- Confirmed: 这个参考离子已经通过手动审计得到确认和验证。
- Reliable: 这个参考离子可能在特定的解剖组织环境中高度保守。
- Unreliable: 这个参考离子具有较高的排名价值,但缺乏可重复性。
- Unavailable: 由于排名价值低且缺乏可重复性,这个参考离子不应用于注释。
Found 6 Reference Ions Near m/z 356.0321
NovoCell ID | m/z | Mass Window | Metabolite | Ranking | Anatomy Context |
---|---|---|---|---|---|
MSI_000018212 Reliable | 356.0321 | 356.032 ~ 356.0321 MzDiff: 0.2 ppm |
Chebulic_acid (BioDeep_00000396672) Formula: C14H12O11 (356.038) |
0.23 (57%) | Vitis vinifera [PO:0009087] mesocarp |
MSI_000036465 Unreliable | 356.029 | 356.029 ~ 356.029 MzDiff: none |
[({[(2s,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}(hydroxy)methylidene)amino]acetic acid (BioDeep_00002221346) Formula: C10H18AsNO8 (355.0248) |
1.33 (100%) | Posidonia oceanica [PO:0005352] xylem |
MSI_000012404 Unreliable | 356.0291 | 356.0291 ~ 356.0291 MzDiff: none |
[({[(2s,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}(hydroxy)methylidene)amino]acetic acid (BioDeep_00002221346) Formula: C10H18AsNO8 (355.0248) |
1.23 (100%) | Plant [PO:0005020] vascular bundle |
MSI_000014192 Unavailable | 356.0291 | 356.0291 ~ 356.0291 MzDiff: none |
[({[(2s,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}(hydroxy)methylidene)amino]acetic acid (BioDeep_00002221346) Formula: C10H18AsNO8 (355.0248) |
-0.39 (100%) | Plant [PO:0005417] phloem |
MSI_000018894 Unreliable | 356.0291 | 356.0291 ~ 356.0291 MzDiff: none |
[({[(2s,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}(hydroxy)methylidene)amino]acetic acid (BioDeep_00002221346) Formula: C10H18AsNO8 (355.0248) |
0.9 (100%) | Plant [PO:0020124] root stele |
MSI_000039660 Unreliable | 356.0293 | 356.0293 ~ 356.0293 MzDiff: none |
[({[(2s,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}(hydroxy)methylidene)amino]acetic acid (BioDeep_00002221346) Formula: C10H18AsNO8 (355.0248) |
2.08 (100%) | Posidonia oceanica [PO:0005417] phloem |
Found 7 Sample Hits
Metabolite | Species | Sample | |
---|---|---|---|
[({[(2s,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}(hydroxy)methylidene)amino]acetic acid Formula: C10H18AsNO8 (355.0248) Adducts: [M+H]+ (Ppm: 8.5) |
Plant (Root) |
MPIMM_035_QE_P_PO_6pmResolution: 30μm, 165x170
|
|
[({[(2s,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}(hydroxy)methylidene)amino]acetic acid Formula: C10H18AsNO8 (355.0248) Adducts: [M+H]+ (Ppm: 0.3) |
Vitis vinifera (Fruit) |
grape_dhb_91_1Resolution: 50μm, 120x114
Grape berries fruit, condition: Ripe |
|
Chebulic_acid Formula: C14H12O11 (356.038) Adducts: [M]+ (Ppm: 15.5) |
Vitis vinifera (Fruit) |
grape_dhb_164_1Resolution: 17μm, 136x122
Grape berries fruit, condition: Late |
|
Chebulic_acid Formula: C14H12O11 (356.038) Adducts: [M]+ (Ppm: 14.9) |
Vitis vinifera (Fruit) |
grape_dhb_163_1Resolution: 17μm, 132x115
Grape berries fruit, condition: Late |
|
Fenoxaprop Formula: C16H12ClNO5 (333.0404) Adducts: [M+Na]+ (Ppm: 8.8) |
Mus musculus (Lung) |
image2Resolution: 40μm, 550x256
Supplementary Figure S6. Ion distribution images for (a) [PC36:4+Na]+ (m/z 804.5514) and (b)
[PC38:6+Na]+ (m/z 828.5515) obtained from mouse lung tissue collected 6 h after administration of D9-
choline and U13C-DPPC–containing CHF5633. Parts-per-million (ppm) mass errors are indicated in
parentheses. (c) Magnification of the boxed region in (a) with selected bronchiolar regions outlined in
white boxes. (d) The corresponding H&E-stained tissue section with the same selected bronchiolar
regions outlined in black boxes. These data demonstrate the co-localisation of the polyunsaturated lipids
PC36:4 and PC38:6 with the bronchiolar regions of the lung. All MSI images were visualised using
total ion current normalisation and hotspot removal (high quantile = 99%). |
|
[({[(2s,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}(hydroxy)methylidene)amino]acetic acid Formula: C10H18AsNO8 (355.0248) Adducts: [M+H]+ (Ppm: 8.7) |
Posidonia oceanica (root) |
20190822_MS1_A19r-19Resolution: 17μm, 303x309
Seagrasses are among the most efficient sinks of carbon dioxide on Earth. While carbon sequestration in terrestrial plants is linked to the microorganisms living in their soils, the interactions of seagrasses with their rhizospheres are poorly understood. Here, we show that the seagrass, Posidonia oceanica excretes sugars, mainly sucrose, into its rhizosphere. These sugars accumulate to µM concentrations—nearly 80 times higher than previously observed in marine environments. This finding is unexpected as sugars are readily consumed by microorganisms. Our experiments indicated that under low oxygen conditions, phenolic compounds from P. oceanica inhibited microbial consumption of sucrose. Analyses of the rhizosphere community revealed that many microbes had the genes for degrading sucrose but these were only expressed by a few taxa that also expressed genes for degrading phenolics. Given that we observed high sucrose concentrations underneath three other species of marine plants, we predict that the presence of plant-produced phenolics under low oxygen conditions allows the accumulation of labile molecules across aquatic rhizospheres. |
|
[({[(2s,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}(hydroxy)methylidene)amino]acetic acid Formula: C10H18AsNO8 (355.0248) Adducts: [M+H]+ (Ppm: 7.9) |
Posidonia oceanica (root) |
MS1_20180404_PO_1200Resolution: 17μm, 193x208
|
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