首页> 外文期刊>Analytical and Bioanalytical Chemistry >Sensitive and selective determination of glutathione in probiotic bacteria by capillary electrophoresis–laser induced fluorescence
【24h】

Sensitive and selective determination of glutathione in probiotic bacteria by capillary electrophoresis–laser induced fluorescence

机译:毛细管电泳-激光诱导荧光灵敏和选择性地测定益生菌中的谷胱甘肽

获取原文
获取原文并翻译 | 示例
           

摘要

Glutathione (GSH) is a thiol with an important function in protecting tissue against the oxidative stress which has been related to carcinogenesis in the colon. For this reason the development of probiotic species producing glutathione could be of great interest. To determine the glutathione content of some probiotic bacteria of the Bifidobacterium and Lactococcus genera, a very sensitive and selective analytical method based on capillary electrophoresis coupled to laser-induced fluorescence detection has been developed. Pretreatment of cell-lysate samples is very simple—precipitation of protein with acetonitrile in 1:2 volume ratio. The fluorophore 5-iodoacetamidofluorescein (5-IAF) was chosen for glutathione derivatisation; it reacts with thiols at pH 12.5, forming a fluorescent adduct which is excited by a laser at 488 nm for detection. The reaction conditions optimised were temperature, time, and 5-IAF/GSH molar ratio. Electrophoresis was performed with a carbonate buffer (25 mmol L−1, pH 9.8) as background electrolyte and a voltage of 30 kV; an electrophoretic run was complete in less than 7 min. There was a good linear relationship between concentration and response in the range 2.5–500 ng mL−1 and the LOD was 0.5 ng mL−1. The glutathione content of probiotic cells was determined by using the standard additions method to reduce matrix effects. The method was fully validated and shown to be of suitable sensitivity and selectivity for determination of GSH in probiotic cell lysates.
机译:谷胱甘肽(GSH)是一种硫醇,在保护组织免受与结肠癌发生有关的氧化应激方面具有重要作用。由于这个原因,产生谷胱甘肽的益生菌物种的发展可能引起人们极大的兴趣。为了确定双歧杆菌和乳球菌属的某些益生菌的谷胱甘肽含量,已经开发了一种基于毛细管电泳和激光诱导荧光检测的非常灵敏和选择性的分析方法。细胞裂解液样品的预处理非常简单-乙腈以1:2的体积比沉淀蛋白质。选择荧光团5-碘乙酰氨基酰荧光素(5-IAF)进行谷胱甘肽衍生化;它与pH值为12.5的硫醇反应,形成荧光加合物,该荧光加合物被488 nm的激光激发进行检测。优化的反应条件是温度,时间和5-IAF / GSH摩尔比。电泳以碳酸盐缓冲液(25 mmol L-1,pH 9.8)作为背景电解质,电压为30 kV;不到7分钟即可完成电泳。在2.5–500 ng mL-1 范围内,浓度与响应之间存在良好的线性关系,LOD为0.5 ng mL-1 。益生菌细胞的谷胱甘肽含量通过使用标准添加方法来减少基质效应来确定。该方法经过充分验证,证明对测定益生菌细胞裂解物中的GSH具有适当的灵敏度和选择性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号