Gustaferro C A, Persing D H
Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota 55905.
J Clin Microbiol. 1992 Apr;30(4):1039-41. doi: 10.1128/jcm.30.4.1039-1041.1992.
We describe a novel procedure for direct covalent coupling of horseradish peroxidase to rRNA and ribotyping by using enhanced chemiluminescence. Compared with their 32P-end-labeled counterparts, chemiluminescent rRNA probes are stable and easy to synthesize and provide results as good as or superior to those obtained with isotopic labeling. Direct chemiluminescent labeling of Escherichia coli rRNA produces a sensitive, universal probe suitable for clinical laboratory use in the investigation of nosocomial outbreaks.
我们描述了一种通过增强化学发光将辣根过氧化物酶直接共价偶联到rRNA并进行核糖体分型的新方法。与32P末端标记的对应物相比,化学发光rRNA探针稳定且易于合成,其提供的结果与同位素标记获得的结果一样好或更优。对大肠杆菌rRNA进行直接化学发光标记可产生一种灵敏的通用探针,适用于临床实验室调查医院内感染暴发。