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加氏乳杆菌温和噬菌体phiadh的一个基因组区域的结构,该区域涵盖一个阻遏基因和同源启动子。

Structure of a genome region of the Lactobacillus gasseri temperate phage phiadh covering a repressor gene and cognate promoters.

作者信息

Engel G, Altermann E, Klein J R, Henrich B

机构信息

Fachereich Biologie, Abteilung Mikrobiologie, Universitat Kaiserslautern, Kaiserslautern, Germany.

出版信息

Gene. 1998 Mar 27;210(1):61-70. doi: 10.1016/s0378-1119(98)00012-2.

DOI:10.1016/s0378-1119(98)00012-2
PMID:9599081
Abstract

By sequencing the DNA regions which flank the intG gene encoding integrase of the temperate Lactobacillus (Lb.) gasseri bacteriophage phiadh, a continuous sequence of 6590 bp was established. It encompasses five newly identified ORFs, of which four are located upstream, and one (orfC) downstream of intG. Proteins corresponding to the expected products of the intG upstream coding regions, orfA (33 kDa), orf2 (14 kDa), rad (12.1 kDa), and tec (7.9 kDa), were identified by in vitro expression of subcloned DNA fragments. Rad shares homology with transcription regulators, including SinR of Bacillus species and the repressor of phage phi105. The gporf2 is similar to predicted products of topologically equivalent coding regions of the Lactococcus lactis phage TP901-1 and the B. subtilis phage phi105. Promoters for the divergently oriented rad and tec genes were mapped within the 435-bp region between them and specify overlapping transcripts with extended 5'-untranslated sequences. As shown with lacZ fusions, Rad repressed transcription from the tec and rad promoters 20- and 5-fold, respectively. In Lb. gasseri, weak expression of cloned rad ws sufficient to mediate immunity towards phiadh.

摘要

通过对编码温和型加氏乳杆菌噬菌体phiadh整合酶的intG基因侧翼的DNA区域进行测序,确定了一段6590 bp的连续序列。它包含五个新鉴定的开放阅读框(ORF),其中四个位于intG上游,一个(orfC)位于intG下游。通过亚克隆DNA片段的体外表达,鉴定出了与intG上游编码区预期产物相对应的蛋白质,即orfA(33 kDa)、orf2(14 kDa)、rad(12.1 kDa)和tec(7.9 kDa)。Rad与转录调节因子具有同源性,包括芽孢杆菌属的SinR和噬菌体phi105的阻遏物。gporf2与乳酸乳球菌噬菌体TP901-1和枯草芽孢杆菌噬菌体phi105拓扑等效编码区的预测产物相似。在它们之间的435 bp区域内定位了向相反方向转录的rad和tec基因的启动子,并确定了具有延长5'非翻译序列的重叠转录本。如lacZ融合实验所示,Rad分别抑制了tec和rad启动子转录20倍和5倍。在加氏乳杆菌中,克隆的rad的弱表达足以介导对phiadh的免疫。

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