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A basidomycetous hydroxynaphthalene-prenylating enzyme exhibits promiscuity toward prenyl donors

ABSTRACT: The fungal prenyltransferase ShPT from Stereum hirsutum was believed to prenylate 4-hydroxybenzyl alcohol and thereby be involved in the vibralactone biosynthesis. In this study, we demonstrate that hydroxynaphthalenes instead of benzyl alcohol or aldehyde were accepted by ShPT for regular...

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Detalles Bibliográficos
Autores principales: Martin, Andreas, Dierlamm, Nele, Zocher, Georg, Li, Shu-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10344970/
https://www.ncbi.nlm.nih.gov/pubmed/37326682
http://dx.doi.org/10.1007/s00253-023-12621-1
Descripción
Sumario:ABSTRACT: The fungal prenyltransferase ShPT from Stereum hirsutum was believed to prenylate 4-hydroxybenzyl alcohol and thereby be involved in the vibralactone biosynthesis. In this study, we demonstrate that hydroxynaphthalenes instead of benzyl alcohol or aldehyde were accepted by ShPT for regular C-prenylation in the presence of both dimethylallyl and geranyl diphosphate. Although the natural substrate of ShPT remains unknown, our results provide one additional prenyltransferase from basidiomycetes, which are less studied, in comparison to those from other sources. Furthermore, this study expands the chemical toolbox for regioselective production of prenylated naphthalene derivatives. KEY POINTS: •Basidiomycetous prenyltransferase •Biochemical characterization •A DMATS prenyltransferase prenylating hydroxynaphthalene derivatives SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-023-12621-1.