Publication | Closed Access
Base Specificity in the Interaction of Polynucleotides with Antibiotic Drugs
478
Citations
37
References
1965
Year
EngineeringMolecular BiologyAntimicrobial ChemotherapyDrug ResistanceBiosynthesisOlivomycin Form ComplexesRna PolymeraseDna ComputingAntimicrobial ResistanceOligonucleotideDna ReplicationAntimicrobial CompoundPharmacologyBiomolecular EngineeringAntibioticsSynthetic BiologyBase SpecificityMedicineEthidium BromideDrug Discovery
Echinomycin, daunomycin, ethidium bromide, nogalamycin, chromomycin, mithramycin, and olivomycin inhibit RNA synthesis by RNA polymerase by interacting with the DNA template. Chromomycin and olivomycin form complexes with DNA, preferably in the helical form, but not with RNA. These complexes require guanine in DNA and the addition of a stoichiometric amount of bivalent cation. None of the other antibiotics requires the presence of any single base in the template for its action.
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