Sarah Schatschneider
Quantitative isotope-dilution high-resolution-mass-apectrometry analysis of multiple intracellular metabolites in Clostridium autoethanogenum with uniformly 13C-labeled standards derived from Spirulina
Schatschneider, Sarah; Abdelrazig, Salah M.A.; Safo, Laudina; Henstra, Anne M.; Millat, Thomas; Kim, Dong-Hyun; Winzer, Klaus; Minton, Nigel P.; Barrett, David A.
Authors
Salah M.A. Abdelrazig
Laudina Safo
Anne M. Henstra
Thomas Millat
Dr DONG-HYUN KIM Dong-hyun.Kim@nottingham.ac.uk
ASSOCIATE PROFESSOR
Dr Klaus Winzer klaus.winzer@nottingham.ac.uk
ASSOCIATE PROFESSOR
Professor NIGEL MINTON NIGEL.MINTON@NOTTINGHAM.AC.UK
PROFESSOR OF APPLIED MOLECULAR MICROBIOLOGY
David A. Barrett
Abstract
We have investigated the applicability of commercially available lyophilized spirulina (Arthrospira platensis), a microorganism uniformly labeled with 13C, as a readily accessible source of multiple 13C-labeled metabolites suitable as internal standards for the quantitative determination of intracellular bacterial metabolites. Metabolites of interest were analyzed by hydrophilic-interaction liquid chromatography coupled with high-resolution mass spectrometry. Multiple internal standards obtained from uniformly (U)-13C-labeled extracts from spirulina were used to enable isotope-dilution mass spectrometry (IDMS) in the identification and quantification of intracellular metabolites. Extraction of the intracellular metabolites of Clostridium autoethanogenum using 2:1:1 chloroform/methanol/water was found to be the optimal method in comparison with freeze–thaw, homogenization, and sonication methods. The limits of quantification were ≤1 μM with excellent linearity for all of the calibration curves (R2 ≥ 0.99) for 74 metabolites. The precision and accuracy were found to be within relative standard deviations (RSDs) of 15% for 49 of the metabolites and within RSDs of 20% for all of the metabolites. The method was applied to study the effects of feeding different levels of carbon monoxide (as a carbon source) on the central metabolism and Wood–Ljungdahl pathway of C. autoethanogenum grown in continuous culture over 35 days. Using LC-IDMS with U-13C spirulina allowed the successful quantification of 52 metabolites in the samples, including amino acids, carboxylic acids, sugar phosphates, purines, and pyrimidines. The method provided absolute quantitative data on intracellular metabolites that was suitable for computational modeling to understand and optimize the C. autoethanogenum metabolic pathways active in gas fermentation.
Citation
Schatschneider, S., Abdelrazig, S. M., Safo, L., Henstra, A. M., Millat, T., Kim, D.-H., Winzer, K., Minton, N. P., & Barrett, D. A. (2018). Quantitative isotope-dilution high-resolution-mass-apectrometry analysis of multiple intracellular metabolites in Clostridium autoethanogenum with uniformly 13C-labeled standards derived from Spirulina. Analytical Chemistry, 90(7), https://doi.org/10.1021/acs.analchem.7b04758
Journal Article Type | Article |
---|---|
Acceptance Date | Mar 13, 2018 |
Online Publication Date | Mar 13, 2018 |
Publication Date | Apr 3, 2018 |
Deposit Date | Apr 10, 2018 |
Publicly Available Date | Apr 10, 2018 |
Journal | Analytical Chemistry |
Print ISSN | 0003-2700 |
Electronic ISSN | 1520-6882 |
Publisher | American Chemical Society |
Peer Reviewed | Peer Reviewed |
Volume | 90 |
Issue | 7 |
DOI | https://doi.org/10.1021/acs.analchem.7b04758 |
Keywords | Isotope dilution mass spectrometry; Spirulina; Arthrospira; Clostridia; Biofuels; Gas fermentation; Metabolites |
Public URL | https://nottingham-repository.worktribe.com/output/923485 |
Publisher URL | https://doi.org/10.1021/acs.analchem.7b04758 |
Contract Date | Apr 10, 2018 |
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Copyright Statement
Copyright information regarding this work can be found at the following address: http://creativecommons.org/licenses/by/4.0
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