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Inside Cover Ribosomal Synthesis of Tricyclic Depsipeptides in Bloom-Forming Cyanobacteria (Angew. Chem. Int. Ed. 402008)

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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.
Inside Cover
Vincent Gandon,* Gilles Lemire, Alexandra Hours,
Louis Fensterbank,* and Max Malacria*
Cage-like depsipeptides are investigated by C. Hertweck, E. Dittmann, and coworkers 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.
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cyanobacteria, 402008, forming, tricyclic, blood, int, cover, angel, synthesis, chem, ribosomal, depsipeptide, insider
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