Wolfe A D, Cook T M, Hahn F E
J Bacteriol. 1971 Oct;108(1):320-7. doi: 10.1128/jb.108.1.320-327.1971.
The antibacterial drug Nitroakridin 3582 inhibited the growth of selected grampositive bacteria more strongly than it inhibited the growth of gram-negative bacilli. Nitroakridin at concentrations of the order of 5 x 10(-5)m induced lysis of Bacillus licheniformis and Micrococcus lysodeikticus. At concentrations less than 10(-4)m, Nitroakridin 3582 reduced the exponential growth rate of Escherichia coli C-2; at 10(-4)m the drug was bacteriostatic, and, at concentrations greater than 10(-4)m, it was bactericidal. Prolonged bacteriostasis resulted in the formation of long filaments by E. coli, Serratia marcescens, Shigella sonnei, and Proteus mirabilis. The reversible effects of Nitroakridin 3582 on the growth of E. coli correlated with partial inhibitions of deoxyribonucleic acid biosynthesis; ribonucleic acid and protein syntheses were inhibited less strongly. Nitroakridin 3582 at concentrations greater than 2 x 10(-4)m, which block deoxyribonucleic acid biosynthesis, produced an accelerated bactericidal action.
抗菌药物硝基吖啶3582对所选革兰氏阳性菌生长的抑制作用比对革兰氏阴性杆菌生长的抑制作用更强。浓度约为5×10⁻⁵m的硝基吖啶可诱导地衣芽孢杆菌和溶壁微球菌裂解。浓度低于10⁻⁴m时,硝基吖啶3582降低了大肠杆菌C - 2的指数生长速率;在10⁻⁴m时,该药物具有抑菌作用,而浓度高于10⁻⁴m时则具有杀菌作用。长时间抑菌导致大肠杆菌、粘质沙雷氏菌、宋内志贺氏菌和奇异变形杆菌形成长丝。硝基吖啶3582对大肠杆菌生长的可逆作用与脱氧核糖核酸生物合成的部分抑制相关;核糖核酸和蛋白质合成的抑制作用较弱。浓度大于2×10⁻⁴m的硝基吖啶3582可阻断脱氧核糖核酸生物合成,产生加速的杀菌作用。