Bandrin S V, Rabinovich P M, Stepanov A I
Genetika. 1983 Sep;19(9):1419-25.
Using transposon Tn5 inactivation technology a collection of Escherichia coli mutants defective in riboflavine biosynthesis was obtained. All mutations were distributed within three linkage groups. With the help of P1-transduction mapping, group I mutations (ribA locus) were localized near cysB locus (28 min of the standard 100 min E. coli map) and mutations of group II (ribB locus) were mapped near tolC locus (66 min). The location of group III mutations was approximately determined by the F' complementation analysis: this linkage group lies in the region of 56-60 min of the E. coli map.
利用转座子Tn5失活技术获得了一批核黄素生物合成缺陷的大肠杆菌突变体。所有突变分布在三个连锁群中。借助P1转导作图,I组突变(ribA位点)定位在cysB位点附近(标准的100分钟大肠杆菌图谱的28分钟处),II组突变(ribB位点)定位在tolC位点附近(66分钟处)。III组突变的位置通过F'互补分析大致确定:该连锁群位于大肠杆菌图谱的56 - 60分钟区域。