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Global Molecular and Morphological Effects of 24-Hour Chromium(VI) Exposure on Shewanella oneidensis MR-1

机译:24小时铬(VI)暴露对拟南芥希瓦氏菌MR-1的全球分子和形态学影响

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The biological impact of 24-h (“chronic”) chromium(VI) [Cr(VI) or chromate] exposure on Shewanella oneidensis MR-1 was assessed by analyzing cellular morphology as well as genome-wide differential gene and protein expression profiles. Cells challenged aerobically with an initial chromate concentration of 0.3 mM in complex growth medium were compared to untreated control cells grown in the absence of chromate. At the 24-h time point at which cells were harvested for transcriptome and proteome analyses, no residual Cr(VI) was detected in the culture supernatant, thus suggesting the complete uptake and/or reduction of this metal by cells. In contrast to the untreated control cells, Cr(VI)-exposed cells formed apparently aseptate, nonmotile filaments that tended to aggregate. Transcriptome profiling and mass spectrometry-based proteomic characterization revealed that the principal molecular response to 24-h Cr(VI) exposure was the induction of prophage-related genes and their encoded products as well as a number of functionally undefined hypothetical genes that were located within the integrated phage regions of the MR-1 genome. In addition, genes with annotated functions in DNA metabolism, cell division, biosynthesis and degradation of the murein (peptidoglycan) sacculus, membrane response, and general environmental stress protection were upregulated, while genes encoding chemotaxis, motility, and transport/binding proteins were largely repressed under conditions of 24-h chromate treatment.
机译:通过分析细胞的形态以及全基因组差异基因和蛋白质表达谱,评估了24小时(“慢性”)铬(VI)[Cr(VI)或铬酸盐]暴露对拟南芥MR-1的生物学影响。将复杂生长培养基中初始铬酸盐浓度为0.3 mM需氧挑战的细胞与不存在铬酸盐的未经处理的对照细胞进行比较。在收获细胞进行转录组和蛋白质组分析的24小时时间点,在培养上清液中未检测到残留的Cr(VI),因此表明细胞完全吸收和/或还原了该金属。与未处理的对照细胞相比,暴露于Cr(VI)的细胞形成了明显的趋于聚集的不活动的细丝。转录组分析和基于质谱的蛋白质组学表征显示,对24-h Cr(VI)暴露的主要分子反应是诱导与噬菌体相关的基因及其编码产物,以及位于其中的许多功能不确定的假设基因MR-1基因组的整合噬菌体区域。此外,具有注释功能的基因在DNA代谢,细胞分裂,壁蛋白(肽聚糖)囊的生物合成和降解,膜反应以及一般的环境胁迫保护中被上调,而编码趋化性,运动性和转运/结合蛋白的基因则被大量上调。在24小时铬酸盐处理条件下被抑制。

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