Togo Chamunorwa Aloius, Wutor Victor Collins, Limson Janice Leigh, Pletschke Brett Ivan
Department of Biochemistry, Rhodes University, Grahamstown, South Africa.
Biotechnol Lett. 2007 Apr;29(4):531-7. doi: 10.1007/s10529-006-9282-5. Epub 2007 Jan 19.
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.
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。