1-Naphthyl phosphate as an enzymatic substrate for enzyme-linked immunomagnetic electrochemistry

被引:56
作者
Gehring, AG [1 ]
Brewster, JD [1 ]
Irwin, PL [1 ]
Tu, SI [1 ]
Van Houten, LJ [1 ]
机构
[1] Agr Res Serv, Eastern Reg Res Ctr, USDA, Wyndmoor, PA 19038 USA
来源
JOURNAL OF ELECTROANALYTICAL CHEMISTRY | 1999年 / 469卷 / 01期
关键词
bacteria; biosensors; detection; Escherichia coli; immunomagnetic beads; osteryoung square wave voltammetry;
D O I
10.1016/S0022-0728(99)00183-7
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We demonstrate substitution of the custom-synthesized alkaline phosphatase (AP) substrate, p-aminophenyl phosphate (pAPP), with the commercially available l-naphthyl phosphate (1-NP) as applied in the enzyme-linked immunomagnetic electrochemical (ELIME) detection of the pathogenic bacterium, Escherichia coli O157:H7. ELIME entails 'sandwiching' bacterial analyte between antibody-coated magnetic beads and an AP-conjugated antibody. The beads (with or without bound bacteria) were localized onto the surface of magnetized graphite ink electrodes in a multi-well plate format. Enzyme substrate (pAPP or 1-NP) was added and conversion to an electroactive product was measured using Osteryoung square wave voltammetry. Using this technique, quantitative detection of E. coli O157:H7 bacterial cells was achieved with a minimum detectable level of less than or equal to 4.7 x 10(3) cells ml(-1) in buffer or porcine carcass wash water within ca. 80 min. (C) 1999 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:27 / 33
页数:7
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