A URA3‐Promoter Deletion in a pYES Vector Increases the Expression Level of a Fungal Lipase in Saccharomyces cerevisiae
- 1 May 1996
- journal article
- Published by Wiley in Annals of the New York Academy of Sciences
- Vol. 782 (1) , 202-207
- https://doi.org/10.1111/j.1749-6632.1996.tb40561.x
Abstract
A simple deletion of the URA3 promoter from a Saccharomyces cerevisiae expression plasmid was performed. The promoter-deleted plasmid is shown to have an increased expression level of a fungal lipase gene. The deletion probably causes a poor expression of the URA3 selection marker, probably resulting in a higher copy number per cell of the plasmid. This higher copy number can increase the transcript level per cell and there by the expression level. In the case of the fungal lipase gene, the expression level with defined inoculum is increased at least three times. The principle is most likely similar to the LEU2d plasmids described previously. A part of the 2-micron origin of the pYES type plasmid was also deleted by the URA3 promoter deletion without affecting transformation frequency. The URA3 promoter can easily be deleted from most pYES type plasmids by the described method.Keywords
This publication has 6 references indexed in Scilit:
- High level of expression of a protective antigen of schistosomes in Saccharomyces cerevisiaeYeast, 1989
- Signals for transcription initiation and termination in the Saccharomyces cerevisiae plasmid 2 micron circle.Molecular and Cellular Biology, 1985
- Yeast promoters URA1 and URA3Journal of Molecular Biology, 1985
- The presence of a defective LEU2 gene on 2 mu DNA recombinant plasmids of Saccharomyces cerevisiae is responsible for curing and high copy numberJournal of Bacteriology, 1983
- Continuous pH-stat titration method for the assay of lipoprotein lipase activity in vitroAnalytical Biochemistry, 1974