Nakamura Y, Uchida H
Mol Gen Genet. 1983;190(2):196-203. doi: 10.1007/BF00330640.
Amber mutants (am3 and am4) of Escherichia coli K12 defective in the synthesis of nusA protein (Friedman 1971) were isolated from a strain harboring an amber suppressor (sup-126) that is active only at low temperatures. These mutants grew at low temperature (30 degrees C) but did not grow at temperatures above 38 degrees C. Complementation experiments with plasmids carrying the nusA+ gene and its derivatives or with plasmids carrying the nusA1 or am4 mutation indicated that the mutations am3, am4 and nusA1 affected the same gene function. Analysis of proteins produced by minicells containing a plasmid demonstrated that the plasmid pYN87, which can complement the nusA1 and amber mutations, codes for three bacterial proteins, a truncated nusA gene product (61 K), argG gene product (48 K) and a 21 K dalton protein, and that the am4 mutation affects the synthesis of only NusA protein. lambda Nam7 (and lambda Nam7Nam53) phages could grow on these amber mutants at 32 degrees C but not on the parental strain. Spontaneous temperature-resistant revertants of the amber mutants simultaneously lost the ability to permit lambda Nam7 phage development, indicating that the two phenotypes are due to a single mutation. These results suggest that the nusA gene function is essential for the growth of E. coli, and that the lambda N function is dispensable for phage development if the nusA gene is defective.
大肠杆菌K12的琥珀突变体(am3和am4)在nusA蛋白合成方面存在缺陷(弗里德曼,1971年),是从携带仅在低温下有活性的琥珀抑制基因(sup - 126)的菌株中分离得到的。这些突变体在低温(30摄氏度)下生长,但在高于38摄氏度的温度下不能生长。用携带nusA +基因及其衍生物的质粒或携带nusA1或am4突变的质粒进行互补实验表明,am3、am4和nusA1突变影响相同的基因功能。对含有质粒的微小细胞产生的蛋白质进行分析表明,能够互补nusA1和琥珀突变的质粒pYN87编码三种细菌蛋白,一种截短的nusA基因产物(61K)、argG基因产物(48K)和一种21K道尔顿的蛋白质,并且am4突变仅影响NusA蛋白的合成。λNam7(和λNam7Nam53)噬菌体在32摄氏度时能够在这些琥珀突变体上生长,但不能在亲本菌株上生长。琥珀突变体的自发温度抗性回复突变体同时丧失了允许λNam7噬菌体发育的能力,表明这两种表型是由单一突变引起的。这些结果表明,nusA基因功能对大肠杆菌的生长至关重要,并且如果nusA基因有缺陷,λN功能对于噬菌体发育是可有可无的。