M/Z: 229.9378
Hit 2 annotations: 6-bromo-3-chloro-1H-indole_[M+H]+
; 2,4-Dichloro-6-nitrophenol_[M+Na]+
- 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 9 Reference Ions Near m/z 229.9378
NovoCell ID | m/z | Mass Window | Metabolite | Ranking | Anatomy Context |
---|---|---|---|---|---|
MSI_000015695 Reliable | 229.9378 | 229.9378 ~ 229.9378 MzDiff: 0.1 ppm |
6-bromo-3-chloro-1H-indole (BioDeep_00000328115) Formula: C8H5BrClN (228.9294) |
3.63 (100%) | Vitis vinifera [PO:0009085] exocarp |
MSI_000007393 | 229.9376 | 229.9374 ~ 229.9379 MzDiff: 2.1 ppm |
2,4-Dichloro-6-nitrophenol (BioDeep_00000173546) Formula: C6H3Cl2NO3 (206.949) |
2.17 (100%) | Rattus norvegicus [UBERON:0004359] corpus epididymis |
MSI_000032520 Unreliable | 229.9378 | 229.9376 ~ 229.938 MzDiff: 1.4 ppm |
6-bromo-3-chloro-1H-indole (BioDeep_00000328115) Formula: C8H5BrClN (228.9294) |
2.85 (100%) | Posidonia oceanica [PO:0005020] vascular bundle |
MSI_000039199 Unreliable | 229.9378 | 229.9377 ~ 229.938 MzDiff: 0.9 ppm |
6-bromo-3-chloro-1H-indole (BioDeep_00000328115) Formula: C8H5BrClN (228.9294) |
0.89 (100%) | Posidonia oceanica [PO:0005059] root endodermis |
MSI_000013507 Unreliable | 229.9382 | 229.9382 ~ 229.9382 MzDiff: none |
6-bromo-3-chloro-1H-indole (BioDeep_00000328115) Formula: C8H5BrClN (228.9294) |
0.94 (100%) | Plant [PO:0005417] phloem |
MSI_000014612 Unreliable | 229.9382 | 229.9382 ~ 229.9382 MzDiff: none |
6-bromo-3-chloro-1H-indole (BioDeep_00000328115) Formula: C8H5BrClN (228.9294) |
0.29 (100%) | Plant [PO:0006036] root epidermis |
MSI_000019100 Unavailable | 229.9382 | 229.9382 ~ 229.9382 MzDiff: none |
6-bromo-3-chloro-1H-indole (BioDeep_00000328115) Formula: C8H5BrClN (228.9294) |
-0.86 (100%) | Plant [PO:0020124] root stele |
MSI_000019355 Unreliable | 229.9382 | 229.9382 ~ 229.9382 MzDiff: none |
6-bromo-3-chloro-1H-indole (BioDeep_00000328115) Formula: C8H5BrClN (228.9294) |
0.87 (100%) | Plant [PO:0025197] stele |
MSI_000035732 Unavailable | 229.9376 | 229.9376 ~ 229.9376 MzDiff: none |
6-bromo-3-chloro-1H-indole (BioDeep_00000328115) Formula: C8H5BrClN (228.9294) |
-0.32 (100%) | Posidonia oceanica [PO:0006203] pericycle |
Found 21 Sample Hits
Metabolite | Species | Sample | |
---|---|---|---|
6-bromo-3-chloro-1H-indole Formula: C8H5BrClN (228.9294) Adducts: [M+H]+ (Ppm: 6.7) |
Plant (Root) |
MPIMM_035_QE_P_PO_6pmResolution: 30μm, 165x170
|
|
6-bromo-3-chloro-1H-indole Formula: C8H5BrClN (228.9294) Adducts: [M+H]+ (Ppm: 4.9) |
Vitis vinifera (Fruit) |
grape_dhb_91_1Resolution: 50μm, 120x114
Grape berries fruit, condition: Ripe |
|
2,4-Dichloro-6-nitrophenol Formula: C6H3Cl2NO3 (206.949) Adducts: [M+Na]+ (Ppm: 1.8) |
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. |
|
2,4-Dichloro-6-nitrophenol Formula: C6H3Cl2NO3 (206.949) Adducts: [M+Na]+ (Ppm: 2.3) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito03_18Resolution: 17μm, 208x104
|
|
