Conformational Analysis, Thermal Rearrangement, and EI‐MS Fragmentation Mechanism of (1(10)<i>E</i>,4<i>E</i>,6<i>S</i>,7<i>R</i>)‐Germacradien‐6‐ol by ¹³C‐Labeling Experiments

Abstract

An uncharacterized terpene cyclase from Streptomyces pratensis was identified as (+)-(1(10)E,4E,6S,7R)-germacradien-6-ol synthase. The enzyme product exists as two interconvertible conformers, resulting in complex NMR spectra. For the complete assignment of NMR data, all fifteen ((13)C1)FPP isotopomers (FPP=farnesyl diphosphate) and ((13)C15)FPP were synthesized and enzymatically converted. The products were analyzed using various NMR techniques, including (13)C, (13)C COSY experiments. The ((13)C)FPP isotopomers were also used to investigate the thermal rearrangement and EI fragmentation of the enzyme product.