Department of Civil, Environmental and Sustainable Engineering, National Science Foundation Water & Environmental Technology Center, Arizona State University, Tempe, Arizona 85287-5306, USA.
J Environ Sci Health A Tox Hazard Subst Environ Eng. 2013;48(8):925-32. doi: 10.1080/10934529.2013.762736.
The objective of the study was to identify the enzymatic-biochemical (enz-bio) signatures of Escherichia coli and Salmonella for rapid detection of these bacteria in drinking water biofilms. The relative potency of lipophilic, glucosidic, and proteolytic activities in biofilms containing single bacterial species and mixture of different bacterial was used to identify the enz-bio signatures of Escherichia coli and Salmonella. The enz-bio signatures identified were: Lipophilic < Glucosidic < Proteolytic (for Escherichia coli); and Glucosidic = Lipophilic < Proteolytic (for Salmonella). The enz-bio assays were performed sequentially for detecting Escherichia coli and Salmonella in pure and mixed biofilm cultures formed on the coupons incubated in a batch reactor. The results obtained were substantiated by culture-based assays indicating comparable data. The enz-bio sensing method described here is a proof of principle and the results of this study provide a platform for the fabrication of a biosensor for bacterial detection in biofilms. The detection time required for the biosensor platform versus culture methods ranged from 10 to 120 min and 24 to 48 h, respectively.
本研究旨在确定大肠杆菌和沙门氏菌的酶生化(enz-bio)特征,以便快速检测饮用水生物膜中的这些细菌。利用含单一细菌物种和不同细菌混合物的生物膜中亲脂性、糖苷和蛋白水解活性的相对效力,来鉴定大肠杆菌和沙门氏菌的 enz-bio 特征。鉴定出的 enz-bio 特征为:亲脂性<糖苷<蛋白水解(大肠杆菌);和糖苷=亲脂性<蛋白水解(沙门氏菌)。enz-bio 分析依次进行,用于检测在分批反应器中孵育的小片中形成的纯和混合生物膜培养物中的大肠杆菌和沙门氏菌。基于培养的检测结果证实了这些数据的可比性。此处描述的 enz-bio 传感方法是原理验证,并且该研究的结果为生物膜中细菌检测的生物传感器的制造提供了平台。生物传感器平台与培养方法的检测时间分别为 10 至 120 分钟和 24 至 48 小时。