- 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 3 Reference Ions Near m/z 357.0559
NovoCell ID | m/z | Mass Window | Metabolite | Ranking | Anatomy Context |
---|---|---|---|---|---|
MSI_000007646 Reliable | 357.0559 | 357.0557 ~ 357.056 MzDiff: 1.1 ppm |
Glycerophosphoinositol (BioDeep_00000004622) Formula: C9H19O11P (334.0665) |
5.17 (100%) | Rattus norvegicus [UBERON:0004359] corpus epididymis |
MSI_000008265 Reliable | 357.0559 | 357.0557 ~ 357.056 MzDiff: 1.1 ppm |
Glycerophosphoinositol (BioDeep_00000004622) Formula: C9H19O11P (334.0665) |
12.96 (100%) | Rattus norvegicus [UBERON:0004360] cauda epididymis |
MSI_000017971 Unreliable | 357.058 | 357.058 ~ 357.058 MzDiff: 0.0 ppm |
Demethyltorosaflavone D (BioDeep_00000267747) Formula: C18H12O8 (356.0532) |
0.83 (100%) | Vitis vinifera [PO:0009087] mesocarp |
Found 17 Sample Hits
Metabolite | Species | Sample | |
---|---|---|---|
Demethyltorosaflavone D Formula: C18H12O8 (356.0532) Adducts: [M+H]+ (Ppm: 7) |
Vitis vinifera (Fruit) |
grape_dhb_91_1Resolution: 50μm, 120x114
Grape berries fruit, condition: Ripe |
|
Glycerophosphoinositol Formula: C9H19O11P (334.0665) Adducts: [M+Na]+ (Ppm: 0) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito03_17Resolution: 17μm, 208x108
1 male adult wild-type rat was obtained from Inserm U1085 - Irset Research Institute (University of Rennes1, France). Animals were age 60 days and were reared under ad-lib conditions. Care and handling of all animals complied with EU directive 2010/63/EU on the protection of animals used for scientific purposes. The whole epididymis was excised from each animal immediately post-mortem, loosely wrapped rapidly in an aluminum foil and a 2.5% (w/v) carboxymethylcellulose (CMC) solution was poured to embed the epididymis to preserve their morphology. To remove air bubbles, the filled aluminum molds was gently freezed by depositing it on isopentane or dry ice, then on the nitrogen vapors and finally by progressively dipping the CMC/sample coated with aluminum foil into liquid nitrogen (or only flush with liquid nitrogen). Frozen tissues were stored at -80 °C until use to avoid degradation. |
|
Glycerophosphoinositol Formula: C9H19O11P (334.0665) Adducts: [M+Na]+ (Ppm: 0) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito03_18Resolution: 17μm, 208x104
|
|
Glycerophosphoinositol Formula: C9H19O11P (334.0665) Adducts: [M+Na]+ (Ppm: 0.2) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito08_43Resolution: 17μm, 298x106
|
|
Glycerophosphoinositol Formula: C9H19O11P (334.0665) Adducts: [M+Na]+ (Ppm: 0.2) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito08_44Resolution: 17μm, 299x111
|
|
Glycerophosphoinositol Formula: C9H19O11P (334.0665) Adducts: [M+Na]+ (Ppm: 0.5) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito08_46Resolution: 17μm, 298x106
|
|
Demethyltorosaflavone D Formula: C18H12O8 (356.0532) Adducts: [M+H]+ (Ppm: 7) |
Vitis vinifera (Fruit) |
grape_dhb_164_1Resolution: 17μm, 136x122
Grape berries fruit, condition: Late |
|
Demethyltorosaflavone D Formula: C18H12O8 (356.0532) Adducts: [M+H]+ (Ppm: 7.3) |
Vitis vinifera (Fruit) |
grape_dhb_163_1Resolution: 17μm, 132x115
Grape berries fruit, condition: Late |
|
Glycerophosphoinositol Formula: C9H19O11P (334.0665) Adducts: [M+Na]+ (Ppm: 0.5) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito08_47Resolution: 17μm, 301x111
|
|
Glycerophosphoinositol Formula: C9H19O11P (334.0665) Adducts: [M+Na]+ (Ppm: 0.8) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito08_48Resolution: 17μm, 294x107
|
|
Glycerophosphoinositol Formula: C9H19O11P (334.0665) Adducts: [M+Na]+ (Ppm: 0.5) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito01_04Resolution: 17μm, 178x91
|
|
Glycerophosphoinositol Formula: C9H19O11P (334.0665) Adducts: [M+Na]+ (Ppm: 0.5) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito01_03Resolution: 17μm, 159x110
|
|
Glycerophosphoinositol Formula: C9H19O11P (334.0665) Adducts: [M+Na]+ (Ppm: 0.2) |
Rattus norvegicus (normal) |
epik_dhb_head_ito01_05Resolution: 17μm, 183x105
|
|
Glycerophosphoinositol Formula: C9H19O11P (334.0665) Adducts: [M+Na]+ (Ppm: 0.2) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito01_06Resolution: 17μm, 183x103
|
|
Glycerophosphoinositol Formula: C9H19O11P (334.0665) Adducts: [M+Na]+ (Ppm: 0.5) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito03_14Resolution: 17μm, 205x103
|
|
Demethyltorosaflavone D Formula: C18H12O8 (356.0532) Adducts: [M+H]+ (Ppm: 7.5) |
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. |
|
Demethyltorosaflavone D Formula: C18H12O8 (356.0532) Adducts: [M+H]+ (Ppm: 6.4) |
Posidonia oceanica (root) |
MS1_20180404_PO_1200Resolution: 17μm, 193x208
|
|