SE163:/S1/M1/D1
From Metabolonote
Sample Set Information
ID | TSE1325 |
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Title | Arabidopsis bile acid:sodium symporter family protein 5 is involved in methionine-derived glucosinolate biosynthesis. |
Description | Glucosinolates (GSLs) are a group of plant secondary metabolites that have repellent activity against herbivore insects and pathogens, and anti-carcinogenic activity in humans. They are produced in plants of the Brassicaceae and other related families. Biosynthesis of GSLs from precursor amino acids takes place in two subcellular compartments; amino acid biosynthesis and side chain elongation occur mainly in the chloroplast, whereas the following core structure synthesis takes place in the cytosol. Although the genes encoding biosynthetic enzymes of GSLs are well known in Arabidopsis thaliana, the transporter genes responsible for translocation of biosynthetic intermediates between the chloroplast and cytosol are as yet unidentified. In this study, we identified the bile acid:sodium symporter family protein 5 (BASS5) gene in Arabidopsis as a candidate transporter gene involved in methionine-derived GSL (Met-GSL) biosynthesis by means of transcriptome co-expression analysis. Knocking out BASS5 resulted in a decrease of Met-GSLs and concomitant increase of methionine. A transient assay using fluorescence fusion proteins indicated a chloroplastic localization of BASS5. These results supported the idea that BASS5 plays a role in translocation across the chloroplast membranes of the biosynthetic intermediates of Met-GSLs. |
Authors | Sawada Y, Toyooka K, Kuwahara A, Sakata A, Nagano M, Saito K, Hirai MY. |
Reference | Plant Cell Physiol. 2009 Sep;50(9):1579-86. doi: 10.1093/pcp/pcp110. Epub 2009 Jul 24. |
Comment |
Sample Information
ID | S1 |
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Title | Arabidopsis thaliana |
Organism - Scientific Name | Arabidopsis thaliana |
Organism - ID | NCBI taxonomy:3702 |
Compound - ID | |
Compound - Source | |
Preparation | Plant growth conditions Wild-type A. thaliana (accession Colombia-0) and T-DNA insertion lines were grown in a pre-fabricated room-type chamber at 22°C and a 16 h photoperiod on agar-solidified 1/2 MS (Murashige–Skoog) medium containing 1% sucrose for transcriptome and metabolome analyses. |
Sample Preparation Details ID | |
Comment |
Analytical Method Information
ID | M1 |
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Title | LC-MS |
Method Details ID | MS1 |
Sample Amount | 1 μL |
Comment |
Analytical Method Details Information
ID | MS1 |
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Title | LC-MS (for widely targeted metabolomics) |
Instrument | UPLC-TQD system (Waters) |
Instrument Type | |
Ionization | ESI |
Ion Mode | positive and negative |
Description | Approximately 50–100 mg of the leaves of wild-type and T-DNA insertion lines (bass5-1 and bass5-2) 3 weeks after germination were used for metabolic profiling with ultra performance liquid chromatography (UPLC)-ZQ (Waters) (for GSL and amino acid analyses) and UPLC-TQD (Waters) (for widely targeted metabolomics) as previously described (Sawada et al. 2009a, Sawada et al. 2009b). Met-GSL and tryptophan-derived indole-GSL are the two major GSL classes of Arabidopsis. The sum of the contents of Met-GSL molecular species (methylthioalkyl and methylsulfinylalkyl GSLs with C4–C8 chains) was indicated as Met-GSL content in Fig. 3C. Similarly, the sum of the contents of indole-GSL molecular species (indol-3-ylmethyl, 1-methoxyindol-3- ylmethyl and 4-methoxyindol-3-ylmethyl GSLs) was indicated as indole-GSL content. Analytical conditions for UPLC-TQD are released in the data repository and distribution site DROP Met at our website PRIMe (http://prime.psc.riken.jp/) (Akiyama et al. 2008). |
Comment_of_details |
Data Analysis Information
ID | D1 |
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Title | Data Processing |
Data Analysis Details ID | DS1 |
Recommended decimal places of m/z | |
Comment |
Data Analysis Details Information
ID | DS1 |
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Title | Data processing |
Description | The metabolites whose accumulation levels changed remarkably (fold change >2 or <0.5, Q-value by the Welch’s t-test <0.1) were identified (Table 1). Q-values were calculated with the ‘qvalue’ package (Storey and Tibshirani 2003) in R (www.r-project.org). |
Comment_of_details |