Biocatalytic Ether Lipid Synthesis by an Archaeal Glycerolprenylase

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<sub>3</sub>PSs). We show that the ultrastable Archaeoglobus fulgidus G<sub>3</sub>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<sub>3</sub>PSs into the biocatalytic alkylation toolbox.

Authors

Institutions

Publication Details

Journal
Angewandte Chemie International Edition
Published
2024-10-02
DOI
https://doi.org/10.1002/anie.202412597
Citations
2
Primary Topic
Plant biochemistry and biosynthesis
Type
article
Field-Weighted Citation Impact
0.47

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Biocatalytic Ether Lipid Synthesis by an Archaeal Glycerolprenylase

Felix Kaspar, Wulf Blankenfeldt, Mario Wolter, Sangwar Wadtey Oung et al.
2 citations
Angewandte Chemie International Edition
Plant biochemistry and biosynthesis
0.47
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
2 citations

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<sub>3</sub>PSs). We show that the ultrastable Archaeoglobus fulgidus G<sub>3</sub>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<sub>3</sub>PSs into the biocatalytic alkylation toolbox.

Angewandte Chemie International EditionVol. 63(46)
Helmholtz Centre for Infection Research (DE), Technische Universität Berlin (DE), University of Gothenburg (SE), Technische Universität Braunschweig (DE)
University College Dublin, Deutsche Forschungsgemeinschaft, Rijksuniversiteit Groningen, Technische Universität Berlin, Deutsches Elektronen-Synchrotron
Clean water and sanitation
Openalex Percentile: Top 35%
Plant biochemistry and biosynthesis
0.47
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.