The impact of respiration and oxidative stress response on recombinant ?-amylase production by Saccharomyces cerevisiae

Studying protein production is important for fundamental research on cell biology and applied research for biotechnology. Yeast Saccharomyces cerevisiae is an attractive workhorse for production of recombinant proteins as it does not secrete many endogenous proteins and it is therefore easy to purif...

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Bibliographic Details
Published inMetabolic engineering communications Vol. 3; p. 205
Main Authors Martinez Ruiz, Jose Luis, Meza, Eugenio, Petranovic Nielsen, Dina, Nielsen, Jens B
Format Journal Article
LanguageEnglish
Published 2016
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ISSN2214-0301
2214-0301
DOI10.1016/j.meteno.2016.06.003

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Summary:Studying protein production is important for fundamental research on cell biology and applied research for biotechnology. Yeast Saccharomyces cerevisiae is an attractive workhorse for production of recombinant proteins as it does not secrete many endogenous proteins and it is therefore easy to purify a secreted product. However, recombinant production at high rates represents a significant metabolic burden for the yeast cells, which results in oxidative stress and ultimately affects the protein production capacity. Here we describe a method to reduce the overall oxidative stress by overexpressing the endogenous HAP1 gene in a S. cerevisiae strain overproducing recombinant α-amylase. We demonstrate how Hap1p can activate a set of oxidative stress response genes and meanwhile contribute to increase the metabolic rate of the yeast strains, therefore mitigating the negative effect of the ROS accumulation associated to protein folding and hence increasing the production capacity during batch fermentations.
ISSN:2214-0301
2214-0301
DOI:10.1016/j.meteno.2016.06.003