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费氏弧菌ATCC7744菌株中lux操纵子的操纵基因鉴定。

Identification of the operator of the lux regulon from the Vibrio fischeri strain ATCC7744.

作者信息

Devine J H, Shadel G S, Baldwin T O

机构信息

Department of Biochemistry and Biophysics, Texas A&M University College Station.

出版信息

Proc Natl Acad Sci U S A. 1989 Aug;86(15):5688-92. doi: 10.1073/pnas.86.15.5688.

Abstract

Escherichia coli that carry a recombinant plasmid bearing the Vibrio fischeri lux regulon express luminescence that mimics the luminescence of V. fischeri. The lux regulon consists of two divergently transcribed operons, the rightward operon (luxICDABE genes) and the leftward operon (luxR gene). The luxR and luxI genes and the control region separating the two operons supply the primary regulatory control over the lux regulon; the regulatory mechanisms result in a dramatic increase in the rate of luciferase synthesis after induction, apparently due to a unique autoregulatory positive feedback mechanism, and in an enormous difference (greater than 10(4] in levels of luminescence in cells before and after induction. The generally accepted model of primary regulation of bioluminescence in V. fischeri involves the interaction of the product of the luxR gene and N-(3-oxohexanoyl)homoserine lactone, the autoinducer produced by the enzyme encoded by luxI, the first gene of the rightward operon, with an operator sequence within the control region to stimulate transcription of the rightward operon in a positive feedback loop. We have used deletion mapping of a transcription reporter vector to determine the approximate location of the operator. By site-directed mutagenesis of the presumed operator, we have demonstrated that the 20-base-pair inverted repeat ACCTGTAGGA/TCGTA CAGGT (where the vertical line is the center of symmetry), which bears striking similarity to the recognition sequence for the pleiotropic repressor protein LexA, is the operator of the lux regulon. We also found that deletion of sequences upstream of the palindrome leads to increased transcription from the rightward promoter (PR), indicative of a cis-acting element that represses transcription in the absence of the LuxR-autoinducer complex. Modifications of the palindrome that eliminate stimulation by LuxR-autoinducer of transcription from PR have no effect on repression by the cis-acting mechanism(s), suggesting that the palindrome is not necessary for repression of the rightward operon. Thus, it appears that the large increase in transcription upon induction of the lux regulon is the result of at least two independent mechanisms, one positive and the other negative.

摘要

携带含有费氏弧菌发光操纵子的重组质粒的大肠杆菌表达的发光现象类似于费氏弧菌的发光。发光操纵子由两个反向转录的操纵子组成,即右向操纵子(luxICDABE基因)和左向操纵子(luxR基因)。luxR和luxI基因以及分隔两个操纵子的控制区域对发光操纵子提供主要的调控控制;这些调控机制导致诱导后荧光素酶合成速率急剧增加,这显然是由于一种独特的自动调节正反馈机制,并且导致诱导前后细胞发光水平存在巨大差异(大于10⁴)。费氏弧菌生物发光初级调控的普遍接受模型涉及luxR基因产物与N-(3-氧代己酰基)高丝氨酸内酯(由右向操纵子的第一个基因luxI编码的酶产生的自诱导物)相互作用,与控制区域内的一个操纵序列结合,以正反馈回路刺激右向操纵子的转录。我们使用转录报告载体的缺失定位来确定操纵子的大致位置。通过对假定的操纵子进行定点诱变,我们证明了20个碱基对的反向重复序列ACCTGTAGGA/TCGTA CAGGT(其中垂直线为对称中心)与多效性阻遏蛋白LexA的识别序列具有惊人的相似性,它就是发光操纵子的操纵子。我们还发现,回文序列上游序列的缺失导致右向启动子(PR)的转录增加,这表明存在一个顺式作用元件,在没有LuxR-自诱导物复合物时抑制转录。消除LuxR-自诱导物对PR转录刺激的回文序列修饰对顺式作用机制的抑制没有影响,这表明回文序列对于右向操纵子的抑制不是必需的。因此,看来发光操纵子诱导后转录的大幅增加是至少两种独立机制的结果,一种是正调控,另一种是负调控。

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