Tuberactinomycin

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Tuberactinomycin[edit | edit source]

Tuberactinomycin is a type of antibiotic that is derived from the bacterium Streptomyces. It is a member of the aminoglycoside family of antibiotics, which are known for their ability to inhibit protein synthesis in bacteria, thereby preventing their growth and reproduction.

History[edit | edit source]

Tuberactinomycin was first isolated in the 1970s from a strain of Streptomyces found in soil samples. Since then, it has been studied for its potential use in the treatment of various bacterial infections.

Mechanism of Action[edit | edit source]

Like other aminoglycosides, tuberactinomycin works by binding to the ribosomes of bacteria, specifically the 30S subunit. This binding interferes with the process of protein synthesis, preventing the bacteria from growing and reproducing.

Clinical Use[edit | edit source]

Tuberactinomycin has been found to be effective against a variety of bacteria, including Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa. However, its use in clinical settings has been limited due to concerns about potential side effects, including ototoxicity and nephrotoxicity.

Research[edit | edit source]

Research into the potential uses of tuberactinomycin is ongoing. Some studies have suggested that it may be particularly effective against multidrug-resistant strains of bacteria, making it a potential option for treating infections that are resistant to other antibiotics.

See Also[edit | edit source]

References[edit | edit source]



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Contributors: Prab R. Tumpati, MD