Degnen G E, Cox E C
J Bacteriol. 1974 Feb;117(2):477-87. doi: 10.1128/jb.117.2.477-487.1974.
A mutator gene, mutD5, whose phenotype is conditional, has been identified in Escherichia coli. By P1 transduction it has been shown to lie at about 5.7 min on the chromosome, being co-transduced with proA and argF. In rich medium, streptomycin- and nalidixic acid-resistant mutation frequencies are 50 to 100 times higher than those in minimal medium. In minimal medium, the mutD5-induced mutation frequencies are still 50 to 100 times above co-isogenic wild-type (mut(+)) levels. Similar results were obtained with all markers tested. Mutant frequencies can be raised by thymidine in the medium at concentrations as low as 0.04 muM, or by the endogenous generation of thymidine from thymine plus a deoxyribosyl donor. Deoxyadenosine, various ribonucleosides, thymine, and 2-deoxyribose do not stimulate mutation. None of these effects are related to growth rate, since growth rate and mutation rate can be decoupled completely.
在大肠杆菌中已鉴定出一种表型为条件型的突变基因mutD5。通过P1转导表明它位于染色体上约5.7分钟处,与proA和argF共转导。在丰富培养基中,抗链霉素和萘啶酸的突变频率比在基本培养基中高50至100倍。在基本培养基中,mutD5诱导的突变频率仍比同基因野生型(mut(+))水平高50至100倍。所有测试的标记都得到了类似的结果。培养基中低至0.04μM的胸苷或由胸腺嘧啶加脱氧核糖基供体内源生成的胸苷可提高突变频率。脱氧腺苷、各种核糖核苷、胸腺嘧啶和2-脱氧核糖不会刺激突变。这些效应均与生长速率无关,因为生长速率和突变率可以完全解耦。