Schwartz R D, Bryson V
J Virol. 1970 Jan;5(1):22-6. doi: 10.1128/JVI.5.1.22-26.1970.
Twenty-one hydroxylamine-induced rII A cistron nonsense mutants were tested for streptomycin (SM)-induced phenotypic suppression by exposing Escherichia coli SBO (nonpermissive host) to phage in the presence and absence of SM. All nine amber, four of six ochre, and five of six opal mutants were phenotypically suppressible by SM. For suppressible mutants, the ratio of the average burst size in the presence of SM to size in the absence of SM ranged from 12 to 242 for the ambers, 3 to 33 for the ochres, and 4 to 14 for the opals. Increased susceptibility of the amber mutants to SM-induced phenotypic suppression relative to the susceptibility of the opal and ochre mutants may reflect a neighboring base effect, such that a 3'-terminal adenine inhibits misreading of a 5'-terminal uracil.
通过在有和没有链霉素(SM)的情况下,将大肠杆菌SBO(非允许宿主)暴露于噬菌体,对21个羟胺诱导的rII A顺反子无义突变体进行了链霉素诱导的表型抑制测试。所有9个琥珀型突变体、6个赭石型突变体中的4个以及6个乳白型突变体中的5个在表型上可被链霉素抑制。对于可抑制的突变体,在有链霉素存在时的平均裂解量与无链霉素时的平均裂解量之比,琥珀型突变体为12至242,赭石型突变体为3至33,乳白型突变体为4至14。相对于乳白型和赭石型突变体,琥珀型突变体对链霉素诱导的表型抑制的易感性增加,这可能反映了相邻碱基效应,即3'末端的腺嘌呤会抑制5'末端尿嘧啶的错读。