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鳗弧菌pJM1介导的铁摄取系统的铁转运基因包含在一个类似转座子的结构中。

Iron transport genes of the pJM1-mediated iron uptake system of Vibrio anguillarum are included in a transposonlike structure.

作者信息

Tolmasky M E, Crosa J H

机构信息

Department of Molecular Microbiology and Immunology L220, School of Medicine, Oregon Health Sciences University, Portland 97201-3098, USA.

出版信息

Plasmid. 1995 May;33(3):180-90. doi: 10.1006/plas.1995.1019.

Abstract

The pJM1 genes encoding the proteins involved in iron transport in the anguibactin iron uptake system were found to be flanked by insertion sequences in a composite transposonlike structure. These Vibrio anguillarum insertion sequences, ISV-A1 and ISV-A2, are related to IS903, IS102, and the ISVs found in Vibrio parahaemoliticus, Vibrio mimicus, and non-O1 Vibrio cholerae flanking various tdh (thermostable direct hemolysin) genes. The inverted repeats at the ends of ISV-A1 and ISV-A2 have no more than three mismatches when compared to the inverted repeats of the other ISVs or IS903 and IS102. ISV-A1 and ISV-A2 are flanked by 9-bp direct repeats, which is the number of bases that are duplicated upon IS903 or IS102 transposition. The similarities found between the V. anguillarum ISVs and the other ISVs as well as IS903 and IS102 suggest that they derive from a common ancestral insertion sequence. At the end of ISV-A1 there is a -35 sequence region followed by a -10 sequence found in the pJM1 sequence immediately outside the ISV. This promoter region is followed by an open reading frame with the potential to encode a polypeptide of 26,985 Da whose function is still unknown. The functionality of this promoter has been demonstrated and expression analysis showed that the promoter is regulated by the iron concentration of the media.

摘要

编码参与anguibactin铁摄取系统中铁转运蛋白的pJM1基因,被发现位于一个复合转座子样结构的插入序列两侧。这些鳗弧菌插入序列ISV-A1和ISV-A2,与IS903、IS102以及在副溶血性弧菌、模仿弧菌和非O1群霍乱弧菌中发现的侧翼为各种tdh(耐热直接溶血素)基因的ISV相关。与其他ISV或IS903和IS102的反向重复序列相比,ISV-A1和ISV-A2末端的反向重复序列错配不超过三个。ISV-A1和ISV-A2两侧是9个碱基对的正向重复序列,这是IS903或IS102转座时复制的碱基数。鳗弧菌ISV与其他ISV以及IS903和IS102之间的相似性表明它们源自一个共同的祖先插入序列。在ISV-A1末端有一个-35序列区域,后面是在ISV外侧的pJM1序列中发现的-10序列。这个启动子区域后面是一个开放阅读框,有可能编码一个26985 Da的多肽,其功能仍然未知。这个启动子的功能已经得到证实,表达分析表明该启动子受培养基中铁浓度的调节。

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