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[大肠杆菌RNA聚合酶与T7噬菌体DNA结合的非特异性常数的动力学测定]

[Kinetic determination of the non-specific constants for the binding of Escherichia coli RNA polymerase to T7 phage DNA].

作者信息

Zavriev S K, Belintsev B N, Shemiakin M F

出版信息

Mol Biol (Mosk). 1982 Jan-Feb;16(1):156-9.

PMID:7040937
Abstract

The kinetics of promoter complex formation of E. coli RNA polymerase with T7 phage DNA was studied under different ionic strengths at DNA concentrations 0.15, 1.5 and 20 microns/ml. Based on the results obtained the non-specific binding constants, Keq, and the promoter complex formation rate constants, kp, were estimated. Within ionic strength range 0 + 125 mM NaCl the Keq and kp vary from 5.10(6) to 9.10(5) M-1 and from 0.8 x 0.26 x 10(9) M-1 S-1, respectively. The results are discussed from the view point of the one-dimensional diffusion sliding of the enzyme along DNA in the process of phomoter site selection.

摘要

在DNA浓度为0.15、1.5和20微克/毫升的情况下,于不同离子强度下研究了大肠杆菌RNA聚合酶与T7噬菌体DNA形成启动子复合物的动力学。根据所得结果估算了非特异性结合常数Keq和启动子复合物形成速率常数kp。在0至125 mM NaCl的离子强度范围内,Keq和kp分别在5×10⁶至9×10⁵ M⁻¹以及0.8至0.26×10⁹ M⁻¹ s⁻¹之间变化。从启动子位点选择过程中酶沿DNA的一维扩散滑动的角度对结果进行了讨论。

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