Gay N J
J Bacteriol. 1984 Jun;158(3):820-5. doi: 10.1128/jb.158.3.820-825.1984.
A strain of Escherichia coli with a mutation in the promoter proximal gene ( uncI ) of the unc operon has been constructed by using a new gene replacement method. The mutation is a deletion of a defined sequence of 196 base pairs. It was constructed by homologous integration and segregation of a ColE1-derived recombinant plasmid containing the mutation, in a temperature-sensitive polA strain. The mutant strain is phenotypically unc+ but has a reduced growth yield compared to a normal sibling strain.
通过一种新的基因置换方法构建了一株在unc操纵子的启动子近端基因(uncI)发生突变的大肠杆菌菌株。该突变是196个碱基对的特定序列缺失。它是通过含有该突变的ColE1衍生重组质粒在温度敏感型polA菌株中的同源整合和分离构建而成。该突变菌株在表型上是unc+,但与正常的同胞菌株相比,其生长产量有所降低。