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alternating - hilic"],"chromatography_protocol":["<p>Liquid chromatography separation was performed using an Agilent 1290 Infinity II UHPLC system. </p><p>For the reversed-phase (RP) system, an ACQUITY UPLC BEH C18 Column (1.7 μm, 2.1 mm × 150 mm) was utilized. </p><p>The RP mobile phase A was 0.1% formic acid in water, and mobile phase B was water/methanol (5:95) containing 10 mmol/L ammonium formate. </p><p>For the HILIC system, an Atlantis Premier BEH Z-HILIC Column (1.7 μm, 2.1 mm × 150 mm) was used. </p><p>The HILIC mobile phase A consisted of 10% acetonitrile in water with 10 mmol/L ammonium acetate, and mobile phase B was water/acetonitrile (10:90) with 10 mmol/L ammonium acetate. </p><p>The auto-sampler temperature was maintained at 6 °C, and the injection volume was set between 1 μL and 2 μL.</p>"],"publication":["Metabolic plasticity of lipid storage and utilization governs fungal persister formation within macrophages."],"submitter_affiliation":["Peking union medical college hospital"],"submitter_name":["Yi Li"],"organism_part":["synthetic","Cell"],"technology_type":["mass spectrometry assay"],"disease":[""],"extraction_protocol":["<p>Metabolites were extracted by adding 500 μL of extraction agent (methanol:water = 3:1, containing internal standards) to 25 mg of the cell pellet sample. </p><p>Two 3.2 mm beads were added, and the mixture was homogenized at 40 Hz for 4 minutes. </p><p>The samples were then sonicated in an ice-water bath for 5 minutes, and this homogenization-sonication cycle was repeated three times. </p><p>Following incubation at -40 °C for 1 hour, the samples were centrifuged at 12000 rpm and 4 °C for 15 minutes. </p><p>A 400 μL aliquot of the supernatant was transferred and dried under vacuum. </p><p>The residue was reconstituted in 200 μL of methanol:acetonitrile:water (1:1:2, v/v/v), filtered, and the liquid was transferred to an autosampler vial for analysis. </p><p>A series of calibration standard solutions and QC samples were also prepared for the quantitative assay and method validation.</p>"],"organism":["synthetic","Candida glabrata"],"full_dataset_link":["https://www.ebi.ac.uk/metabolights/MTBLS15358"],"author":["Su Yanyu.","Li Yingxing.","Yi Li. Peking Union Medical College Hospital. liyi67@pumch.cn."],"data_transformation_protocol":["<p>Raw data files generated by LC-MS/MS were processed using the SCIEX Analyst Work Station Software (version 1.7.3). </p><p>During data preprocessing, metabolites were filtered to retain only those with no more than 50% missing values in a single group or across all groups. </p><p>Missing values were then imputed using the minimum value multiplied by a random number between 0.1 and 0.5. </p><p>Prior to statistical and multivariate pattern recognition analyses, the data were scaled and logarithmically transformed using an in-house R script and the ropls package (v1.34.0).</p>"],"study_factor":["Treatment","Strain"],"submitter_email":["liyi67@pumch.cn"],"sample_collection_protocol":["<p>Three experimental groups of <em>Candida glabrata</em> strains were prepared for targeted metabolomics analysis: wild-type (WT), the ΔASN2 mutant, and the asparagine-supplemented ΔASN2 mutant (ASN2R). Fungal cells were cultured in Dulbecco's Modified Eagle Medium (DMEM) for 3 hours to induce metabolic responses. For the ASN2R group, the DMEM culture medium was additionally supplemented with 1 mM L-asparagine. Each of the three conditions consisted of 6 independent biological replicates. Following the 3-hour incubation period, the fungal cells were rapidly harvested by centrifugation, washed with cold PBS to halt metabolism, and the resulting cell pellets were immediately snap-frozen in liquid nitrogen and stored at -80°C until subsequent metabolite extraction.