4.7 Article

Engineering of vesicle trafficking improves heterologous protein secretion in Saccharomyces cerevisiae

Journal

METABOLIC ENGINEERING
Volume 14, Issue 2, Pages 120-127

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ymben.2012.01.002

Keywords

Vesicle trafficking; Sec1p; Sly1p; Heterologous protein secretion; Saccharomyces cerevisiae

Funding

  1. The Knut and Alice Wallenberg Foundation
  2. EU [212766]
  3. European Research Council [247013]
  4. Chalmers Foundation
  5. NIH

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The yeast Saccharomyces cerevisiae is a widely used platform for the production of heterologous proteins of medical or industrial interest. However, heterologous protein productivity is often restricted due to the limitations of the host strain. In the protein secretory pathway, the protein trafficking between different organelles is catalyzed by the soluble NSF (N-ethylmaleimide-sensitive factor) receptor (SNARE) complex and regulated by the Secl/Munc18 (SM) proteins. In this study, we report that over-expression of the SM protein encoding genes SEC1 and SLY1, improves the protein secretion in S. cerevisiae. Engineering Sec1p, the SM protein that is involved in vesicle trafficking from Golgi to cell membrane, improves the secretion of heterologous proteins human insulin precursor and alpha-amylase, and also the secretion of an endogenous protein invertase. Enhancing Sly1p, the SM protein regulating the vesicle fusion from endoplasmic reticulum (ER) to Golgi, increases alpha-amylase production only. Our study demonstrates that strengthening the protein trafficking in ER-to-Golgi and Golgi-to-plasma membrane process is a novel secretory engineering strategy for improving heterologous protein production in S. cerevisiae. (C) 2012 Elsevier Inc. All rights reserved.

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