High-cell density shake-flask expression and rapid purification of the large fragment of Thermus aquaticus DNA polymerase I using a new chemically and temperature inducible expression plasmid in Escherichia coli

Author:

Brandis John W.,Johnson Kenneth A.

Publisher

Elsevier BV

Subject

Biotechnology

Reference19 articles.

1. Rapid quench kinetic analysis of polymerases, adenosinetriphosphatases, and enzyme intermediates;Johnson;Methods Enzymol.,1995

2. Recombinant protein expression in Escherichia coli;Baneyx;Curr. Opin. Biotechnol.,1999

3. Strategies for achieving high-level expression of genes in Escherichia coli;Makrides;Microbiol. Rev.,1996

4. Improved M13 phage and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors;Yanish-Perron;Gene,1985

5. Cloning of the gene for thermostable Thermus aquaticus YT-1 DNA polymerase and its expression in Escherichia coli;Patrushev;Mol. Biol. (Mosk),1993

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