Beilstein Journal of Organic Chemistry (Aug 2016)

Mechanistic investigations on six bacterial terpene cyclases

  • Patrick Rabe,
  • Thomas Schmitz,
  • Jeroen S. Dickschat

DOI
https://doi.org/10.3762/bjoc.12.173
Journal volume & issue
Vol. 12, no. 1
pp. 1839 – 1850

Abstract

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The products obtained by incubation of farnesyl diphosphate (FPP) with six purified bacterial terpene cyclases were characterised by one- and two-dimensional NMR spectroscopic methods, allowing for a full structure elucidation. The absolute configurations of four terpenes were determined based on their optical rotary powers. Incubation experiments with 13C-labelled isotopomers of FPP in buffers containing water or deuterium oxide allowed for detailed insights into the cyclisation mechanisms of the bacterial terpene cyclases.

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