z-logo
Premium
Inside Cover: Ribosomal Synthesis of Tricyclic Depsipeptides in Bloom‐Forming Cyanobacteria (Angew. Chem. Int. Ed. 40/2008)
Author(s) -
Ziemert Nadine,
Ishida Keishi,
Liaimer Anton,
Hertweck Christian,
Dittmann Elke
Publication year - 2008
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.200890196
Subject(s) - depsipeptide , cyanobacteria , ribosomal rna , stereochemistry , chemistry , biology , bacteria , biochemistry , gene , genetics
Cage‐like depsipeptides are investigated by C. Hertweck, E. Dittmann, and co‐workers in their Communication on page 7756 ff. The cyanobacterial protease inhibitors microviridin B and J are synthesized from ribosomally produced prepeptides that are transformed into tricyclic depsipeptides. The picture shows a microviridin‐producing cyanobacteria toxic bloom on a lake surface, together with a schematic representation of ribosomal protein biosynthesis and tricyclic depsipeptide cage structures.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom