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大肠杆菌B-r中染色体复制的起源与序列

Origin and sequence of chromosome replication in Escherichia coli B-r.

作者信息

Helmstetter C E

出版信息

J Bacteriol. 1968 May;95(5):1634-41. doi: 10.1128/jb.95.5.1634-1641.1968.

Abstract

The initial rates of induced synthesis of tryptophanase, beta-galactosidase, and d-serine deaminase were measured in relation to the chromosome replication cycle of Escherichia coli B/r. Exponentially growing cultures were exposed briefly to (14)C-thymidine or the appropriate inducers (or both), and the amount of label or enzyme (or both) in cells of different ages was found by measuring these quantities in their progeny. The rates of induced synthesis of the three enzymes increased abruptly at about 4, 20, and 34 min, respectively, after the start of a round of replication lasting 40 min. By matching this sequence to the ind, lac, and Dsd loci on the genetic map of E. coli K-12, it was estimated that replication began at about 8 o'clock (60 min) and proceeded clockwise. In rapidly growing cells, the sequence during the division cycle was consistent with the concept that rounds of replication overlapped.

摘要

测定了色氨酸酶、β-半乳糖苷酶和d-丝氨酸脱氨酶诱导合成的初始速率与大肠杆菌B/r染色体复制周期的关系。将指数生长的培养物短暂暴露于¹⁴C-胸腺嘧啶或适当的诱导剂(或两者),通过测量不同年龄细胞后代中的标记物或酶(或两者)的量来确定不同年龄细胞中的标记物或酶(或两者)的量。在持续40分钟的一轮复制开始后,三种酶的诱导合成速率分别在约4、20和34分钟时突然增加。通过将这个序列与大肠杆菌K-12遗传图谱上的ind、lac和Dsd位点进行匹配,估计复制大约在8点(60分钟)开始并顺时针进行。在快速生长的细胞中,分裂周期中的序列与复制轮次重叠的概念一致。

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