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Index >> Bacterial Cheomotherapy >>Rifamycins

Rifamycins

Rifamycins - Rifamycins differ from the previously mentioned compounds acting on DNA in that they specifically inhibit the function of bacterial RNA polymerase, without affecting mammalian RNA polymerase. They are produced by strains of Streptomyces mediterranei. They show good activity against gram positive bacteria and Mycobacterium tuberculosis, but are much less active against gram negative bacteria.

Rifampicin is a semi synthetic member of the rifamycins. It inhibits DNA dependent RNA polymerase, probably by interfering with the initiation of RNA synthesis, after the attachment of the polymerase but before nucleotide bond formation. The antibacterial action of rifampicin is due to the fact that it inhibits bacterial RNA synthesis without affecting RNA synthesis in the host.

Rifampicin has also been found to inhibit the multiplication of several mammalian viruses, e. g. vaccinia, cowpox, adenovirus and the trachoma virus. The concentra­tion required for antiviral activity is, however, much higher than for antibacterial activity. It does not appear to inhibit viral RNA polymerase.

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