<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/MTBLS14102/m_MTBLS14102_LC-MS_positive_reverse-phase_metabolite_profiling_v2_maf.tsv</Tabular><Tabular>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14102/m_MTBLS14102_LC-MS_negative_reverse-phase_metabolite_profiling_v2_maf.tsv</Tabular><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14102/s_MTBLS14102.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14102/i_Investigation.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14102/a_MTBLS14102_LC-MS_positive_reverse-phase_metabolite_profiling-1.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14102/a_MTBLS14102_LC-MS_negative_reverse-phase_metabolite_profiling.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/MTBLS14102</ftp_download_link><metabolite_identification_protocol>&lt;p>The pretreatment of LC/MS raw data was performed by Progenesis QI software, and a three-dimensional data matrix in CSV format was exported. The information in this three-dimensional matrix included: sample information, metabolite name and mass spectral response intensity. Internal standard peaks, as well as any known false positive peaks (including noise, column bleed, and derivatized reagent peaks), were removed from the data matrix, deredundant and peak pooled. At the same time, the metabolites were identified by searching database, and the main databases were the HMDB (http://www.hmdb.ca/), Metlin (https://metlin.scripps.edu/) and the self-compiled Majorbio Database (MJDB) of Majorbio Biotechnology Co., Ltd. (Shanghai, China) The data matrix obtained by searching database was uploaded to the Majorbio cloud platform (https://cloud.majorbio.com) for data analysis. Fistly, the data matrix was pre-processed, as Your Personal Adviser of Life Science and Technology Services follows: At least 80% of the metabolic features detected in any set of samples were retained. After filtering, the minimum value in the data matrix was selected to fill the missing value and each metabolic signature was normalized to the sum. To reduce the errors caused by sample preparation and instrument instability, the response intensities of the sample mass spectrometry peaks were normalized using the sum normalization method, to obtain the normalized data matrix. Meanwhile, the variables of QC samples with relative standard deviation (RSD) &amp;gt; 30% were excluded and log10 logarithmicized, to obtain the final data matrix for subsequent analysis.Perform variance analysis on the matrix file after data preprocessing. The R package “ropls”(Version 1.6.2) was used to perform principal component analysis (PCA) and orthogonal least partial squares discriminant analysis (OPLS-DA), and 7-cycle interactive validation evaluating the stability of the model. The metabolites with VIP&amp;gt;1, p&amp;lt;0.05 were determined as significantly different metabolites based on the Variable importance in the projeciton (VIP) obtained by the OPLS-DA model and the p-value generated by student’s t test. Differential metabolites among two groups were mapped into their biochemical pathways through metabolic enrichment and pathway analysis based on KEGG database (http://www. genome.jp/kegg/). These metabolites could be classified according to the pathways they involved or the functions they performed. Enrichment analysis was used to analyze a group of metabolites in a function node whether appears or not. The principle was that the annotation analysis of a single metabolite develops into an annotation analysis of a group of metabolites. Python packages “scipy.stats” (https://docs.scipy.org/doc/scipy/ ) was used to perform enrichment analysis to obtain the most relevant biological pathways for experimental treatments.&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>The LC-MS/MS analysis of sample was conducted on a UHPLC-Orbitrap Exploris 240 system equipped with an ACQUITY HSS T3 column (100 mm × 2.1 mm i.d., 1.8 μm) at Majorbio Bio-Pharm Technology Co. Ltd. (Shanghai, China). The mobile phases consisted of 0.1% formic acid in water:acetonitrile (2:98, v/v) (solvent A) and 0.1% formic acid in acetonitrile (solvent B). The flow rate was 0.40 mL/min and the column temperature was 40℃. The injection volume was 5 μL.