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Optimization of cold methanol quenching for quantitative metabolomics of Penicillium chrysogenum
A sampling procedure for quantitative metabolomics in Penicillium chrysogenum based on cold aqueous methanol quenching was re-evaluated and optimized to reduce metabolite leakage during sample treatment. The optimization study included amino acids and intermediates of the glycolysis and the TCA-cycl...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397231/ https://www.ncbi.nlm.nih.gov/pubmed/22833711 http://dx.doi.org/10.1007/s11306-011-0367-3 |
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author | de Jonge, Lodewijk P. Douma, Rutger D. Heijnen, Joseph J. van Gulik, Walter M. |
author_facet | de Jonge, Lodewijk P. Douma, Rutger D. Heijnen, Joseph J. van Gulik, Walter M. |
author_sort | de Jonge, Lodewijk P. |
collection | PubMed |
description | A sampling procedure for quantitative metabolomics in Penicillium chrysogenum based on cold aqueous methanol quenching was re-evaluated and optimized to reduce metabolite leakage during sample treatment. The optimization study included amino acids and intermediates of the glycolysis and the TCA-cycle. Metabolite leakage was found to be minimal for a methanol content of the quenching solution (QS) of 40% (v/v) while keeping the temperature of the quenched sample near −20°C. The average metabolite recovery under these conditions was 95.7% (±1.1%). Several observations support the hypothesis that metabolite leakage from quenched mycelia of P. chrysogenum occurs by diffusion over the cell membrane. First, a prolonged contact time between mycelia and the QS lead to a somewhat higher extent of leakage. Second, when suboptimal quenching liquids were used, increased metabolite leakage was found to be correlated with lower molecular weight and with lower absolute net charge. The finding that lowering the methanol content of the quenching liquid reduces metabolite leakage in P. chrysogenum contrasts with recently published quenching studies for two other eukaryotic micro-organisms. This demonstrates that it is necessary to validate and, if needed, optimize the quenching conditions for each particular micro-organism. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11306-011-0367-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-3397231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-33972312012-07-23 Optimization of cold methanol quenching for quantitative metabolomics of Penicillium chrysogenum de Jonge, Lodewijk P. Douma, Rutger D. Heijnen, Joseph J. van Gulik, Walter M. Metabolomics Original Article A sampling procedure for quantitative metabolomics in Penicillium chrysogenum based on cold aqueous methanol quenching was re-evaluated and optimized to reduce metabolite leakage during sample treatment. The optimization study included amino acids and intermediates of the glycolysis and the TCA-cycle. Metabolite leakage was found to be minimal for a methanol content of the quenching solution (QS) of 40% (v/v) while keeping the temperature of the quenched sample near −20°C. The average metabolite recovery under these conditions was 95.7% (±1.1%). Several observations support the hypothesis that metabolite leakage from quenched mycelia of P. chrysogenum occurs by diffusion over the cell membrane. First, a prolonged contact time between mycelia and the QS lead to a somewhat higher extent of leakage. Second, when suboptimal quenching liquids were used, increased metabolite leakage was found to be correlated with lower molecular weight and with lower absolute net charge. The finding that lowering the methanol content of the quenching liquid reduces metabolite leakage in P. chrysogenum contrasts with recently published quenching studies for two other eukaryotic micro-organisms. This demonstrates that it is necessary to validate and, if needed, optimize the quenching conditions for each particular micro-organism. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11306-011-0367-3) contains supplementary material, which is available to authorized users. Springer US 2011-10-07 2012 /pmc/articles/PMC3397231/ /pubmed/22833711 http://dx.doi.org/10.1007/s11306-011-0367-3 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Original Article de Jonge, Lodewijk P. Douma, Rutger D. Heijnen, Joseph J. van Gulik, Walter M. Optimization of cold methanol quenching for quantitative metabolomics of Penicillium chrysogenum |
title | Optimization of cold methanol quenching for quantitative metabolomics of Penicillium chrysogenum |
title_full | Optimization of cold methanol quenching for quantitative metabolomics of Penicillium chrysogenum |
title_fullStr | Optimization of cold methanol quenching for quantitative metabolomics of Penicillium chrysogenum |
title_full_unstemmed | Optimization of cold methanol quenching for quantitative metabolomics of Penicillium chrysogenum |
title_short | Optimization of cold methanol quenching for quantitative metabolomics of Penicillium chrysogenum |
title_sort | optimization of cold methanol quenching for quantitative metabolomics of penicillium chrysogenum |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397231/ https://www.ncbi.nlm.nih.gov/pubmed/22833711 http://dx.doi.org/10.1007/s11306-011-0367-3 |
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