Extension of the Terpene Chemical Space: the Very First Biosynthetic Steps
Review article, 2022

The structural diversity of terpenes is particularly notable and many studies are carried out to increase it further. In the terpene biosynthetic pathway this diversity is accessible from only two common precursors, i. e. isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Methods recently developed (e. g. the Terpene Mini Path) have allowed DMAPP and IPP to be obtained from a two-step enzymatic conversion of industrially available isopentenol (IOH) and dimethylallyl alcohol (DMAOH) into their corresponding diphosphates. Easily available IOH and DMAOH analogues then offer quick access to modified terpenoids thus avoiding the tedious chemical synthesis of unnatural diphosphates. The aim of this minireview is to cover the literature devoted to the use of these analogues for widening the accessible terpene chemical space.

Author

Julie Couillaud

Aix Marseille University

Chalmers, Biology and Biological Engineering, Systems and Synthetic Biology

Katia Duquesne

Aix Marseille University

Gilles Iacazio

Aix Marseille University

ChemBioChem

1439-4227 (ISSN) 1439-7633 (eISSN)

Vol. 23 9 e202100642

Subject Categories

Economic Geography

Biocatalysis and Enzyme Technology

Organic Chemistry

DOI

10.1002/cbic.202100642

PubMed

34905641

More information

Latest update

7/4/2022 1