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2
Effects of Incubation Conditions on Cr(VI) Reduction by c-type Cytochromes in Intact Shewanella oneidensis MR-1 Cells.培养条件对完整的希瓦氏菌MR-1细胞中c型细胞色素还原六价铬的影响
Front Microbiol. 2016 May 19;7:746. doi: 10.3389/fmicb.2016.00746. eCollection 2016.
3
Cadmium resistance mechanism in Escherichia coli P4 and its potential use to bioremediate environmental cadmium.大肠杆菌P4中的镉抗性机制及其在生物修复环境镉方面的潜在用途。
Appl Microbiol Biotechnol. 2015 Dec;99(24):10745-57. doi: 10.1007/s00253-015-6901-x. Epub 2015 Aug 18.
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Shotgun proteomic analysis unveils survival and detoxification strategies by Caulobacter crescentus during exposure to uranium, chromium, and cadmium.鸟枪法蛋白质组学分析揭示了新月柄杆菌在暴露于铀、铬和镉期间的生存及解毒策略。
J Proteome Res. 2014 Apr 4;13(4):1833-47. doi: 10.1021/pr400880s. Epub 2014 Mar 7.
5
Proteomics reveals a core molecular response of Pseudomonas putida F1 to acute chromate challenge.蛋白质组学揭示了铜绿假单胞菌 F1 对急性铬酸盐胁迫的核心分子反应。
BMC Genomics. 2010 May 19;11:311. doi: 10.1186/1471-2164-11-311.
6
A nitric oxide-inducible lactate dehydrogenase enables Staphylococcus aureus to resist innate immunity.一种一氧化氮诱导型乳酸脱氢酶使金黄色葡萄球菌能够抵抗先天免疫。
Science. 2008 Mar 21;319(5870):1672-6. doi: 10.1126/science.1155207.
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Biosorption of Cr (VI) using a bacterial biofilm supported on granular activated carbon and on zeolite.利用负载在颗粒活性炭和沸石上的细菌生物膜对六价铬进行生物吸附。
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8
Effect of chromate stress on Escherichia coli K-12.铬酸盐胁迫对大肠杆菌K-12的影响。
J Bacteriol. 2006 May;188(9):3371-81. doi: 10.1128/JB.188.9.3371-3381.2006.
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Whole-genome transcriptional analysis of heavy metal stresses in Caulobacter crescentus.新月柄杆菌中重金属胁迫的全基因组转录分析。
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通过差异蛋白质表达评估海洋菌株NIOMR8对铬酸盐刺激的反应。

Response to chromate challenge by marine sp. NIOMR8 evaluated by differential protein expression.

作者信息

Pereira Elroy Joe, Damare Samir, Furtado Bliss, Ramaiah Nagappa

机构信息

1Biological Oceanography Division, CSIR-National Institute of Oceanography, Dona Paula, Goa 403004 India.

Present Address: Department of Microbiology, Copernicus University, Toruń, Poland.

出版信息

3 Biotech. 2018 Dec;8(12):500. doi: 10.1007/s13205-018-1522-6. Epub 2018 Nov 26.

DOI:10.1007/s13205-018-1522-6
PMID:30498673
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6261127/
Abstract

Liquid Chromatography-Mass Spectrometry-Quadrupole Time of Flight (LC/MS QToF) protein profiling of marine-derived NIOMR8 was carried out to evaluate proteins conferring chromate (Cr) resistance and possible metabolic pathways that were altered as a result. Expressional (up or down-regulation) responses to varying Cr (0, 50, 100, 150, and 200 µg mL) concentrations varied, with as many as 346 proteins identified. Most number of proteins-their numbers in parentheses-were up-regulated when grown in medium with 50 µg mL (162) and, down-regulated in medium with 100 (281) or 200 µg mL Cr (280). Among these, eight proteins were commonly up-regulated, while 58 were commonly down-regulated across all conditions of Cr. Expression of protein moieties in metabolic pathways like translation (38), transcription (14), replication (18) and repair (4), metabolism of carbohydrates (26), amino acids (27), nucleotides (17), and membrane transport (21) was evidenced. Up-regulation patterns suggest that reduction of molecular oxygen (5), DNA repair (4) and peptide misfolding (7) were the potential protective mechanisms employed to counter Cr stress. Additionally, proteins associated with biofilm and cell wall biogenesis highlight their hypothetical involvement in toxicity tolerance. Results also indicate that at higher concentrations of Cr, down-regulation of functional proteins impedes normal cellular functions.

摘要

采用液相色谱 - 质谱联用 - 四极杆飞行时间质谱(LC/MS QToF)对海洋来源的NIOMR8进行蛋白质谱分析,以评估赋予铬(Cr)抗性的蛋白质以及由此改变的可能代谢途径。对不同Cr(0、50、100、150和200 μg/mL)浓度的表达(上调或下调)反应各不相同,共鉴定出多达346种蛋白质。当在含有50 μg/mL(162种)的培养基中生长时,上调的蛋白质数量最多;而在含有100 μg/mL(281种)或200 μg/mL Cr(280种)的培养基中生长时,下调的蛋白质数量最多。其中,有8种蛋白质在所有Cr条件下均普遍上调,而58种蛋白质在所有Cr条件下均普遍下调。在翻译(38种)、转录(14种)、复制(18种)和修复(4种)、碳水化合物代谢(26种)、氨基酸代谢(27种)、核苷酸代谢(17种)和膜转运(21种)等代谢途径中的蛋白质部分表达得到了证实。上调模式表明,分子氧还原(5种)、DNA修复(4种)和肽错误折叠(7种)是对抗Cr胁迫所采用的潜在保护机制。此外,与生物膜和细胞壁生物合成相关的蛋白质突出了它们在毒性耐受中的假设作用。结果还表明,在较高Cr浓度下,功能蛋白的下调会阻碍正常细胞功能。