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大肠杆菌K-12 tyrP基因启动子操纵区的分子分析

Molecular analysis of the promoter operator region of the Escherichia coli K-12 tyrP gene.

作者信息

Kasian P A, Davidson B E, Pittard J

出版信息

J Bacteriol. 1986 Aug;167(2):556-61. doi: 10.1128/jb.167.2.556-561.1986.

Abstract

The nucleotide sequence of the tyrP promoter region from Escherichia coli has been determined. Two TYR R boxes have been identified, and one of these was shown to overlap the -35 region of a major tyrP promoter (p1). S1 nuclease mapping of in vivo transcripts revealed that transcription from p1 is stimulated by phenylalanine and to a lesser extent by leucine. The demonstration that mutants in which TyrR-tyrosine-mediated repression of tyrP has been abolished have single base changes in the TYR R box which overlaps p1 suggests that TyrR-tyrosine-mediated repression of tyrP also involves p1. TyrR-independent stimulation of tyrP expression by Casamino Acids involves a second promoter 140 bases upstream of p1. There are no TYR R boxes in this region. The sequences of 10 TYR R boxes preceding the genes tyrP, tyrR, and aroG and the operons aroF tyrA and aroL aroM are compared and discussed.

摘要

已确定大肠杆菌tyrP启动子区域的核苷酸序列。已鉴定出两个TYR R框,其中一个被证明与主要tyrP启动子(p1)的-35区域重叠。体内转录本的S1核酸酶图谱显示,p1的转录受苯丙氨酸刺激,受亮氨酸的刺激程度较小。在与p1重叠的TYR R框中具有单碱基变化的突变体中,tyrP的TyrR-酪氨酸介导的阻遏作用已被消除,这表明tyrP的TyrR-酪氨酸介导的阻遏作用也涉及p1。酪蛋白氨基酸对tyrP表达的TyrR非依赖性刺激涉及p1上游140个碱基处的第二个启动子。该区域没有TYR R框。对tyrP、tyrR和aroG基因以及aroF tyrA和aroL aroM操纵子之前的10个TYR R框的序列进行了比较和讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec57/212925/c506cbe44ef4/jbacter00207-0140-a.jpg

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