Transcriptome profiles for high‐cell‐density recombinant and wild‐type Escherichia coli
Authors:
- 1 March 2005
- journal article
- research article
- Published by Wiley in Biotechnology and Bioengineering
- Vol. 90 (2) , 127-153
Abstract
The transcriptome profiles for wild‐type (plasmid‐free) and recombinant (plasmid‐bearing) Escherichia coli during well‐controlled synchronized high‐cell‐density fed‐batch cultures were analyzed by DNA microarrays. It was observed that the growth phase significantly affected the transcriptome profiles, and the transcriptome profiles were significantly different for the recombinant and wild‐type cultures. The response of the wild‐type and recombinant cultures to an isopropyl‐1‐thio‐β‐d‐galactopyranoside‐ (IPTG‐) addition was examined, where IPTG induced recombinant protein production in the plasmid‐bearing cultures. The IPTG‐addition significantly altered the transcriptome response of the wild‐type cultures entering the stationary phase. The IPTG‐induced recombinant protein production resulted in a significant down‐regulation of many energy synthesis genes (atp, nuo, cyo), as well as nearly all transcription‐ and translation‐related genes (rpo, rpl, rpm, rps, rrf, rrl, rrs). Numerous phage (psp, hfl) and transposon‐related genes (tra, ins) were significantly regulated in the recombinant cultures due to the IPTG‐induction. These results indicate that the signaling mechanism, associated with the recombinant protein production, may induce a metabolic burden in the form of a phage defense mechanism. Taken together, these results indicated that recombinant protein production initiated a cascade of transcriptome responses that down‐regulated the very genes needed to sustain productivity.Keywords
This publication has 48 references indexed in Scilit:
- Global gene expression in Escherichia coli biofilmsMolecular Microbiology, 2003
- Microarray expression profiling: capturing a genome‐wide portrait of the transcriptomeMolecular Microbiology, 2003
- Combined transcriptome and proteome analysis of Escherichia coli during high cell density cultureBiotechnology and Bioengineering, 2003
- Global RNA Half-Life Analysis inEscherichia coliReveals Positional Patterns of Transcript DegradationGenome Research, 2003
- Transcriptome analysis of all two‐component regulatory system mutants of Escherichia coli K‐12Molecular Microbiology, 2002
- Genome‐wide analysis of deoxyadenosine methyltransferase‐mediated control of gene expression in Escherichia coliMolecular Microbiology, 2002
- DNA Microarray-Mediated Transcriptional Profiling of the Escherichia coli Response to Hydrogen PeroxideJournal of Bacteriology, 2001
- Response of Escherichia coli cell membranes to induction of λc1857 prophage by heat shockMolecular Microbiology, 1991
- Plasmid‐encoded protein: The principal factor in the “metabolic burden” associated with recombinant bacteriaBiotechnology and Bioengineering, 1990
- Stringent response in Escherichia coli induces expression of heat shock proteinsJournal of Molecular Biology, 1985