SE194:/S5/M1

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Sample Set Information

ID SE194
Title LC-MS based untargeted metabolome analysis of soil samples
Description Untargeted metabolome analysis using reverse-phase liquid chromatography (LC) coupled to high-resolution mass spectrometry (MS) was conducted for comparing chemical profiles from five soil samples.
Authors Sakurai N 1,2, Mardani-Korrani H 3, Nakayasu M 4, Matsuda K 5, Ochiai K 6, Kobayashi M 6 , Tahara Y 7, Onodera T 8, Aoki Y 9, Motobayashi T 3, Komatsuzaki M 10, Ihara M 5, Shibata D 2, Fujii Y 3, Sugiyama A 4. 1 National Institute of Genetics, Mishima Japan, 2 Kazusa DNA Research Institute, Kisarazu Japan, 3 Tokyo University of Agriculture and Technology, Fuchu, Japan, 4 RISH, Kyoto University, Uji, Japan, 5 Kindai University, Nara, Japan, 6 Graduate School of Agriculture, Kyoto University, Kyoto, Japan, 7 Research and Development Center for Five-Sense Devices, Kyushu University, Fukuoka, Japan, 8 Faculty of Information Science and Electrical Engineering, Kyushu University, Fukuoka, Japan, 9 Tohoku Medical Megabank Organization, Tohoku University, Sendai, Japan, 10 Ibaraki University, Ami, Japan.
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Sample Information

ID S5
Title KUAS-R
Organism - Scientific Name
Organism - ID
Compound - ID
Compound - Source
Preparation Soil from Kyoto University of Advanced Science (KUAS) used for plant culture in a root box.
Sample Preparation Details ID
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Analytical Method Information

ID M1
Title LC-MS, ESI, Positive
Method Details ID MS1
Sample Amount 5 mg soil / 20 uL injection
Comment


Analytical Method Details Information

ID MS1
Title LC-FTICR-MS, ESI Positive
Instrument Agilent1200 HPLC (Agilent), LTQ-FT (Thermo Fisher Scientific)
Instrument Type LC-FTICR-MS
Ionization ESI
Ion Mode Positive
Description - Extraction

Frozen soil sample (300 mg) was extracted with 900 µL of methanol containing 25 µM of 7-hydroxy-5-methylflavone as an internal standard. After homogenizing the samples by mixing twice for 2 min each time using a Mixer Mill MM 300 (QIAGEN K.K., Tokyo, Japan) at 25 Hz, the homogenates were centrifuged (17,400 xg for 5 min at 4C). After recovery of the supernatant from each homogenate, it was filtered through a 0.2-µm polytetrafluoroethylene (PTFE) membrane (Millipore). Hydrophobic compounds in the filtrate were removed by absorption to a C18 silica column (MonoSpin C18, GL Science, Tokyo, Japan). The eluate was used for the untargeted metabolome analysis using LC-MS. Mock samples were prepared as above without adding the soil materials.

- LC-MS

The untargeted metabolome analysis was performed using an Agilent 1100 system (Agilent, Palo Alto, CA) coupled to a Finnigan LTQ-FT (Thermo Fisher Scientific). An aliquot (20 µL) of a methanol solution was applied to a TSK-gel column ODS-100V (4.6 x 250 mm, 5 µm; TOSOH Corporation, Tokyo, Japan). Water (HPLC grade; solvent A) and acetonitrile (HPLC grade; solvent B) were used as the mobile phase with 0.1% v/v formic acid added to both solvents. The gradient program was as follows: 3% B (0 min), 97% B (90 min), 97% B (100 min), 3% B (100.1 min) and 3% B (107 min). The flow rate was set to 0.25 mL/min (0–100 min) and 0.5 mL/min (100.1–107 min). The column oven temperature was set to 40C. The mass range was m/z 100–1500. The electrospray-ionization (ESI) settings were a spray voltage of 4.0 kV and capillary temperature of 300 °C. The nitrogen sheath gas and auxiliary gas were set at 40 and 15 arbitrary units, respectively. The MSn analysis was performed with ESI positive mode as follows: Full mass scan with FT-ICR at a resolution of 100,000 and a mass scan range 100-1500, and MS2 scans by collision-induced dissociation for the most intense five ions of the full mass scan with ion trap (IT). To monitor the HPLC eluate, a photodiode array detector was used with a wavelength range of 200–650 nm. Data were acquired and browsed using Xcalibur software version 2.0.7 (Thermo Fisher Scientific).

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