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大肠杆菌B/r F的dnaA和dnaC突变体中染色体复制的起始

Initiation of chromosome replication in dnaA and dnaC mutants of Escherichia coli B/r F.

作者信息

Helmstetter C E, Krajewski C A

出版信息

J Bacteriol. 1982 Feb;149(2):685-93. doi: 10.1128/jb.149.2.685-693.1982.

Abstract

Regulatory aspects of chromosome replication were investigated in dnaA5 and dnaC2 mutants of the Escherichia coli B/r F. When cultures growing at 25 degrees C were shifted to 41 degrees C for extended periods and then returned to 25 degrees C, the subsequent synchronous initiations of chromosome replication were spaced at fixed intervals. When chloramphenicol was added coincident with the temperature downshift, the extend of chromosome replication in the dnaA mutant was greater than that in the dnaC mutant, but the time intervals between initiations were the same in both mutants. Furthermore, the time interval between the first two initiation events was unaffected by alterations in the rate of rifampin-sensitive RNA synthesis or cell mass increase. In the dnaC2 mutant, the capacities for both initiations were achieved in the absence of extensive DNA replication at 25 degrees C as long as protein synthesis was permitted, but the cells did not progress toward the second initiation at 25 degrees C when both protein synthesis and DNA replication were prevented. Cells of the dnaA5 mutant did not achieve the capacity for the second initiation event in the absence of extensive chromosome replication, although delayed initiation may have taken place. A plausible hypothesis to explain the data is that the minimum interval is determined by the time required for formation of a supercoiled, membrane-attached structure in the vicinity of oriC which is required for initiation of DNA synthesis.

摘要

对大肠杆菌B/r F的dnaA5和dnaC2突变体中染色体复制的调控方面进行了研究。当在25℃生长的培养物长时间转移到41℃,然后再回到25℃时,随后染色体复制的同步起始以固定间隔进行。当在温度下降时同时加入氯霉素,dnaA突变体中染色体复制的程度大于dnaC突变体,但两个突变体中起始之间的时间间隔相同。此外,前两个起始事件之间的时间间隔不受利福平敏感RNA合成速率或细胞质量增加变化的影响。在dnaC2突变体中,只要允许蛋白质合成,在25℃下即使没有广泛的DNA复制也能实现两次起始的能力,但当蛋白质合成和DNA复制都被阻止时,细胞在25℃下不会进入第二次起始。尽管可能发生了延迟起始,但在没有广泛染色体复制的情况下,dnaA5突变体的细胞没有获得第二次起始事件的能力。一个解释这些数据的合理假说是,最小间隔由在oriC附近形成超螺旋、膜附着结构所需的时间决定,而这种结构是DNA合成起始所必需的。

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