<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/MTBLS13818/m_MTBLS13818_LC-MS_positive_reverse-phase_metabolite_profiling_v2_maf.tsv</Tabular><Tabular>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS13818/m_MTBLS13818_LC-MS_negative_reverse-phase_metabolite_profiling_v2_maf.tsv</Tabular><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS13818/s_MTBLS13818.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS13818/i_Investigation.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS13818/a_MTBLS13818_LC-MS_positive_reverse-phase_metabolite_profiling.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS13818/a_MTBLS13818_LC-MS_negative_reverse-phase_metabolite_profiling.txt</Txt><Raw>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS13818/FILES/RAW_FILES/Pos-BP20241925-PGM326.raw</Raw><Raw>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS13818/FILES/RAW_FILES/Neg-BP20241925-PGM326.raw</Raw></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/MTBLS13818</ftp_download_link><metabolite_identification_protocol>&lt;p>Metabolite identification was performed by matching exact mass (mass tolerance &amp;lt; 10 ppm) and MS/MS spectra (mass tolerance &amp;lt; 0.01 Da) against public databases including HMDB, MassBank, and GNPS, as well as an in-house Bepu Metabolite Library (BP-DB).&lt;/p></metabolite_identification_protocol><repository>MetaboLights</repository><study_status>Public</study_status><ptm_modification></ptm_modification><instrument_platform>Liquid Chromatography MS - negative - reverse-phase</instrument_platform><instrument_platform>Liquid Chromatography MS - positive - reverse-phase</instrument_platform><chromatography_protocol>&lt;p>Throughout the entire analytical process, samples were maintained at 4 °C in the autosampler. Separation was performed on a SHIMADZU-LC30 ultra-high performance liquid chromatography (UHPLC) system equipped with an ACQUITY UPLC HSS T3 column (2.1 × 100 mm, 1.8 µm; Waters, Milford, MA, USA). The injection volume was 6 µL, the column temperature was set at 40 °C, and the flow rate was 0.3 mL/min. Mobile phase A consisted of 0.1% formic acid in water, and mobile phase B was 0.1% formic acid in acetonitrile. The gradient elution program was applied as follows: 0–2 min, 0% B; 2–6 min, 0% to 48% B; 6–10 min, 48% to 100% B; 10–12 min, 100% B; 12–12.1 min, 100% to 0% B; and 12.1–15 min, 0% B.&lt;/p></chromatography_protocol><publication>Butyric acid derived from porcine-derived antioxidant probiotic PGM326 enhances intestinal cell differentiation by promoting oxidative phosphorylation.</publication><submitter_affiliation>Peking University</submitter_affiliation><submitter_name>Duo Keai</submitter_name><organism_part>The intestinal contents of piglets</organism_part><technology_type>mass spectrometry assay</technology_type><disease></disease><extraction_protocol>&lt;p>The samples were thawed at 4 °C and vortexed thoroughly. An aliquot of 600 μL from each sample was transferred to a microcentrifuge tube and dried under vacuum in a high-speed centrifugal concentrator. Then, 1 mL of pre-cooled methanol-water (4:1, v/v) was added, followed by mixing and sonication in an ice bath for 20 min. After standing at -20 °C for 1 h, the mixture was centrifuged at 16,000 × g and 4 °C for 20 min. The resulting supernatant was collected and concentrated to dryness again under vacuum. For LC–MS analysis, the residue was reconstituted in 100 μL of pre-chilled methanol-water (1:1, v/v), centrifuged at 20,000 × g and 4 °C for 15 min, and an appropriate volume of the supernatant was injected for analysis.