S. J., Galan-Bataller, R., Lurshay, T. C., Hancox, C., Williamson, J. J., Heap, J. T., Reeve, H. A., & Morra, S. (in press). Scalable bioreactor production of an O2‐protected [FeFe]‐hydrogenase enables simple aerobic handling for clean chemical synthesis. ChemCatChem, https://doi.org/10.1002/cctc.202400193

Journal Article Type Article
Acceptance Date Mar 27, 2024
Online Publication Date Mar 28, 2024
Deposit Date Apr 19, 2024
Publicly Available Date May 3, 2024
Journal ChemCatChem
Print ISSN 1867-3880
Electronic ISSN 1867-3899
Publisher Wiley
Peer Reviewed Peer Reviewed
DOI https://doi.org/10.1002/cctc.202400193
Keywords hydrogenase; cofactor recycling; industrial biotechnology; biocatalysis; sustainable chemistry
Public URL https://nottingham-repository.worktribe.com/output/33548831
Publisher URL https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/cctc.202400193
Additional Information Received: 2024-01-30; Accepted: 2024-03-27; Published: 2024-03-28

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