Cargando…

Continuous Flow Bioamination of Ketones in Organic Solvents at Controlled Water Activity using Immobilized ω‐Transaminases

Compared with biocatalysis in aqueous media, the use of enzymes in neat organic solvents enables increased solubility of hydrophobic substrates and can lead to more favorable thermodynamic equilibria, avoidance of possible hydrolytic side reactions and easier product recovery. ω‐Transaminases from A...

Descripción completa

Detalles Bibliográficos
Autores principales: Böhmer, Wesley, Volkov, Alexey, Engelmark Cassimjee, Karim, Mutti, Francesco G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217232/
https://www.ncbi.nlm.nih.gov/pubmed/32421034
http://dx.doi.org/10.1002/adsc.201901274
_version_ 1783532576382648320
author Böhmer, Wesley
Volkov, Alexey
Engelmark Cassimjee, Karim
Mutti, Francesco G.
author_facet Böhmer, Wesley
Volkov, Alexey
Engelmark Cassimjee, Karim
Mutti, Francesco G.
author_sort Böhmer, Wesley
collection PubMed
description Compared with biocatalysis in aqueous media, the use of enzymes in neat organic solvents enables increased solubility of hydrophobic substrates and can lead to more favorable thermodynamic equilibria, avoidance of possible hydrolytic side reactions and easier product recovery. ω‐Transaminases from Arthrobacter sp. (AsR−ωTA) and Chromobacterium violaceum (Cv−ωTA) were immobilized on controlled porosity glass metal‐ion affinity beads (EziG) and applied in neat organic solvents for the amination of 1‐phenoxypropan‐2‐one with 2‐propylamine. The reaction system was investigated in terms of type of carrier material, organic solvents and reaction temperature. Optimal conditions were found with more hydrophobic carrier materials and toluene as reaction solvent. The system's water activity (a(w)) was controlled via salt hydrate pairs during both the biocatalyst immobilization step and the progress of the reaction in different non‐polar solvents. Notably, the two immobilized ωTAs displayed different optimal values of a(w), namely 0.7 for EziG(3)−AsR−ωTA and 0.2 for EziG(3)−Cv−ωTA. In general, high catalytic activity was observed in various organic solvents even when a high substrate concentration (450–550 mM) and only one equivalent of 2‐propylamine were applied. Under batch conditions, a chemical turnover (TTN) above 13000 was obtained over four subsequent reaction cycles with the same batch of EziG‐immobilized ωTA. Finally, the applicability of the immobilized biocatalyst in neat organic solvents was further demonstrated in a continuous flow packed‐bed reactor. The flow reactor showed excellent performance without observable loss of enzymatic catalytic activity over several days of operation. In general, ca. 70% conversion was obtained in 72 hours using a 1.82 mL flow reactor and toluene as flow solvent, thus affording a space‐time yield of 1.99 g L(−1) h(−1). Conversion reached above 90% when the reaction was run up to 120 hours. [Image: see text]
format Online
Article
Text
id pubmed-7217232
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-72172322020-05-13 Continuous Flow Bioamination of Ketones in Organic Solvents at Controlled Water Activity using Immobilized ω‐Transaminases Böhmer, Wesley Volkov, Alexey Engelmark Cassimjee, Karim Mutti, Francesco G. Adv Synth Catal Full Papers Compared with biocatalysis in aqueous media, the use of enzymes in neat organic solvents enables increased solubility of hydrophobic substrates and can lead to more favorable thermodynamic equilibria, avoidance of possible hydrolytic side reactions and easier product recovery. ω‐Transaminases from Arthrobacter sp. (AsR−ωTA) and Chromobacterium violaceum (Cv−ωTA) were immobilized on controlled porosity glass metal‐ion affinity beads (EziG) and applied in neat organic solvents for the amination of 1‐phenoxypropan‐2‐one with 2‐propylamine. The reaction system was investigated in terms of type of carrier material, organic solvents and reaction temperature. Optimal conditions were found with more hydrophobic carrier materials and toluene as reaction solvent. The system's water activity (a(w)) was controlled via salt hydrate pairs during both the biocatalyst immobilization step and the progress of the reaction in different non‐polar solvents. Notably, the two immobilized ωTAs displayed different optimal values of a(w), namely 0.7 for EziG(3)−AsR−ωTA and 0.2 for EziG(3)−Cv−ωTA. In general, high catalytic activity was observed in various organic solvents even when a high substrate concentration (450–550 mM) and only one equivalent of 2‐propylamine were applied. Under batch conditions, a chemical turnover (TTN) above 13000 was obtained over four subsequent reaction cycles with the same batch of EziG‐immobilized ωTA. Finally, the applicability of the immobilized biocatalyst in neat organic solvents was further demonstrated in a continuous flow packed‐bed reactor. The flow reactor showed excellent performance without observable loss of enzymatic catalytic activity over several days of operation. In general, ca. 70% conversion was obtained in 72 hours using a 1.82 mL flow reactor and toluene as flow solvent, thus affording a space‐time yield of 1.99 g L(−1) h(−1). Conversion reached above 90% when the reaction was run up to 120 hours. [Image: see text] John Wiley and Sons Inc. 2020-02-17 2020-04-27 /pmc/articles/PMC7217232/ /pubmed/32421034 http://dx.doi.org/10.1002/adsc.201901274 Text en © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Böhmer, Wesley
Volkov, Alexey
Engelmark Cassimjee, Karim
Mutti, Francesco G.
Continuous Flow Bioamination of Ketones in Organic Solvents at Controlled Water Activity using Immobilized ω‐Transaminases
title Continuous Flow Bioamination of Ketones in Organic Solvents at Controlled Water Activity using Immobilized ω‐Transaminases
title_full Continuous Flow Bioamination of Ketones in Organic Solvents at Controlled Water Activity using Immobilized ω‐Transaminases
title_fullStr Continuous Flow Bioamination of Ketones in Organic Solvents at Controlled Water Activity using Immobilized ω‐Transaminases
title_full_unstemmed Continuous Flow Bioamination of Ketones in Organic Solvents at Controlled Water Activity using Immobilized ω‐Transaminases
title_short Continuous Flow Bioamination of Ketones in Organic Solvents at Controlled Water Activity using Immobilized ω‐Transaminases
title_sort continuous flow bioamination of ketones in organic solvents at controlled water activity using immobilized ω‐transaminases
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217232/
https://www.ncbi.nlm.nih.gov/pubmed/32421034
http://dx.doi.org/10.1002/adsc.201901274
work_keys_str_mv AT bohmerwesley continuousflowbioaminationofketonesinorganicsolventsatcontrolledwateractivityusingimmobilizedōtransaminases
AT volkovalexey continuousflowbioaminationofketonesinorganicsolventsatcontrolledwateractivityusingimmobilizedōtransaminases
AT engelmarkcassimjeekarim continuousflowbioaminationofketonesinorganicsolventsatcontrolledwateractivityusingimmobilizedōtransaminases
AT muttifrancescog continuousflowbioaminationofketonesinorganicsolventsatcontrolledwateractivityusingimmobilizedōtransaminases