Frolova L Y, Meldrays Y A, Kochkina L L, Giller S A, Eremeyev A V, Grayevskaya N A, Kisselev L L
Nucleic Acids Res. 1977 Mar;4(3):523-38. doi: 10.1093/nar/4.3.523.
Ten new derivatives of the antibiotic rifamycin with variable side chains at position 3 were synthesized. The inhibitory activity of these derivatives against DNA-polymerases isolated from avian myeloblastosis virus, E. coli and calf thymus were studied at various conditions. 3-(2,4,6-trinitrophenylhydrazone-(methyl) rifamycin SV is a strong inhibitor for all the polymerases tested and belongs to the C class inhibitors of reverse transcriptase. 3-(monoallylhydrazone-(methyl) rifamycin SV possesses a selective action on polymerases: at 0.1 mg/ml concentration it almost completely inhibits the reverse transcriptase and less than half of the bacterial and eukaryotic enzymes. A drug is found which strongly inhibits the DNA-polymerases from E. coli and calf thymus and weakly the viral enzyme. The inhibitory effect on reverse transcriptase is independent of the choice of template-primer; it could be overcome by the addition of excess enzyme but not of excess template-primer; the inhibition could be completely reversed by dilution of the drug-enzyme mixture. From Lineweaver-Burk analysis, the inhibition is noncompetitive with respect to the template-primer and, thus the drugs bind to the site different from the active site for the template-primer. From protective action of the template-primer and other data it might be suggested that the rifamycin derivatives act at an early step(s) in DNA synthesis catalyzed by reverse transcriptase. The obtained data are in agreement with the results for other derivatives of rifamycin SV described in literature.
合成了10种在3位带有可变侧链的抗生素利福霉素新衍生物。在不同条件下研究了这些衍生物对从禽成髓细胞瘤病毒、大肠杆菌和小牛胸腺中分离出的DNA聚合酶的抑制活性。3-(2,4,6-三硝基苯腙-(甲基)利福霉素SV是所有测试聚合酶的强抑制剂,属于逆转录酶的C类抑制剂。3-(单烯丙基腙-(甲基)利福霉素SV对聚合酶具有选择性作用:在0.1mg/ml浓度下,它几乎完全抑制逆转录酶,而对细菌和真核酶的抑制作用不到一半。发现了一种药物,它强烈抑制大肠杆菌和小牛胸腺的DNA聚合酶,而对病毒酶的抑制作用较弱。对逆转录酶的抑制作用与模板引物的选择无关;加入过量的酶可以克服这种抑制作用,但加入过量的模板引物则不能;通过稀释药物-酶混合物可以完全逆转这种抑制作用。从Lineweaver-Burk分析来看,这种抑制作用相对于模板引物是非竞争性的,因此这些药物结合在与模板引物活性位点不同的位点上。从模板引物的保护作用和其他数据可以推测,利福霉素衍生物在逆转录酶催化的DNA合成的早期步骤起作用。所获得的数据与文献中描述的利福霉素SV的其他衍生物的结果一致。