Protective action of bacterial melanin against DNA damage in full UV spectrums by a sensitive plasmid-based noncellular system

Jing Geng , Sheng-Bing Yu , Xia Wan , Xiao-Juan Wang , Ping Shen , Ping Zhou , Xiang-Dong Chen
{"title":"Protective action of bacterial melanin against DNA damage in full UV spectrums by a sensitive plasmid-based noncellular system","authors":"Jing Geng ,&nbsp;Sheng-Bing Yu ,&nbsp;Xia Wan ,&nbsp;Xiao-Juan Wang ,&nbsp;Ping Shen ,&nbsp;Ping Zhou ,&nbsp;Xiang-Dong Chen","doi":"10.1016/j.jprot.2007.12.013","DOIUrl":null,"url":null,"abstract":"<div><p>The purpose of this study was to introduce a simple and sensitive plasmid-based noncellular system to evaluate the photoprotection of bacterial melanin on DNA damage against ultraviolet (UV) radiation. Plasmid DNA was used to assess the role of melanin in different ranges of UV using a series of <em>in vitro</em> assays. Fluorometric measurements suggested that melanin could efficiently scavenge reactive oxygen species (ROS) generated by UVA irradiation in solution, and the scavenging capability was proportional to the pigment concentration. The protective effect of melanin on plasmid DNA under UVB irradiation was confirmed by the transformation efficiency of the protected DNA, which was at least 10-fold higher than that of the non melanin protected DNA. After the UVC irradiation, the DNA damage of strand breaks was quantified by laser-induced fluorescence capillary electrophoresis. The percentage of supercoiled plasmid was reduced from 80% to less than 5% without melanin protection. In contrast, the percentage of supercoiled DNA only decreased to about 40% in the presence of melanin under the same radiation conditions. All these results demonstrated that bacterial melanin did protect DNA from being damaged throughout full UV irradiation. This system, avoiding the potential interference by cellular DNA repair machinery and intracellular substances, may provide a sensitive <em>in vitro</em> means to evaluate the functions of melanin and other photoprotective compounds from different sources.</p></div>","PeriodicalId":15257,"journal":{"name":"Journal of biochemical and biophysical methods","volume":"70 6","pages":"Pages 1151-1155"},"PeriodicalIF":0.0000,"publicationDate":"2008-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.jprot.2007.12.013","citationCount":"38","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of biochemical and biophysical methods","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0165022X0700190X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 38

Abstract

The purpose of this study was to introduce a simple and sensitive plasmid-based noncellular system to evaluate the photoprotection of bacterial melanin on DNA damage against ultraviolet (UV) radiation. Plasmid DNA was used to assess the role of melanin in different ranges of UV using a series of in vitro assays. Fluorometric measurements suggested that melanin could efficiently scavenge reactive oxygen species (ROS) generated by UVA irradiation in solution, and the scavenging capability was proportional to the pigment concentration. The protective effect of melanin on plasmid DNA under UVB irradiation was confirmed by the transformation efficiency of the protected DNA, which was at least 10-fold higher than that of the non melanin protected DNA. After the UVC irradiation, the DNA damage of strand breaks was quantified by laser-induced fluorescence capillary electrophoresis. The percentage of supercoiled plasmid was reduced from 80% to less than 5% without melanin protection. In contrast, the percentage of supercoiled DNA only decreased to about 40% in the presence of melanin under the same radiation conditions. All these results demonstrated that bacterial melanin did protect DNA from being damaged throughout full UV irradiation. This system, avoiding the potential interference by cellular DNA repair machinery and intracellular substances, may provide a sensitive in vitro means to evaluate the functions of melanin and other photoprotective compounds from different sources.

基于敏感质粒的非细胞系统在全紫外光谱下细菌黑色素对DNA损伤的保护作用
本研究的目的是建立一种简单、灵敏的基于质粒的非细胞系统来评估细菌黑色素对紫外线(UV)损伤的光保护作用。质粒DNA用于评估黑色素在不同紫外范围内的作用,使用一系列的体外测定。荧光测定表明,黑色素能有效清除溶液中UVA辐射产生的活性氧(ROS),清除能力与色素浓度成正比。在UVB照射下,黑色素对质粒DNA的保护作用通过保护DNA的转化效率得到证实,其转化效率至少比未受黑色素保护的DNA高10倍。紫外辐射后,采用激光诱导荧光毛细管电泳定量检测DNA链断裂损伤。在没有黑色素保护的情况下,超卷曲质粒的比例从80%降低到5%以下。相比之下,在相同的辐射条件下,在黑色素存在的情况下,超卷曲DNA的百分比仅下降到40%左右。所有这些结果表明,细菌黑色素确实可以保护DNA免受紫外线照射的损害。该系统避免了细胞DNA修复机制和细胞内物质的潜在干扰,可能为评估来自不同来源的黑色素和其他光保护化合物的功能提供一种敏感的体外手段。
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