Biocatalytic Ether Lipid Synthesis by an Archaeal Glycerolprenylase

Abstract Although ethers are common in secondary natural products, they are an underrepresented functional group in primary metabolism. As such, there are comparably few enzymes capable of constructing ether bonds in a general fashion. However, such enzymes are highly sought after for synthetic applications as they typically operate with higher regioselectivity and under milder conditions than traditional organochemical approaches. To expand the repertoire of well characterized ether synthases, we herein report on a promiscuous archaeal prenyltransferase from the scarcely researched family of geranylgeranylglyceryl phosphate synthases (GGGPSs or G 3 PSs). We show that the ultrastable Archaeoglobus fulgidus G 3 PS makes various ( E )‐ and ( Z )‐configured prenyl glycerol ethers from the corresponding pyrophosphates while exerting perfect control over the configuration at the glycerol unit. Based on experimental and computational data, we propose a mechanism for this enzyme which involves an intermediary prenyl carbocation equivalent. As such, this study provides the fundamental understanding and methods to introduce G 3 PSs into the biocatalytic alkylation toolbox.

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Publication Details

Journal
Angewandte Chemie
Published
2024-10-02
DOI
https://doi.org/10.1002/ange.202412597
Primary Topic
Microbial Metabolic Engineering and Bioproduction
Type
article
Field-Weighted Citation Impact
0.00

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article

Biocatalytic Ether Lipid Synthesis by an Archaeal Glycerolprenylase

Felix Kaspar, Wulf Blankenfeldt, Mario Wolter, Sangwar Wadtey Oung et al.
Angewandte Chemie
Microbial Metabolic Engineering and Bioproduction
article

Biocatalytic Ether Lipid Synthesis by an Archaeal Glycerolprenylase

Felix Kaspar, Wulf Blankenfeldt, Mario Wolter, Sangwar Wadtey Oung, Charity S. G. Ganskow, Christoph R. Jacob, Sophie Staar, Philipp Klahn, Lea Eilert, Anett Schallmey, Sebastian Kemper
article en

Abstract

Abstract Although ethers are common in secondary natural products, they are an underrepresented functional group in primary metabolism. As such, there are comparably few enzymes capable of constructing ether bonds in a general fashion. However, such enzymes are highly sought after for synthetic applications as they typically operate with higher regioselectivity and under milder conditions than traditional organochemical approaches. To expand the repertoire of well characterized ether synthases, we herein report on a promiscuous archaeal prenyltransferase from the scarcely researched family of geranylgeranylglyceryl phosphate synthases (GGGPSs or G 3 PSs). We show that the ultrastable Archaeoglobus fulgidus G 3 PS makes various ( E )‐ and ( Z )‐configured prenyl glycerol ethers from the corresponding pyrophosphates while exerting perfect control over the configuration at the glycerol unit. Based on experimental and computational data, we propose a mechanism for this enzyme which involves an intermediary prenyl carbocation equivalent. As such, this study provides the fundamental understanding and methods to introduce G 3 PSs into the biocatalytic alkylation toolbox.

Angewandte ChemieVol. 136(46)
Helmholtz Centre for Infection Research (DE), Technische Universität Berlin (DE), University of Gothenburg (SE), Technische Universität Braunschweig (DE)
Deutsche Forschungsgemeinschaft
Clean water and sanitation
Openalex Percentile: Top 85%
Microbial Metabolic Engineering and Bioproduction
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