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Plasmid maintenance in Escherichia coli recombinant cultures is dramatically, steadily, and specifically influenced by features of the encoded proteins
Author(s) -
Corchero José L.,
Villaverde Antonio
Publication year - 1998
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/(sici)1097-0290(19980620)58:6<625::aid-bit8>3.0.co;2-k
Subject(s) - plasmid , recombinant dna , biology , plasmid preparation , escherichia coli , gene , population , microbiology and biotechnology , genetics , demography , sociology , pbr322
A set of eight closely related plasmid constructs carrying CI857‐controlled recombinant genes has been used as a model to study plasmid stability in Escherichia coli, in the absence of antibiotic selection. Plasmid loss rates and relative interdivision times of plasmid‐bearing cells and plasmid‐free cells have been analyzed throughout prolonged cultures. Whereas the calculated plasmid loss rates are not consistent for a given plasmid and set of conditions, the relative growth fitness of plasmid‐bearing cells is highly reproducible. In the absence of gene expression, plasmid maintenance is influenced by the length of the cloned segment, the growth temperature, and the plasmid copy number, but not by the plasmid size. At high, inducing temperatures, the effects of the metabolic burden are eclipsed by the toxicity exhibited by the different proteins produced, which is determined by structural features. Despite the multifactorial nature of the negative pressures acting independently on plasmid‐bearing cells, the relative cell fitness in a mixed cell population is very reproducible for a given vector, resulting in a monotonous spread of the plasmid‐free cells in recombinant cultures. © 1998 John Wiley & Sons, Inc. Biotechnol Bioeng 58: 625–632, 1998.