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Biocatalytic Ether Lipid Synthesis by an Archaeal Glycerolprenylase.
Kaspar, Felix; Eilert, Lea; Staar, Sophie; Oung, Sangwar Wadtey; Wolter, Mario; Ganskow, Charity S G; Kemper, Sebastian; Klahn, Philipp; Jacob, Christoph R; Blankenfeldt, Wulf; Schallmey, Anett.
Afiliação
  • Kaspar F; Institute for Biochemistry, Biotechnology and Bioinformatics, Technische Universität Braunschweig, Spielmannstraße 7, 38106, Braunschweig, Germany.
  • Eilert L; Department Structure and Function of Proteins, Helmholtz Centre for Infection Research, Inhoffenstraße 7, 38124, Braunschweig, Germany.
  • Staar S; Institute for Biochemistry, Biotechnology and Bioinformatics, Technische Universität Braunschweig, Spielmannstraße 7, 38106, Braunschweig, Germany.
  • Oung SW; Institute of Physical and Theoretical Chemistry, Technische Universität Braunschweig, Gaußstraße 17, 38106, Braunschweig, Germany.
  • Wolter M; Institute of Physical and Theoretical Chemistry, Technische Universität Braunschweig, Gaußstraße 17, 38106, Braunschweig, Germany.
  • Ganskow CSG; Department of Chemistry and Molecular Biology, University of Gothenburg, Medicinaregatan 7B, 413 90, Gothenburg, Sweden.
  • Kemper S; Institute for Chemistry, Technische Universität Berlin, Straße des 17. Juni 135, 10623, Berlin, Germany.
  • Klahn P; Department of Chemistry and Molecular Biology, University of Gothenburg, Medicinaregatan 7B, 413 90, Gothenburg, Sweden.
  • Jacob CR; Institute of Physical and Theoretical Chemistry, Technische Universität Braunschweig, Gaußstraße 17, 38106, Braunschweig, Germany.
  • Blankenfeldt W; Institute for Biochemistry, Biotechnology and Bioinformatics, Technische Universität Braunschweig, Spielmannstraße 7, 38106, Braunschweig, Germany.
  • Schallmey A; Department Structure and Function of Proteins, Helmholtz Centre for Infection Research, Inhoffenstraße 7, 38124, Braunschweig, Germany.
Angew Chem Int Ed Engl ; : e202412597, 2024 Oct 02.
Article em En | MEDLINE | ID: mdl-39359010
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 G3PSs). We show that the ultrastable Archaeoglobus fulgidus G3PS 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 G3PSs into the biocatalytic alkylation toolbox.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article