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2
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J Bacteriol. 1985 Jul;163(1):69-74. doi: 10.1128/jb.163.1.69-74.1985.
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本文引用的文献

1
Contribution of membrane-binding and enzymatic domains of penicillin binding protein 5 to maintenance of uniform cellular morphology of Escherichia coli.青霉素结合蛋白5的膜结合结构域和酶结构域对维持大肠杆菌细胞形态一致性的作用。
J Bacteriol. 2002 Jul;184(13):3630-9. doi: 10.1128/JB.184.13.3630-3639.2002.
2
Reconstruction of Escherichia coli mrcA (PBP 1a) mutants lacking multiple combinations of penicillin binding proteins.缺乏多种青霉素结合蛋白组合的大肠杆菌mrcA(PBP 1a)突变体的重建。
J Bacteriol. 2001 Oct;183(20):6148-9. doi: 10.1128/JB.183.20.6148-6149.2001.
3
Contributions of PBP 5 and DD-carboxypeptidase penicillin binding proteins to maintenance of cell shape in Escherichia coli.青霉素结合蛋白5和DD-羧肽酶青霉素结合蛋白对大肠杆菌细胞形态维持的作用
J Bacteriol. 2001 May;183(10):3055-64. doi: 10.1128/JB.183.10.3055-3064.2001.
4
Escherichia coli mutants lacking all possible combinations of eight penicillin binding proteins: viability, characteristics, and implications for peptidoglycan synthesis.缺乏八种青霉素结合蛋白所有可能组合的大肠杆菌突变体:生存能力、特性及对肽聚糖合成的影响
J Bacteriol. 1999 Jul;181(13):3981-93. doi: 10.1128/JB.181.13.3981-3993.1999.
5
Growth of the stress-bearing and shape-maintaining murein sacculus of Escherichia coli.大肠杆菌承受压力和维持形状的胞壁质囊的生长
Microbiol Mol Biol Rev. 1998 Mar;62(1):181-203. doi: 10.1128/MMBR.62.1.181-203.1998.
6
AmpC and AmpH, proteins related to the class C beta-lactamases, bind penicillin and contribute to the normal morphology of Escherichia coli.AmpC和AmpH是与C类β-内酰胺酶相关的蛋白质,它们结合青霉素并有助于大肠杆菌的正常形态。
J Bacteriol. 1997 Oct;179(19):6112-21. doi: 10.1128/jb.179.19.6112-6121.1997.
7
A simple gel electrophoretic method for analyzing the muropeptide composition of bacterial peptidoglycan.一种用于分析细菌肽聚糖中胞壁肽组成的简单凝胶电泳方法。
J Bacteriol. 1996 Jul;178(13):3962-6. doi: 10.1128/jb.178.13.3962-3966.1996.
8
Penicillin-binding protein 7/8 of Escherichia coli is a DD-endopeptidase.大肠杆菌的青霉素结合蛋白7/8是一种DD-内肽酶。
Eur J Biochem. 1994 Sep 1;224(2):597-604. doi: 10.1111/j.1432-1033.1994.00597.x.
9
Identification and cloning of the gene encoding penicillin-binding protein 7 of Escherichia coli.大肠杆菌青霉素结合蛋白7编码基因的鉴定与克隆。
J Bacteriol. 1995 Apr;177(8):2074-9. doi: 10.1128/jb.177.8.2074-2079.1995.
10
Tight regulation, modulation, and high-level expression by vectors containing the arabinose PBAD promoter.由含有阿拉伯糖PBAD启动子的载体进行严格调控、调节和高水平表达。
J Bacteriol. 1995 Jul;177(14):4121-30. doi: 10.1128/jb.177.14.4121-4130.1995.

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.

DOI:10.1016/j.ab.2003.11.007
PMID:14769329
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3086757/
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。