Bursztyn H, Sgaramella V, Ciferri O, Lederberg J
J Bacteriol. 1975 Dec;124(3):1630-4. doi: 10.1128/jb.124.3.1630-1634.1975.
Cells of rough (but not smooth) strains of Salmonella typhimurium become competent for transfection by phage P22 deoxyribonucleic acid after treatment with 0.1 M CaCl2. The yield of infectious centers is about 10(-8) per genome equivalent of deoxyribonucleic acid. However, different sorts of rough strains vary in their ability to become competent in a fashion that can be correlated with the level of the genetic block in cell wall lipopolysaccharide synthesis. The most amenable strains are blocked by defects in the addition of galactose units I and II of the lipopolysaccharide by the inability to synthesize uridine 5'-diphosphate-galactose (galE point mutants and gal deletion mutants). Strains blocked only in the addition of galactose I, glucose I, or heptose II have low levels of transfectability, whereas strains with either more complete or more deficient lipopolysaccharide core are not competent for transfection. When normal lipopolysaccharide synthesis is restored either genetically or by furnishing exogenous galactose (galE point mutants that can still use it), the cells are not longer competent for transfection.
鼠伤寒沙门氏菌粗糙型(而非光滑型)菌株的细胞在用0.1M氯化钙处理后,会变得能够被噬菌体P22脱氧核糖核酸转染。每基因组当量的脱氧核糖核酸产生的感染中心产量约为10^(-8)。然而,不同类型的粗糙型菌株在变得具有感受态的能力方面存在差异,这种差异与细胞壁脂多糖合成中的遗传阻断水平相关。最易转染的菌株因无法合成尿苷5'-二磷酸半乳糖(galE点突变体和gal缺失突变体),导致脂多糖的半乳糖单元I和II添加缺陷而被阻断。仅在半乳糖I、葡萄糖I或庚糖II添加方面受阻的菌株转染能力较低,而脂多糖核心更完整或更缺陷的菌株则不具备转染能力。当通过遗传手段或提供外源性半乳糖(仍能利用它的galE点突变体)恢复正常脂多糖合成时,细胞不再具有转染能力。