4.4 Article

Chemometric evaluation of Saccharomyces cerevisiae metabolic profiles using LC-MS

Journal

METABOLOMICS
Volume 11, Issue 1, Pages 210-224

Publisher

SPRINGER
DOI: 10.1007/s11306-014-0689-z

Keywords

Metabolic profiling; Untargeted metabolomics; Metabolite identification; Saccharomyces cerevisiae; Multivariate curve resolution-alternating least squares; Partial least squares-discriminant analysis; Liquid chromatography-mass spectrometry

Funding

  1. European Research Council under the European Union's Seventh Framework Programme (FP)/ERC [32073]

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A new liquid chromatography mass spectrometry (LC-MS) metabolomics strategy coupled to chemometric evaluation, including variable and biomarker selection, has been assessed as a tool to discriminate between control and stressed Saccharomyces cerevisiae yeast samples. Metabolic changes occurring during yeast culture at different temperatures (30 and 42 A degrees C) were analysed and the complex data generated in profiling experiments were evaluated by different chemometric multivariate approaches. Multivariate curve resolution alternating least squares (MCR-ALS) was applied to full spectral scan LC-MS preprocessed data multisets arranged in augmented column-wise data matrices. The results showed that sectioning the MS-chromatograms in different windows and analysing them by MCR-ALS enabled the proper resolution of very complex coeluted chromatographic peaks. The investigation of possible relationships between MCR-ALS resolved chromatographic peak areas and culture temperature was then investigated by partial least squares discriminant analysis (PLS-DA). Selection of most relevant resolved chromatographic peaks associated to yeast culture temperature changes was achieved according to PLS-DA-Variable Importance in Projection scores. A metabolite identification workflow was developed utilizing MCR-ALS resolved pure MS spectra and high-resolution accurate mass measurements to confirm assigned structures based on entries in metabolite databases. A total of 65 metabolites were identified. A preliminary interpretation of these results indicates that the strategy described in this study can be proposed as a general tool to facilitate biomarker identification and modelling in similar untargeted metabolomic studies.

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