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鱼发光杆菌lumP和lux操纵子调控区的核苷酸序列及功能分析。

Nucleotide sequence and functional analysis of regulatory region of the lumP and the lux operon from Photobacterium leiognathi.

作者信息

Lin J W, Chao Y F, Weng S F

机构信息

Institute of Molecular Biology, National Chung Hsing University, Taichung, Taiwan, ROC.

出版信息

Biochem Biophys Res Commun. 1995 May 25;210(3):938-47. doi: 10.1006/bbrc.1995.1747.

Abstract

The lumP gene is linked to the lux operon, but runs in the opposite direction in Photobacterium leiognathi PL741. The gene order of the lumP and the lux operon is < -lumP-R & R-luxC-luxD-luxA-luxB-luxN-luxE- > (R & R: regulatory region). The nucleotide sequence of the regulatory region (827-bp) between the lumP and the lux operon was determined. Sequence analysis illustrates that the regulatory region includes two divergent promoter systems, PR-promoter system for the lux operon (R-operon) and PL-promoter system for the lumP or lum operon (L-operon). Functional analysis of the regulatory region shows that the PR- and PL-promoter systems both are able to lead the gene expression. The deletion experiment result elicits that the PR- and PL-promoter are coordinatively and negatively regulated; the PR- and PL-promoter might be competing for recognition by RNA polymerase to initiate transcription. The fact of the LumP responsible for the spectral blue shift in P. leiognathi implied that the lumP gene closedly linked to the lux operon is for coordinative regulation with the lux operon. In addition, the glucose repression on the PR-promoter system shows that the expression of the lux operon is regulated by cAMP-CRP induction in E. coli.

摘要

lumP基因与lux操纵子相连,但在鱼发光杆菌PL741中其转录方向相反。lumP基因和lux操纵子的基因顺序为< -lumP-R & R-luxC-luxD-luxA-luxB-luxN-luxE- >(R & R:调控区)。测定了lumP基因与lux操纵子之间调控区(827 bp)的核苷酸序列。序列分析表明,该调控区包含两个不同的启动子系统,即lux操纵子(R操纵子)的PR启动子系统和lumP或lum操纵子(L操纵子)的PL启动子系统。对调控区的功能分析表明,PR启动子系统和PL启动子系统均能引导基因表达。缺失实验结果表明,PR启动子和PL启动子受到协同负调控;PR启动子和PL启动子可能竞争RNA聚合酶的识别以启动转录。鱼发光杆菌中LumP导致光谱蓝移这一事实表明,与lux操纵子紧密相连的lumP基因用于与lux操纵子进行协同调控。此外,PR启动子系统上的葡萄糖抑制作用表明,lux操纵子的表达在大肠杆菌中受cAMP-CRP诱导调控。

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