Evidence map›Paper›PMID 41501181›Full record

ArticleNature chemical biology2026

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

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

Abstract read
In one paragraph

Article in Nature chemical biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. A Hidden Binding Pocket in the β- ketoacyl-ACP Synthase FabB.bioRxiv : the preprint server for biology · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Damian L Ludig *Institute of Organic Chemistry and Chemical Biology, Buchmann Institute for Molecular Life Sciences, Goethe Universität Frankfurt am Main, Frankfurt, Germany.ORCID http://orcid.org/0000-0002-0042-6322
Xiaoxin Zhai *Division of Biotechnology, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, PR China.
Alexander RittnerInstitute of Organic Chemistry and Chemical Biology, Buchmann Institute for Molecular Life Sciences, Goethe Universität Frankfurt am Main, Frankfurt, Germany.
Christian GusendaInstitute of Organic Chemistry and Chemical Biology, Buchmann Institute for Molecular Life Sciences, Goethe Universität Frankfurt am Main, Frankfurt, Germany.ORCID http://orcid.org/0009-0002-9159-0271
Maximilian HeinzInstitute of Organic Chemistry and Chemical Biology, Buchmann Institute for Molecular Life Sciences, Goethe Universität Frankfurt am Main, Frankfurt, Germany.ORCID http://orcid.org/0009-0007-1422-4813
Svenja BerlageInstitute of Organic Chemistry and Chemical Biology, Buchmann Institute for Molecular Life Sciences, Goethe Universität Frankfurt am Main, Frankfurt, Germany.ORCID http://orcid.org/0009-0003-5400-0356
Ning GaoDivision of Biotechnology, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, PR China.
Adrian J JervisUnilever Research & Development, Port Sunlight, Wirral, UK.ORCID http://orcid.org/0000-0003-2386-3354
Yongjin J ZhouDivision of Biotechnology, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, PR China. zhouyongjin@dicp.ac.cn.ORCID http://orcid.org/0000-0002-2369-3079
Martin GriningerInstitute of Organic Chemistry and Chemical Biology, Buchmann Institute for Molecular Life Sciences, Goethe Universität Frankfurt am Main, Frankfurt, Germany. grininger@chemie.uni-frankfurt.de.ORCID http://orcid.org/0000-0002-7269-0667

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) GR3854/10-1 to M.G.National Natural Science Foundation of China (National Science Foundation of China) 22425807
6 · The paper itself

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

Indexed as

Fatty AcidsFatty Acid SynthasesProtein EngineeringSaccharomyces cerevisiaeAnimalsFatty AcidsFatty Acid Synthases

Identifiers

PMID41501181
PMCPMC13303079

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.