Article ID Journal Published Year Pages File Type
23788 Journal of Biotechnology 2012 9 Pages PDF
Abstract

Novel shuttle vectors named pEBP were constructed to allow the gene expression in different bacterial hosts including Escherichia coli, Bacillus subtilis and Pseudomonas putida. These vectors share the inducible promoters PT7 and PXyl and a cos site to enable packaging of plasmid DNA into phage, and carry different multiple cloning sites and antibiotic resistance genes. Vector pEBP41 generally replicates episomally while pEBP18 replicates episomally in Gram-negative bacteria only, but integrates into the chromosome of B. subtilis. Plasmid copy numbers determined for E. coli and P. putida were in the range of 5–50 per cell. The functionality of pEBP18 and pEBP41 was confirmed by expression of two lipolytic enzymes, namely lipase A from B. subtilis and cutinase from the eukaryotic fungus Fusarium solani pisi in three different host strains. Additionally, we report here the construction of a T7 RNA polymerase-based expression strain of P. putida.

► Novel shuttle vectors were constructed for gene expression in different bacteria. ► Inducible expression occurs from promoters PT7 and Pxyl. ► Functionality was confirmed by expression of lipolytic enzymes. ► A T7 RNA polymerase-based expression strain of Pseudomonas putida was constructed.

Related Topics
Physical Sciences and Engineering Chemical Engineering Bioengineering
Authors
, , , , , , , ,