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Isolation and structure revision of the actin-binding macrolide rhizopodin from Myxococcus stipitatus (Myxobacteria)
Authors:Rolf Jansen  Heinrich Steinmetz  Wolf-Dieter Schubert  Simone C. Albrecht
Affiliation:a Work Group of Microbial Drugs, Helmholtz Centre for Infection Research, Inhoffenstrasse 7, D-38124 Braunschweig-Stöckheim, Germany
b Department of Chemical Biology, Helmholtz Centre for Infection Research, Inhoffenstrasse 7, D-38124 Braunschweig-Stöckheim, Germany
c Department of Structural Biology, Helmholtz Centre for Infection Research, Inhoffenstrasse 7, D-38124 Braunschweig-Stöckheim, Germany
Abstract:Rhizopodin was isolated as cytostatic and weakly antifungal macrolide (1) and later characterized as potent actin-depolymerizing agent. It is produced by the myxobacterium Myxococcus stipitatus, which enables a fermentative supply of the drug for biological studies. We here report a revised structure that characterizes rhizopodin (2) as the first known dimeric bis-lactone exhibiting side chains that terminate in N-methyl-vinylformamide groups, which are otherwise found in smaller marine toxins also targeting the actin cytoskeleton. Compound 2 might function as bivalent inhibitor forming ternary complexes with actin which would explain its high efficacy.
Keywords:Myxobacteria   Myxococcus stipitatus   Actin polymerization inhibitor   Bivalent inhibitor   Dilactone   N-Methyl-vinylformamide
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