&lt;/p></chromatography_protocol><publication>Intercropping with Peucedanum praeruptorum enhances the growth and quality of Pseudostellaria heterophylla.</publication><submitter_name>Qing-Song Yuan</submitter_name><submitter_affiliation>Guizhou University of Traditional Chinese Medicine</submitter_affiliation><organism_part>Root exudates</organism_part><technology_type>mass spectrometry assay</technology_type><disease></disease><extraction_protocol>&lt;p>100 mg solid sample was added to a 2 mL centrifuge tube and a 6 mm diameter grinding bead was added. 800 μL of extraction solution (methanol: water = 4:1 (v:v) containing four internal standards ( 0.02 mg/mL L-2-chlorophenylalanine, etc.) were used for metabolite extraction. Samples were ground by the Wonbio-96c ( Shanghai wanbo biotechnology co, LTD) frozen tissue grinder for 6 min (-10°C, 50 Hz), followed by low-temperature ultrasonic extraction for 30 min (5°C, 40 kHz). The samples were left at -20°C for 30 min, centrifuged for 15 min (4°C, 13000 g), and the supernatant was transferred to the injection vial for LC-MS/MS analysis.&lt;/p></extraction_protocol><organism>Hydroponic sample</organism><full_dataset_link>https://www.ebi.ac.uk/metabolights/MTBLS14102</full_dataset_link><author>Qingsong Yuan. Guizhou University of Traditional Chinese Medicine. yqs198609031006@126.com.</author><author>Chuanzhi Kang.</author><author>Xue Jiang.</author><author>Lingling Wang.</author><author>Yanhong Wang.</author><author>Tao Zhou. Guizhou University of Traditional Chinese Medicine. taozhou88@163.com.</author><author>Jiayue Ran.</author><author>Yanping Gao.</author><author>Xiaohong Ou.</author><author>Zan Li.</author><author>Xianyan Xie. 3515895880@qq.com.</author><author>Yangjun Tan.</author><data_transformation_protocol>&lt;p>The pretreatment of LC/MS raw data was performed by Progenesis QI software, and a three-dimensional data matrix in CSV format was exported. The information in this three-dimensional matrix included: sample information, metabolite name and mass spectral response intensity. Internal standard peaks, as well as any known false positive peaks (including noise, column bleed, and derivatized reagent peaks), were removed from the data matrix, deredundant and peak pooled. At the same time, the metabolites were identified by searching database, and the main databases were the HMDB (http://www.hmdb.ca/), Metlin (https://metlin.scripps.edu/) and the self-compiled Majorbio Database (MJDB) of Majorbio Biotechnology Co., Ltd. (Shanghai, China) The data matrix obtained by searching database was uploaded to the Majorbio cloud platform (https://cloud.majorbio.com) for data analysis. Fistly, the data matrix was pre-processed, as Your Personal Adviser of Life Science and Technology Services follows: At least 80% of the metabolic features detected in any set of samples were retained. After filtering, the minimum value in the data matrix was selected to fill the missing value and each metabolic signature was normalized to the sum. To reduce the errors caused by sample preparation and instrument instability, the response intensities of the sample mass spectrometry peaks were normalized using the sum normalization method, to obtain the normalized data matrix. Meanwhile, the variables of QC samples with relative standard deviation (RSD) &amp;gt; 30% were excluded and log10 logarithmicized, to obtain the final data matrix for subsequent analysis.Perform variance analysis on the matrix file after data preprocessing. The R package “ropls”(Version 1.6.2) was used to perform principal component analysis (PCA) and orthogonal least partial squares discriminant analysis (OPLS-DA), and 7-cycle interactive validation evaluating the stability of the model. The metabolites with VIP&amp;gt;1, p&amp;lt;0.05 were determined as significantly different metabolites based on the Variable importance in the projeciton (VIP) obtained by the OPLS-DA model and the p-value generated by