The yeast has been a successful host for the production of heterologous proteins for over 30 years. Currently, the galactose-/lactose-inducible and glucose-repressible promoter (P ) is the most widely used promoter to drive recombinant protein expression in However, P is not fully repressed in the presence of glucose and significant protein expression still occurs. Thus, P is not suitable in processes where tight regulation of heterologous gene expression is required. In this study, we devised a novel promoter system that is both strong and tightly controllable. We first tested several different endogenous promoters for their ability to express recombinant proteins. A novel hybrid promoter (termed P) was created by combining segments of two promoters, namely, the strong constitutive P promoter and the carbon source-sensitive P promoter. We demonstrate that P is tightly repressed in the presence of glucose or glycerol and becomes derepressed upon depletion of these compounds by the growing cells. We further illustrate the utility of P-controlled protein expression in shake flask and high-cell-density bioreactor cultivation strategies. The P hybrid promoter is a strong derepressible promoter for use in autoinduction of one-step fermentation processes for the production of heterologous proteins in The yeast is an important host for the expression of recombinant proteins at both laboratory and industrial scales. However, the system lacks a tightly regulated promoter that permits controlled expression of heterologous proteins. In this study, we report the engineering of a highly regulated strong hybrid promoter (termed P) for use in P is tightly repressed by glucose or glycerol in the medium but strongly promotes gene expression once the carbon source has been consumed by the cells. This feature permits heterologous protein expression to be "autoinduced" at any scale without the addition of a gratuitous inducer molecule or changing feed solutions.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6606884 | PMC |
http://dx.doi.org/10.1128/AEM.00542-19 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!