<HashMap><database>MetaboLights</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Tabular>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14589/m_MTBLS14589_LC-MS_negative_hilic_metabolite_profiling_v2_maf.tsv</Tabular><Tabular>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14589/m_MTBLS14589_LC-MS_positive_hilic_metabolite_profiling_v2_maf.tsv</Tabular><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14589/s_MTBLS14589.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14589/a_MTBLS14589_LC-MS_negative_hilic_metabolite_profiling.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14589/a_MTBLS14589_LC-MS_positive_hilic_metabolite_profiling.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14589/i_Investigation.txt</Txt></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><ftp_download_link>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14589</ftp_download_link><metabolite_identification_protocol>&lt;p>The R package and the BiotreeDB (V3.0, China) were applied in metabolite annotation. Candidate metabolites (VIP > 1 and adjusted P &lt; 0.05) were regarded as potential biomarkers.&lt;/p></metabolite_identification_protocol><repository>MetaboLights</repository><study_status>Public</study_status><ptm_modification></ptm_modification><instrument_platform>Liquid Chromatography MS - positive - hydrophilic interaction</instrument_platform><instrument_platform>Liquid Chromatography MS - negative - hydrophilic interaction - Thermo Orbitrap Exploris 120</instrument_platform><chromatography_protocol>&lt;p>Chromatographic separation was carried out on a UHPLC system with a Waters Acquity UPLC BEH Amide column (1.7 µm, 2.1 × 50 mm). Mobile phases A (0.1% formic acid in water) and B (0.1% formic acid in acetonitrile) used a gradient elution (0–10 min: 5–95% B) at 0.3 mL/min; column temperature was 4°C, and injection volume was 2 µL.&lt;/p></chromatography_protocol><publication>Fermented brewers' grains modulate serum and pectoral muscle metabolome to regulate flavor quality formation in broilers.</publication><submitter_affiliation>Liaocheng University</submitter_affiliation><submitter_name>Yuanfeng Li</submitter_name><organism_part>muscle</organism_part><technology_type>mass spectrometry assay</technology_type><disease></disease><extraction_protocol>&lt;p>Samples were extracted using 400 μL of extraction solution (MeOH:ACN, 1:1 (v/v). The process included homogenizing samples on ice for 5 min, centrifuging at 12,000 rpm for 10 min at 4°C, and collecting supernatants for analysis.&lt;/p></extraction_protocol><organism>Gallus gallus</organism><full_dataset_link>https://www.ebi.ac.uk/metabolights/MTBLS14589</full_dataset_link><author>Li Yuanfeng. Liaocheng University. Liaocheng University, Liaocheng, Shandong, China. 309271207@qq.com.</author><data_transformation_protocol>&lt;p>The raw mass spectrometry data were converted to mzXML format using ProteoWizard software (ProteoWizard Software Foundation, USA) for data standardization, then processed with an in-house R program based on XCMS for peak alignment, retention time correction, and data normalization to ensure consistency for downstream analysis.&lt;/p></data_transformation_protocol><study_factor>Dietary treatment</study_factor><submitter_email>309271207@qq.com</submitter_email><sample_collection_protocol>&lt;p>After euthanasia, the right pectoralis major muscle was rapidly dissected. Tissue blocks (0.5 cm × 0.5 cm × 0.5 cm) were collected from the middle part, avoiding fascia and adipose tissue. Samples were rinsed with pre-cooled sterile saline, dried with filter paper, snap-frozen in liquid nitrogen, and stored at −80 °C until metabolomic analysis.