Efficient heterocyclisation by (di)terpene synthases

Biblio

Publication Type:

Journal Article

Source:

Chem Commun (Camb), Volume 51, Issue 70, Number 70, p.13485-7 (2015)

ISBN:

1364-548X (Electronic)<br/>1359-7345 (Linking)

Accession Number:

26214384

Abstract:

<p>While cyclic ether forming terpene synthases are known, the basis for such heterocyclisation is unclear. Here it is reported that numerous (di)terpene synthases, particularly including the ancestral ent-kaurene synthase, efficiently produce isomers of manoyl oxide from the stereochemically appropriate substrate. Accordingly, such heterocyclisation is easily accomplished by terpene synthases. Indeed, the use of single residue changes to induce production of the appropriate substrate in the upstream active site leads to efficient bifunctional enzymes producing isomers of manoyl oxide, representing novel enzymatic activity.</p>

Notes:

Mafu, S<br/>Potter, K C<br/>Hillwig, M L<br/>Schulte, S<br/>Criswell, J<br/>Peters, R J<br/>eng<br/>R01 GM076324/GM/NIGMS NIH HHS/<br/>England<br/>2015/07/28 06:00<br/>Chem Commun (Camb). 2015 Aug 18;51(70):13485-7. doi: 10.1039/c5cc05754j.