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整合宿主因子是牙龈卟啉单胞菌中pYGK衍生质粒复制所必需的。

Integration host factor is required for replication of pYGK-derived plasmids in Aggregatibacter actinomycetemcomitans.

作者信息

Torres-Escobar Ascención, Juárez-Rodríguez María D, Demuth Donald R

机构信息

Research Group in Oral Health and Systemic Disease, University of Louisville School of Dentistry, Louisville, KY, USA.

出版信息

FEMS Microbiol Lett. 2014 Aug;357(2):184-94. doi: 10.1111/1574-6968.12510. Epub 2014 Jul 17.

Abstract

In this study, we show that integration host factor protein (IHF) is required for replication of pYGK plasmids in Aggregatibacter actinomycetemcomitans. YGK plasmids were not replicated in A. actinomycetemcomitans strains lacking either the α- or β- subunit of IHF. However, the deletion mutants were complemented, and plasmid replication was restored when the promoter region and gene for either ihfA or ihfB was cloned into pYGK. We also identified two motifs that resemble the consensus IHF-binding site in a 813-bp fragment containing the pYGK origin of replication. Using electrophoretic mobility shift assays, purified IHFα-IHFβ protein complex was shown to bind to probes containing either of these motifs. To our knowledge, this is the first report showing that plasmid replication is IHF-dependent in the family Pasteurellaceae. In addition, using site-direct mutagenesis, the XbaI and KpnI restriction sites in the suicide vector pJT1 were modified to generate plasmid pJT10. The introduction of these new unique sites in pJT10 facilitates the transfer of transcriptional or translational lacZ fusion constructs for the generation of single-copy chromosomal insertion of the reporter construct. Plasmid pJT10 and its derivatives will be useful for genetic studies in Aggregatibacter (Actinobacillus) and probably other genera of Pasteurellaceae, including Haemophilus, Pasteurella, and Mannheimia.

摘要

在本研究中,我们发现整合宿主因子蛋白(IHF)是牙龈卟啉单胞菌中pYGK质粒复制所必需的。在缺乏IHFα亚基或β亚基的牙龈卟啉单胞菌菌株中,YGK质粒无法复制。然而,当将ihfA或ihfB的启动子区域和基因克隆到pYGK中时,缺失突变体得到了互补,质粒复制得以恢复。我们还在包含pYGK复制起点的813 bp片段中鉴定出两个类似于IHF共有结合位点的基序。通过电泳迁移率变动分析表明,纯化的IHFα-IHFβ蛋白复合物能与包含这些基序之一的探针结合。据我们所知,这是第一份表明巴斯德氏菌科中质粒复制依赖于IHF的报告。此外,通过定点诱变,对自杀载体pJT1中的XbaI和KpnI限制酶切位点进行了修饰,构建了质粒pJT10。在pJT10中引入这些新的独特位点有助于转录或翻译lacZ融合构建体的转移,从而实现报告构建体的单拷贝染色体插入。质粒pJT10及其衍生物将有助于牙龈卟啉单胞菌(放线杆菌属)以及可能包括嗜血杆菌属、巴斯德氏菌属和曼氏杆菌属在内的其他巴斯德氏菌科属的遗传学研究。

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