syn-Elimination of glutamylated threonine in lanthipeptide biosynthesis

Methyllanthionine (MeLan) containing macrocycles are key structural features of lanthipeptides. They are formed typically by anti-elimination of l-Thr residues followed by cyclization of l-Cys residues onto the (Z)-dehydrobutyrine (Dhb) intermediates. In this report we demonstrate that the biosynthesis of lanthipeptides containing the d-allo-l-MeLan macrocycle such as the morphogenetic lanthipeptide SapT proceeds through (E)-Dhb intermediates formed by net syn-elimination of l-Thr.

Automated summary

This report demonstrates that the biosynthesis of lanthipeptides containing the d-allo-l-MeLan macrocycle proceeds through (E)-Dhb intermediates formed by net syn-elimination of l-Thr.