A conditional expression vector for the cyanobacteriaSynechocystis sp. strains PCC6803 and PCC6714 orSynechococcus sp. strains PCC7942 and PCC6301
- 1 March 1994
- journal article
- Published by Springer Nature in Current Microbiology
- Vol. 28 (3) , 145-148
- https://doi.org/10.1007/bf01571055
Abstract
An expression vector, pFC1, has been constructed based on the promiscuous plasmid RSF1010, which provides autonomous replication in several cyanobacteria of the generaSynechocystis andSynechococcus [Mermet-Bouvier et al., Curr Microbiol 26:323–327]. pFC1 harbors the λcI857 repressor-encoding gene andp R promoter, followed by the λcro ribosome-binding site and ATG translation initiation codon. The latter is located within the uniqueNdeI restriction site (CATATG) of pFC1 and can be exposed after cleavage with this enzyme for in-frame fusion with the protein-coding sequence to be expressed. TheEscherichia coli lacZ reporter gene cloned in pFC1 appeared to be highly expressed in heat-inducedE. coli or cyanobacterial cells. In every case, β-galactosidase amounted to at least 10% of soluble proteins.Keywords
This publication has 21 references indexed in Scilit:
- Genetic analysis of photosynthesis in prokaryotes and lower eukaryotesCurrent Opinion in Genetics & Development, 1992
- Plasmid vectors for selecting IS1-promoted deletions in cloned DNA: sequence analysis of the omega interposonGene, 1991
- A promoter-probe vector-host system for the cyanobacterium, Synechocystis PCC6803Gene, 1989
- Transfer of broad host-range plasmids to sulphate-reducing bacteriaFEMS Microbiology Letters, 1989
- Complete nucleotide sequence and gene organization of the broad-host-range plasmid RSF1010Gene, 1989
- Controlled gene expression utilising Lambda phage regulatory signals in a cyanobacterium hostMolecular Genetics and Genomics, 1986
- In vitro insertional mutagenesis with a selectable DNA fragmentGene, 1984
- New versatile plasmid vectors for expression of hybrid proteins coded by a cloned gene fused to lacA gene sequences encoding an enzymatically active carboxy-terminal portion of β-galactosidaseGene, 1983
- A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye BindingAnalytical Biochemistry, 1976
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976