Long‐term adaptation of Saccharomyces cerevisiae to the burden of recombinant insulin production. Issue 10 (14th May 2013)

• Record Type: Journal Article
• Authors: Kazemi Seresht, Ali; Cruz, Ana Luisa; de Hulster, Erik; Hebly, Marit; Palmqvist, Eva Akke; van Gulik, Walter; Daran, Jean‐Marc; Pronk, Jack; Olsson, Lisbeth
• Is Part Of: Biotechnology and bioengineering. Volume 110:Issue 10(2013:Oct.)
• Page Start: 2749
• Page End: 2763
• Publication Date: 2013-05-14
• Subjects: Biotechnology -- Periodicals; Bioengineering -- Periodicals; 660.6
• DOI: 10.1002/bit.24927
• Languages: English
• ISSNs: 0006-3592

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <sec id="bit24927-sec-0001" sec-type="section"> <p>High‐level production of heterologous proteins is likely to impose a metabolic burden on the host cell and can thus affect various aspects of cellular physiology. A data‐driven approach was applied to study the secretory production of a human insulin analog precursor (IAP) in <italic>Saccharomyces cerevisiae</italic> during prolonged cultivation (80 generations) in glucose‐limited aerobic chemostat cultures. Physiological characterization of the recombinant cells involved a comparison with cultures of a congenic reference strain that did not produce IAP, and time‐course analysis of both strains aimed at identifying the metabolic adaptation of the cells towards the burden of IAP production. All cultures were examined at high cell density conditions (30 g/L dry weight) to increase the industrial relevance of the results. The burden of heterologous protein production in the recombinant strain was explored by global transcriptome analysis and targeted metabolome analysis, including the analysis of intracellular amino acid pools, glycolytic metabolites, and TCA intermediates. The cellular re‐arrangements towards IAP production were categorized in direct responses, for example, enhanced metabolism of amino acids as precursors for the formation of IAP, as well as indirect responses, for example, changes in the central carbon metabolism. As part of the long‐term adaptation, a metabolic re‐modeling of the IAP‐expressing strain was observed, indicating an augmented negative selection pressure on glycolytic overcapacity, and the emergence of mitochondrial dysfunction. The evoked metabolic re‐modeling of the cells led to less optimal conditions with respect to the expression and processing of the target protein and thus decreased the cellular expression capacity for the secretory production of IAP during prolonged cultivation. Biotechnol. Bioeng. 2013;110: 2749–2763. © 2013 Wiley Periodicals, Inc.</p> </sec> </abstract>