Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
18749 | Enzyme and Microbial Technology | 2006 | 4 Pages |
Abstract
Using a linear fed batch culture system, we obtained a yield of 296 mgDNA L−1 of a non-expressing plasmid containing a gene therapy sequence in Escherichia coli DH1 bioreactor culture. We propose that we exploited a transient increase in specific plasmid content, first observed during the adaptation from batch to chemostat culture, by inducing a progressive down-regulation of growth rate during our fed batch culture.
Keywords
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Bioengineering
Authors
A. Rozkov, C.A. Avignone-Rossa, P.F. Ertl, P. Jones, R.D. O’Kennedy, J.J. Smith, J.W. Dale, M.E. Bushell,