student’s t test. Differential metabolites among two groups were mapped into their biochemical pathways through metabolic enrichment and pathway analysis based on KEGG database (http://www. genome.jp/kegg/). These metabolites could be classified according to the pathways they involved or the functions they performed. Enrichment analysis was used to analyze a group of metabolites in a function node whether appears or not. The principle was that the annotation analysis of a single metabolite develops into an annotation analysis of a group of metabolites. Python packages “scipy.stats” (https://docs.scipy.org/doc/scipy/ ) was used to perform enrichment analysis to obtain the most relevant biological pathways for experimental treatments.&lt;/p></data_transformation_protocol><study_factor>Treatment</study_factor><submitter_email>yqs198609031006@126.com</submitter_email><sample_collection_protocol>&lt;p>At July 1, 2024, fifty milliliters of P. heterophylla culture solution from hydroponic experiments were frozen in liquid nitrogen and lyophilized.&lt;/p></sample_collection_protocol><omics_type>Metabolomics</omics_type><study_design>intercropping</study_design><study_design>photosynthetic</study_design><study_design>Root exudates</study_design><study_design>untargeted analysis</study_design><study_design>Hydroponic sample</study_design><study_design>Pseudostellaria heterophylla</study_design><study_design>Multiomics</study_design><study_design>Peucedanum</study_design><study_design>UHPLC-Orbitrap Exploris 480</study_design><study_design>pooled sample</study_design><study_design>Agilent 1100 Series HPLC System</study_design><curator_keywords>intercropping</curator_keywords><curator_keywords>photosynthetic</curator_keywords><curator_keywords>Root exudates</curator_keywords><curator_keywords>untargeted analysis</curator_keywords><curator_keywords>Hydroponic sample</curator_keywords><curator_keywords>Pseudostellaria heterophylla</curator_keywords><curator_keywords>Multiomics</curator_keywords><curator_keywords>Peucedanum</curator_keywords><curator_keywords>UHPLC-Orbitrap Exploris 480</curator_keywords><curator_keywords>pooled sample</curator_keywords><curator_keywords>Agilent 1100 Series HPLC System</curator_keywords><mass_spectrometry_protocol>&lt;p>The UPLC system was coupled to a UHPLC-Orbitrap Exploris 240 system Mass Spectrometer equipped with an electrospray ionization (ESI) source operating in positive mode and negative mode. The optimal conditions were set as followed: source temperature at 400℃ ; sheath gas flow rate at 40 arb; Aux gas flow rate at 10 arb; ion-spray voltage floating (ISVF) at -2800V in negative mode and 3500V in positive mode, respectively; Normalized collision energy , 20-40-60V rolling for MS/MS. Data acquisition was performed with the Data Dependent Acquisition (DDA) mode. The detection was carried out over a mass range of 70-1050 m/z.&lt;/p></mass_spectrometry_protocol><metabolite_name>Diphenyl Phosphate</metabolite_name><metabolite_name>Indole-3-Propionic Acid</metabolite_name><metabolite_name>2-Fluoroadenosine</metabolite_name><metabolite_name>Thr-Phe</metabolite_name><metabolite_name>Docosapentaenoic Acid</metabolite_name><metabolite_name>L-Aspartyl-L-Phenylalanine</metabolite_name><metabolite_name>Uridine Monophosphate</metabolite_name><metabolite_name>Janthitrem C</metabolite_name><metabolite_name>Soyacerebroside I</metabolite_name><metabolite_name>5-Hydroxy-2-Oxo-4-Ureido-2,5-Dihydro-1H Imidazole-5-Carboxylate</metabolite_name><metabolite_name>Etorphine</metabolite_name><metabolite_name>Quercetin-4'-Glucuronide</metabolite_name><metabolite_name>Glutamyltyrosine</metabolite_name><metabolite_name>Surfactin A</metabolite_name><metabolite_name>Trimellitic Anhydride</metabolite_name><metabolite_name>Ochratoxin B</metabolite_name><metabolite_name>Bz-Arg-Oet</metabolite_name><metabolite_name>N-Arachidonoyl Glutamine</metabolite_name><metabolite_name>Glu-Leu</metabolite_name><metabolite_name>Bms-707035</metabolite_name><metabolite_name>Carboxyifosfamide</metabolite_name><metabolite_name>Prolylproline</metabolite_name><metabolite_name>Phosphatidyl-D-Serine</metabolite_name><metabolite_name>Pe(32:1)</metabolite_name><metabolite_name>Gpetn(16:0/16:1)</metabolite_name><metabolite_name>Lithocholic