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编码核苷转运系统的大肠杆菌nupC基因的克隆及相邻插入元件IS 186的鉴定。

Cloning of the nupC gene of Escherichia coli encoding a nucleoside transport system, and identification of an adjacent insertion element, IS 186.

作者信息

Craig J E, Zhang Y, Gallagher M P

机构信息

Institute of Cell and Molecular Biology, University of Edinburgh, UK.

出版信息

Mol Microbiol. 1994 Mar;11(6):1159-68. doi: 10.1111/j.1365-2958.1994.tb00392.x.

Abstract

Escherichia coli is known to contain more than one active transport system for nucleoside uptake. In the present study we report the sequence of a gene encoding a second nucleoside transport system, nupC (in addition to nupG). An open reading frame (ORF) of 1200 bp was identified that codes for a hydrophobic polypeptide of 43,560 Da and an NupC fusion protein was shown to be membrane associated. The native NupC protein is also identified, following over-expression. NupC exhibits short regions of homology to several membrane-associated proteins, including LacY and Cyd. Analysis of the nupC promoter region revealed the presence of at least two putative CRP-binding sites, centred at -40bp and -89bp, which probably flank a CytR-binding site. In addition, an adjacent IS 186 element was identified and found to reside within a putative terminator structure, downstream from the nupC ORF. This arrangement is shown to reflect the previously established gene order on the E. coli chromosome.

摘要

已知大肠杆菌含有不止一种用于核苷摄取的主动转运系统。在本研究中,我们报告了编码第二种核苷转运系统nupC(除nupG之外)的基因序列。鉴定出一个1200 bp的开放阅读框(ORF),其编码一个43,560 Da的疏水多肽,并且一个NupC融合蛋白显示与膜相关。在过表达后也鉴定出了天然的NupC蛋白。NupC与几种膜相关蛋白,包括LacY和Cyd,存在短的同源区域。对nupC启动子区域的分析揭示,存在至少两个假定的CRP结合位点,位于-40 bp和-89 bp处,它们可能位于一个CytR结合位点的两侧。此外,鉴定出一个相邻的IS 186元件,发现其位于nupC ORF下游的一个假定终止子结构内。这种排列显示反映了大肠杆菌染色体上先前确立的基因顺序。

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