Young K D
Department of Microbiology and Immunology, School of Medicine, University of North Dakota, Grand Forks, North Dakota 58202-9037, USA.
J Bacteriol. 1996 Jul;178(13):3962-6. doi: 10.1128/jb.178.13.3962-3966.1996.
The muropeptide composition of bacterial peptidoglycan is currently most efficiently determined by reverse-phase high-pressure liquid chromatography (HPLC). Though sensitive, the HPLC procedure is technically demanding and has been applied to a relatively small number of bacterial strains and species. We have found that fluorescence-assisted carbohydrate electrophoresis (FACE) is a simple, rapid method by which reducing muropeptides from multiple peptidoglycan samples can be visualized. Individual reducing muropeptides were covalently labeled with the fluorescent molecule 8-aminonaphthalene-1,3,6-trisulfonic acid, after which they were separated by electrophoresis through a 35% polyacrylamide gel and visualized by exposure to UV light. FACE detected the appropriate numbers of reducing muropeptides in the proper proportions for four bacteria: Escherichia coli, Pseudomonas aeruginosa, Enterobacter cloacae, and Yersinia enterocolitica. As little as 2 to 5 pmol per muropeptide was detected when the intensity of the fluorescent signal was measured with a charge-coupled device camera, at a level of sensitivity between 50 and 250 times higher than that of the classic HPLC technique. Thus, FACE may be used to identify interesting peptidoglycan samples prior to more-extensive analysis by HPLC, or FACE may eventually replace HPLC for some applications.
目前,细菌肽聚糖的胞壁肽组成最有效的测定方法是反相高压液相色谱法(HPLC)。尽管HPLC方法灵敏,但技术要求高,且仅应用于相对少数的细菌菌株和种类。我们发现,荧光辅助碳水化合物电泳(FACE)是一种简单、快速的方法,通过该方法可以可视化多个肽聚糖样品中的还原性胞壁肽。单个还原性胞壁肽用荧光分子8-氨基萘-1,3,6-三磺酸进行共价标记,然后通过35%聚丙烯酰胺凝胶电泳进行分离,并通过紫外线照射进行可视化。FACE检测到四种细菌(大肠杆菌、铜绿假单胞菌、阴沟肠杆菌和小肠结肠炎耶尔森菌)中适当数量和比例的还原性胞壁肽。当使用电荷耦合器件相机测量荧光信号强度时,每胞壁肽低至2至5皮摩尔即可被检测到,灵敏度比经典HPLC技术高50至250倍。因此,FACE可用于在通过HPLC进行更广泛分析之前识别有趣的肽聚糖样品,或者在某些应用中,FACE最终可能会取代HPLC。