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大肠杆菌RNA聚合酶E σ70和E σ38全酶的启动子选择性。DNA超螺旋的影响。

Promoter selectivity of Escherichia coli RNA polymerase E sigma 70 and E sigma 38 holoenzymes. Effect of DNA supercoiling.

作者信息

Kusano S, Ding Q, Fujita N, Ishihama A

机构信息

Department of Molecular Genetics, National Institute of Genetics, Shizuoka, Japan.

出版信息

J Biol Chem. 1996 Jan 26;271(4):1998-2004. doi: 10.1074/jbc.271.4.1998.

Abstract

The functional specificity was compared between two sigma factors, sigma 70 (the major sigma at exponentially growing phase) and sigma 38 (the essential sigma at stationary growth phase), of Escherichia coli RNA polymerase. The core enzyme binding affinity of sigma 38 was less than half the level of sigma 70 as measured by gel filtration column chromatography or by titrating the concentration of sigma required for the maximum transcription in the presence of a fixed amount of core enzyme. In addition, the holoenzyme concentration required for the maximum transcription of a fixed amount of templates was higher for E sigma 38 than E sigma 70. The transcription by E sigma 38 was, however, enhanced with the use of templates with low superhelical density, in good agreement with the decrease in DNA superhelicity in the stationary growth phase. We thus propose that the selective transcription of stationary-specific genes by E sigma 38 holoenzyme requires either a specific reaction condition(s) or a specific factor(s) such as template DNA with low superhelical density.

摘要

对大肠杆菌RNA聚合酶的两种σ因子,即σ70(指数生长期的主要σ因子)和σ38(稳定生长期的必需σ因子)的功能特异性进行了比较。通过凝胶过滤柱色谱法或在固定量的核心酶存在下滴定最大转录所需的σ浓度来测量,σ38与核心酶的结合亲和力不到σ70的一半。此外,对于固定量的模板,Eσ38进行最大转录所需的全酶浓度高于Eσ70。然而,使用超螺旋密度低的模板时,Eσ38的转录会增强,这与稳定生长期DNA超螺旋度的降低高度一致。因此,我们提出Eσ38全酶对稳定期特异性基因的选择性转录需要特定的反应条件或特定因子,如超螺旋密度低的模板DNA。

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