&lt;/p></extraction_protocol><organism>bacillus</organism><full_dataset_link>https://www.ebi.ac.uk/metabolights/MTBLS13818</full_dataset_link><author>Yitong Zhang. Hunan Normal University. 3277185620@qq.com.</author><author>Huansheng Yang. Hunan Normal University. yhs@hunnu.edu.cn.</author><data_transformation_protocol>&lt;p>Raw data were processed using the MSDIAL software for peak alignment, retention time correction, and peak area extraction.&lt;/p></data_transformation_protocol><study_factor>Group</study_factor><submitter_email>keaiduoduo998@126.com</submitter_email><sample_collection_protocol>&lt;p>Strain PGM326, a porcine-derived antioxidant probiotic, was purified and cultured for more than three generations. The bacterial cells were then centrifuged at 4 °C (10000 × g, 5 min) to collect the strain PGM326-CFS (cell-free supernatant), which was subsequently sent to BiotechBio Corporation for metabolomic analysis.&lt;/p>&lt;p>&lt;br>&lt;/p></sample_collection_protocol><omics_type>Metabolomics</omics_type><study_design>Bacillus PGM326</study_design><study_design>Antioxidant probiotic</study_design><study_design>LCMS</study_design><curator_keywords>Bacillus PGM326</curator_keywords><curator_keywords>Antioxidant probiotic</curator_keywords><curator_keywords>LCMS</curator_keywords><mass_spectrometry_protocol>&lt;p>Each sample was analyzed in both positive (+) and negative (-) ion modes using electrospray ionization (ESI). After UPLC separation, mass spectrometry was performed on a Q-Exactive Plus mass spectrometer (Thermo Scientific) equipped with a HESI ion source. The ionization parameters were set as follows: spray voltage: 3.8 kV (+) and 3.2 kV (-); capillary temperature: 320 °C; sheath gas: 30 arb; aux gas: 5 arb; probe heater temperature: 350 °C; S-lens RF level: 50. Mass spectrometry data were acquired under the following settings: acquisition time: 15 min; full scan range: m/z 75–1050; MS1 resolution: 70,000 at m/z 200; AGC target: 3e6; maximum ion injection time (IT) for MS1: 100 ms. For MS/MS analysis, the top 10 most intense precursor ions from each full scan were selected for fragmentation. The MS2 settings were: resolution: 17,500 at m/z 200; AGC target: 1e5; maximum IT: 50 ms; activation type: HCD; isolation window: 2 m/z; normalized collision energy (stepped): 20, 30, 40.&lt;/p></mass_spectrometry_protocol><metabolite_name>α-D-Glucose</metabolite_name><metabolite_name>6-(2-Carboxyethyl)-7-hydroxy-2,2-dimethyl-4-chromanone glucoside</metabolite_name><metabolite_name>(R)-Dihydromaleimide</metabolite_name><metabolite_name>Guanosine</metabolite_name><metabolite_name>dAMP / 2'-Deoxyadenosine 5'-monophosphate</metabolite_name><metabolite_name>(S,S)-Np-Histidinylalanine</metabolite_name><metabolite_name>Edulisin I</metabolite_name><metabolite_name>Isopropyl beta-D-glucoside</metabolite_name><metabolite_name>L-N-(3-Carboxypropyl)glutamine</metabolite_name><metabolite_name>cadralazine</metabolite_name><metabolite_name>Methylpyrazine</metabolite_name><metabolite_name>O-Acetylserine</metabolite_name><metabolite_name>1-(Hydroxymethyl)-5,5-dimethyl-2,4-imidazolidinedione</metabolite_name><metabolite_name>Penmacric acid</metabolite_name><metabolite_name>Bilobetin</metabolite_name><metabolite_name>Uroporphyrinogen I</metabolite_name><metabolite_name>Tartronate semialdehyde</metabolite_name><metabolite_name>Conivaptan</metabolite_name><metabolite_name>Pantothenamide</metabolite_name><metabolite_name>8-Hydroxyadenine</metabolite_name><metabolite_name>L-Xylulose</metabolite_name><metabolite_name>Isoplumbagin</metabolite_name><metabolite_name>Leucyl-Histidine</metabolite_name><metabolite_name>4-Acetamido-2-aminobutanoic