Clorobiocin
Clorobiocin is a natural product and antibiotic that is derived from the Streptomyces species of bacteria. It is a member of the aminocoumarin class of antibiotics, which also includes novobiocin and coumermycin A1. Clorobiocin is known for its ability to inhibit DNA gyrase, an enzyme that is essential for DNA replication in bacteria.
History[edit | edit source]
Clorobiocin was first isolated in the 1950s from a strain of Streptomyces bacteria. The compound was initially identified for its potent antibacterial activity, and subsequent studies revealed its unique mechanism of action.
Mechanism of Action[edit | edit source]
Clorobiocin inhibits DNA gyrase by binding to the enzyme's ATP-binding site, thereby preventing the enzyme from introducing negative supercoils into DNA. This inhibitory action disrupts DNA replication and leads to cell death. Clorobiocin's mechanism of action is similar to that of other aminocoumarin antibiotics.
Clinical Use[edit | edit source]
While clorobiocin has potent antibacterial activity, it is not currently used in clinical practice. This is primarily due to the compound's poor bioavailability and the development of drug resistance by certain bacterial strains. However, clorobiocin continues to be studied for its potential use in treating multidrug-resistant bacterial infections.
Research[edit | edit source]
Research into clorobiocin has focused on understanding its mechanism of action and exploring its potential use in treating multidrug-resistant bacterial infections. Studies have also investigated the possibility of modifying the clorobiocin molecule to improve its bioavailability and overcome drug resistance.
See Also[edit | edit source]
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Contributors: Prab R. Tumpati, MD