Tully M, Yudkin M D
J Bacteriol. 1977 Jul;131(1):49-56. doi: 10.1128/jb.131.1.49-56.1977.
Sixty-two point mutations were isolated in Escherichia coli by means of transduction with mutagenized phage P1. Twenty-two deletions extending into cysB but able to recombine with at least some of the point mutations were isolated on a transmissible E. coli plasmid. Mapping of the point mutations against the deletions divided the former into 16 deletion groups. Nine merodiploids were constructed in which the chromosome carried one of the three point mutations most distal to the trp operon and in which a plasmid carried one of the three point mutations most proximal to the trp operon. All of these showed a Cys-phenotype. It follows that mutations at the two extreme ends of the region belong to the same complementation group.
通过用诱变噬菌体P1进行转导,在大肠杆菌中分离出62个点突变。在一个可转移的大肠杆菌质粒上分离出22个延伸至cysB但能与至少一些点突变重组的缺失。将点突变与缺失进行定位,将前者分为16个缺失组。构建了9个部分二倍体,其中染色体携带距trp操纵子最远的三个点突变之一,质粒携带距trp操纵子最近的三个点突变之一。所有这些都表现出半胱氨酸表型。由此可见,该区域两端的突变属于同一互补群。