Hansen F G, Nielsen J, Riise E, von Meyenburg K
Mol Gen Genet. 1981;183(3):463-72. doi: 10.1007/BF00268766.
The genes for the eight subunits of the membrane bound ATP synthase of Escherichia coli (Ca++, Mg++ dependent ATPase, EC 3.6.1.3) were mapped through genetic, physical and functional analysis of specialized transducing phages lambda asn (von Meyenburg et al. 1978). The ATP synthase genes, designated atp1, are located at 83.2 min in a segment of the chromosome between 3.5 and 11.3 kb left (counterclockwise) of the origin of replication oriC. The counterclockwise order of the genes for the eight subunits, the expression of which starts from a control region at 3.5 kb-L, was found to be: a, (c, b, delta), alpha, gamma, (epsilon, beta) which in the notation of Downie el al. (1981) reads atp B (EFH) A G (C D). The analysis was in part based on the isolation of new types of atp (unc, Suc-) mutations. We made use of the fact that specialized transducing phages lambda asn carrying oriC can establish themselves as minichromosomes rendering asnA cells Asn+, and that the resulting Asn+ cells grow slowly if the lambda asn carries part or all of the atp operon. Selecting for fast growing strains mutations were isolated on the lambda asn which either eliminated atp genes or affected their expression ("promoter" mutations). The relationship between these atp mutations and the cop mutations of Ogura et al. (1980), which also appear to map in front of or within the atp genes, is discussed.
通过对特殊转导噬菌体λasn进行遗传、物理和功能分析,绘制了大肠杆菌膜结合ATP合酶(Ca++、Mg++依赖性ATP酶,EC 3.6.1.3)八个亚基的基因图谱(von Meyenburg等人,1978年)。ATP合酶基因,命名为atp1,位于染色体上83.2分钟处,在复制起点oriC左侧(逆时针方向)3.5至11.3 kb的一段区域内。发现八个亚基的基因按逆时针顺序排列,其表达从3.5 kb-L处的一个控制区域开始,顺序为:a,(c,b,δ),α,γ,(ε,β),用Downie等人(1981年)的符号表示为atp B(EFH)A G(C D)。该分析部分基于新型atp(unc,Suc-)突变的分离。我们利用了携带oriC的特殊转导噬菌体λasn可以将自身建立为微型染色体,使asnA细胞变为Asn+这一事实,并且如果λasn携带部分或全部atp操纵子,所产生的Asn+细胞生长缓慢。通过选择快速生长的菌株,在λasn上分离出了要么消除atp基因要么影响其表达的突变(“启动子”突变)。还讨论了这些atp突变与Ogura等人(1980年)的cop突变之间的关系,后者似乎也定位在atp基因之前或之内。