4.7 Article

Quantitative metabolomics analysis of amino acid metabolism in recombinant Pichia pastoris under different oxygen availability conditions

期刊

MICROBIAL CELL FACTORIES
卷 11, 期 -, 页码 -

出版社

BIOMED CENTRAL LTD
DOI: 10.1186/1475-2859-11-83

关键词

Pichia pastoris; Metabolite quantification; Recombinant protein production; Hypoxia; Amino acids; Metabolic burden

资金

  1. Spanish program on Chemical Process Technologies of the Spanish Ministry of Science and Innovation [CTQ2010-15131]
  2. Generalitat de Catalunya [2009-SGR-281]
  3. Spanish Ministry scholarship [TME2009-00591]

向作者/读者索取更多资源

Background: Environmental and intrinsic stress factors can result in the global alteration of yeast physiology, as evidenced by several transcriptional studies. Hypoxia has been shown to have a beneficial effect on the expression of recombinant proteins in Pichia pastoris growing on glucose. Furthermore, transcriptional profiling analyses revealed that oxygen availability was strongly affecting ergosterol biosynthesis, central carbon metabolism and stress responses, in particular the unfolded protein response. To contribute to the better understanding of the effect and interplay of oxygen availability and foreign protein secretion on central metabolism, a first quantitative metabolomic analysis of free amino acids pools in a recombinant P. pastoris strain growing under different oxygen availability conditions has been performed. Results: The values obtained indicate significant variations in the intracellular amino acid pools due to different oxygen availability conditions, showing an overall increase of their size under oxygen limitation. Notably, even while foreign protein productivities were relatively low (about 40-80 mu g Fab/g(DCW).h), recombinant protein production was found to have a limited but significant impact on the intracellular amino acid pools, which were generally decreased in the producing strain compared with the reference strain. However, observed changes in individual amino acids pools were not correlated with their corresponding relative abundance in the recombinant protein sequence, but to the overall cell protein amino acid compositional variations. Conclusions: Overall, the results obtained, combined with previous transcriptomic and proteomic analyses provide a systematic metabolic fingerprint of the oxygen availability impact on recombinant protein production in P. pastoris.

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