- 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 18 Reference Ions Near m/z 556.0354
NovoCell ID | m/z | Mass Window | Metabolite | Ranking | Anatomy Context |
---|---|---|---|---|---|
MSI_000054209 Unreliable | 556.0406 | 556.0401 ~ 556.041 MzDiff: 3.6 ppm |
6-{[5,7-dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]oxy}-3,4-dihydroxy-5-(sulfooxy)oxane-2-carboxylic acid (BioDeep_00002235437) Formula: C22H20O15S (556.0523) |
3.16 (60%) | MALDI - CHCA [NOVOCELL:BACKGROUND] blank |
MSI_000010996 Unreliable | 556.0285 | 556.0285 ~ 556.0285 MzDiff: none |
C.I. Direct Red 45 (BioDeep_00000034529) Formula: C24H17N3O7S3 (555.0229) |
2.68 (100%) | Mus musculus [UBERON:0012378] muscle layer of urinary bladder |
MSI_000011003 Unreliable | 556.0372 | 556.0372 ~ 556.0372 MzDiff: none |
trans-zeatin riboside triphosphate (BioDeep_00000011186) Formula: C15H24N5O14P3 (591.0533) |
2.65 (100%) | Mus musculus [UBERON:0012378] muscle layer of urinary bladder |
MSI_000010456 Unavailable | 556.0404 | 556.0404 ~ 556.0404 MzDiff: 0.1 ppm |
trans-zeatin riboside triphosphate (BioDeep_00000011186) Formula: C15H24N5O14P3 (591.0533) |
-1.47 (100%) | Bathymodiolus [UBERON:0009120] gill filament |
MSI_000009499 Unavailable | 556.0285 | 556.0285 ~ 556.0285 MzDiff: none |
C.I. Direct Red 45 (BioDeep_00000034529) Formula: C24H17N3O7S3 (555.0229) |
-0.59 (100%) | Mus musculus [UBERON:0004645] urinary bladder urothelium |
MSI_000009553 Unavailable | 556.0372 | 556.0372 ~ 556.0372 MzDiff: none |
trans-zeatin riboside triphosphate (BioDeep_00000011186) Formula: C15H24N5O14P3 (591.0533) |
-0.89 (100%) | Mus musculus [UBERON:0004645] urinary bladder urothelium |
MSI_000012195 Unavailable | 556.0404 | 556.0404 ~ 556.0404 MzDiff: 0.1 ppm |
trans-zeatin riboside triphosphate (BioDeep_00000011186) Formula: C15H24N5O14P3 (591.0533) |
-1 (100%) | Bathymodiolus [UBERON:2000211] gill lamella |
MSI_000013019 Unavailable | 556.0405 | 556.0405 ~ 556.0405 MzDiff: none |
C.I. Direct Red 45 (BioDeep_00000034529) Formula: C24H17N3O7S3 (555.0229) |
-0.62 (100%) | Plant [PO:0005020] vascular bundle |
MSI_000013823 Unreliable | 556.0405 | 556.0405 ~ 556.0405 MzDiff: none |
C.I. Direct Red 45 (BioDeep_00000034529) Formula: C24H17N3O7S3 (555.0229) |
0.07 (100%) | Plant [PO:0005417] phloem |
MSI_000015205 Unavailable | 556.0405 | 556.0405 ~ 556.0405 MzDiff: none |
C.I. Direct Red 45 (BioDeep_00000034529) Formula: C24H17N3O7S3 (555.0229) |
-0.62 (100%) | Plant [PO:0006036] root epidermis |
MSI_000018590 Unreliable | 556.0405 | 556.0405 ~ 556.0405 MzDiff: none |
C.I. Direct Red 45 (BioDeep_00000034529) Formula: C24H17N3O7S3 (555.0229) |
1.71 (100%) | Plant [PO:0020124] root stele |
MSI_000020205 Unavailable | 556.0405 | 556.0405 ~ 556.0405 MzDiff: none |
C.I. Direct Red 45 (BioDeep_00000034529) Formula: C24H17N3O7S3 (555.0229) |
-0.55 (100%) | Plant [PO:0025197] stele |
MSI_000024963 Unreliable | 556.0284 | 556.0284 ~ 556.0284 MzDiff: none |
C.I. Direct Red 45 (BioDeep_00000034529) Formula: C24H17N3O7S3 (555.0229) |
1.75 (100%) | Mus musculus [UBERON:0004269] upper arm connective tissue |
MSI_000032926 Unavailable | 556.04 | 556.04 ~ 556.04 MzDiff: none |
Not Annotated | -0.05 (0%) | Posidonia oceanica [PO:0005020] vascular bundle |
MSI_000033801 Unreliable | 556.04 | 556.04 ~ 556.04 MzDiff: none |
Not Annotated | 0.55 (0%) | Posidonia oceanica [PO:0005352] xylem |
MSI_000040226 Unavailable | 556.0407 | 556.0407 ~ 556.0407 MzDiff: none |
6-{[5,7-dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]oxy}-3,4-dihydroxy-5-(sulfooxy)oxane-2-carboxylic acid (BioDeep_00002235437) Formula: C22H20O15S (556.0523) |
-0.08 (100%) | Posidonia oceanica [PO:0005417] phloem |
MSI_000050398 Unreliable | 556.0399 | 556.0399 ~ 556.0399 MzDiff: none |
C.I. Direct Red 45 (BioDeep_00000034529) Formula: C24H17N3O7S3 (555.0229) |
0 (100%) | Mytilus edulis [UBERON:0009120] gill filament |
MSI_000051134 Unreliable | 556.0399 | 556.0399 ~ 556.0399 MzDiff: none |
C.I. Direct Red 45 (BioDeep_00000034529) Formula: C24H17N3O7S3 (555.0229) |
0 (100%) | Mytilus edulis [UBERON:2001856] gill ray |
Found 5 Sample Hits
Metabolite | Species | Sample | |
---|---|---|---|
trans-zeatin riboside triphosphate Formula: C15H24N5O14P3 (591.0533) Adducts: [M+H-2H2O]+ (Ppm: 4) |
Mus musculus (Urinary bladder) |
HR2MSI_mouse_urinary_bladder - S096Resolution: 10μm, 260x134
Mass spectrometry imaging of phospholipids in mouse urinary bladder (imzML dataset) |
|
m/z_556.04 Formula: - (n/a) Adducts: (Ppm: 0) |
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. |
|
m/z_556.0401 Formula: - (n/a) Adducts: (Ppm: 0) |
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. |
|
5-Amino-1-[carboxy(methyl)amino]pentane-1,1,2,2,3,3,4,4,5-nonacarboxylic acid Formula: C16H16N2O20 (556.0296) Adducts: [M]+ (Ppm: 11.3) |
Mytilus edulis (mantle) |
20190201_MS38_Crassostrea_Mantle_350-1500_DHB_pos_A28_10um_270x210Resolution: 10μm, 270x210
|
|
C.I. Direct Red 45 Formula: C24H17N3O7S3 (555.0229) Adducts: [M+H]+ (Ppm: 17.6) |
Mytilus edulis (gill) |
20190202_MS38_Crassostrea_Gill_350-1500_DHB_pos_A25_11um_305x210Resolution: 11μm, 305x210
single cell layer |
|