2019
DOI: 10.3390/metabo9040068
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Drying Enhances Signal Intensities for Global GC–MS Metabolomics

Abstract: We report here that a straightforward change of the standard derivatization procedure for GC–MS metabolomics is leading to a strong increase in metabolite signal intensity. Drying samples between methoxymation and trimethylsilylation significantly increased signals by two- to tenfold in extracts of yeast cells, plant and animal tissue, and human urine. This easy step reduces the cost of sample material and the need for expensive new hardware.

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Cited by 15 publications
(11 citation statements)
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“…These steps break apart the salt crystals and release water into the toluene to enhance salt drying and metabolite extraction. Finally, following a recently described method for improving GC-MS metabolite detection regardless of sample type (33), we included an additional step between the methoximation and trimethylsilylation derivatization reactions and evaporated the first derivatization reagent under N 2 gas (see Fig. 1B for total signal improvements of each step for the metabolite mixture).…”
Section: Resultsmentioning
confidence: 99%
“…These steps break apart the salt crystals and release water into the toluene to enhance salt drying and metabolite extraction. Finally, following a recently described method for improving GC-MS metabolite detection regardless of sample type (33), we included an additional step between the methoximation and trimethylsilylation derivatization reactions and evaporated the first derivatization reagent under N 2 gas (see Fig. 1B for total signal improvements of each step for the metabolite mixture).…”
Section: Resultsmentioning
confidence: 99%
“…Metabolite derivatization was performed by adding 80 µL of methoxyamine hydrochloride dissolved in pyridine (20 mg mL -1 ) to the dried pellet and incubating for 90 min at 37 °C using a thermal rotating incubator under constant rotation at 1350 rpm. Following recent advancements in signal improvement 58 , the pyridine was removed from the sample at room temperature under a gentle flow of N 2 gas (approximately 1 hour). Following the addition of 100 µL of N,O-B is(trimethylsilyl)trifluoroacetamide, each extract was vortexed, and incubated for another 30 min at 37 °C using a thermal rotating incubator under constant rotation at 1350 rpm.…”
Section: Methodsmentioning
confidence: 99%
“…This feature makes the identification of unknown compounds in GC-MS more straightforward than the LC-MS approach. Nonetheless, GC-MS can only be used to analyze volatile compounds; thus, a derivatization step is often necessary during the analysis of key metabolites, such as amino acids, sugars, and fatty acids [ 59 , 60 ].…”
Section: Application Of Metabolomics In the Study Of Biological Responses To Environmental Toxicantsmentioning
confidence: 99%
“…In addition to the HILIC approach, GC-MS analysis with derivatization has long been the preferred method for the analysis of polar primary metabolites. Amino acids and carbohydrates have also been analyzed using various silylation agents, when methylation agents are often preferred for the analysis of fatty acids [ 59 , 81 , 89 ]. Furthermore, metabolites that can be analyzed via GC-MS are often involved in key metabolic pathways related to energy production, such as glycolysis, TCA cycle, and free fatty acid metabolism, in model organisms [ 90 , 91 ].…”
Section: Metabolomics Workflowmentioning
confidence: 99%