Hammelburger J W, Orr G A
J Bacteriol. 1983 Nov;156(2):789-99. doi: 10.1128/jb.156.2.789-799.1983.
sn-Glycerol 3-phosphorothioate was found to be bacteriocidal to strains of Escherichia coli which have a functional sn-glycerol 3-phosphate transport system. This effect was manifest in strains 7 and 8, which are constitutive mutants for the utilization and transport of sn-glycerol 3-phosphate (glpRc2). Strain E15, which is considered to be wild type for the glycerol phosphate functional units, was affected by the phosphorothioate analog only under conditions that are known to induce the transport system for sn-glycerol 3-phosphate. In addition, another strain of E. coli, strain 6, which is isogenic with strain E15 but has an impaired sn-glycerol 3-phosphate transport system (glpT13), was not affected by similar concentrations of sn-glycerol 3-phosphorothioate. Transport studies in which [3H]glycerol phosphate and its phosphorothioate analog were used demonstrated that the latter compound was taken up via the specific active transport system for sn-glycerol 3-phosphate; the Km values were 9 and 11 microM, respectively. The rates of macromolecular synthesis were found to be inhibited severely by sn-glycerol 3-phosphorothioate at a concentration at which sn-glycerol 3-phosphate had no effect (5 microM). At a lower concentration of the analog (0.5 microM), the rates of protein synthesis and RNA synthesis (52 and 58% below control values after 90 min, respectively) were more sensitive than the rates of DNA synthesis and cell wall synthesis (18% below control values after 3 h for DNA; transient decrease in the cell wall values after 90 min). The levels of the nucleoside triphosphates were not affected by the presence of the phospholipid precursor or its analog at a concentration of 5 microM. The phospholipid composition was significantly altered in the presence of bacteriocidal concentrations (5 microM) of sn-glycerol 3-phosphorothioate. The amount of phosphatidylglycerol in the membranes decreased from 13.5 to 3.5%. Concomitant with this decrease in phosphatidylglycerol content was a fourfold increase in the 32P content of cardiolipin (from 6.8 to 24.2%), whereas the phosphatidylethanolamine content showed only a minor reduction (8%) after 3 h. The rates of synthesis of all of the phospholipids decreased in the presence of 5 microM sn-glycerol 3-phosphorothioate, with the most significant effects observed for phosphatidylglycerol (63% after 3 h). Phosphatidylglycerol showed increased rates of turnover after 90 min (21%) and 3 h (11%), with concomitant increases in the levels of cardiolipin of more than twofold. Our data suggest that a considerably greater proportion of phosphatidylglycerol turnover may be recover in cardiolipin than is metabolized via other pathways (e.g., the membrane-derived oligosaccharide pathway).
已发现sn-甘油3-硫代磷酸酯对具有功能性sn-甘油3-磷酸转运系统的大肠杆菌菌株具有杀菌作用。这种作用在菌株7和8中表现明显,它们是sn-甘油3-磷酸利用和转运的组成型突变体(glpRc2)。菌株E15被认为是甘油磷酸功能单元的野生型,仅在已知诱导sn-甘油3-磷酸转运系统的条件下才受硫代磷酸酯类似物的影响。此外,另一株大肠杆菌菌株6与菌株E15同基因,但sn-甘油3-磷酸转运系统受损(glpT13),不受类似浓度的sn-甘油3-硫代磷酸酯影响。使用[3H]甘油磷酸及其硫代磷酸酯类似物进行的转运研究表明,后一种化合物是通过sn-甘油3-磷酸的特异性主动转运系统摄取的;Km值分别为9和11 microM。发现sn-甘油3-硫代磷酸酯在sn-甘油3-磷酸无作用的浓度(5 microM)下严重抑制大分子合成速率。在较低浓度的类似物(0.5 microM)下,蛋白质合成和RNA合成速率(90分钟后分别比对照值低52%和58%)比DNA合成和细胞壁合成速率更敏感(DNA在3小时后比对照值低18%;90分钟后细胞壁值短暂下降)。核苷三磷酸水平不受5 microM浓度的磷脂前体或其类似物的影响。在杀菌浓度(5 microM)的sn-甘油3-硫代磷酸酯存在下,磷脂组成发生了显著变化。膜中磷脂酰甘油的量从13.5%降至3.5%。伴随着磷脂酰甘油含量的这种下降,心磷脂的32P含量增加了四倍(从6.8%增至24.2%),而磷脂酰乙醇胺含量在3小时后仅略有下降(8%)。在5 microM sn-甘油3-硫代磷酸酯存在下,所有磷脂的合成速率均下降,其中磷脂酰甘油受到的影响最为显著(3小时后为63%)。90分钟(21%)和3小时(11%)后,磷脂酰甘油的周转速率增加,同时心磷脂水平增加了两倍多。我们的数据表明,与通过其他途径(如膜衍生寡糖途径)代谢相比,磷脂酰甘油周转中相当大比例可能在心磷脂中得以恢复。