acid</metabolite_name><metabolite_name>dCYD / 2'-Deoxycytidine</metabolite_name><metabolite_name>4R,5R,6S-Trihydroxy-2-hydroxymethyl-2-cyclohexen-1-one 6-(2-hydroxy-6-methylbenzoate)</metabolite_name><metabolite_name>Citrusin E</metabolite_name><metabolite_name>O-Acetylethanolamine</metabolite_name><metabolite_name>L-2-Amino-3-(1-pyrazolyl)propanoic acid</metabolite_name><metabolite_name>1-Isothiocyanato-6-(methylsulfinyl)hexane</metabolite_name><metabolite_name>D-Glucuronic acid</metabolite_name><metabolite_name>D-1-Amino-2-pyrrolidinecarboxylic acid</metabolite_name><metabolite_name>Melleolide D</metabolite_name><metabolite_name>N-Acetyl-b-neuraminic acid</metabolite_name><metabolite_name>Pterolactam</metabolite_name><metabolite_name>2',3' cyclic CMP</metabolite_name><metabolite_name>Lysyl-Lysine</metabolite_name><metabolite_name>Telbivudine</metabolite_name><metabolite_name>(2S,3'S)-alpha-Amino-2-carboxy-5-oxo-1-pyrrolidinebutanoic acid</metabolite_name><metabolite_name>xi-3-Hydroxy-2-oxobutanoic acid</metabolite_name><metabolite_name>Threoninyl-glutamate</metabolite_name><metabolite_name>Hydroxyminaline</metabolite_name><metabolite_name>Methyl N-methylanthranilate</metabolite_name><metabolite_name>trans-Aconitic acid</metabolite_name><metabolite_name>DL-Ornithino-L-alanine</metabolite_name><metabolite_name>Glucosylisomaltol</metabolite_name><metabolite_name>L-Cyclo(alanylglycyl)</metabolite_name><metabolite_name>Cephalexin</metabolite_name><metabolite_name>3-O-Caffeoyl-4-O-methylquinic acid</metabolite_name><metabolite_name>Artonin R</metabolite_name><metabolite_name>L-Homocystine</metabolite_name><metabolite_name>Gulonic acid</metabolite_name><metabolite_name>3,4-Dihydroxy-2-hydroxymethyl-1-pyrrolidinepropanamide</metabolite_name><metabolite_name>Xanthosine</metabolite_name><metabolite_name>T hymidine glycol</metabolite_name><metabolite_name>(2S,4S)-Pinnatanine</metabolite_name><metabolite_name>Valyl-Alanine</metabolite_name><metabolite_name>Di-2-furanylmethane</metabolite_name><metabolite_name>2,5-Furandicarboxylic acid</metabolite_name><metabolite_name>Glucosylgalactosyl hydroxylysine</metabolite_name><metabolite_name>trifluoroacetic acid</metabolite_name><metabolite_name>5'-O-Desmethyl omeprazole</metabolite_name><metabolite_name>S-Japonin</metabolite_name><metabolite_name>2-Hydroxy-4-oxopentanoic acid</metabolite_name><metabolite_name>L-Agaritine</metabolite_name><metabolite_name>L-Pinitol</metabolite_name><metabolite_name>N-(1-Deoxy-1-fructosyl)threonine</metabolite_name><metabolite_name>(S)-N-(4,5-Dihydro-1-methyl-4-oxo-1H-imidazol-2-yl)alanine</metabolite_name><metabolite_name>L-Valine</metabolite_name><metabolite_name>5-Taurinomethyl-2-thiouridine</metabolite_name><metabolite_name>L-prolyl-L-glycine</metabolite_name></additional><is_claimable>false</is_claimable><name>Butyric acid derived from porcine-derived antioxidant probiotic PGM326 enhances intestinal cell differentiation by promoting oxidative phosphorylation</name><description>&lt;p>This study not only identified an efficient host-homologous antioxidant probiotic, PGM326, but also systematically elucidated its mechanism of exerting antioxidant function by synthesizing BA to promote OXPHOS in intestinal epithelial cells, thereby enhancing cell differentiation. This provides a systematic solution for developing host-homologous, mechanism-defined antioxidant microecological feed 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