Willetts N S
J Bacteriol. 1972 Nov;112(2):773-8. doi: 10.1128/jb.112.2.773-778.1972.
The location of the origin of transfer on the map of Flac has been determined by two different techniques. The first showed that no transfer cistrons were transferred early by a transposition Hfr strain with a known point of chromosomal integration into Flac, and the second used a series of transfer-deficient Hfr deletion strains to map a locus required in cis for chromosome transfer by an incoming Flac factor. Both techniques gave results consistent with a location for the origin of transfer between traJ and the phi(R) (11) locus.
在Flac图谱上转移起点的位置已通过两种不同技术确定。第一种方法表明,具有已知染色体整合点并导入Flac的转座高频重组(Hfr)菌株不会早期转移任何转移顺反子;第二种方法使用了一系列转移缺陷型Hfr缺失菌株,来定位由导入的Flac因子进行染色体转移时顺式所需的一个位点。两种技术所得结果均与转移起点位于traJ和phi(R)(11)位点之间的位置相符。