Huang W M
J Virol. 1979 Dec;32(3):917-24. doi: 10.1128/JVI.32.3.917-924.1979.
3-Decynoyl-N-acetylcysteamine (3-decynoyl-NAC) is an analog which specifically causes the immediate cessation of the biosynthesis of unsaturated fatty acids in Escherichia coli, whereas the synthesis of saturated fatty acids is actually stimulated. As a result, the cell membrane accumulates saturated fatty acids in its phospholipid. Addition of the inhibitor at the time of infection of E. coli by T4 phage had no effect on normal phage replication and development, implying that the synthesis of unsaturated fatty acids per se has little effect on T4 DNA replication. However, if the integrity and composition of the bacterial membrane was grossly perturbed by first treating the cells with the inhibitor for 60 min before infection, the proper initiation and the attainment of a rapid rate of T4 DNA synthesis were not observed. Under these conditions, a full complement of T4 early proteins was synthesized. The membrane associability of the known DNA delay proteins induced by wild-type T4 phage in the treated cells resembled that expected of a culture of untreated cells infected with a DNA delay mutant. When any one of three DNA delay mutants was used to infect 3-decynoyl-NAC-treated cells, T4 DNA replication was aborted. These findings suggest that some kind of specific interactions among the initiation proteins defined by the DNA delay mutants and the bacterial membrane may be necessary to facilitate the normal initiation and rapid rate of T4 DNA replication. A model for the involvement of the three different initiation proteins and the subsequent attainment of rapid DNA synthesis is discussed.
3-癸炔酰-N-乙酰半胱胺(3-癸炔酰-NAC)是一种类似物,它能特异性地使大肠杆菌中不饱和脂肪酸的生物合成立即停止,而饱和脂肪酸的合成实际上受到刺激。结果,细胞膜在其磷脂中积累了饱和脂肪酸。在T4噬菌体感染大肠杆菌时添加该抑制剂对正常噬菌体的复制和发育没有影响,这意味着不饱和脂肪酸的合成本身对T4 DNA复制影响很小。然而,如果在感染前先用抑制剂处理细胞60分钟,使细菌膜的完整性和组成受到严重干扰,就无法观察到T4 DNA合成的正常起始和快速合成速率。在这些条件下,合成了完整的T4早期蛋白质。野生型T4噬菌体在处理过的细胞中诱导产生的已知DNA延迟蛋白的膜结合能力类似于用DNA延迟突变体感染的未处理细胞培养物的预期情况。当用三种DNA延迟突变体中的任何一种感染3-癸炔酰-NAC处理过的细胞时,T4 DNA复制就会中止。这些发现表明,DNA延迟突变体所定义的起始蛋白与细菌膜之间的某种特定相互作用可能是促进T4 DNA正常起始和快速复制速率所必需的。文中讨论了三种不同起始蛋白的参与以及随后实现快速DNA合成的模型。