Issue 20, 2011

Templating effects in aristolochene synthase catalysis: elimination versus cyclisation

Abstract

Analysis of the products generated by mutants of aristolochene synthase from P. roqueforti (PR-AS) revealed the prominent structural role played by the aliphatic residue Leu 108 in maintaining the productive conformation of farnesyl diphosphate to ensure C1–C10 (σ-bond) ring-closure and hence (+)-aristolochene production.

Graphical abstract: Templating effects in aristolochene synthase catalysis: elimination versus cyclisation

Supplementary files

Article information

Article type
Communication
Submitted
16 Jul 2011
Accepted
11 Aug 2011
First published
12 Aug 2011

Org. Biomol. Chem., 2011,9, 6920-6923

Templating effects in aristolochene synthase catalysis: elimination versus cyclisation

J. A. Faraldos, V. González, M. Senske and R. K. Allemann, Org. Biomol. Chem., 2011, 9, 6920 DOI: 10.1039/C1OB06184D

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