Akasaka S, Takimoto K, Yamamoto K
Division of Industrial Health, Osaka Prefectural Institute of Public Health, Japan.
Mol Gen Genet. 1992 Nov;235(2-3):173-8. doi: 10.1007/BF00279358.
Escherichia coli K12 strain KS40 and plasmid pKY241 were designed for easy screening of supF mutations in plasmid pZ189. KS40 is a nalidixic acid-resistant (gyrA) derivative of MBM7070 (lacZ(am)CA7020). Using in vitro mutagenesis, an amber mutation was introduced into the cloned gyrA structural gene, of E. coli, to give pKY241, a derivative of pACYC184. When KS40 containing pKY241 (designated KS40/pKY241) is transformed with pZ189, nalidixic acid-resistant GyrA protein is produced from the chromosomal gyrA gene and wild-type GyrA protein from pKY241 because of the suppression of the gyrA amber mutation by supF. It is known that the wild-type, otherwise nalidixic acid-sensitive, phenotype is dominant over the nalidixic acid-resistant phenotype. Thus, KS40/pKY241 gives rise to nalidixic acid-sensitive colonies when it carries a pZ189 plasmid with an active supF suppressor tRNA. If the supF gene on the plasmid carries an inactivating mutation then KS40/pKY241 will form nalidixic acid-resistant colonies. By using this system, the spontaneous mutational frequency of the supF gene on pZ189 was calculated to be 3.06 x 10(-7) per replication. Among 51 independent supF mutations analyzed by DNA sequencing, 63% were base substitutions, 25% IS element insertions, 9.6% deletions and 1.9% single-base frameshifts. The base substitutions included both transversions (84.8%) and transitions (15.2%), the largest single group being G:C to T:A transversions (45.4% of the base substitutions). These results demonstrate that the KS40/pKY241 system we have developed can be used to characterize the DNA sequence changes induced by mutagens that give very low mutational frequencies.
大肠杆菌K12菌株KS40和质粒pKY241旨在便于筛选质粒pZ189中的supF突变。KS40是MBM7070(lacZ(am)CA7020)的耐萘啶酸(gyrA)衍生物。通过体外诱变,将琥珀突变引入克隆的大肠杆菌gyrA结构基因中,得到pKY241,它是pACYC184的衍生物。当用pZ189转化含有pKY241的KS40(命名为KS40/pKY241)时,由于supF对gyrA琥珀突变的抑制作用,染色体gyrA基因产生耐萘啶酸的GyrA蛋白,pKY241产生野生型GyrA蛋白。已知野生型(否则对萘啶酸敏感)表型比耐萘啶酸表型占优势。因此,当KS40/pKY241携带带有活性supF抑制tRNA的pZ189质粒时,会产生对萘啶酸敏感的菌落。如果质粒上的supF基因携带失活突变,那么KS40/pKY241将形成耐萘啶酸的菌落。通过使用该系统,计算出pZ189上supF基因的自发突变频率为每复制3.06×10⁻⁷ 。在通过DNA测序分析的51个独立的supF突变中,63%是碱基替换,25%是IS元件插入,9.6%是缺失,1.9%是单碱基移码。碱基替换包括颠换(84.8%)和转换(15.2%),最大的单一组是G:C到T:A颠换(占碱基替换的45.4%)。这些结果表明,我们开发的KS40/pKY241系统可用于表征由诱变剂诱导的具有极低突变频率的DNA序列变化。