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PMID: 8187762 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The initiation mass for DNA replication in Escherichia coli K-12 is dependent on growth rate.

The EMBO journal ·Vol. 13 ·No. 9 ·1994-05-01 ·Pages 2097-102

Wold S, Skarstad K, Steen HB, Stokke T, Boye E

Abstract

It is widely accepted that the initiation mass of Escherichia coli is constant and independent of growth rate, and therefore is an important parameter in the regulation of initiation of DNA replication. We have used flow cytometry to measure the initiation mass of E. coli K-12 cells as a function of growth rate. The average initiation mass was determined by two methods: (i) from a mathematical relationship between average cell mass, cell age at initiation and number of origins present in the cells, and (ii) directly from the cell mass distribution. The light scattering signal from individual cells and the protein content per cell were employed as measures of cell mass. The initiation mass was found to increase monotonically with decreasing growth rate, being 1.6 times higher (light scattering) or 2.1 times higher (protein content) at 0.3 than at 2.5 doublings per hour. We conclude that the initiation mass is dependent on growth rate. This finding indicates that the control for timing of initiation is not governed by a direct connection between mass accumulation and the molecule(s) determining initiation of replication.

MeSH Terms
Cell Division/drug effects,physiology DNA Replication DNA, Bacterial/biosynthesis Escherichia coli/drug effects,genetics,growth & development Flow Cytometry Rifampin/pharmacology Time Factors
Chemicals
DNA, Bacterial Rifampin
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Wold S
Department of Biophysics, Institute for Cancer Research, Montebello, Oslo, Norway.
Skarstad K
Steen H B
Stokke T
Boye E
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32 references, click to expand
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Article Info
Journal
The EMBO journal
Abbr.
EMBO J
ISSN
0261-4189
Published
1994-05-01
Pages
2097-102
Language
English
Region
England
NLM ID
8208664
PMCID
PMC395061
Subset
IM
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