Multienzyme cascade synthesis of ω-amino fatty acids from vegetable-derived precursors for use as nylon monomers

Abstract

Omega-amino fatty acids (ω-AmFAs) are non-natural organic molecules with amino and carboxyl groups located at the ends of unbranched carbon chains. They are widely used in the synthesis of polymers such as polyesters and polyamides, as well as in the production of chemical products such as biofuels and pharmaceutical intermediates. In recent years, the production of such materials and other chemicals via the fermentation of renewable resources using engineered microorganisms has become a hot spot of research, as examples of emerging green and low-carbon technologies. Traditional petrochemical synthesis methods of nylon monomers often face problems such as environmental pollution, increased energy consumption and high cost. By contrast, the catalytic production of ω-AmFAs from fatty acids such as oleic acid, ricinoleic acid and lauric acid found in vegetable oils using a multienzyme cascade has the unique advantages of being environmentally friendly and having high process economics. This paper reviews multienzyme synthesis strategies of ω-AmFAs used as nylon monomers.

Graphical abstract: Multienzyme cascade synthesis of ω-amino fatty acids from vegetable-derived precursors for use as nylon monomers

Article information

Article type
Tutorial Review
Submitted
06 dek 2024
Accepted
27 mar 2025
First published
28 mar 2025
This article is Open Access
Creative Commons BY-NC license

RSC Sustainability, 2025, Advance Article

Multienzyme cascade synthesis of ω-amino fatty acids from vegetable-derived precursors for use as nylon monomers

Y. Zhou, R. Lu, X. Gao, L. Lin, Y. Wei and X. Ji, RSC Sustainability, 2025, Advance Article , DOI: 10.1039/D4SU00764F

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements