Ohwada T, Sagisaka S
Institute of Low Temperature Science, Hokkaido University, Sapporo, Japan.
Arch Biochem Biophys. 1987 Nov 15;259(1):157-63. doi: 10.1016/0003-9861(87)90481-4.
Osmotic treatment with sodium chloride of Escherichia coli B growing in the logarithmic phase induced an immediate increase in ATP concentration in response to increased concentrations of added solute in its growth medium in the first 10 min of the addition. After that, ATP concentration decreased gradually. Sodium arsenate and potassium fluoride almost abolished the ATP increase. The time course of the increase was quite different from that of cells treated with inhibitors of protein synthesis. The osmotic treatment did not decrease the viability of cells. In addition, there was no degradation of RNA by 5 min after sodium chloride addition, and, further, the lag time of ATP increase was extended by an inhibitor of nucleotide synthesis. These results indicated that a major fraction of the stress-increased ATP resulted from de novo synthesis, and that it was mainly dependent upon the reaction of substrate-level phosphorylation, which is regulated by turgor pressure.
对数生长期的大肠杆菌B用氯化钠进行渗透处理时,在添加溶质后的最初10分钟内,随着生长培养基中添加溶质浓度的增加,ATP浓度立即升高。之后,ATP浓度逐渐下降。砷酸钠和氟化钾几乎完全消除了ATP的升高。这种升高的时间进程与用蛋白质合成抑制剂处理的细胞有很大不同。渗透处理并未降低细胞的活力。此外,添加氯化钠后5分钟内RNA没有降解,而且,核苷酸合成抑制剂延长了ATP升高的延迟时间。这些结果表明,应激增加的ATP主要来自从头合成,并且主要依赖于由膨压调节的底物水平磷酸化反应。