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      Increasing pentose phosphate pathway flux enhances recombinant protein production in Pichia pastoris

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          Abstract

          Production of heterologous proteins in Pichia pastoris (syn. Komagataella sp.) has been shown to exert a metabolic burden on the host metabolism. This burden is associated with metabolite drain, which redirects nucleotides and amino acids from primary metabolism. On the other hand, recombinant protein production affects energy and redox homeostasis of the host cell. In a previous study, we have demonstrated that overexpression of single genes of the oxidative pentose phosphate pathway (PPP) had a positive influence on recombinant production of cytosolic human superoxide dismutase (hSOD). In this study, different combinations of these genes belonging to the oxidative PPP were generated and analyzed. Thereby, a 3.8-fold increase of hSOD production was detected when glucose-6-phosphate dehydrogenase ( ZWF1) and 6-gluconolactonase ( SOL3) were simultaneously overexpressed, while the combinations of other genes from PPP had no positive effect on protein production. By measuring isotopologue patterns of 13C-labelled metabolites, we could detect an upshift in the flux ratio of PPP to glycolysis upon ZWF1 and SOL3 co-overexpression, as well as increased levels of 6-phosphogluconate. The substantial improvement of hSOD production by ZWF1 and SOL3 co-overexpression appeared to be connected to an increase in PPP flux. In conclusion, we show that overexpression of SOL3 together with ZWF1 enhanced both the PPP flux ratio and hSOD accumulation, providing evidence that in P. pastoris Sol3 limits the flux through PPP and recombinant protein production.

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          The online version of this article (doi:10.1007/s00253-016-7363-5) contains supplementary material, which is available to authorized users.

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          Most cited references34

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          Genome sequence of the recombinant protein production host Pichia pastoris.

          The methylotrophic yeast Pichia pastoris is widely used for the production of proteins and as a model organism for studying peroxisomal biogenesis and methanol assimilation. P. pastoris strains capable of human-type N-glycosylation are now available, which increases the utility of this organism for biopharmaceutical production. Despite its biotechnological importance, relatively few genetic tools or engineered strains have been generated for P. pastoris. To facilitate progress in these areas, we present the 9.43 Mbp genomic sequence of the GS115 strain of P. pastoris. We also provide manually curated annotation for its 5,313 protein-coding genes.
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            Plasmid-encoded protein: the principal factor in the "metabolic burden" associated with recombinant bacteria.

            Experimental elucidation of the metabolic load placed on bacteria by the expression of foreign protein is presented. The host/vector system is Escherichia coli RR1/pBR329 (amp(r), cam(r), and let(r)). Plasmid content results, which indicate that the plasmid copy number monotonically increases with decreasing growth rate, are consistent with the literature on ColE1-like plasmids. More significantly, we have experimentally quantified the reduction in growth rate brought about by the expression of chloramphenicol-acetyl-transferase (CAT) and beta-lactamase. Results indicate a nearly linear decrease in growth rate with increasing foreign protein content. Also, the change in growth rate due to foreign protein expression depends on the growth rate of the cells. The observed linear relationship is media independent and, to our knowledge, previously undocumented. Furthermore, the induction of CAT, mediated by the presence of chloramphenicol, is shown to occur only at low growth rates, which further increases the metabolic load.Results are vdelineated with the aid of a structured kinetic model representing the metabolism of recombinant E. coli. In this article, several previous hypotheses and model predictions are justified and validated. This work provides an important step in the development of comprehensive, methabolically-structured, kinetic models capable of prediciting optimal conditions for maximizing product yield.
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              Metabolic load and heterologous gene expression.

              The expression of a foreign protein(s) in a recombinant host cell or organism often utilizes a significant amount of the host cell's resources, removing those resources away from host cell metabolism and placing a metabolic load (metabolic drain, metabolic burden) on the host. As a consequence of the imposed metabolic load, the biochemistry and physiology of the host may be dramatically altered. The numerous physiological changes that may occur often lowers the amount of the target foreign protein that is produced and eventually recovered from the recombinant organism. In this review the physiological changes to host cells, the causes of the phenomenon of metabolic load, and several strategies to avoid some of the problems associated with metabolic load are elaborated and discussed.
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                Author and article information

                Contributors
                +43-1-47654-6813 , brigitte.gasser@boku.ac.at
                Journal
                Appl Microbiol Biotechnol
                Appl. Microbiol. Biotechnol
                Applied Microbiology and Biotechnology
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0175-7598
                1432-0614
                28 March 2016
                28 March 2016
                2016
                : 100
                : 5955-5963
                Affiliations
                [ ]Department of Biotechnology, BOKU, University of Natural Resources and Life Sciences Vienna, Muthgasse 18, 1190 Vienna, Austria
                [ ]Austrian Centre of Industrial Biotechnology, Muthgasse 11, 1190 Vienna, Austria
                [ ]Department of Chemistry, BOKU, University of Natural Resources and Life Sciences Vienna, Muthgasse 18, 1190 Vienna, Austria
                Article
                7363
                10.1007/s00253-016-7363-5
                4909809
                27020289
                e892d468-9a7c-41a4-b4e7-9d856cadc7e4
                © The Author(s) 2016

                Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 25 September 2015
                : 13 January 2016
                : 30 January 2016
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100002428, Austrian Science Fund;
                Award ID: FWF W1224
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100004955, Österreichische Forschungsförderungsgesellschaft;
                Award ID: Comet-ACIB
                Award Recipient :
                Categories
                Applied Microbial and Cell Physiology
                Custom metadata
                © Springer-Verlag Berlin Heidelberg 2016

                Biotechnology
                recombinant protein,pentose phosphate pathway,metabolic flux analysis,zwf1,sol3
                Biotechnology
                recombinant protein, pentose phosphate pathway, metabolic flux analysis, zwf1, sol3

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