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噬菌体SPO1基因33和34。枯草芽孢杆菌RNA聚合酶调控亚基编码基因的定位与一级结构。

Bacteriophage SPO1 genes 33 and 34. Location and primary structure of genes encoding regulatory subunits of Bacillus subtilis RNA polymerase.

作者信息

Costanzo M, Brzustowicz L, Hannett N, Pero J

出版信息

J Mol Biol. 1984 Dec 15;180(3):533-47. doi: 10.1016/0022-2836(84)90026-3.

Abstract

Bacteriophage SPO1 gene 33 and 34 products are required for SPO1 late gene transcription. Both proteins bind to the core RNA polymerase of the Bacillus subtilis host to direct the recognition of SPO1 late gene promoters, whose sequences differ from those of SPO1 early and middle gene promoters. We have located and cloned the genes for these two regulatory proteins, and have engineered their expression in Escherichia coli by placing them under the control of the bacteriophage lambda PL promoter. Nucleotide sequence analysis indicated that genes 33 and 34 overlap by 4 base-pairs and encode highly charged, slightly basic proteins of molecular weight 11,902 and 23,677, respectively.

摘要

噬菌体SPO1的晚期基因转录需要基因33和34的产物。这两种蛋白质都与枯草芽孢杆菌宿主的核心RNA聚合酶结合,以指导对SPO1晚期基因启动子的识别,这些启动子的序列与SPO1早期和中期基因启动子的序列不同。我们已经定位并克隆了这两种调节蛋白的基因,并通过将它们置于噬菌体λPL启动子的控制下,在大肠杆菌中对其表达进行了工程改造。核苷酸序列分析表明,基因33和34重叠4个碱基对,分别编码分子量为11902和23677的高电荷、略带碱性的蛋白质。

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