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利用微生物修饰玻碳电极对大肠杆菌β-D-葡萄糖醛酸酶活性进行新型检测及其在粪便污染监测中的潜力。

Novel detection of Escherichia coli beta-D-glucuronidase activity using a microbially-modified glassy carbon electrode and its potential for faecal pollution monitoring.

作者信息

Togo Chamunorwa Aloius, Wutor Victor Collins, Limson Janice Leigh, Pletschke Brett Ivan

机构信息

Department of Biochemistry, Rhodes University, Grahamstown, South Africa.

出版信息

Biotechnol Lett. 2007 Apr;29(4):531-7. doi: 10.1007/s10529-006-9282-5. Epub 2007 Jan 19.

Abstract

The electrochemical detection of Escherichia coli beta-D-glucuronidase activity as a means of monitoring water pollution by faecal material was investigated using separate Moraxella- and Pseudomonas putida-modified glassy carbon electrodes. The former was more sensitive and selective. The Moraxella-modified biosensor was 100 times more rapid and sensitive than the spectrophotometric detection of beta-D-glucuronidase activity. The experimental limit of detection of the biosensor was two c.f.u. per 100 ml polluted water sample within 20 min. The biosensor gave a linear response to commercial beta-D-glucuronidase concentration between 0.2 ng and 2 microg ml(-1). The biosensor detected activity of beta-D-glucuronidase from viable but non-culturable (VBNC) cells and can therefore serve as a presence or absence device for rapid water quality monitoring.

摘要

使用分别经莫拉克斯氏菌和恶臭假单胞菌修饰的玻碳电极,研究了将电化学检测大肠杆菌β-D-葡萄糖醛酸酶活性作为监测粪便物质水污染手段的方法。前者更灵敏且更具选择性。经莫拉克斯氏菌修饰的生物传感器比分光光度法检测β-D-葡萄糖醛酸酶活性快100倍且更灵敏。该生物传感器的实验检测限为每100 ml受污染水样中2个菌落形成单位,检测时间为20分钟。该生物传感器对商业β-D-葡萄糖醛酸酶浓度在0.2 ng至2 μg ml(-1)之间呈线性响应。该生物传感器可检测存活但不可培养(VBNC)细胞的β-D-葡萄糖醛酸酶活性,因此可作为快速水质监测的存在或不存在检测装置。

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