2,4-Dichloro-6-nitrophenol Formula: C6H3Cl2NO3 (206.949) Adducts: [M+Na]+ (Ppm: 3.6) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito08_43Resolution: 17μm, 298x106
|
|
2,4-Dichloro-6-nitrophenol Formula: C6H3Cl2NO3 (206.949) Adducts: [M+Na]+ (Ppm: 3.6) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito08_44Resolution: 17μm, 299x111
|
|
2,4-Dichloro-6-nitrophenol Formula: C6H3Cl2NO3 (206.949) Adducts: [M+Na]+ (Ppm: 1.4) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito08_46Resolution: 17μm, 298x106
|
|
6-bromo-3-chloro-1H-indole Formula: C8H5BrClN (228.9294) Adducts: [M+H]+ (Ppm: 4.9) |
Vitis vinifera (Fruit) |
grape_dhb_164_1Resolution: 17μm, 136x122
Grape berries fruit, condition: Late |
|
6-bromo-3-chloro-1H-indole Formula: C8H5BrClN (228.9294) Adducts: [M+H]+ (Ppm: 4.9) |
Vitis vinifera (Fruit) |
grape_dhb_163_1Resolution: 17μm, 132x115
Grape berries fruit, condition: Late |
|
2,4-Dichloro-6-nitrophenol Formula: C6H3Cl2NO3 (206.949) Adducts: [M+Na]+ (Ppm: 2.7) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito08_47Resolution: 17μm, 301x111
|
|
2,4-Dichloro-6-nitrophenol Formula: C6H3Cl2NO3 (206.949) Adducts: [M+Na]+ (Ppm: 2.7) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito08_48Resolution: 17μm, 294x107
|
|
2,4-Dichloro-6-nitrophenol Formula: C6H3Cl2NO3 (206.949) Adducts: [M+Na]+ (Ppm: 1.4) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito01_04Resolution: 17μm, 178x91
|
|
2,4-Dichloro-6-nitrophenol Formula: C6H3Cl2NO3 (206.949) Adducts: [M+Na]+ (Ppm: 1.8) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito01_03Resolution: 17μm, 159x110
|
|
2,4-Dichloro-6-nitrophenol Formula: C6H3Cl2NO3 (206.949) Adducts: [M+Na]+ (Ppm: 3.1) |
Rattus norvegicus (normal) |
epik_dhb_head_ito01_05Resolution: 17μm, 183x105
|
|
2,4-Dichloro-6-nitrophenol Formula: C6H3Cl2NO3 (206.949) Adducts: [M+Na]+ (Ppm: 1.8) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito01_06Resolution: 17μm, 183x103
|
|
2,4-Dichloro-6-nitrophenol Formula: C6H3Cl2NO3 (206.949) Adducts: [M+Na]+ (Ppm: 1.4) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito03_14Resolution: 17μm, 205x103
|
|
6-bromo-3-chloro-1H-indole Formula: C8H5BrClN (228.9294) Adducts: [M+H]+ (Ppm: 4.1) |
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. |
|
6-bromo-3-chloro-1H-indole Formula: C8H5BrClN (228.9294) Adducts: [M+H]+ (Ppm: 4.5) |
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. |
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6-bromo-3-chloro-1H-indole Formula: C8H5BrClN (228.9294) Adducts: [M+H]+ (Ppm: 5.8) |
Posidonia oceanica (root) |
20190613_MS1_A19r-18Resolution: 17μm, 246x264
|
|
6-bromo-3-chloro-1H-indole Formula: C8H5BrClN (228.9294) Adducts: [M+H]+ (Ppm: 3.6) |
Posidonia oceanica (root) |
20190828_MS1_A19r-22Resolution: 17μm, 292x279
|
|
6-bromo-3-chloro-1H-indole Formula: C8H5BrClN (228.9294) Adducts: [M+H]+ (Ppm: 4.5) |
Posidonia oceanica (root) |
MS1_20180404_PO_1200Resolution: 17μm, 193x208
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