Acid Glycine Conjugate</metabolite_name><metabolite_name>Aureothin</metabolite_name><metabolite_name>Pregnenolone Sulfate</metabolite_name><metabolite_name>Triphasiol</metabolite_name><metabolite_name>Oxidized Dithiothreitol</metabolite_name><metabolite_name>Lipoxin A4</metabolite_name><metabolite_name>Ethyl Myristate</metabolite_name><metabolite_name>Leu-Tyr</metabolite_name><metabolite_name>Prednisone</metabolite_name><metabolite_name>Petunidin</metabolite_name><metabolite_name>Scopoletin</metabolite_name><metabolite_name>Porphobilinogen</metabolite_name><metabolite_name>Indole-3-Carboxilic Acid-O-Sulphate</metabolite_name><metabolite_name>3-Hydroxyanthranilic Acid</metabolite_name><metabolite_name>Ayapin</metabolite_name><metabolite_name>Gpetn(18:1/16:1)</metabolite_name><metabolite_name>1-Methylxanthine</metabolite_name><metabolite_name>Ile-Tyr</metabolite_name><metabolite_name>N-Acetyl-L-Methionine</metabolite_name><metabolite_name>Eugenin</metabolite_name><metabolite_name>Glucoconringiin</metabolite_name><metabolite_name>Ethotoin</metabolite_name><metabolite_name>1-Oleoylglycerophosphoserine</metabolite_name><metabolite_name>Emideltide</metabolite_name><metabolite_name>Levobunolol</metabolite_name><metabolite_name>3-Methylthiopropyl-Desulfoglucosinolate</metabolite_name><metabolite_name>Gpetn(22:5/22:5)</metabolite_name><metabolite_name>Eicosopentanoic Acid</metabolite_name><metabolite_name>P-Coumaric Acid Sulfate</metabolite_name><metabolite_name>Bolton-Hunter Reagent</metabolite_name><metabolite_name>Homovanillic Acid Sulfate</metabolite_name><metabolite_name>Ps(6 Keto-Pgf1Alpha/18:3(6Z,9Z,12Z))</metabolite_name><metabolite_name>Deoxycholylisoleucine</metabolite_name><metabolite_name>Starch Acetate</metabolite_name><metabolite_name>Cinncassiol A</metabolite_name><metabolite_name>6-Keto-Prostaglandin F1A</metabolite_name><metabolite_name>Tridecanedioic Acid</metabolite_name><metabolite_name>Cinncassiol E</metabolite_name><metabolite_name>Isopropylmaleic Acid</metabolite_name><metabolite_name>(+/-)-Tryptophan</metabolite_name><metabolite_name>Val-Ile</metabolite_name><metabolite_name>Dehydroeburicoic Acid</metabolite_name><metabolite_name>3-Furoic Acid</metabolite_name><metabolite_name>Amoxicilloyl</metabolite_name><metabolite_name>Phosphate</metabolite_name><metabolite_name>Octadecenedioic Acid</metabolite_name><metabolite_name>Veranisatin C</metabolite_name><metabolite_name>2-Furoic Acid</metabolite_name><metabolite_name>Flavin Mononucleotide</metabolite_name><metabolite_name>Imidazolone A</metabolite_name><metabolite_name>Thiodi-Glycolic Acid</metabolite_name><metabolite_name>2-Lysophosphatidylcholine</metabolite_name><metabolite_name>Bisnoryangonin</metabolite_name><metabolite_name>Val-Phe</metabolite_name><metabolite_name>Benzotript</metabolite_name><metabolite_name>Pc(35:2)</metabolite_name><metabolite_name>Succinyldisalicylic Acid</metabolite_name><metabolite_name>Cinncassiol C2</metabolite_name><metabolite_name>5-Deoxyribose-1-Phosphate</metabolite_name><metabolite_name>Flavin Adenine Dinucleotide</metabolite_name><metabolite_name>Pg(36:2)</metabolite_name><metabolite_name>Piperonylic Acid</metabolite_name><metabolite_name>Dehydroisocoproporphyrinogen</metabolite_name><metabolite_name>Phenylalanyl-Phenylalanyl-Arginine Chloromethyl Ketone</metabolite_name><metabolite_name>N-Sulfo-D-Glucosamine</metabolite_name><metabolite_name>Carboxy-Ethyl-Hydroxychroman</metabolite_name><metabolite_name>Cyclo-Dopa 5-O-Glucoside</metabolite_name><metabolite_name>Artonol B</metabolite_name><metabolite_name>Etoricoxib</metabolite_name><metabolite_name>Ps(Dime(13,5)/Monome(13,5))</metabolite_name><metabolite_name>1-Methyl-1,2-Dihydropyridine-3-Carboxamide</metabolite_name><metabolite_name>Petasitenine</metabolite_name><metabolite_name>Allylisopropylacetamide</metabolite_name><metabolite_name>Pipecuronium</metabolite_name><metabolite_name>Ala-Ile</metabolite_name><metabolite_name>Leu-Val</metabolite_name><metabolite_name>Isopentyl