Improved Secretion of Heterologous Proteins bySaccharomyces cerevisiae: Effects of Promoter Substitution in Alpha-Factor Fusions

Publisher Website
Google Scholar
Abstract
The effects of promoter strength on secretion of a heterologous protein, somatomedin-C (SMC), by the yeast Saccharomyces cerevisiae were studied by using the promoters of the MF.alpha.1, ACT, and CYC1 genes to control expression of alpha-factor/SMC gene fusions. When a low-copy centromere vector was used to carry the gene fusions in yeast transformants, the greatest secretion was obtained with the MF.alpha.1 promoter construction and the least with the CYC1 promoter construction. Unexpectedly, using two types of multicopy vectors, the greatest secretion was obtained with the CYC1 promoter construction and the least with the MF.alpha.1 promoter construction. The decrease in secretion by the strongest promoter construction (MF.alpha.1 promoter) on multicopy vectors was associated with (i) a decrease in SMC mRNA during growth, (ii) a decrease in vector copy number, (iii) a decrease in vector stability, and (iv) a decrease in transformation frequency. The results demonstrate that, unlike in intracellular expression, promoter strength is not simply related to secretion expression levels. Selection against oversecreting cells during growth may explain the reduced secretion efficiency of strong promoter constructions.