TY - JOUR
T1 - Quantitative metabolomics of the thermophilic methylotroph Bacillus methanolicus
AU - Carnicer, Marc
AU - Vieira, Gilles
AU - Brautaset, Trygve
AU - Portais, Jean Charles
AU - Heux, Stephanie
N1 - Funding Information:
The authors are grateful to Serguei Sokol and Fabien Letisse for critical discus‑ sions and suggestions. MetaToul (Metabolomics & Fluxomics Facitilies, Tou‑ louse, France, http://www.metatoul.fr) and its staff members Edern Cahoreau, Lara Gales, Lindsay Peyriga and Hanna Barbier are gratefully acknowledged for technical support and access to mass spectrometry facilities. MetaToul is part of the national infrastructure MetaboHUB‑ANR‑11‑INBS‑0010 (The French National infrastructure for metabolomics and fluxomics, http://www.metabo‑ hub.fr). MetaToul is supported by grants from the Région Midi‑Pyrénées, the European Regional Development Fund, SICOVAL, the Infrastructures en Biologie Sante et Agronomie (IBiSa, France), the Centre National de la Recherche Scienti-fique (CNRS) and the Institut National de la Recherche Agronomique (INRA). This work was funded by PROMYSE European project (FP7‑KBBE‑2011‑3‑6‑04).
Publisher Copyright:
© 2016 The Author(s).
PY - 2016/6/1
Y1 - 2016/6/1
N2 - Background: The gram-positive bacterium Bacillus methanolicus MGA3 is a promising candidate for methanol-based biotechnologies. Accurate determination of intracellular metabolites is crucial for engineering this bacteria into an efficient microbial cell factory. Due to the diversity of chemical and cell properties, an experimental protocol validated on B. methanolicus is needed. Here a systematic evaluation of different techniques for establishing a reliable basis for metabolome investigations is presented. Results: Metabolome analysis was focused on metabolites closely linked with B. methanolicus central methanol metabolism. As an alternative to cold solvent based procedures, a solvent-free quenching strategy using stainless steel beads cooled to 20 °C was assessed. The precision, the consistency of the measurements, and the extent of metabolite leakage from quenched cells were evaluated in procedures with and without cell separation. The most accurate and reliable performance was provided by the method without cell separation, as significant metabolite leakage occurred in the procedures based on fast filtration. As a biological test case, the best protocol was used to assess the metabolome of B. methanolicus grown in chemostat on methanol at two different growth rates and its validity was demonstrated. Conclusion: The presented protocol is a first and helpful step towards developing reliable metabolomics data for thermophilic methylotroph B. methanolicus. This will definitely help for designing an efficient methylotrophic cell factory.
AB - Background: The gram-positive bacterium Bacillus methanolicus MGA3 is a promising candidate for methanol-based biotechnologies. Accurate determination of intracellular metabolites is crucial for engineering this bacteria into an efficient microbial cell factory. Due to the diversity of chemical and cell properties, an experimental protocol validated on B. methanolicus is needed. Here a systematic evaluation of different techniques for establishing a reliable basis for metabolome investigations is presented. Results: Metabolome analysis was focused on metabolites closely linked with B. methanolicus central methanol metabolism. As an alternative to cold solvent based procedures, a solvent-free quenching strategy using stainless steel beads cooled to 20 °C was assessed. The precision, the consistency of the measurements, and the extent of metabolite leakage from quenched cells were evaluated in procedures with and without cell separation. The most accurate and reliable performance was provided by the method without cell separation, as significant metabolite leakage occurred in the procedures based on fast filtration. As a biological test case, the best protocol was used to assess the metabolome of B. methanolicus grown in chemostat on methanol at two different growth rates and its validity was demonstrated. Conclusion: The presented protocol is a first and helpful step towards developing reliable metabolomics data for thermophilic methylotroph B. methanolicus. This will definitely help for designing an efficient methylotrophic cell factory.
KW - Bacillus methanolicus
KW - Methanol
KW - Quantitative metabolomics
KW - Quenching
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U2 - 10.1186/s12934-016-0483-x
DO - 10.1186/s12934-016-0483-x
M3 - Article
C2 - 27251037
AN - SCOPUS:84971439930
SN - 1475-2859
VL - 15
JO - Microbial Cell Factories
JF - Microbial Cell Factories
IS - 1
M1 - 92
ER -