Institute of Terrestrial Ecology, Soil Biology, Eidgenössische Technische Hochschule Zürich, Grabenstrasse 3, CH-8952 Schlieren, Switzerland, and Lehrstuhl für Mikrobiologie, Technische Universität München, Arcisstrasse 21, D-8000 Munich 2, Germany.
Appl Environ Microbiol. 1993 Aug;59(8):2753-7. doi: 10.1128/aem.59.8.2753-2757.1993.
Detection of mRNA of the thiostrepton resistance gene (tsr) harbored by plasmid pIJ673 in Streptomyces violacelatus was achieved by whole-cell hybridization with digoxigenin-labeled in vitro transcripts followed by an antibody-alkaline phosphatase detection of the digoxigenin reporter molecule. Prior to hybridization, the cells had to be permeabilized by lysozyme, the detergent Nonidet P-40, and toluene. The permeability of the S. violacelatus cells for probes and the antibody-alkaline phosphatase conjugate was demonstrated by hybridization with digoxigenin-labeled, 16S rRNA-targeted oligonucleotides.
采用地高辛标记的体外转录物进行全细胞杂交,并用碱性磷酸酶检测地高辛报告分子,从而检测到链霉菌属紫色素中由质粒 pIJ673 携带的硫链丝菌素抗性基因 (tsr) 的 mRNA。在杂交之前,必须通过溶菌酶、非离子去污剂 NP-40 和甲苯使细胞通透。通过与地高辛标记的、针对 16S rRNA 的寡核苷酸杂交,证明了探针和抗体-碱性磷酸酶缀合物对链霉菌属紫色素细胞的通透性。