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Overview
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Midecamycin is an naturally occurring, broad-spectrum acetoxy-substituted macrolide antibiotic similar in structure to erythromycin. An acetoxy group is substituted on position 9 of the 16-membered ring and on position 4 of the terminal sugar. It is naturally produced by Streptomyces mycarofaciens. It interrupts protein synthesis of Gram-positive and Gram-negative bacteria. Its metabolites present little to no antimicrobial activity. It is very soluble in methanol, ethanol, and acidic solutions and soluble in DMSO.
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Background
Midecamycin inhibits bacterial growth by targeting the 50S ribosomal subunit preventing peptide bond formation and translocation during protein synthesis. Resistance to Midecamycin is commonly attributed to mutations in 50S rRNA preventing Midecamycin binding allowing the cell to synthesize proteins free of error.
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- Properties
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Overview