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Table · dataset · 2026

Identification and Cyclization Mechanism of Fungal (+)-β-Chamigrene Synthase

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Chamigranes are a unique class of sesquiterpenoids featuring a spiro[5.5]undecane framework, yet their biosynthesis in fungi has remained elusive for decades.

Description

In this study, we identify and characterize ChamTS, a sesquiterpene synthase from the basidiomycetous fungus <i>Cerrena albocinnamomea</i>, which specifically catalyzes the formation of (+)-β-chamigrane. <i>In vitro</i> isotope-labeling experiments unveiled the cyclization pathway of ChamTS, revealing an initial 1,6-cyclization followed by a 1,5-proton shift and spirocycle-forming rearrangement.

This work provides a foundation for the biosynthetic production and further engineering of β-chamigrane-type terpenoids.

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figshareoai:figshare.com:article/3381910610 d agoJSON v1
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