4.7 Article

Disruption of vacuolar protein sorting components of the HOPS complex leads to enhanced secretion of recombinant proteins in Pichia pastoris

Journal

MICROBIAL CELL FACTORIES
Volume 18, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/s12934-019-1155-4

Keywords

Komagataella; Vacuolar protein sorting; Recombinant protein production; Yeast; Protein secretion; Secretion enhancing factor

Funding

  1. Austrian Federal Ministry of Digital and Economic Affairs (bmdw)
  2. Federal Ministry of Traffic, Innovation and Technology (bmvit)
  3. Styrian Business Promotion Agency SFG
  4. Standortagentur Tirol
  5. Government of Lower Austria
  6. ZIT-Technology Agency of the City of Vienna through the COMET-Funding Program
  7. Biomin Holding GmbH
  8. Boehringer-Ingelheim RCV
  9. Lonza AG
  10. Biocrates Life Sciences AG
  11. Validogen GmbH
  12. Sandoz GmbH

Ask authors/readers for more resources

BackgroundThe yeast Pichia pastoris is a widely used host for the secretion of heterologous proteins. Despite being an efficient producer, we observed previously that certain recombinant proteins were mistargeted to the vacuole on their route to secretion. Simultaneous disruption of one vacuolar sorting pathway together with vacuolar proteases prevented this mis-sorting and resulted in higher levels of secreted heterologous protein. Inspired by the positive results, we now set out to investigate the influence of further parts of the vacuolar pathway, namely the Cvt-pathway and the homotypic fusion and protein sorting (HOPS) complex.ResultsStrains impaired in the Cvt pathway (atg11, atg8) had no effect on secretion of the model protein carboxylesterase (CES), but resulted in lower secretion levels of the antibody fragment HyHEL-Fab. Disruption of genes involved in the HOPS complex led to vacuole-like compartments of the B category of vps mutants, which are characteristic for the deleted genes YPT7, VPS41 and VAM6. In particular ypt7 and vam6 strains showed an improvement in secreting the model proteins HyHEL-Fab and CES. Additional disruption of the vacuolar protease Pep4 and the potential protease Vps70 led to even further enhanced secretion in ypt7 and vam6 strains. Nevertheless, intracellular product accumulation was still observed. Therefore, the secretory route was strengthened by overexpression of early or late secretory genes in the vacuolar sorting mutants. Thereby, overexpression of Sbh1, a subunit of the ER translocation pore, significantly increased HyHEL-Fab secretion, leading up to fourfold higher extracellular Fab levels in the ypt7 strain. The beneficial impact on protein secretion and the suitability of these strains for industrial applicability was confirmed in fed-batch cultivations.ConclusionsDisruption of genes involved in the HOPS complex, especially YPT7, has a great influence on the secretion of the two different model proteins HyHEL-Fab and CES. Therefore, disruption of HOPS genes shows a high potential to increase secretion of other recombinant proteins as well. Secretion of HyHEL-Fab was further enhanced when overexpressing secretion enhancing factors. As the positive effect was also present in fed-batch cultivations, these modifications likely have promising industrial relevance.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available