Sample Set Information
ID
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SE42
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Title
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Metabolic profiling of flavonoids in Lotus japonicus
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Description
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Metabolic profiling of flavonoids in leaf, stem, flower of Lotus japonicus Miyakojima MG-20 and Gifu B-129.
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Authors
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Hideyuki Suzuki 1, Ryosuke Sasaki 1, Yoshiyuki Ogata 1, Yukiko Nakamura 2 4, Nozomu Sakurai 1, Mariko Kitajima 3, Hiromitsu Takayama 3, Shigehiko Kanaya 2, Koh Aoki 1, Daisuke Shibata 1, Kazuki Saito 3, 1: Kazusa DNA Research Institute, 2: Nara Institute of Science and Technology, 3: hiba University, 4: Ehime Women’s College
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Reference
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Phytochemistry, 2008, 69(1), 99-111
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Comment
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Seed coats of L. japonicus were scratched by glass paper and fed water for 1 d. The seedlings were transferred to a mixture of vermiculite and a commercial soil, Powersoil (mix ratio 1.3–1, Kureha Chemical Ind., Tokyo, Japan, and Kanto Hiryou Ind., Saitama, Japan), and grown for 90–120 days (from March to June) in 2005, in a greenhouse under natural sunlight. From 7-day-old plants, cotyledons and hypocotyls were collected separately and served as leaf and stem samples, respectively. From 14-, 21-, 30-, 60, and 90-day-old plants, leaves and stems were collected. The tissues for one experimental replicate were collected from 12 independent plants for 7-, 14-, and 21-day-old stages, or from one independent plant for 30-, 60-, and 90-day-old stages.
|
The web resources and information related to the species used in this study are available at Plant Genome Database Japan (PGDBj).
http://pgdbj.jp/plantdb/plantinfo.html?ln=en&cmd=entry&ppid=t34305
Sample Information
ID
|
S03
|
Title
|
Lotus japonicus B-129 stem
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Organism - Scientific Name
|
Lotus japonicus
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Organism - ID
|
NCBI taxonomy:34305
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Compound - ID
|
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Compound - Source
|
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Preparation
|
|
Sample Preparation Details ID
|
SS1
|
Comment
|
|
Sample Preparation Details Information
ID
|
SS1
|
Title
|
Growth condition
|
Description
|
Seed coats of L. japonicus were scratched by glass paper and fed water for 1 d. The seedlings were transferred to a mixture of vermiculite and a commercial soil, Powersoil (mix ratio 1.3–1, Kureha Chemical Ind., Tokyo, Japan, and Kanto Hiryou Ind., Saitama, Japan), and grown for 90–120 days (from March to June) in 2005, in a greenhouse under natural sunlight. From 7-day-old plants, cotyledons and hypocotyls were collected separately and served as leaf and stem samples, respectively. From 14-, 21-, 30-, 60, and 90-day-old plants, leaves and stems were collected. The tissues for one experimental replicate were collected from 12 independent plants for 7-, 14-, and 21-day-old stages, or from one independent plant for 30-, 60-, and 90-day-old stages.
|
Comment_of_details
|
|
Analytical Method Details Information
ID
|
MS3
|
Title
|
LC-FT-ICR-MS ESI positive method 3
|
Instrument
|
Agilent1100 HPLC (Agilent), LTQ-FT (Thermo Fisher Scientific)
|
Instrument Type
|
LC-FTICR-MS
|
Ionization
|
ESI
|
Ion Mode
|
Positive
|
Description
|
Harvested sample is frozen by liquid N2 and resulting powder (100mg) are solved in 300uL 80% methanol solution. 20uL sample is injected into HPLC after 0.2um membrane filter treatment. HPLC conditions: Agilent 1100 series (Agilent), Column: TSKgel-100V (4.6 x 250 mm, 5 micrometer; TOSOH), Solvent: A; 0.1% formic acid aq. B; ACN (addition 0.1% formic acid fc.), Gradient: (B);3 to 42% (0.0 to 45.0 min), 42 to 95% (45.0 to 45.1 min), 95% (45.1 to 50.0 min), 3% (50.1 to 57.0 min), Column temp.: 30 degree C, Flow rate=0.5mL/min, PDA: 200-650 nm (2 nm step). FT-ICR-MS conditions: Filter 1: FTMS + c norm !corona !pi o(200.0-1500.0);2: ITMS + c norm !corona !pi o(200.0-1500.0);3: ITMS + c norm !corona !pi Dep MS/MS Most intense ion from (2). Rejected mass=143.00;145.00;171.00;173.00;198.00;199.00;235.00;271.50;376.00;391.00;609.00;810.50;1105.50.
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Comment_of_details
|
MTLC0364
|
Data Analysis Information
ID
|
D01
|
Title
|
PowerGet data analysis
|
Data Analysis Details ID
|
DS1
|
Recommended decimal places of m/z
|
6|ITMS 2
|
Comment
|
|
Data Analysis Details Information
ID
|
DS1
|
Title
|
PowerGet analysis for annotation of peaks
|
Description
|
Raw data files are converted to text file by MSGet software without cut off value and peaks are extracted from the text files by PowerFT. The replicates data are aligned by PowerMatch with blank data. The alignment is manually edited. Assigned peaks observed in multiple replicate samples are selected for annotation process.
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Comment_of_details
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