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尿素在大肠杆菌的乳糖操纵子(LAC)和色氨酸操纵子(TNA)中发挥作用的两种不同机制。

Two different mechanisms for urea action at the LAC and TNA operons in Escherichia coli.

作者信息

Blazy B, Ullmann A

机构信息

Unité de Biochimie des Régulations Cellulaires, Institut Pasteur, Paris, France.

出版信息

Mol Gen Genet. 1990 Feb;220(3):419-24. doi: 10.1007/BF00391748.

Abstract

Urea, at concentrations which do not interfere with bacterial growth, specifically inhibits the expression of catabolite sensitive operons. To search for the target and the mechanism of urea action we measured lactose (lac) and tryptophanase (tna) specific mRNA synthesis in vivo and in vitro. We show that urea acts by two different mechanisms at these two catabolite sensitive operons, resembling the manner in which catabolite repression regulates lac and tna. At the lac promoter, urea abolishes transcription initiation or blocks an early step in mRNA elongation without interfering with the binding of RNA polymerase and catabolite gene activator protein (CAP). At the tna promoter, urea does not abolish transcription initiation but could interfere with tnaC translation.

摘要

在不干扰细菌生长的浓度下,尿素可特异性抑制分解代谢敏感操纵子的表达。为了寻找尿素作用的靶点和机制,我们在体内和体外测量了乳糖(lac)和色氨酸酶(tna)特异性mRNA的合成。我们发现,尿素在这两个分解代谢敏感操纵子上通过两种不同机制发挥作用,类似于分解代谢阻遏调节lac和tna的方式。在lac启动子处,尿素可消除转录起始或阻断mRNA延伸的早期步骤,而不干扰RNA聚合酶和分解代谢基因激活蛋白(CAP)的结合。在tna启动子处,尿素不会消除转录起始,但可能会干扰tnaC的翻译。

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