Pacelli L Z, Edmiston S H, Mount D W
J Bacteriol. 1979 Jan;137(1):568-73. doi: 10.1128/jb.137.1.568-573.1979.
We describe the isolation and characterization of amber mutations in the lexA gene of Escherichia coli K-12. These mutations, designated spr(Am), were isolated and characterized in a lexA tif sfi genetic background. They abolished the sensitivity of the strain to UV light and resulted in high rates of synthesis of recA protein. Phage lambda+ failed to lysogenize the strains as observed with similar strains carrying non-amber spr mutations described previously, thereby indicating a constitutive expression of the phage induction pathway. Introduction of an amber suppressor mutation into a strain bearing the spr(Am) mutation restored expression of the LexA mutant phenotype. We conclude that spr mutations either inactivate or prevent synthesis of the lexA gene product and that loss of this product results in constitutive expression of the E. coli induction system in the tif sfi genetic background.
我们描述了大肠杆菌K-12 lexA基因中琥珀突变的分离和特性。这些突变被命名为spr(Am),是在lexA tif sfi遗传背景下分离和鉴定的。它们消除了菌株对紫外线的敏感性,并导致recA蛋白的高合成率。如先前所述,携带非琥珀spr突变的类似菌株一样,λ+噬菌体无法使这些菌株溶源化,从而表明噬菌体诱导途径的组成型表达。将琥珀抑制突变引入携带spr(Am)突变的菌株中可恢复LexA突变表型的表达。我们得出结论,spr突变使lexA基因产物失活或阻止其合成,并且该产物的缺失导致tif sfi遗传背景下大肠杆菌诱导系统的组成型表达。