Elliott J, Arber W
Mol Gen Genet. 1978 Apr 25;161(1):1-8. doi: 10.1007/BF00266608.
Escherichia coli pel- mutants inhibit the penetration of bacteriophage lambda DNA into the cell. Using P1 mediated cotransduction, we mapped pel- mutations between markers fadD and eda in the interval of minute 40 of the revised E. coli K-12 map. This places pel in the same region as genes kdgR and ptsM. Mutations in kdgR usually do not alter the Pel phenotype, and vice versa. In contrast, about 30% of ptsM- mutants are also pel-, and all pel- mutants isolated are ptsM-. These results suggest that pel and ptsM are one and the same gene. This interpretation would identify the bacterial product required for injection of phage lambda DNA as a component of the phosphoenolpyruvate-dependent phosphotransferase system specific for mannose, glucosamine, glucose and fructose. However, the experimental results do not exclude an alternative explanation: that pel and ptsM identify two closely linked genes which would be simultaneously affected at high frequency by a particular mutational event.
大肠杆菌pel-突变体抑制噬菌体λDNA进入细胞。利用P1介导的共转导,我们将pel-突变定位在修正后的大肠杆菌K-12图谱第40分钟区间的fadD和eda标记之间。这使得pel与kdgR和ptsM基因位于同一区域。kdgR的突变通常不会改变Pel表型,反之亦然。相比之下,约30%的ptsM-突变体也是pel-,并且分离得到的所有pel-突变体都是ptsM-。这些结果表明pel和ptsM是同一个基因。这种解释将把噬菌体λDNA注入所需的细菌产物鉴定为磷酸烯醇丙酮酸依赖性磷酸转移酶系统中对甘露糖、氨基葡萄糖、葡萄糖和果糖具有特异性的一个组分。然而,实验结果并不排除另一种解释:即pel和ptsM鉴定出两个紧密连锁的基因,它们会因特定的突变事件而同时受到高频影响。