&lt;/p></sample_collection_protocol><omics_type>Metabolomics</omics_type><study_design>Thermo Scientific Vanquish UHPLC System</study_design><study_design>Metabolomics</study_design><study_design>pooled quality control sample</study_design><study_design>Untargeted metabolites</study_design><study_design>wet-fermented brewer's grains</study_design><study_design>untargeted analysis</study_design><study_design>Thermo Scientific Orbitrap Exploris 120</study_design><study_design>muscle</study_design><study_design>nutrition intervention</study_design><study_design>Gallus gallus</study_design><study_design>experimental sample</study_design><curator_keywords>Thermo Scientific Vanquish UHPLC System</curator_keywords><curator_keywords>Metabolomics</curator_keywords><curator_keywords>pooled quality control sample</curator_keywords><curator_keywords>Untargeted metabolites</curator_keywords><curator_keywords>wet-fermented brewer's grains</curator_keywords><curator_keywords>untargeted analysis</curator_keywords><curator_keywords>Thermo Scientific Orbitrap Exploris 120</curator_keywords><curator_keywords>muscle</curator_keywords><curator_keywords>nutrition intervention</curator_keywords><curator_keywords>Gallus gallus</curator_keywords><curator_keywords>experimental sample</curator_keywords><mass_spectrometry_protocol>&lt;p>The Orbitrap Exploris 120 mass spectrometer was used for its ability to acquire MS/MS spectra on information-dependent acquisition (IDA) mode in the control of the acquisition software (Xcalibur, Thermo). In this mode, the acquisition software continuously evaluates the full scan MS spectrum. The ESI source conditions were set as following:sheath gas flow rate as 50 Arb, Aux gas flow rate as 15 Arb, capillary temperature 320 ℃, full MS resolution as 60000, MS/MS resolution as 15000, collision energy: SNCE 20/30/40, spray voltage as 3.8 kV (positive) or -3.4 kV (negative), respectively.&lt;/p></mass_spectrometry_protocol><metabolite_name>Dimethyl (9E,18E)-1,10-bis(.beta.-D-glucopyranosyloxy)-6,15-dioxo-4a,5,6,8,13a,14,15,17-octahydro-1H,10H-dipyrano[3,4-d:3',4'-k][1,8]dioxacyclotetradecine-4,13-dicarboxylate</metabolite_name><metabolite_name>(2-{[3-(hexadecanoyloxy)-2-[octadeca-9.12-dienoyloxy]propyl phosphono]oxy}ethyl)trimethylazanium</metabolite_name><metabolite_name>Glutathione disulfide</metabolite_name><metabolite_name>LPG(18:1(9Z))</metabolite_name><metabolite_name>PG(16:0/18:1)</metabolite_name><metabolite_name>(2-aminoethoxy)[2-[icosa-5.8.11.14-tetraenoyloxy]-3-[octadec-11-enoyloxy]propoxy]phosphinic acid</metabolite_name><metabolite_name>2-Oleoyl-1-palmitoyl-sn-glycero-3-phosphoserine</metabolite_name><metabolite_name>Taurohyodeoxycholic acid</metabolite_name><metabolite_name>Tauroursodeoxycholic acid</metabolite_name><metabolite_name>1-Stearoyl-2-arachidonoyl-sn-glycero-3-phospho-(1'-sn-glycerol)</metabolite_name><metabolite_name>Nis(monooleoylglycero)phosphate (S,R Isomer)</metabolite_name><metabolite_name>(2-aminoethoxy)[2-[octadec-9-enoyloxy]-3-(octadecanoyloxy)propoxy]phosphinic acid</metabolite_name><metabolite_name>(2-aminoethoxy)[2-[icosa-5.8.11-trienoyloxy]-3-(octadecanoyloxy)propoxy]phosphinic acid</metabolite_name><metabolite_name>(2-aminoethoxy)[2-[docosa-4.7.10.13.16.19-hexaenoyloxy]-3-[hexadec-1-en-1-yloxy]propoxy]phosphinic acid</metabolite_name><metabolite_name>[2-[docosa-4.7.10.13.16.19-hexaenoyloxy]-3-(octadecanoyloxy)propoxy]({[2.3.4.5.6-pentahydroxycyclohexyl]oxy})phosphinic acid</metabolite_name><metabolite_name>1-Stearoyl-2-arachidonoyl-sn-glycero-3-phospho-(1'-myo-inositol)</metabolite_name><metabolite_name>1,2-Distearoyl-sn-glycero-3-phospho-L-serine</metabolite_name><metabolite_name>Taurocholic acid</metabolite_name><metabolite_name>2-amino-3-({[3-(hexadecanoyloxy)-2-(octadecanoyloxy)propoxy](hydroxy)phosphoryl}oxy)propanoic