Foster T J
Mol Gen Genet. 1976 Feb 2;143(3):339-44. doi: 10.1007/BF00269413.
Strains of Escherichia coli K12 heterozygous for the R100-1 tetracycline resistance region were constructed. They carried the wild-type Tetr genes in the chromosome and single site Tets mutations on plasmids. Some heterozygotes could not express tetracycline resistance fully after induction. The mutant tet allele was thus partially dominant. When heterozygotes carrying the dominant tet mutant were plated on agar containing 20 mg/ml tetracycline, mutants which grew normally occurred at a frequency of 1-4 X 10(-4). Analysis of these dominance relief mutants showed that in 53/56 isolates the dominant tet allele was lost forming either Tra+ or Tra- deletion mutants of the plasmid. The mutation frequency was not affected either by the host chromosomal recA mutation or by the temperature of growth of the culture.
构建了对R100 - 1四环素抗性区域杂合的大肠杆菌K12菌株。它们在染色体上携带野生型Tetr基因,在质粒上携带单一位点的Tets突变。一些杂合子在诱导后不能完全表达四环素抗性。因此,突变的tet等位基因具有部分显性。当携带显性tet突变体的杂合子接种在含有20mg/ml四环素的琼脂平板上时,正常生长的突变体出现频率为1 - 4×10(-4)。对这些显性缓解突变体的分析表明,在56个分离株中的53个中,显性tet等位基因丢失,形成了质粒的Tra +或Tra -缺失突变体。突变频率不受宿主染色体recA突变或培养物生长温度的影响。