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应对铜绿假单胞菌中铬(VI)毒性的蛋白质组学变化。

Proteomic changes in response to chromium(VI) toxicity in Pseudomonas aeruginosa.

机构信息

Faculty of Science, Department of Biology, Ankara University, Beşevler, Ankara, Turkey.

出版信息

Bioresour Technol. 2010 Apr;101(7):2134-40. doi: 10.1016/j.biortech.2009.11.008. Epub 2009 Nov 30.

Abstract

A proteomic approach was used to identify proteins involved in Cr(VI) stress response of Pseudomonas aeruginosa to toxic Cr(VI). Cytosolic and membrane fractions from bacteria exposed to 300 mg l(-1) Cr(VI) were prepared, 2D gel electrophoresis in combination with MALDI-TOF MS and LC-MS/MS was used to identify proteins whose expression level increased or decreased upon exposure to Cr(VI). Overexpressed proteins include stress proteins, proteins involved in protein biosynthesis, proteins responsible for energy production, proteins involved in free radicals detoxification by the glutathione system, outer membrane proteins, MucD, while downregulated proteins were isocitrate dehydrogenase and 30S ribosomal protein S1. Under Cr(VI) exposure, upregulation of MucD (role in exopolysaccharide production) and outer membrane proteins concluded that bacteria have access to more than one resistance mechanism against toxic metal ions. We propose that the mechanisms of Cr(VI) resistance include production of exopolysaccharide and complexing of metal ions outside the cell.

摘要

采用蛋白质组学方法鉴定铜绿假单胞菌应对六价铬毒性的蛋白质,以研究其对六价铬的应激反应。制备暴露于 300mg/L 六价铬的细菌胞质和膜部分,通过 2D 凝胶电泳结合 MALDI-TOF MS 和 LC-MS/MS 鉴定表达水平在暴露于六价铬后增加或减少的蛋白质。过表达的蛋白质包括应激蛋白、参与蛋白质生物合成的蛋白质、负责能量产生的蛋白质、参与谷胱甘肽系统清除自由基的蛋白质、外膜蛋白、MucD,而下调的蛋白质是异柠檬酸脱氢酶和 30S 核糖体蛋白 S1。在六价铬暴露下,MucD(在胞外多糖产生中的作用)和外膜蛋白的上调表明细菌具有多种抵抗有毒金属离子的机制。我们提出,六价铬抗性的机制包括胞外多糖的产生和细胞外金属离子的络合。

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