A non-natural biosynthesis pathway toward 2-methylisoborneol

Chem Commun (Camb). 2022 Mar 31;58(27):4316-4319. doi: 10.1039/d2cc00636g.

Abstract

The biosynthesis of 2-methylisoborneol was reconstituted by elongation of dimethylallyl diphosphate (DMAPP) with (S)- and (R)-2-methylisopentenyl diphosphate (2-Me-IPP) using farnesyl diphosphate synthase (FPPS), followed by terpene cyclisation. The stereochemical course of the FPPS reaction was studied in detail using stereoselectively deuterated 2-Me-IPP isotopomers.

MeSH terms

  • Camphanes* / chemical synthesis
  • Diphosphates / metabolism
  • Geranyltranstransferase* / metabolism
  • Terpenes / chemistry
  • Terpenes / metabolism

Substances

  • Camphanes
  • Diphosphates
  • Terpenes
  • 2-methylisoborneol
  • Geranyltranstransferase