Debrouwere L, Zabeau M, Van Montagu M, Schell J
Mol Gen Genet. 1980;179(1):75-80. doi: 10.1007/BF00268448.
The lambda ral function modulates the restriction and modification activities of the Escherichia coli K12 and B restriction enzymes (Zabeau et al., 1980). In order to further analyse this function, ral deficient mutants have been isolated, using a method which exploits the property of the strong mutagen N-methyl-N'-nitro-N-nitrosoguanidine (N.G.) to induce multiple closely linked mutations. Hence, mutagenized phages carrying mutations in one locus were frequently found to contain additional mutations in adjacent loci. This very efficient mutagenesis procedure enabled us to isolate 27 independent Ral deficient mutants. Seven mutants were found to affect the ral gene directly and were located between the genes N anc cIII. Detailed mapping of two of these mutants showed that the lambda ral gene is located at position 70.6-70.9% on the physical map. The isolation and characterization of these mutants further supports the conclusion that ral is a gene different from the N gene, and demonstrates that the ral gene product is responsible for both counteracting restriction and enhancing modification.
λral 功能调节大肠杆菌 K12 和 B 限制酶的限制和修饰活性(扎博等,1980 年)。为了进一步分析该功能,利用强诱变剂 N-甲基-N'-硝基-N-亚硝基胍(N.G.)诱导多个紧密连锁突变的特性,分离出了 ral 缺陷型突变体。因此,经常发现携带一个位点突变的诱变噬菌体在相邻位点含有额外的突变。这种非常有效的诱变程序使我们能够分离出 27 个独立的 Ral 缺陷型突变体。发现七个突变体直接影响 ral 基因,它们位于基因 N 和 cIII 之间。对其中两个突变体的详细定位表明,λral 基因位于物理图谱上的 70.6 - 70.9% 位置。这些突变体的分离和表征进一步支持了 ral 是一个不同于 N 基因的基因的结论,并证明 ral 基因产物负责对抗限制和增强修饰。