Minas W, Sahar E, Gutnick D
Department of Microbiology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Ramat Aviv, Israel.
Arch Microbiol. 1988;150(5):432-7. doi: 10.1007/BF00422282.
Flow cytometry (FCM) in conjunction with immunocytochemical-labeling was used to analyze and screen a population of Escherichia coli clones containing a genomic library from the oil-degrading microorganism Acinetobacter calcoaceticus RAG-1 surface antigens. Reconstruction experiments using mixed populations indicated that RAG-1 cells could be clearly distinguished at a ratio of one RAG-1 cell to 500 Escherichia coli cells. Using this technique two clones, WM143 and WM191, were isolated and shown by restriction endonuclease cleavage and Southern hybridization to contain plasmids carrying inserts of RAG-1 DNA of 9.4 and 9.8 kb respectively.
采用流式细胞术(FCM)结合免疫细胞化学标记法,对含有来自石油降解微生物醋酸钙不动杆菌RAG-1表面抗原基因组文库的大肠杆菌克隆群体进行分析和筛选。使用混合群体进行的重建实验表明,当RAG-1细胞与大肠杆菌细胞的比例为1:500时,RAG-1细胞能够被清晰区分。利用该技术分离出了两个克隆,即WM143和WM191,通过限制性内切酶切割和Southern杂交表明,它们分别含有携带9.4 kb和9.8 kb RAG-1 DNA插入片段的质粒。