acid</metabolite_name><metabolite_name>[2-[docosa-7.10.13.16-tetraenoyloxy]-3-(octadecanoyloxy)propoxy]({[2.3.4.5.6-pentahydroxycyclohexyl]oxy})phosphinic acid</metabolite_name><metabolite_name>2-Arachidonoyl-1-palmitoyl-sn-glycero-3-phosphoethanolamine</metabolite_name><metabolite_name>Maltotriose</metabolite_name><metabolite_name>2-amino-3-({hydroxy[2-(icosanoyloxy)-3-(octadecanoyloxy)propoxy]phosphoryl}oxy)propanoic acid</metabolite_name><metabolite_name>1-Stearoyl-2-arachidonoyl-sn-glycero-3-phosphoserine</metabolite_name><metabolite_name>Chebulinic acid</metabolite_name><metabolite_name>Taurochenodeoxycholic acid</metabolite_name><metabolite_name>2-amino-3-({hydroxy[2-(icosanoyloxy)-3-[octadec-11-enoyloxy]propoxy]phosphoryl}oxy)propanoic acid</metabolite_name><metabolite_name>PS(18:0/18:2)</metabolite_name><metabolite_name>Cholesteryl sulfate</metabolite_name><metabolite_name>Asparasaponin I</metabolite_name><metabolite_name>Nicotinamide adenine dinucleotide (NAD)</metabolite_name><metabolite_name>2-amino-3-({hydroxy[2-[icosa-5.8.11-trienoyloxy]-3-(octadecanoyloxy)propoxy]phosphoryl}oxy)propanoic acid</metabolite_name><metabolite_name>Ethanox 310</metabolite_name><metabolite_name>PE(18:0/18:2)</metabolite_name><metabolite_name>Taurodeoxycholic acid</metabolite_name><metabolite_name>LPC(13:0)</metabolite_name><metabolite_name>Tauro-gamma-muricholic acid</metabolite_name><metabolite_name>[3-(hexadecanoyloxy)-2-[icosa-5.8.11-trienoyloxy]propoxy]({[2.3.4.5.6-pentahydroxycyclohexyl]oxy})phosphinic acid</metabolite_name><metabolite_name>1-Stearoyl-2-oleoyl-sn-glycero-3-phospho-(1'-sn-glycerol)</metabolite_name><metabolite_name>PI(16:0/18:1)</metabolite_name><metabolite_name>2-Linoleoyl-1-palmitoyl-sn-glycero-3-phosphoethanolamine</metabolite_name><metabolite_name>20-((6-O-Hexopyranosylhexopyranosyl)oxy)-14-hydroxypregn-5-en-3-yl 2,6-dideoxy-4-O-(6-deoxy-3-O-methyl-4-O-((2E)-2-methylbut-2-enoyl)hexopyranosyl)-3-O-methylhexopyranoside</metabolite_name><metabolite_name>ADP-ribose</metabolite_name><metabolite_name>2-Docosahexaenoyl-1-stearoyl-sn-glycero-3-phosphoserine</metabolite_name><metabolite_name>Cyclic adenosine diphosphate-ribose (cADPR)</metabolite_name><metabolite_name>PC(16:0/20:4)</metabolite_name><metabolite_name>1-palmitoyl-2-linoleoyl-sn-glycero-3-phospho-(1'-rac-glycerol)</metabolite_name><metabolite_name>(2-aminoethoxy)[2-[docosa-4.7.10.13.16.19-hexaenoyloxy]-3-[octadeca-1.9-dien-1-yloxy]propoxy]phosphinic acid</metabolite_name><metabolite_name>Tauro-beta-muricholic acid</metabolite_name><metabolite_name>(2-aminoethoxy)[2-[docosa-4.7.10.13.16-pentaenoyloxy]-3-(octadecanoyloxy)propoxy]phosphinic acid</metabolite_name></additional><is_claimable>false</is_claimable><name>Fermented brewers' grains modulate serum and pectoral muscle metabolome to regulate flavor quality formation in broilers</name><description>&lt;p>This study was designed to systematically assess the impact of wet-fermented brewer's grains (WFBG) on pectoral muscle metabolic profiles and key regulatory pathways in broiler chickens. In this 21-day experiment, a total of 281 DEMs were identified, with 29 upregulated and 252 downregulated DEMs (P &lt; 0.05). These DEMs were mainly enriched in 61 metabolic pathways, involving amino acid anabolism, lipid metabolism, and flavor precursor transformation pathways. This study elucidated the metabolomic mechanism by which WFBG regulated broiler meat quality and filled the research gap regarding the effects of WFBG on flavor formation and muscle nutrition in broilers. The findings provided a theoretical basis and practical reference for the large-scale application of WFBG in broiler diet formulation. &lt;/p></description><dates><publication>2026-05-27</publication><submission>2026-05-27</submission></dates><accession>MTBLS14589</accession><cross_references/></HashMap>