Yoshida H, Kojima T, Yamagishi J, Nakamura S
Research Laboratories, Dainippon Pharmaceutical Co. Ltd., Osaka, Japan.
Mol Gen Genet. 1988 Jan;211(1):1-7. doi: 10.1007/BF00338386.
DNA fragments of 8.5 kb containing the gyrA gene were cloned from Escherichia coli KL-16 and from four spontaneous gyrA mutants which showed various levels of resistance to quinolones. The gyrA gene was situated at about 4 kb in front of the nrdA gene and transcribed counterclockwise on the E. coli chromosome. It encoded a polypeptide of 875 amino acids with a molecular weight of about 97,000. The four gyrA mutations were located strikingly close to one another within a small region near the N-terminus of the gyrA polypeptide, i.e., nucleotide changes from C to T, from C to G, from G to T and from G to T at nucleotides 248, 248, 318 and 199, respectively, resulting in amino acid changes from Ser to Leu, from Ser to Trp, from Gln to His and from Ala to Ser at amino acids 83, 83, 106 and 67, respectively. These mutations were situated in the relatively hydrophilic regions of the GyrA polypeptide and close to Tyr at amino acid 122 which has been shown to be the site covalently bound to DNA.
从大肠杆菌KL-16以及四个对喹诺酮类药物呈现不同耐药水平的自发gyrA突变体中克隆出了包含gyrA基因的8.5 kb DNA片段。gyrA基因位于nrdA基因前方约4 kb处,在大肠杆菌染色体上逆时针转录。它编码一个由875个氨基酸组成的多肽,分子量约为97,000。这四个gyrA突变在gyrA多肽N端附近的一个小区域内彼此非常靠近,即分别在核苷酸248、248、318和199处发生从C到T、从C到G、从G到T以及从G到T的核苷酸变化,导致在氨基酸83、83、106和67处分别发生从Ser到Leu、从Ser到Trp、从Gln到His以及从Ala到Ser的氨基酸变化。这些突变位于GyrA多肽相对亲水的区域,且靠近已被证明是与DNA共价结合位点的氨基酸122处的Tyr。