Evaluation of interaction among arsenic and Brevibacterium sp. strain CS2 and its proteins profiling

IF 6.6 Q1 ENGINEERING, ENVIRONMENTAL
Shahid Sher , Sajjad Ullah , Dilara Abbas Bukhari , Syed Zajif Hussain , Abdul Rehman
{"title":"Evaluation of interaction among arsenic and Brevibacterium sp. strain CS2 and its proteins profiling","authors":"Shahid Sher ,&nbsp;Sajjad Ullah ,&nbsp;Dilara Abbas Bukhari ,&nbsp;Syed Zajif Hussain ,&nbsp;Abdul Rehman","doi":"10.1016/j.hazl.2024.100119","DOIUrl":null,"url":null,"abstract":"<div><p>In this study, <em>Brevibacterium</em> sp. strain CS2 was used to evaluate the mechanisms of arsenic interaction with the bacterium and its enzymatic and protein profiling under arsenic stress. The bacterium was capable to resist the arsenate 280 mM and arsenite 40 mM as per MIC. The whole genome, available on NCBI, was analyzed for genes associated with arsenic, which confirmed the genes for both arsenic oxidation (<em>aioB</em>) and arsenic reduction <em>arsR, arsC, ACR3,</em> and <em>arsB</em>. The sharpening and shifting of FTIR spectra in the ranges of 3278–2851 cm<sup>−1</sup> are due to hydroxyl and amide stretching. SEM analysis showed no significant changes in morphology in arsenic stress while EDX analysis proved the arsenite interaction by showing arsenic peaks in the graph. Both glutathione and non-protein thiol showed different responses in the absence and presence of arsenic stress. Protein bands such as 25, 30, 32, 37, 42, 48, and 100 kDa were expressed more in arsenic-treated samples as compared to the control one. The presence of arsenic oxidizing genes, the ability to resist arsenic, and the varied response of enzymes and proteins in arsenic stress make the bacterium a suitable agent for arsenic eradication from contaminated sites.</p></div>","PeriodicalId":93463,"journal":{"name":"Journal of hazardous materials letters","volume":null,"pages":null},"PeriodicalIF":6.6000,"publicationDate":"2024-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666911024000182/pdfft?md5=27bd3a4ed884d7017ea2d68da54e0627&pid=1-s2.0-S2666911024000182-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of hazardous materials letters","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666911024000182","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, ENVIRONMENTAL","Score":null,"Total":0}
引用次数: 0

Abstract

In this study, Brevibacterium sp. strain CS2 was used to evaluate the mechanisms of arsenic interaction with the bacterium and its enzymatic and protein profiling under arsenic stress. The bacterium was capable to resist the arsenate 280 mM and arsenite 40 mM as per MIC. The whole genome, available on NCBI, was analyzed for genes associated with arsenic, which confirmed the genes for both arsenic oxidation (aioB) and arsenic reduction arsR, arsC, ACR3, and arsB. The sharpening and shifting of FTIR spectra in the ranges of 3278–2851 cm−1 are due to hydroxyl and amide stretching. SEM analysis showed no significant changes in morphology in arsenic stress while EDX analysis proved the arsenite interaction by showing arsenic peaks in the graph. Both glutathione and non-protein thiol showed different responses in the absence and presence of arsenic stress. Protein bands such as 25, 30, 32, 37, 42, 48, and 100 kDa were expressed more in arsenic-treated samples as compared to the control one. The presence of arsenic oxidizing genes, the ability to resist arsenic, and the varied response of enzymes and proteins in arsenic stress make the bacterium a suitable agent for arsenic eradication from contaminated sites.

砷与 Brevibacterium sp. 菌株 CS2 之间相互作用的评估及其蛋白质分析
本研究利用 Brevibacterium sp. 菌株 CS2 评估砷与该细菌的相互作用机制,以及砷胁迫下该细菌的酶和蛋白质谱。根据 MIC,该细菌能够抵抗 280 mM 的砷酸盐和 40 mM 的亚砷酸盐。对 NCBI 提供的全基因组进行了分析,以寻找与砷有关的基因,结果证实了砷氧化(aioB)和砷还原的基因 arsR、arsC、ACR3 和 arsB。傅立叶变换红外光谱在 3278-2851 cm-1 范围内的锐化和移动是由羟基和酰胺伸展引起的。扫描电子显微镜分析表明,在砷应力作用下,形态没有明显变化,而电离辐射X分析则通过在图中显示砷峰证明了亚砷酸盐之间的相互作用。谷胱甘肽和非蛋白质硫醇在没有砷胁迫和有砷胁迫的情况下表现出不同的反应。与对照组相比,砷处理过的样品中 25、30、32、37、42、48 和 100 kDa 等蛋白质条带的表达量更高。砷氧化基因的存在、抗砷能力以及砷胁迫下酶和蛋白质的不同反应,使该细菌成为消除受污染地区砷污染的合适菌剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of hazardous materials letters
Journal of hazardous materials letters Pollution, Health, Toxicology and Mutagenesis, Environmental Chemistry, Waste Management and Disposal, Environmental Engineering
CiteScore
10.30
自引率
0.00%
发文量
0
审稿时长
20 days
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信