苯并苯胺生物碱对逆转录酶活性的抑制作用。

Lloydia Pub Date : 1979-03-01
M L Sethi
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引用次数: 0

摘要

苯并苯胺类生物碱、fagaronine 4、o -甲基fagaronine 5、nitidine 1、allonitidine 3和methoxydihydronitidine 2对RNA肿瘤病毒的逆转录酶具有抑制活性。当多核苷酸-寡脱氧核苷酸复合物作为模板引物时,这些生物碱对酶的抑制作用为6-60微克/毫升。结果表明,苯并苯胺生物碱与模板引物(特别是A:T碱基对)相互作用,而不与酶蛋白相互作用。反转录酶抑制的动力学反应表明,生物碱可能与模板引物相互作用,使DNA聚合酶的合成瞬间停止。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibition of reverse transcriptase activity by benzophenanthridine alkaloids.

Benzophenanthridine alkaloids, fagaronine 4, O-methylfagaronine 5,nitidine 1, allonitidine 3 and methoxydihydronitidine 2 have been shown to possess inhibitory activity against reverse transcriptase of RNA tumor viruses. The enzyme inhibition (50%) by these alkaloids was found in the range of 6-60 microgram per milliliter of the reaction mixture when polynucleotide-oligodeoxynucleotide complexes were used as template primers. The results suggested that the benzophenanthridine alkaloids interacted with the template primers (particularly of the A:T base pairs) and not with the enzyme proteins. Kinetics reaction of the reverse transciptase inhibition showed that the alkaloids stopped the DNA polymerase synthesis instantly, probably by interacting with the template primer.

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