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Primed abortive initiation of RNA synthesis by E. coli RNA polymerase on T7 DNA. Steady state kinetic studies.

机译:通过大肠杆菌RNA聚合酶在T7 DNA上引发RNA合成引发的流产启动。稳态动力学研究。

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摘要

Ternary complexes of T7 DNA, RNA polymerase and the antibiotic rifampicin carry out the promoter specific abortive initiation when dinucleoside monophosphates were employed as primers. Primed abortive initiation, leading to synthesis of trinucleoside diphosphates, only occured with combinations of primers and substrates complementary to a promoter region of 8 base pairs centered around the origin of transcription. The steady state kinetics of three abortive initiations at T7 promoter A3 were studied in detail. The reactions appeared to be truly ordered. Affinity constants, maximal velocities and elementary step rate constants were thus obtained. The stimulation by dinucleoside monophosphate primers is brought about by positively effecting the function of the substrate site rather then by their higher affinity to the primer site of the transcriptional complex.
机译:当将二磷酸核苷单磷酸用作引物时,T7 DNA,RNA聚合酶和抗生素利福平的三元复合物会进行启动子特异性的流产启动。引发的流产引发,导致三磷酸核苷二磷酸的合成,仅在引物和底物的组合与以转录起点为中心的8个碱基对的启动子区域互补时发生。详细研究了在T7启动子A3处三个流产引发的稳态动力学。反应似乎是有序的。由此获得亲和常数,最大速度和基本步速常数。通过积极影响底物位点的功能,而不是通过它们对转录复合物引物位点的更高亲和力,可以实现二核苷单磷酸引物的刺激。

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