scholarly journals Secretory helpers for enhanced production of heterologous proteins in Yarrowia lipolytica

2021 ◽  
Vol 32 ◽  
pp. e00669
Author(s):  
Paulina Korpys-Woźniak ◽  
Piotr Kubiak ◽  
Ewelina Celińska
2020 ◽  
Vol 104 (22) ◽  
pp. 9785-9800
Author(s):  
Paulina Korpys-Woźniak ◽  
Piotr Kubiak ◽  
Wojciech Białas ◽  
Ewelina Celińska

Abstract Overproduction of recombinant secretory proteins triggers numerous physiological perturbations. Depending on a given heterologous protein characteristics, the producer cell is faced with different challenges which lead to varying responses in terms of its physiology and the target protein production rate. In the present study, we used steady-state-maintained Yarrowia lipolytica cells to investigate the impact of different heterologous proteins on the physiological behavior of the host cells. Such an approach allowed to uncouple the impact of the overproduction of a particular protein from the phenomena that result from growth phase or are caused by the heterogeneity of the analyzed populations. Altogether, eight variants of recombinant strains, individually overproducing heterologous proteins of varying molecular weight (27–65 kDa) and reporting activity (enzymatic and fluorescent) were subjected to chemostat cultivations. The steady-state-maintained cells were analyzed in terms of the substrate utilization, biomass and metabolites production, as well as the reporter protein synthesis. Simplified distribution of carbon and nitrogen between the respective products, as well as expression analysis of the heterologous genes were conducted. The here-obtained data suggest that using a more transcriptionally active promoter results in channeling more C flux towards the target protein, giving significantly higher specific amounts and production rates of the target polypeptide, at the cost of biomass accumulation, and with no significant impact on the polyols production. The extent of the reporter protein’s post-translational modifications, i.e., the number of disulfide bonds and glycosylation pattern, strongly impacts the synthesis process. Specific responses in terms of the protein formation kinetics, the gene expression levels, and transcript-to-protein linearity were observed. Key Points • Eight expression systems, producing different reporter proteins were analyzed. • The cells were maintained in steady-state by continuous chemostat culturing. • Protein- and promoter-specific effects were observed.


2016 ◽  
Vol 41 ◽  
pp. 114-121 ◽  
Author(s):  
Aakanksha Vatsal ◽  
Chirag Potdar ◽  
Smita S. Zinjarde ◽  
V. Ravi Kumar ◽  
Bhasker D. Kulkarni ◽  
...  

1998 ◽  
Vol 180 (24) ◽  
pp. 6736-6742 ◽  
Author(s):  
Young-Sun Sohn ◽  
Cheon Seok Park ◽  
Sun-Bok Lee ◽  
Dewey D. Y. Ryu

ABSTRACT The Yarrowia lipolytica PMR1 gene (YlPMR1) is a Saccharomyces cerevisiae PMR1 homolog which encodes a putative secretory pathway Ca2+-ATPase. In this study, we investigated the effects of a YlPMR1 disruption on the processing and secretion of native and foreign proteins in Y. lipolytica and found variable responses by theYlPMR1-disrupted mutant depending on the protein. The secretion of 32-kDa mature alkaline extracellular protease (AEP) was dramatically decreased, and incompletely processed precursors were observed in the YlPMR1-disrupted mutant. A 36- and a 52-kDa premature AEP were secreted, and an intracellular 52-kDa premature AEP was also detected. The acid extracellular protease activity of theYlPMR1-disrupted mutant was increased by 60% compared to that of the wild-type strain. The inhibitory effect of mutations in secretory pathway Ca2+-ATPase genes on the secretion of rice α-amylase was also observed in the Y. lipolytica andS. cerevisiae PMR1-disrupted mutants. Unlike rice α-amylase, the secretion of Trichoderma reeseiendoglucanase I (EGI) was not influenced by the YlPMR1disruption. However, the secreted EGI from theYlPMR1-disrupted mutant had different characteristics than that of the control. While wild-type cells secreted the hyperglycosylated form of EGI, hyperglycosylation was completely absent in the YlPMR1-disrupted mutant. Our results indicate that the effects of the YlPMR1 disruption as manifested by the phenotypic response depend on the characteristics of the reporter protein in the recombinant yeast strain evaluated.


2008 ◽  
Vol 74 (24) ◽  
pp. 7759-7766 ◽  
Author(s):  
T. Payne ◽  
C. Finnis ◽  
L. R. Evans ◽  
D. J. Mead ◽  
S. V. Avery ◽  
...  

ABSTRACT The yeast Saccharomyces cerevisiae has been successfully established as a commercially viable system for the production of recombinant proteins. Manipulation of chaperone gene expression has been utilized extensively to increase recombinant protein production from S. cerevisiae, focusing predominantly on the products of the protein disulfide isomerase gene PDI1 and the hsp70 gene KAR2. Here we show that the expression of the genes SIL1, LHS1, JEM1, and SCJ1, all of which are involved in regulating the ATPase cycle of Kar2p, is increased in a proprietary yeast strain, developed by several rounds of random mutagenesis and screening for increased production of recombinant human albumin (rHA). To establish whether this expression contributes to the enhanced-production phenotype, these genes were overexpressed both individually and in combination. The resultant strains showed significantly increased shake-flask production levels of rHA, granulocyte-macrophage colony-stimulating factor, and recombinant human transferrin.


2016 ◽  
Vol 47 (2) ◽  
pp. 417-423 ◽  
Author(s):  
Magdalena Rakicka ◽  
Anita Rywińska ◽  
Krzysztof Cybulski ◽  
Waldemar Rymowicz

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