pH induced damage and repair in E. coli

Javed Musarrat, Masood Ahmad
{"title":"pH induced damage and repair in E. coli","authors":"Javed Musarrat,&nbsp;Masood Ahmad","doi":"10.1016/0167-8817(88)90032-6","DOIUrl":null,"url":null,"abstract":"<div><p><em>Escherichia coli</em> lost its colony-forming ability when suspended in Tris/NaOH or Tris/Mg<sup>2+</sup> buffers of pH 10.0 and 4.0, respectively. A significant decrease in the survival of radiation-sensitive mutants <em>recA</em>, <em>polA, res, rer</em> and <em>lexA</em> was observed as compared to their wild-type counterpart under these conditions. The alkali-injured cells were found to recover when incubated at 37°C for 2 h in 0.05 M phosphate buffer of pH 8.0, whereas no such liquid holding recovery was observed in <em>recA</em> and <em>lexA</em> mutants. Recovery in phosphate buffer was not affected by metabolic inhibitors. As a result of alkali treatment, the sensitivity of bacteria to ultraviolet light (UV) was enhanced. However, on incubation for 2 h in recovery buffer at 37°C, the bacteria regained partial UV resistance. Bacteria exposed to alkaline environment exhibited an enhanced level of mutagenesis. Contrary to the treated wild-type, the mutants <em>recA</em> and <em>lexA</em> did not exhibit any increase in the mutation frequency. Alkali treatment to GC → AT transition mutants of <em>Salmonella typhimurium</em>, TA102 and TA104 resulted in the highest number of revertants per plate.</p></div>","PeriodicalId":100936,"journal":{"name":"Mutation Research/DNA Repair Reports","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1988-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0167-8817(88)90032-6","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mutation Research/DNA Repair Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0167881788900326","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5

Abstract

Escherichia coli lost its colony-forming ability when suspended in Tris/NaOH or Tris/Mg2+ buffers of pH 10.0 and 4.0, respectively. A significant decrease in the survival of radiation-sensitive mutants recA, polA, res, rer and lexA was observed as compared to their wild-type counterpart under these conditions. The alkali-injured cells were found to recover when incubated at 37°C for 2 h in 0.05 M phosphate buffer of pH 8.0, whereas no such liquid holding recovery was observed in recA and lexA mutants. Recovery in phosphate buffer was not affected by metabolic inhibitors. As a result of alkali treatment, the sensitivity of bacteria to ultraviolet light (UV) was enhanced. However, on incubation for 2 h in recovery buffer at 37°C, the bacteria regained partial UV resistance. Bacteria exposed to alkaline environment exhibited an enhanced level of mutagenesis. Contrary to the treated wild-type, the mutants recA and lexA did not exhibit any increase in the mutation frequency. Alkali treatment to GC → AT transition mutants of Salmonella typhimurium, TA102 and TA104 resulted in the highest number of revertants per plate.

pH诱导大肠杆菌的损伤和修复
当大肠杆菌分别悬浮在pH为10.0和4.0的Tris/NaOH或Tris/Mg2+缓冲液中时,大肠杆菌失去了集落形成能力。在这些条件下,与野生型相比,辐射敏感突变体recA、polA、res、rer和lexA的存活率显著降低。在pH 8.0的0.05 M磷酸盐缓冲液中,37°C孵育2小时,发现碱损伤细胞恢复,而在recA和lexA突变体中没有这种液体保存恢复。磷酸盐缓冲液的恢复不受代谢抑制剂的影响。碱处理提高了细菌对紫外光的敏感性。然而,在37°C的恢复缓冲液中孵育2小时后,细菌恢复了部分紫外线抗性。暴露于碱性环境中的细菌表现出更高的诱变水平。与处理过的野生型相反,突变体recA和lexA的突变频率没有增加。对鼠伤寒沙门菌、TA102和TA104的GC→AT过渡突变体进行碱处理后,每个培养皿的回复菌数量最多。
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
自引率
0.00%
发文量
0
×
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