Suppr超能文献

胱氨酸在暴露于过氧化氢的大肠杆菌细胞细胞毒性反应中的作用。

Action of cystine in the cytotoxic response of Escherichia coli cells exposed to hydrogen peroxide.

作者信息

Cantoni O, Brandi G, Albano A, Cattabeni F

机构信息

Institute of Pharmacology and Pharmacognosy, University of Urbino, Italy.

出版信息

Free Radic Res. 1995 Mar;22(3):275-83. doi: 10.3109/10715769509147545.

Abstract

Cystine markedly enhanced the cytotoxic response of Escherichia coli cells to concentrations of hydrogen peroxide resulting in mode one killing, but displayed little effect in mode two killed cells. The effect of cystine was concentration-dependent over a range of 5-50 microM and did not further increase at higher levels. Cystine had similar effects in other bacterial systems. In order to sensitize the cells to the oxidative injury, the amino acid must be present during exposure to the oxidant since no enhancement of the cytotoxic response can be observed in cystine pre-loaded cells. In addition, no further enhancement of cytotoxicity could be detected when cystine was added before and left during challenge with the oxidant. The enhancing effect of cystine on oxidative injury of E. coli cells appears to be directly mediated by the amino acid and in fact cysteic acid, the most likely oxidation product, had no effect on the killing of bacterial cells elicited by hydrogen peroxide. Other disulfide compounds such as oxidized glutathione, cystamine and dithionitrobenzoic acid only slightly increased the susceptibility of bacteria to the oxidant. The effect of the disulfides was not concentration-dependent over a range of 200-800 microM and was statistically significant only for cystamine. Taken together, these results indicate that cystine markedly increases the cytotoxic response of bacteria to hydrogen peroxide and suggest that the amino acid might impair the cellular defence machinery against hydrogen peroxide. This effect may involve a thiol-disulfide exchange reaction at the cell membrane level.

摘要

胱氨酸显著增强了大肠杆菌细胞对导致第一种杀伤模式的过氧化氢浓度的细胞毒性反应,但对第二种杀伤模式的细胞几乎没有影响。在5 - 50微摩尔范围内,胱氨酸的作用呈浓度依赖性,在更高水平时不会进一步增加。胱氨酸在其他细菌系统中也有类似作用。为了使细胞对氧化损伤敏感,氨基酸必须在暴露于氧化剂期间存在,因为在预先加载胱氨酸的细胞中未观察到细胞毒性反应增强。此外,在氧化剂攻击前添加并在攻击期间保留胱氨酸时,未检测到细胞毒性的进一步增强。胱氨酸对大肠杆菌细胞氧化损伤的增强作用似乎直接由该氨基酸介导,事实上,最可能的氧化产物半胱磺酸对过氧化氢引起的细菌细胞杀伤没有影响。其他二硫化合物,如氧化型谷胱甘肽、胱胺和二硫代硝基苯甲酸,仅略微增加了细菌对氧化剂的敏感性。在200 - 800微摩尔范围内,二硫化合物的作用不呈浓度依赖性,且仅胱胺的作用具有统计学意义。综上所述,这些结果表明胱氨酸显著增加了细菌对过氧化氢的细胞毒性反应,并表明该氨基酸可能损害细胞对过氧化氢的防御机制。这种作用可能涉及细胞膜水平的硫醇 - 二硫键交换反应。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验