Low-Copy Plasmids can Perform as Well as or Better Than High-Copy Plasmids for Metabolic Engineering of Bacteria
- 1 October 2000
- journal article
- Published by Elsevier in Metabolic Engineering
- Vol. 2 (4), 328-338
- https://doi.org/10.1006/mben.2000.0161
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- Expression of prokaryotic 1‐deoxy‐d‐xylulose‐5‐phosphatases in Escherichia coli increases carotenoid and ubiquinone biosynthesisFEBS Letters, 1999
- Construction and characterization of F plasmid-based expression vectorsBiotechnology & Bioengineering, 1998
- mRNA stability and plasmid copy number effects on gene expression from an inducible promoter systemBiotechnology & Bioengineering, 1998
- The deoxyxylulose phosphate pathway of terpenoid biosynthesis in plants and microorganismsChemistry & Biology, 1998
- Tight regulation, modulation, and high-level expression by vectors containing the arabinose PBAD promoterJournal of Bacteriology, 1995
- Guanosine pentaphosphate phosphohydrolase of Escherichia coli is a long-chain exopolyphosphatase.Proceedings of the National Academy of Sciences, 1993
- Plasmid presence changes the relative levels of many host cell proteins and ribosome components in recombinant Escherichia coliBiotechnology & Bioengineering, 1991
- Plasmid‐encoded protein: The principal factor in the “metabolic burden” associated with recombinant bacteriaBiotechnology & Bioengineering, 1990
- [3] Design and construction of expression plasmid vectors in escherichia coliMethods in Enzymology, 1990
- Persistence of pBR322-related plasmids inEscherichia coligrown in chemostat culturesFEMS Microbiology Letters, 1984