Extension of the Terpene Chemical Space: the Very First Biosynthetic Steps
Reviewartikel, 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.

Författare

Julie Couillaud

Aix-Marseille Université

Chalmers, Biologi och bioteknik, Systembiologi

Katia Duquesne

Aix-Marseille Université

Gilles Iacazio

Aix-Marseille Université

ChemBioChem

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

Vol. 23 9 e202100642

Ämneskategorier

Ekonomisk geografi

Biokatalys och enzymteknik

Organisk kemi

DOI

10.1002/cbic.202100642

PubMed

34905641

Mer information

Senast uppdaterat

2022-07-04