A simplified method for reconstituting active E. coli DNA polymerase III.
10.1007/s13238-011-1032-3
- Author:
Shi-Qiang LIN
1
;
Li-Jun BI
;
Xian-En ZHANG
Author Information
1. National Laboratory of Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China.
- Publication Type:Journal Article
- MeSH:
Cloning, Molecular;
DNA Polymerase III;
chemistry;
genetics;
metabolism;
DNA Replication;
DNA, Bacterial;
biosynthesis;
genetics;
Escherichia coli;
enzymology;
genetics;
Plasmids;
metabolism;
Polymerization;
Protein Engineering;
methods;
Protein Subunits;
chemistry;
genetics;
metabolism;
Recombinant Proteins;
chemistry;
genetics;
metabolism
- From:
Protein & Cell
2011;2(4):303-307
- CountryChina
- Language:English
-
Abstract:
Genome duplication in E. coli is carried out by DNA polymerase III, an enzyme complex consisting of ten subunits. Investigations of the biochemical and structural properties of DNA polymerase III require the expression and purification of subunits including α, ge, θ, γ, δ', δ, and β separately followed by in vitro reconstitution of the pol III core and clamp loader. Here we propose a new method for expressing and purifying DNA polymerase III components by utilizing a protein co-expression strategy. Our results show that the subunits of the pol III core and those of the clamp loader can be coexpressed and purified based on inherent interactions between the subunits. The resulting pol III core, clamp loader and sliding clamp can be reconstituted effectively to perform DNA polymerization. Our strategy considerably simplifies the expression and purification of DNA polymerase III and provides a feasible and convenient method for exploring other multi-subunit systems.
