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Ti质粒pTiR10中表达两种ABC型通透酶和traR基因的OccR激活型及TraR激活型启动子的定位

Localization of OccR-activated and TraR-activated promoters that express two ABC-type permeases and the traR gene of Ti plasmid pTiR10.

作者信息

Fuqua C, Winans S C

机构信息

Department of Biology, Trinity University, San Antonio, Texas 78212, USA.

出版信息

Mol Microbiol. 1996 Jun;20(6):1199-210. doi: 10.1111/j.1365-2958.1996.tb02640.x.

Abstract

Conjugation of Agrobacterium tumefaciens wide-host-range octopine-type Ti plasmids is regulated by the LuxR-type transcriptional activator TraR in conjunction with an acylated homoserine lactone designated AAI. Expression of traR in octopine-type Ti plasmids is stimulated by OccR in response to octopine, an opine released from crown gall tumours, and is also positively autoregulated by TraR and AAI. Genetic and physical mapping of these promoters indicates that the OccR-activated promoter lies 14.5 kb upstream of traR, while the TraR-activated promoter lies 6 kb upstream. The upstream portion of the 14.5 kb operon contains seven previously characterized genes that direct the uptake and catabolism of octopine. The TraR-activated promoter lies just downstream from the octopine catabolic genes, and transcribes six genes in addition to traR, including five genes (ophABCDE) that show strong homology to oligo-peptide permeases of Salmonella typhimurium and Bacillus subtilis. Several TraR-regulated promoters overlap with 18 bp inverted repeats called tra boxes. In contrast, the traR autoregulatory promoter is not associated with a consensus tra box.

摘要

根癌土壤杆菌广宿主范围章鱼碱型Ti质粒的接合由LuxR型转录激活因子TraR与一种名为AAI的酰化高丝氨酸内酯共同调控。章鱼碱型Ti质粒中traR的表达受OccR的刺激,以响应章鱼碱(一种从冠瘿瘤释放的冠瘿碱),并且也受到TraR和AAI的正自调控。这些启动子的遗传和物理图谱表明,OccR激活的启动子位于traR上游14.5 kb处,而TraR激活的启动子位于上游6 kb处。14.5 kb操纵子的上游部分包含七个先前已鉴定的基因,这些基因指导章鱼碱的摄取和分解代谢。TraR激活的启动子位于章鱼碱分解代谢基因的下游,除traR外还转录六个基因,包括五个与鼠伤寒沙门氏菌和枯草芽孢杆菌的寡肽通透酶具有高度同源性的基因(ophABCDE)。几个TraR调控的启动子与称为tra盒的18 bp反向重复序列重叠。相反,traR自调控启动子与共有tra盒无关。

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