</p>"],"omics_type":["Metabolomics"],"study_design":["synthetic","Metabolomics","AB SCIEX Triple Quad 6500+","targeted analysis","liquid chromatography-mass spectrometry","Agilent 1290 Infinity II UHPLC","Candida glabrata","experimental blank","targeted metabolite profiling","Cell"],"curator_keywords":["synthetic","Metabolomics","AB SCIEX Triple Quad 6500+","targeted analysis","liquid chromatography-mass spectrometry","Agilent 1290 Infinity II UHPLC","Candida glabrata","experimental blank","targeted metabolite profiling","Cell"],"mass_spectrometry_protocol":["<p>Mass spectrometry data were acquired using an AB Sciex Triple Quad 6500+ mass spectrometer equipped with an IonDrive Turbo V ESI ion source. </p><p>The data acquisition was conducted in Multiple Reaction Monitoring (MRM) mode. </p><p>The specific ion source parameters were set as follows: IonSpray Voltage at +5500 V / -4500 V to accommodate both positive and negative ionization modes. </p><p>Curtain Gas was set at 35 psi, Temperature at 400 °C, Ion Source Gas 1 at 50 psi, and Ion Source Gas 2 at 50 psi.</p>"],"metabolite_name":["D-Fructose","L-Phenylalanine","Glycolic Acid","D-Ribulose 5-phosphate","Glucaric acid","Uridine-5'-diphosphate","Guanosine-5'-triphosphate","L-Argininosuccinic Acid","Mannose 6-phosphate","Adenosine 5'-diphosphoribose","Thiamine pyrophosphate","Thymidine-5'-phosphate","L-Threonine","Uridine diphosphate glucose","Ribose-5-Phosphate","L-Histidine","alpha-Ketoglutaric acid","2-Oxobutanoic acid","L-Leucine","3',5'-cyclic AMP","L-Citrulline","alpha-Ketoisovaleric acid","Guanosine Diphosphate-Fucose","Nicotinamide riboside","Vanillylmandelic acid","Glucose-1-phosphate","L-Proline","L-Methionine","D-Glucuronic acid","Flavin mononucleotide","Guanosine Diphosphate-Mannose","Uridine-5'-monophosphate","Nicotinamide","Trehalose-6-phosphate","Glucosamine","N-Acetylglucosamine 6-phosphate","D-Glucose-6-phosphate","2-Picolinic acid","Pyruvic acid","Glycine","Guanine","Gamma-Aminobutyric Acid","L-Asparagine","Ribulose 1,5-bisphosphate","Adenosine-5'-Monophosphate","Mevalonic acid","Pyroglutamic acid","L-Tryptophan","Coenzyme A","Glucosamine 6-phosphate","Glutathione","Creatinine","Fructose-6-phosphate","Phosphoenolpyruvic acid","6-Phosphogluconic acid","Citric acid","S-Adenosylmethionine","L-Glutamine","Adenosine-5'-diphosphate","Uridine diphosphate glucuronic acid","Nicotinamide adenine dinucleotide phosphate","Choline","Lipoamide","L-Valine","Uracil","Succinyl-CoA","Dihydronicotinamide adenine dinucleotide phosphate","Guanosine","Glyceraldehyde 3-phosphate","Creatine","L-Ornithine","L-Isoleucine","S-Adenosyl-homocysteine","Erythrose 4-phosphate","Orotic acid","Itaconic acid","Glycerophosphoric acid","Methylmalonic acid","Betaine","Maleic acid","L-Alanine","Malic acid","Succinic semialdehyde","Cytosine","Glyceric acid","3-Phosphoglyceric acid","Flavin adenine dinucleotide","6-phosphogluconolactone","2,3-Diphosphoglyceric acid","Gluconic acid","N-Acetyl-Neuraminic Acid","L-Cystine","3-Ureidopropionic acid","Nicotinamide adenine dinucleotid","2-Phosphoglyceric acid","Oxalic acid","Oxalacetic acid","Fructose-1,6-diphosphate","Uridine","Succinic acid","Hypoxanthine","L-Aspartic acid","L-Lysine","Nicotinamide mononucleotide","2'-Deoxyadenosine-5'-monophosphate","Guanosine-5'-Monophosphate","L-Arginine","D-Glucose","2-Oxoadipic acid","Hippuric acid","Guanosine-5'-diphosphate","L-Cysteic acid","4-Hydroxyphenylpyruvic acid","Isocitric acid","L-Cysteine","UDP-N-acetylglucosamine","2-Aminobenzoic acid","L-Lactic acid","Quinolinic acid","2-Hydroxybutyric acid","cis-Aconitic acid","Deoxyuridine monophosphate","L-Glutamic acid","Adenosine","Adenosine-5'-triphosphate","Indole-3-acetic acid","N,N-Dimethylglycine","Adenine","Sedoheptulose 7-phosphate","1,4-Dihydronicotinamide adenine dinucleotide","Acetyl-CoA","Phosphoribosyl pyrophosphate","3-Hydroxypropionic acid","2-Hydroxyglutaric acid","Homogentisic acid","N-Acetylglucosamine 1-phosphate","D-Ribose","L-Tyrosine","Fumaric acid","Citraconic acid","L-Serine","Inosine","Trans-Aconitic acid","3-Hydroxybutyric acid","Glutaryl-CoA","Glutathione Disulfide"],"additional_accession":[]},"is_claimable":false,"name":"targeted metabolomic analysis of carbon and energy intermediates in WT Candida glabrata, ΔASN2_Cgl, and asparagine-supplemented ΔASN2_Cgl cells","description":"Targeted metabolomic analysis of carbon and energy intermediates in WT Candida glabrata, ΔASN2_Cgl, and asparagine-supplemented ΔASN2_Cgl 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