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首页> 外文期刊>Journal of Basic Microbiology: An International Journal on Morphology, Physiology, Genetics, and Ecology of Microorganisms >Comparative proteome analysis reveals proteins involved in salt adaptation in Photobacterium damselae subsp piscicida
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Comparative proteome analysis reveals proteins involved in salt adaptation in Photobacterium damselae subsp piscicida

机译:比较蛋白质组学分析揭示了与damselae亚种piscicida亚种的盐适应有关的蛋白质

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摘要

Proteomic approaches were applied to investigate whether Photobacterium damselae subsp. piscicida (Phdp) can directly sense and respond to growth conditions under different salinities, 0.85% and 3.5% NaCl concentrations, mimicking the osmotic conditions in host and marine water bodies, respectively. Proteins significantly altered were analyzed by two-dimensional gel electrophoresis (2-DE), liquid chromatography-electrospray ionization-quadrupole-time-of-flight tandem mass spectrometry (LC-ESI-Q-TOF MS/MS) and bioinformatics analysis, thus resulting in 16 outer membrane proteins (OMPs), 12 inner membrane proteins (IMPs), and 20 cytoplasmic proteins (CPs). Quantitative real-time PCR was also applied to monitor the mRNA expression level of these target proteins. Cluster of orthologous groups of protein (COG) analysis revealed that when shifting from 3.5% to 0.85% salinity, the majority of the up-regulated proteins were involved in posttranslational modification, protein turnover, and chaperones, while the down-regulated proteins were mainly related to energy production and conversion, compatible solutes (carbohydrates, amino acids and their derivatives) biogenesis and transport. Differentially expressed proteins identified in the current study could be used to elucidate the salt adaptation mechanisms of Phdp during their transition between host cells and the marine habitats.
机译:蛋白质组学的方法被用来调查是否有光细菌的damselae亚种。 piscicida(Phdp)可以直接感应和响应不同盐度,0.85%和3.5%NaCl浓度下的生长条件,分别模仿宿主和海洋水体的渗透条件。通过二维凝胶电泳(2-DE),液相色谱-电喷雾电离-四极杆飞行时间串联质谱(LC-ESI-Q-TOF MS / MS)和生物信息学分析来分析显着改变的蛋白质产生16种外膜蛋白(OMP),12种内膜蛋白(IMP)和20种胞质蛋白(CP)。实时定量PCR还用于监测这些靶蛋白的mRNA表达水平。直系同源蛋白质组(COG)分析的聚类分析表明,当盐度从3.5%转变为0.85%时,大多数上调的蛋白质参与翻译后修饰,蛋白质更新和伴侣,而下调的蛋白质主要参与翻译与能量产生和转化,相容性溶质(碳水化合物,氨基酸及其衍生物)的生物发生和运输有关。在当前研究中鉴定出的差异表达蛋白可用于阐明Phdp在宿主细胞和海洋生境之间过渡期间的盐适应机制。

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