Bradley D, Park J V, Soll L
J Bacteriol. 1981 Feb;145(2):704-12. doi: 10.1128/jb.145.2.704-712.1981.
We selected mutants of lambda pSu+2 which had an increased ability to suppress on Escherichia coli trp B9601 amber mutation on translationally stringent rpsL594 streptomycin-resistant ribosomes. tRNA2Gin Su+2 molecules produced from eight independent mutants were purified, and their ribonucleic acid sequences were determined. Two types of mutations were mapped to the tRNA2Gin Su+2(glnV) gene by this method. Both altered the pseudouridine at position 37 of the tRNA anticodon loop. Seven of the isolates were transitions (pseudouridine to cytosine), and one was a transversion (pseudouridine to adenine). These mutations resulted in Su+ transfer ribonucleic acid molecules that exhibited higher transmission coefficients than their parent Su+2 transfer ribonucleic acids. As judged by their suppressor spectra on T4 amber mutants, which were almost identical to that of Su+2, the two mutant Su+ transfer ribonucleic acids inserted glutamine at amber sites.
我们挑选了λ pSu + 2的突变体,这些突变体在翻译严格的rpsL594抗链霉素核糖体上对大肠杆菌trp B9601琥珀突变的抑制能力增强。从八个独立突变体产生的tRNA2Gin Su + 2分子被纯化,并测定了它们的核糖核酸序列。通过这种方法,两种类型的突变被定位到tRNA2Gin Su + 2(glnV)基因上。两者都改变了tRNA反密码子环第37位的假尿苷。七个分离株是转换(假尿苷到胞嘧啶),一个是颠换(假尿苷到腺嘌呤)。这些突变产生的Su + 转移核糖核酸分子比其亲本Su + 2转移核糖核酸表现出更高的传递系数。根据它们对T4琥珀突变体的抑制谱判断,这两种突变的Su + 转移核糖核酸在琥珀位点插入谷氨酰胺,其抑制谱与Su + 2几乎相同。