A basidomycetous hydroxynaphthalene-prenylating enzyme exhibits promiscuity toward prenyl donors

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-prenyla...

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Veröffentlicht in:Applied microbiology and biotechnology 2023-08, Vol.107 (15), p.4845-4852
Hauptverfasser: Martin, Andreas, Dierlamm, Nele, Zocher, Georg, Li, Shu-Ming
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Sprache:eng
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Zusammenfassung: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
ISSN:0175-7598
1432-0614
DOI:10.1007/s00253-023-12621-1