Yoshizawa Y, Yamamoto N
Department of Microbiology and Immunology, Hahnemann University School of Medicine, Philadelphia, PA 19102.
Microbiol Immunol. 1989;33(6):449-57. doi: 10.1111/j.1348-0421.1989.tb01994.x.
An Escherichia coli mutant, C18, which plates at an efficiency of 5.0 x 10(-4) under anaerobic condition, was isolated among spontaneous nalidixic-acid-resistant mutants. This strict aerobic mutation was mapped by P1 cotransduction with a gyrA linked transposon Tn10 and found to be at the gyrA gene. A low degree of superhelicity of pBR322 DNA isolated from C18 was demonstrated by agarose gel electrophoresis with various concentrations of ethidium bromide. The superhelical density of pBR322 isolated from C18 was 80% of the value of pBR322 isolated from wild-type bacteria cultured under aerobic condition, and 50% cultured under anaerobic condition. These results lead us to conclude that a certain mutation of the gyrA gene causes a decrease in DNA superhelicity and prevents anaerobic growth.
在自发的耐萘啶酸突变体中分离出一株大肠杆菌突变体C18,它在厌氧条件下的平板接种效率为5.0×10⁻⁴。通过与gyrA连锁转座子Tn10进行P1共转导,对这种严格需氧突变进行定位,发现其位于gyrA基因处。用不同浓度溴化乙锭进行琼脂糖凝胶电泳,结果表明从C18中分离出的pBR322 DNA超螺旋程度较低。从C