大肠杆菌RNA聚合酶全酶与噬菌体T7 DNA的结合。T7启动子A处开放复合物形成速率的测定。 - Suppr

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超能文献

Binding of Escherichia coli RNA polymerase holoenzyme to bacteriophage T7 DNA. Measurements of the rate of open complex formation at T7 promoter A.

作者信息

Rosenberg S, Kadesch T R, Chamberlin M J

出版信息

J Mol Biol. 1982 Feb 15;155(1):31-51. doi: 10.1016/0022-2836(82)90490-9.

DOI:10.1016/0022-2836(82)90490-9

PMID:7042986

Abstract

摘要

相似文献

Binding of Escherichia coli RNA polymerase holoenzyme to bacteriophage T7 DNA. Measurements of the rate of open complex formation at T7 promoter A.大肠杆菌RNA聚合酶全酶与噬菌体T7 DNA的结合。T7启动子A处开放复合物形成速率的测定。

J Mol Biol. 1982 Feb 15;155(1):31-51. doi: 10.1016/0022-2836(82)90490-9.

Binding of Escherichia coli RNA polymerase holoenzyme to bacteriophage T7 DNA. Measurements of binding at bacteriophage T7 promoter A1 using a template competition assay.大肠杆菌RNA聚合酶全酶与噬菌体T7 DNA的结合。使用模板竞争分析法对噬菌体T7启动子A1处的结合进行测量。

J Mol Biol. 1982 Feb 15;155(1):1-29. doi: 10.1016/0022-2836(82)90489-2.

Binding of Escherichia coli ribonucleic acid polymerase holoenzyme to a bacteriophage T7 promoter-containing fragment: evaluation of promoter binding constants as a function of solution conditions.大肠杆菌核糖核酸聚合酶全酶与含噬菌体T7启动子片段的结合：作为溶液条件函数的启动子结合常数评估

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Binding of Escherichia coli ribonucleic acid polymerase holoenzyme to a bacteriophage T7 promoter-containing fragment: selectivity exists over a wide range of solution conditions.大肠杆菌核糖核酸聚合酶全酶与含有噬菌体T7启动子的片段的结合：在广泛的溶液条件范围内存在选择性。

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On the promoter complex formation rate of E. coli RNA polymerases with T7 phage DNA.关于大肠杆菌RNA聚合酶与T7噬菌体DNA的启动子复合物形成速率

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Bacteriophage T7 E promoter: identification and measurement of kinetics of association with Escherichia coli RNA polymerase.噬菌体T7 E启动子：与大肠杆菌RNA聚合酶结合动力学的鉴定与测定

Biochemistry. 1985 Apr 23;24(9):2219-27. doi: 10.1021/bi00330a016.

[Transcription initiation: influence of ionic strength and actinomycin D on the kinetics of the open promoter complex formation between Escherichia coli RNA-polymerase and T7 DNA].[转录起始：离子强度和放线菌素D对大肠杆菌RNA聚合酶与T7 DNA之间开放启动子复合物形成动力学的影响]

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[RNA polymerase of a rifampicin-resistant mutant of Escherichia coli has an altered selectivity to phage T7 DNA promoters].[大肠杆菌利福平抗性突变体的RNA聚合酶对噬菌体T7 DNA启动子的选择性发生改变]

Mol Biol (Mosk). 1988 Mar-Apr;22(2):384-92.

Studies of the binding of Escherichia coli RNA polymerase to DNA. V. T7 RNA chain initiation by enzyme-DNA complexes.大肠杆菌RNA聚合酶与DNA结合的研究。V. 酶-DNA复合物引发的T7 RNA链起始

J Mol Biol. 1972 Sep 28;70(2):221-37. doi: 10.1016/0022-2836(72)90535-9.

[The effect of mutation in the beta-subunit of Escherichia coli RNA polymerase on the selectivity of complex formation with T7 DNA promoters].[大肠杆菌RNA聚合酶β亚基突变对与T7 DNA启动子形成复合物的选择性的影响]

Dokl Akad Nauk SSSR. 1989;309(2):487-91.

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Solute probes of conformational changes in open complex (RPo) formation by Escherichia coli RNA polymerase at the lambdaPR promoter: evidence for unmasking of the active site in the isomerization step and for large-scale coupled folding in the subsequent conversion to RPo.大肠杆菌RNA聚合酶在λPR启动子上形成开放复合物（RPo）过程中构象变化的溶质探针：异构化步骤中活性位点暴露以及随后转化为RPo过程中大规模耦合折叠的证据。

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Mutations affecting two different steps in transcription initiation at the phage lambda PRM promoter.影响噬菌体λ PRM启动子转录起始两个不同步骤的突变。

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RNA polymerase II ternary transcription complexes generated in vitro.体外生成的RNA聚合酶II三元转录复合物。

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Sequence distributions associated with DNA curvature are found upstream of strong E. coli promoters.与DNA弯曲相关的序列分布在大肠杆菌强启动子的上游被发现。

Nucleic Acids Res. 1987 Jan 26;15(2):785-96. doi: 10.1093/nar/15.2.785.

Association of RNA polymerase having increased Km for ATP and UTP with hyperexpression of the pyrB and pyrE genes of Salmonella typhimurium.对ATP和UTP具有增加的米氏常数的RNA聚合酶与鼠伤寒沙门氏菌pyrB和pyrE基因的过表达之间的关联。

J Bacteriol. 1986 Jun;166(3):857-65. doi: 10.1128/jb.166.3.857-865.1986.

Promoter recognition and promoter strength in the Escherichia coli system.大肠杆菌系统中的启动子识别与启动子强度

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Topography of intermediates in transcription initiation of E.coli.

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