Ohkawa T
Eur J Biochem. 1975 Dec 1;60(1):57-66. doi: 10.1111/j.1432-1033.1975.tb20975.x.
In a thymine-deprived culture, the mutant cells (deficient in dTDP-glucose pyrophosphorylase activity and named Ter-15) lose viability at a faster rate, form longer filaments for the first 60 min and lose thymidine nucleotides and dTDP-sugar pools at a faster rate for the first 15 min than those of the parent cells, but the dTDP-sugar pool in the parent cells is maintained at high concentration for the first 90 min during thymine starvation. In the recovery of cell growth after re-addition of thymine into the thymine-deprived culture, parent cells recommence growth immediately, but the mutant cells (Ter-15) show a lag-phase for 45 min after which time their growth recommences. The rate of dTTP synthesis for the first 10 to 15 min after re-addition of thymine to thymine-deprived cultures of parent and mutant (Ter-15) cells is three-fold higher than that of thymine nondeprived culture (control), but the rates of dTMP and dTDP-sugar syntheses are the same as those of the control. The total DNA synthesis after re-addition of thymine is equal to that of the control, and the period of thymine starvation other than the number of viable cells during thymine starvation plays an important role. After separation of the filament cells from normal-sized cells by sucrose gradient centrifugation, the initial rate of DNA synthesis of filament cells is three-fold faster than that of normal-sized cells. These results show that the dependency of DNA synthesis upon dTTP concentration is maintained after re-addition of thymine into thymine-deprived culture.
在胸腺嘧啶缺乏的培养环境中,突变细胞(缺乏dTDP - 葡萄糖焦磷酸化酶活性,命名为Ter - 15)比亲代细胞更快地丧失活力,在最初的60分钟内形成更长的丝状结构,并且在最初的15分钟内比亲代细胞更快地丧失胸苷核苷酸和dTDP - 糖库,但在胸腺嘧啶饥饿的最初90分钟内,亲代细胞中的dTDP - 糖库保持在高浓度。在向胸腺嘧啶缺乏的培养物中重新添加胸腺嘧啶后细胞生长的恢复过程中,亲代细胞立即重新开始生长,但突变细胞(Ter - 15)显示出45分钟的延迟期,之后其生长才重新开始。在向亲代和突变(Ter - 15)细胞的胸腺嘧啶缺乏培养物中重新添加胸腺嘧啶后的最初10至15分钟内,dTTP合成速率比未缺乏胸腺嘧啶的培养物(对照)高两倍,但dTMP和dTDP - 糖的合成速率与对照相同。重新添加胸腺嘧啶后的总DNA合成与对照相等,并且胸腺嘧啶饥饿的时间而非胸腺嘧啶饥饿期间存活细胞的数量起着重要作用。通过蔗糖梯度离心将丝状细胞与正常大小的细胞分离后,丝状细胞的DNA合成初始速率比正常大小的细胞快两倍。这些结果表明,在向胸腺嘧啶缺乏的培养物中重新添加胸腺嘧啶后,DNA合成对dTTP浓度的依赖性得以维持。