- 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 515.0354
NovoCell ID | m/z | Mass Window | Metabolite | Ranking | Anatomy Context |
---|---|---|---|---|---|
MSI_000053838 Reliable | 515.0354 | 515.0351 ~ 515.0356 MzDiff: 2.0 ppm |
[14-hydroxy-7-methoxy-3,10-dioxo-13-(sulfooxy)-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl]oxidanesulfonic acid (BioDeep_00002294449) Formula: C15H8O14S2 (475.9356) |
4.18 (100%) | MALDI - CHCA [NOVOCELL:BACKGROUND] blank |
MSI_000016710 Unreliable | 515.0372 | 515.0371 ~ 515.0372 MzDiff: 0.2 ppm |
UDP-L-rhamnose (BioDeep_00000003571) Formula: C15H24N2O16P2 (550.0601) |
0.18 (50%) | Vitis vinifera [PO:0009086] endocarp |
MSI_000013530 Unreliable | 515.0371 | 515.0371 ~ 515.0371 MzDiff: none |
2-Deoxy-5-hydroxymethylcytidine-5-triphosphate (BioDeep_00000008457) Formula: C10H18N3O14P3 (497.0002) |
0.86 (100%) | Plant [PO:0005417] phloem |
MSI_000018844 Unreliable | 515.0371 | 515.0371 ~ 515.0371 MzDiff: none |
2-Deoxy-5-hydroxymethylcytidine-5-triphosphate (BioDeep_00000008457) Formula: C10H18N3O14P3 (497.0002) |
1.16 (100%) | Plant [PO:0020124] root stele |
MSI_000019684 Unavailable | 515.0371 | 515.0371 ~ 515.0371 MzDiff: none |
2-Deoxy-5-hydroxymethylcytidine-5-triphosphate (BioDeep_00000008457) Formula: C10H18N3O14P3 (497.0002) |
-0.14 (100%) | Plant [PO:0025197] stele |
MSI_000040239 Unavailable | 515.0352 | 515.0352 ~ 515.0352 MzDiff: none |
[14-hydroxy-7-methoxy-3,10-dioxo-13-(sulfooxy)-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl]oxidanesulfonic acid (BioDeep_00002294449) Formula: C15H8O14S2 (475.9356) |
-0.1 (100%) | Posidonia oceanica [PO:0005417] phloem |
Found 10 Sample Hits
Metabolite | Species | Sample | |
---|---|---|---|
2-Deoxy-5-hydroxymethylcytidine-5-triphosphate Formula: C10H18N3O14P3 (497.0002) Adducts: [M+NH4]+ (Ppm: 6) |
Plant (Root) |
MPIMM_035_QE_P_PO_6pmResolution: 30μm, 165x170
|
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UDP-L-rhamnose Formula: C15H24N2O16P2 (550.0601) Adducts: [M+H-2H2O]+ (Ppm: 17.6) |
Vitis vinifera (Fruit) |
grape_dhb_91_1Resolution: 50μm, 120x114
Grape berries fruit, condition: Ripe |
|
[14-hydroxy-7-methoxy-3,10-dioxo-13-(sulfooxy)-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl]oxidanesulfonic acid Formula: C15H8O14S2 (475.9356) Adducts: [M+K]+ (Ppm: 7.4) |
Vitis vinifera (Fruit) |
grape_dhb_164_1Resolution: 17μm, 136x122
Grape berries fruit, condition: Late |
|
UDP-L-rhamnose Formula: C15H24N2O16P2 (550.0601) Adducts: [M+H-2H2O]+ (Ppm: 17.8) |
Vitis vinifera (Fruit) |
grape_dhb_163_1Resolution: 17μm, 132x115
Grape berries fruit, condition: Late |
|
[14-hydroxy-7-methoxy-3,10-dioxo-13-(sulfooxy)-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl]oxidanesulfonic acid Formula: C15H8O14S2 (475.9356) Adducts: [M+K]+ (Ppm: 4.5) |
Posidonia oceanica (root) |
20190614_MS1_A19r-20Resolution: 17μm, 262x276
Seagrasses are one of the most efficient natural sinks of carbon dioxide (CO2) on Earth. Despite covering less than 0.1% of coastal regions, they have the capacity to bury up to 10% of marine organic matter and can bury the same amount of carbon 35 times faster than tropical rainforests. On land, the soil’s ability to sequestrate carbon is intimately linked to microbial metabolism. Despite the growing attention to the link between plant production, microbial communities, and the carbon cycle in terrestrial ecosystems, these processes remain enigmatic in the sea. Here, we show that seagrasses excrete organic sugars, namely in the form of sucrose, into their rhizospheres. Surprisingly, the microbial communities living underneath meadows do not fully use this sugar stock in their metabolism. Instead, sucrose piles up in the sediments to mM concentrations underneath multiple types of seagrass meadows. Sediment incubation experiments show that microbial communities living underneath a meadow use sucrose at low metabolic rates. Our metagenomic analyses revealed that the distinct community of microorganisms occurring underneath meadows is limited in their ability to degrade simple sugars, which allows these compounds to persist in the environment over relatively long periods of time. Our findings reveal how seagrasses form blue carbon stocks despite the relatively small area they occupy. Unfortunately, anthropogenic disturbances are threatening the long-term persistence of seagrass meadows. Given that these sediments contain a large stock of sugars that heterotopic bacteria can degrade, it is even more important to protect these ecosystems from degradation. |
|
[14-hydroxy-7-methoxy-3,10-dioxo-13-(sulfooxy)-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl]oxidanesulfonic acid Formula: C15H8O14S2 (475.9356) Adducts: [M+K]+ (Ppm: 3.5) |
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. |
|
[14-hydroxy-7-methoxy-3,10-dioxo-13-(sulfooxy)-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl]oxidanesulfonic acid Formula: C15H8O14S2 (475.9356) Adducts: [M+K]+ (Ppm: 3.7) |
Posidonia oceanica (root) |
MS1_20180404_PO_1200Resolution: 17μm, 193x208
|
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2-Deoxy-5-hydroxymethylcytidine-5-triphosphate Formula: C10H18N3O14P3 (497.0002) Adducts: [M+NH4]+ (Ppm: 3.3) |
Mytilus edulis (mantle) |
20190201_MS38_Crassostrea_Mantle_350-1500_DHB_pos_A28_10um_270x210Resolution: 10μm, 270x210
|
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2-Deoxy-5-hydroxymethylcytidine-5-triphosphate Formula: C10H18N3O14P3 (497.0002) Adducts: [M+NH4]+ (Ppm: 2.4) |
Mytilus edulis (gill) |
20190202_MS38_Crassostrea_Gill_350-1500_DHB_pos_A25_11um_305x210Resolution: 11μm, 305x210
single cell layer |
|
2-Deoxy-5-hydroxymethylcytidine-5-triphosphate Formula: C10H18N3O14P3 (497.0002) Adducts: [M+NH4]+ (Ppm: 2.5) |
Mytilus edulis (mantle) |
20190216_MS38_Mytilus_mantle_350-1500_DHB_pos_A26_10um_275x210Resolution: 10μm, 275x210
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