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来自南非克利普河重金属抗性细菌的pcoA、pcoR和chrB基因部分长度蛋白质序列的表征与结构预测

Characterization and structure prediction of partial length protein sequences of pcoA, pcoR and chrB genes from heavy metal resistant bacteria from the Klip River, South Africa.

作者信息

Chihomvu Patience, Stegmann Peter, Pillay Michael

机构信息

Department of Biotechnology, Vaal University of Technology, Private Bag X021, Vanderbijlpark 1900, South Africa.

出版信息

Int J Mol Sci. 2015 Apr 1;16(4):7352-74. doi: 10.3390/ijms16047352.

Abstract

The Klip River has suffered from severe anthropogenic effects from industrial activities such as mining. Long-term exposure to heavy metal pollution has led to the development of heavy metal resistant strains of Pseudomonas sp. KR23, Lysinibacillus sp. KR25, and E. coli KR29. The objectives of this study were to characterize the genetics of copper and chromate resistance of the isolates. Copper and chromate resistance determinants were cloned and sequenced. Open reading frames (ORFs) related to the genes CopA and CopR were identified in E. coli KR29, PcoA in Lysinibacillus sp. KR25 and none related to chromate resistance were detected. The 3D-models predicted by I-TASSER disclose that the PcoA proteins consist of β-sheets, which form a part of the cupredoxin domain of the CopA copper resistance family of genes. The model for PcoR_29 revealed the presence of a helix turn helix; this forms part of a DNA binding protein, which is part of a heavy metal transcriptional regulator. The bacterial strains were cured using ethidium bromide. The genes encoding for heavy metal resistance and antibiotic resistance were found to be located on the chromosome for both Pseudomonas sp. (KR23) and E. coli (KR29). For Lysinibacillus (KR25) the heavy metal resistance determinants are suspected to be located on a mobile genetic element, which was not detected using gel electrophoresis.

摘要

克利普河受到了采矿等工业活动带来的严重人为影响。长期暴露于重金属污染导致了假单胞菌属KR23、赖氨酸芽孢杆菌属KR25和大肠杆菌KR29等重金属抗性菌株的产生。本研究的目的是对分离菌株的铜和铬抗性遗传学特征进行表征。克隆并测序了铜和铬抗性决定簇。在大肠杆菌KR29中鉴定出了与CopA和CopR基因相关的开放阅读框(ORF),在赖氨酸芽孢杆菌属KR25中鉴定出了PcoA,未检测到与铬抗性相关的基因。I-TASSER预测的三维模型显示,PcoA蛋白由β-折叠组成,这些β-折叠构成了CopA铜抗性基因家族的铜蓝蛋白结构域的一部分。PcoR_29的模型显示存在螺旋-转角-螺旋结构;这构成了一种DNA结合蛋白的一部分,该蛋白是重金属转录调节因子的一部分。使用溴化乙锭对细菌菌株进行了治愈处理。发现假单胞菌属(KR23)和大肠杆菌(KR29)中编码重金属抗性和抗生素抗性的基因都位于染色体上。对于赖氨酸芽孢杆菌(KR25),重金属抗性决定簇疑似位于一个移动遗传元件上,而凝胶电泳未检测到该元件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24a8/4425021/07348c0ad8f1/ijms-16-07352-g001.jpg

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