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Fusion of Formate Dehydrogenase and Alanine Dehydrogenase as an Amino Donor Regenerating System Coupled to Transaminases
Fusion enzymes are attractive tools for facilitating the assembly of biocatalytic cascades for chemical synthesis. This approach can offer great advantages for cooperative redox cascades that need the constant supply of a donor molecule. In this work, we have developed a self‐sufficient bifunctional...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9828552/ https://www.ncbi.nlm.nih.gov/pubmed/36066500 http://dx.doi.org/10.1002/cbic.202200428 |
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author | Marchini, Valentina Benítez‐Mateos, Ana I. Hutter, Sofia L. Paradisi, Francesca |
author_facet | Marchini, Valentina Benítez‐Mateos, Ana I. Hutter, Sofia L. Paradisi, Francesca |
author_sort | Marchini, Valentina |
collection | PubMed |
description | Fusion enzymes are attractive tools for facilitating the assembly of biocatalytic cascades for chemical synthesis. This approach can offer great advantages for cooperative redox cascades that need the constant supply of a donor molecule. In this work, we have developed a self‐sufficient bifunctional enzyme that can be coupled to transaminase‐catalyzed reactions for the efficient recycling of the amino donor (L‐alanine). By genetic fusion of an alanine dehydrogenase (AlaDH) and a formate dehydrogenase (FDH), a redox‐complementary system was applied to recycle the amino donor and the cofactor (NADH), respectively. AlaDH and FDH were assembled in both combinations (FDH‐AlaDH and AlaDH‐FDH), with a 2.5‐fold higher enzymatic activity of the latter system. Then, AlaDH‐FDH was coupled to two different S‐selective transaminases for the synthesis of vanillyl amine (10 mM) reaching up to 99 % conversion in 24 h in both cases. Finally, the multienzyme system was reused for at least 3 consecutive cycles when implemented in dialysis‐assisted biotransformations. |
format | Online Article Text |
id | pubmed-9828552 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98285522023-01-10 Fusion of Formate Dehydrogenase and Alanine Dehydrogenase as an Amino Donor Regenerating System Coupled to Transaminases Marchini, Valentina Benítez‐Mateos, Ana I. Hutter, Sofia L. Paradisi, Francesca Chembiochem Research Articles Fusion enzymes are attractive tools for facilitating the assembly of biocatalytic cascades for chemical synthesis. This approach can offer great advantages for cooperative redox cascades that need the constant supply of a donor molecule. In this work, we have developed a self‐sufficient bifunctional enzyme that can be coupled to transaminase‐catalyzed reactions for the efficient recycling of the amino donor (L‐alanine). By genetic fusion of an alanine dehydrogenase (AlaDH) and a formate dehydrogenase (FDH), a redox‐complementary system was applied to recycle the amino donor and the cofactor (NADH), respectively. AlaDH and FDH were assembled in both combinations (FDH‐AlaDH and AlaDH‐FDH), with a 2.5‐fold higher enzymatic activity of the latter system. Then, AlaDH‐FDH was coupled to two different S‐selective transaminases for the synthesis of vanillyl amine (10 mM) reaching up to 99 % conversion in 24 h in both cases. Finally, the multienzyme system was reused for at least 3 consecutive cycles when implemented in dialysis‐assisted biotransformations. John Wiley and Sons Inc. 2022-09-29 2022-11-04 /pmc/articles/PMC9828552/ /pubmed/36066500 http://dx.doi.org/10.1002/cbic.202200428 Text en © 2022 The Authors. ChemBioChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Marchini, Valentina Benítez‐Mateos, Ana I. Hutter, Sofia L. Paradisi, Francesca Fusion of Formate Dehydrogenase and Alanine Dehydrogenase as an Amino Donor Regenerating System Coupled to Transaminases |
title | Fusion of Formate Dehydrogenase and Alanine Dehydrogenase as an Amino Donor Regenerating System Coupled to Transaminases |
title_full | Fusion of Formate Dehydrogenase and Alanine Dehydrogenase as an Amino Donor Regenerating System Coupled to Transaminases |
title_fullStr | Fusion of Formate Dehydrogenase and Alanine Dehydrogenase as an Amino Donor Regenerating System Coupled to Transaminases |
title_full_unstemmed | Fusion of Formate Dehydrogenase and Alanine Dehydrogenase as an Amino Donor Regenerating System Coupled to Transaminases |
title_short | Fusion of Formate Dehydrogenase and Alanine Dehydrogenase as an Amino Donor Regenerating System Coupled to Transaminases |
title_sort | fusion of formate dehydrogenase and alanine dehydrogenase as an amino donor regenerating system coupled to transaminases |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9828552/ https://www.ncbi.nlm.nih.gov/pubmed/36066500 http://dx.doi.org/10.1002/cbic.202200428 |
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