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高效液相色谱法与荧光团辅助碳水化合物电泳法分析大肠杆菌肽聚糖组成的比较

Comparison of high-performance liquid chromatography and fluorophore-assisted carbohydrate electrophoresis methods for analyzing peptidoglycan composition of Escherichia coli.

作者信息

Li Shi-Yan, Höltje Joachim-Volker, Young Kevin D

机构信息

Department of Microbiology and Immunology, University of North Dakota School of Medicine, Grand Forks, ND 58202-9037, USA.

出版信息

Anal Biochem. 2004 Mar 1;326(1):1-12. doi: 10.1016/j.ab.2003.11.007.

Abstract

Currently, reversed-phase high-performance liquid chromatography (HPLC) is the method of choice for determining the types and amounts of muropeptide subunits comprising bacterial peptidoglycan. Although effective and sensitive, the technique does not lend itself to high throughput screening, and its complexity and equipment requirements may dissuade some investigators from pursuing certain types of cell wall experiments. Previously, we showed that muropeptides can be labeled with a fluorescent dye and separated by fluorophore-assisted carbohydrate electrophoresis (FACE), a simple and rapid gel procedure that might serve as a prelude to more intense analysis by HPLC. To validate the utility of FACE, we used both techniques to perform a side-by-side analysis of the peptidoglycan of eight mutants and their Escherichia coli parent strain. FACE and HPLC both detected the seven major muropeptides, which represent more than 95% of the total muropeptides present in this organism. In addition, FACE returned the same relative and quantitative results in 92% of 72 measurements, indicating that the procedure gives an accurate overview of peptidoglycan composition. The results also suggest a possible biochemical activity for the AmpC and AmpH proteins of E. coli, and the use of FACE as an in vitro enzyme assay detected possible substrate preferences for the endopeptidase penicillin binding protein 4.

摘要

目前,反相高效液相色谱法(HPLC)是测定构成细菌肽聚糖的胞壁肽亚基类型和数量的首选方法。尽管该技术有效且灵敏,但它并不适用于高通量筛选,其复杂性和设备要求可能会使一些研究人员放弃进行某些类型的细胞壁实验。此前,我们表明胞壁肽可以用荧光染料标记,并通过荧光辅助碳水化合物电泳(FACE)进行分离,这是一种简单快速的凝胶程序,可作为通过HPLC进行更深入分析的前奏。为了验证FACE的实用性,我们使用这两种技术对八个突变体及其大肠杆菌亲本菌株的肽聚糖进行了并行分析。FACE和HPLC都检测到了七种主要的胞壁肽,它们占该生物体中总胞壁肽的95%以上。此外,在72次测量中,FACE在92%的测量中得到了相同的相对和定量结果,表明该程序能够准确概述肽聚糖的组成。结果还表明大肠杆菌的AmpC和AmpH蛋白可能具有生化活性,并且使用FACE作为体外酶测定法检测到了内肽酶青霉素结合蛋白4可能的底物偏好。

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