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大肠杆菌RNA聚合酶与噬菌体T5启动子的相互作用:复合物形成和解离的速率及其与体外和体内转录活性的相关性。

Interaction of E. coli RNA polymerase with promotors of coliphage T5: the rates of complex formation and decay and their correlation with in vitro and in vivo transcriptional activity.

作者信息

von Gabain A, Bujard H

出版信息

Mol Gen Genet. 1977 Dec 9;157(3):301-11. doi: 10.1007/BF00268667.

Abstract

The genome of virulent coliphage T5 contains about 30 sites which form stable complexes with E. coli RNA polymerase. Some of these sites bind RNA polymerase with high rates, others form extremely stable complexes as compared with promotors of other E. coli systems. The transcriptional activity of these promotors in vivo and in vitro reflects the rate of complex formation with RNA polymerase rather than the stability of the enzyme/promotor complex. The fastest, i.e. the most active promotors are found in the "early" region of gene expression followed by promotors of the "preearly" class. The few binding sites for the E. coli holoenzyme within the "late" region react more slowly with the enzyme.

摘要

烈性大肠杆菌噬菌体T5的基因组包含约30个位点,这些位点可与大肠杆菌RNA聚合酶形成稳定的复合物。其中一些位点能快速结合RNA聚合酶,与其他大肠杆菌系统的启动子相比,另一些位点则形成极其稳定的复合物。这些启动子在体内和体外的转录活性反映了与RNA聚合酶形成复合物的速率,而非酶/启动子复合物的稳定性。在基因表达的“早期”区域发现了最快,即最活跃的启动子,其次是“早前期”类别的启动子。“晚期”区域内大肠杆菌全酶的少数结合位点与该酶的反应较慢。

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