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One‐Step Biocatalytic Synthesis of Sustainable Surfactants by Selective Amide Bond Formation

Lubberink, Max; Finnigan, William; Schnepel, Christian; Baldwin, Christopher R.; Turner, Nicholas J.; Flitsch, Sabine L.

Authors

Max Lubberink

William Finnigan

Christopher R. Baldwin

Nicholas J. Turner

Sabine L. Flitsch



Abstract

N-alkanoyl-N-methylglucamides (MEGAs) are non-toxic surfactants widely used as commercial ingredients, but more sustainable syntheses towards these compounds are highly desirable. Here, we present a biocatalytic route towards MEGAs and analogues using a truncated carboxylic acid reductase construct tailored for amide bond formation (CARmm-A). CARmm-A is capable of selective amide bond formation without the competing esterification reaction observed in lipase catalysed reactions. A kinase was implemented to regenerate ATP from polyphosphate and by thorough reaction optimisation using design of experiments, the amine concentration needed for amidation was significantly reduced. The wide substrate scope of CARmm-A was exemplified by the synthesis of 24 commercially relevant amides, including selected examples on a preparative scale. This work establishes acyl-phosphate mediated chemistry as a highly selective strategy for biocatalytic amide bond formation in the presence of multiple competing alcohol functionalities.

Citation

Lubberink, M., Finnigan, W., Schnepel, C., Baldwin, C. R., Turner, N. J., & Flitsch, S. L. (2022). One‐Step Biocatalytic Synthesis of Sustainable Surfactants by Selective Amide Bond Formation. Angewandte Chemie International Edition, 61(30), Article e202205054. https://doi.org/10.1002/anie.202205054

Journal Article Type Article
Acceptance Date May 20, 2022
Online Publication Date Jun 8, 2022
Publication Date Jul 25, 2022
Deposit Date Jan 1, 2025
Journal Angewandte Chemie International Edition
Print ISSN 1433-7851
Electronic ISSN 1521-3773
Publisher Wiley
Peer Reviewed Peer Reviewed
Volume 61
Issue 30
Article Number e202205054
DOI https://doi.org/10.1002/anie.202205054
Public URL https://durham-repository.worktribe.com/output/3263628