Engineering metazoan fatty acid synthase to control chain length applied in yeast

Metazoan fatty acid (FA) synthases (mFASs) facilitate the de novo synthesis of C16- and C18-FAs through iterative extensions within the FA cycle and hydrolytic release. Here we re-engineer mFAS to fine-tune the interplay between FA extension and FA hydrolytic release for the targeted production of short- and medium-chain fatty acids. Single amino acid exchanges in the ketosynthase domain can redirect FA product profiles from predominantly C8 (G113W) to C8/C10 (G113F) and C12/C14 (G113M). Integration of a thioreductase domain enables the production of medium-chain fatty aldehydes and alcohols. We apply our approach for controlling chain length in FA biosynthesis to the microbial production of C10- and C12-FAs, translate it into a yeast cell factory and achieve C10/C12-FAs titers of 674 mg l<sup>-1</sup> and 67% purity of total free FAs. Our work demonstrates a modular platform for programmable FA synthesis and paves the way toward sustainable bioproduction of valuable oleochemicals.

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Journal
Nature Chemical Biology
Published
2026-01-07
DOI
https://doi.org/10.1038/s41589-025-02105-w
Primary Topic
Microbial Metabolic Engineering and Bioproduction
Type
article
Field-Weighted Citation Impact
0.00

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article

Engineering metazoan fatty acid synthase to control chain length applied in yeast

Martin Grininger, Adrian J. Jervis, Yongjin J. Zhou, Xiaoxin Zhai et al.
Nature Chemical Biology
Microbial Metabolic Engineering and Bioproduction
article

Engineering metazoan fatty acid synthase to control chain length applied in yeast

Martin Grininger, Adrian J. Jervis, Yongjin J. Zhou, Xiaoxin Zhai, Alexander Rittner, Damian Ludig, Christian Gusenda, Svenja Berlage, Ning Gao, Maximilian Heinz
article en

Abstract

Metazoan fatty acid (FA) synthases (mFASs) facilitate the de novo synthesis of C16- and C18-FAs through iterative extensions within the FA cycle and hydrolytic release. Here we re-engineer mFAS to fine-tune the interplay between FA extension and FA hydrolytic release for the targeted production of short- and medium-chain fatty acids. Single amino acid exchanges in the ketosynthase domain can redirect FA product profiles from predominantly C8 (G113W) to C8/C10 (G113F) and C12/C14 (G113M). Integration of a thioreductase domain enables the production of medium-chain fatty aldehydes and alcohols. We apply our approach for controlling chain length in FA biosynthesis to the microbial production of C10- and C12-FAs, translate it into a yeast cell factory and achieve C10/C12-FAs titers of 674 mg l<sup>-1</sup> and 67% purity of total free FAs. Our work demonstrates a modular platform for programmable FA synthesis and paves the way toward sustainable bioproduction of valuable oleochemicals.

Nature Chemical Biology
Goethe University Frankfurt (DE), Unilever (United Kingdom) (GB), Dalian Institute of Chemical Physics (CN), Chinese Academy of Sciences (CN), Frankfurt Institute for Advanced Studies (DE), University of Chinese Academy of Sciences (CN), China National Petroleum Corporation (China) (CN)
Deutsche Forschungsgemeinschaft, National Natural Science Foundation of China, Goethe-Universität Frankfurt am Main, Chinesisch-Deutsche Zentrum für Wissenschaftsförderung
Responsible consumption and production
Openalex Percentile: Top 96%
Microbial Metabolic Engineering and Bioproduction
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