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Chemo-biocatalytic one-pot two-step conversion of cyclic amine to lactam using whole cell monoamine oxidase

Zajkoska, Petra, Cárdenas-Fernández, Max, Lye, Gary J, Rosenberg, Michal, Turner, Nicholas J, Rebroš, Martin (2016) Chemo-biocatalytic one-pot two-step conversion of cyclic amine to lactam using whole cell monoamine oxidase. Journal of Chemical Technology & Biotechnology, 92 (7). pp. 1558-1565. ISSN 0268-2575. E-ISSN 1097-4660. (doi:10.1002/jctb.5146) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:88161)

The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided.
Official URL:
https://doi.org/10.1002/jctb.5146

Abstract

BACKGROUNDMost biocatalysts currently involved in one‐pot chemoenzymatic cascades are pure enzymes, while whole cells and crude enzyme extracts remain unexplored. This work aims to develop a chemo‐biocatalytic one‐pot two‐step system involving whole cell monoamine oxidase (MAO, EC 1.4.3.4) coupled with a Cu‐based oxidative system (CuI/H2O2) for the transformation of 1,2,3,4‐tetrahydroisoquinoline (THIQ) to 3,4‐dihydroisoquinolin‐1(2H)‐one (DHIO).RESULTSMAO‐N variants D9 and D11 were tested as whole cell and crude lysate biocatalysts for biological oxidation. Whole Escherichia coli OverExpress C43(DE3) cells expressing MAO‐N D9 showed the best performance (Vmax = 36.58 mmol L−1 h−1, KM = 8.124 mmol L−1, maximum specific productivity 89.3 μmol min−1 g−1DCW) and were employed in combination with CuI/H2O2 in a sequential one‐pot two‐step process. The biotransformation was scaled‐up to the initial volume of 25 mL and after triple THIQ feeding, 48.2 mmol L−1 of the intermediate 3,4‐dihydroisoquinoline (DHIQ) was obtained with a yield of 71.3%. Afterwards, chemical catalysts (1 mol% CuI and 10 eq. H2O2) were added to the biologically produced DHIQ, which was transformed to ∼30 mmol L−1 DHIO at 69.4% overall yield.CONCLUSIONAs MAO‐N variants have wide substrate specificity, this work broadens the portfolio of one‐pot chemoenzymatic processes employing whole cell biocatalysts, representing an alternative to using pure enzymes.

Item Type: Article
DOI/Identification number: 10.1002/jctb.5146
Divisions: Divisions > Division of Natural Sciences > Biosciences
Depositing User: Max Cardenas Fernandez
Date Deposited: 14 May 2021 15:42 UTC
Last Modified: 05 Nov 2024 12:54 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/88161 (The current URI for this page, for reference purposes)

University of Kent Author Information

Cárdenas-Fernández, Max.

Creator's ORCID: https://orcid.org/0000-0003-1422-5369
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