A series of new expression vectors (pPro) have been constructed for the regulated expression of genes in Escherichia coli. The pPro vectors contain the prpBCDE promoter (PprpB) responsible for expression of the propionate catabolic genes (prpBCDE) and prpR encoding the positive regulator of this promoter. The efficiency and regulatory properties of the prpR-PprpB system were measured by placing the gene encoding the green fluorescent protein (gfp) under the control of the inducible PprpB of E. coli. This system provides homogenous expression in individual cells, highly regulatable expression over a wide range of propionate concentrations, and strong expression (maximal 1,500-fold induction) at high propionate concentrations. Since the prpBC...
Background Production of recombinant proteins in bacteria for academic and commercial purposes is a ...
Experiments requiring strong repression and precise control of cloned genes can be difficult to cond...
In this study, we introduced an efficient subcloning and expression system with two inducible prokar...
A series of new expression vectors (pPro) have been constructed for the regulated expression of gene...
A new expression system containing the Salmonella enterica prpBCDE promoter (PprpB) responsible for ...
We have developed an expression system (Salmonella-based pPro system) containing the Salmonella ente...
The expression and regulatory properties of a propionate-regulated overexpression system (Salmonella...
We examined expression of two plant genes encoding coclaurine N-methyltransferase (CMT) and norcocla...
The ugp promoter (pugp) responsible for expression of the binding-protein-dependent sn-glycerol-3-ph...
The pGinger suite of expression plasmids comprises 43 plasmids that will enable precise constitutive...
Plassmeier J, Busche T, Molck S, et al. A propionate-inducible expression system based on the Coryne...
International audienceEscherichia coli is an important experimental, medical and industrial cell fac...
International audienceEscherichia coli is an important experimental, medical and industrial cell fac...
peer reviewedEscherichia coli is an important experimental, medical and industrial cell factory for ...
Abstract Background Besides Escherichia coli, Bacillus subtilis is an important bacterial species fo...
Background Production of recombinant proteins in bacteria for academic and commercial purposes is a ...
Experiments requiring strong repression and precise control of cloned genes can be difficult to cond...
In this study, we introduced an efficient subcloning and expression system with two inducible prokar...
A series of new expression vectors (pPro) have been constructed for the regulated expression of gene...
A new expression system containing the Salmonella enterica prpBCDE promoter (PprpB) responsible for ...
We have developed an expression system (Salmonella-based pPro system) containing the Salmonella ente...
The expression and regulatory properties of a propionate-regulated overexpression system (Salmonella...
We examined expression of two plant genes encoding coclaurine N-methyltransferase (CMT) and norcocla...
The ugp promoter (pugp) responsible for expression of the binding-protein-dependent sn-glycerol-3-ph...
The pGinger suite of expression plasmids comprises 43 plasmids that will enable precise constitutive...
Plassmeier J, Busche T, Molck S, et al. A propionate-inducible expression system based on the Coryne...
International audienceEscherichia coli is an important experimental, medical and industrial cell fac...
International audienceEscherichia coli is an important experimental, medical and industrial cell fac...
peer reviewedEscherichia coli is an important experimental, medical and industrial cell factory for ...
Abstract Background Besides Escherichia coli, Bacillus subtilis is an important bacterial species fo...
Background Production of recombinant proteins in bacteria for academic and commercial purposes is a ...
Experiments requiring strong repression and precise control of cloned genes can be difficult to cond...
In this study, we introduced an efficient subcloning and expression system with two inducible prokar...