Beta-D-Glucoside</metabolite_name><metabolite_name>Glutamylphenylalanine</metabolite_name><metabolite_name>Betalamic Acid</metabolite_name><metabolite_name>Dodecanedioic Acid</metabolite_name><metabolite_name>L-Proline, 1-Acetyl-4-Hydroxy-, Cis-</metabolite_name><metabolite_name>Patuletin 7-Glucoside</metabolite_name><metabolite_name>Dg(Pgf2Alpha/I-22:0/0:0)</metabolite_name><metabolite_name>Oxandrolone</metabolite_name><metabolite_name>Nirvanol</metabolite_name><metabolite_name>3-Methylxanthine</metabolite_name><metabolite_name>8-Oxoguanine</metabolite_name><metabolite_name>N-(4-Aminobutyl)-N-Ethylisoluminol</metabolite_name><metabolite_name>Citric Acid</metabolite_name><metabolite_name>Phe-Glu</metabolite_name><metabolite_name>Ps(Dime(13,5)/Dime(11,5))</metabolite_name><metabolite_name>5-Hydroxyferulic Acid</metabolite_name><metabolite_name>Linalool (8-Hydroxydihydro-)</metabolite_name><metabolite_name>Dg(Pgd2/A-15:0/0:0)</metabolite_name><metabolite_name>Glucose Aspartate</metabolite_name><metabolite_name>4,7-Dihydro-5-(4-Methyl-3-Pentenyl)-1,2,3-Trithiepin</metabolite_name><metabolite_name>Aerobactin</metabolite_name><metabolite_name>5-Methoxytryptamine</metabolite_name><metabolite_name>Glyceric Acid</metabolite_name><metabolite_name>Trifluoroacetyl-L-Lysyl-L-Alaninanilide</metabolite_name><metabolite_name>Mycophenolic Acid</metabolite_name><metabolite_name>Gibberellin A53</metabolite_name><metabolite_name>N-Acetylaspartic Acid</metabolite_name><metabolite_name>Cerebroside B</metabolite_name><metabolite_name>3-Hydroxybenzoic Acid</metabolite_name><metabolite_name>7-Methoxycoumarin-3-Carbonyl Azide</metabolite_name><metabolite_name>Ceranapril</metabolite_name><metabolite_name>Elsibucol</metabolite_name><metabolite_name>N-[2-(3,4-Dihydroxyphenyl)Ethyl]Icosa-5,8,11,14-Tetraenamide</metabolite_name><metabolite_name>Pregn-4-Ene-3,20-Dione, 11,17,18,21-Tetrahydroxy-, (11Beta)-</metabolite_name><metabolite_name>26-Deoxyactein</metabolite_name><metabolite_name>Glu-Phe</metabolite_name><metabolite_name>Abt-510</metabolite_name><metabolite_name>Dg(Pgd2/I-19:0/0:0)</metabolite_name><metabolite_name>Kynurenic Acid</metabolite_name><metabolite_name>Kanokoside D</metabolite_name><metabolite_name>negletein 6-[Rhamnosyl-(1->2)-Fucoside]</metabolite_name><metabolite_name>3'-Adenylic Acid</metabolite_name><metabolite_name>Gibberellin A24</metabolite_name><metabolite_name>Thr-Ile</metabolite_name><metabolite_name>Prostaglandin A1</metabolite_name><metabolite_name>Myricetin 3-(6-Acetylgalactoside)</metabolite_name><metabolite_name>Benzo(F)Quinolin-3(2H)-One, 8-Chloro-1,4,4A,5,6,10B-Hexahydro-4-Methyl-, Trans-</metabolite_name><metabolite_name>Delprostenato</metabolite_name><metabolite_name>Phe-Ser</metabolite_name><metabolite_name>Melagatran</metabolite_name><metabolite_name>Ile-Glu</metabolite_name><metabolite_name>Isopropyl-Beta-D-Thiogalactopyranoside</metabolite_name><metabolite_name>Bendamustine</metabolite_name><metabolite_name>Obtusilactone A</metabolite_name><metabolite_name>3-[4-Hydroxy-3-[3-(4-Hydroxyphenyl)Prop-2-Enoyloxy]Phenyl]Prop-2-Enoic Acid</metabolite_name><metabolite_name>Betalone</metabolite_name><metabolite_name>14,16-Nonacosanedione</metabolite_name><metabolite_name>Gamma-Glutamylisoleucine</metabolite_name><metabolite_name>2-Hydroxynevirapine</metabolite_name><metabolite_name>4-Nitrophenyl Beta-D-Glucopyranosiduronic Acid</metabolite_name><metabolite_name>3-Nitrotyrosine</metabolite_name><metabolite_name>2,3-Thioepoxy Madol</metabolite_name><metabolite_name>N-Methyl-4,6,7-Trihydroxy-1,2,3,4-Tetrahydroisoquinoline</metabolite_name><metabolite_name>Alongside</metabolite_name><metabolite_name>2-Hydroxy-4-Methylthiobutyric Acid</metabolite_name><metabolite_name>Methyl 5-Hydroxyoxindole-3-Acetate</metabolite_name><metabolite_name>Theogallin</metabolite_name><metabolite_name>Fosphenytoin</metabolite_name><metabolite_name>4-Hydroxy-5-(3',4'-Dihydroxyphenyl)-Valeric Acid-O-Glucuronide</metabolite_name><metabolite_name>Bax Inhibitor Peptide V5</metabolite_name><metabolite_name>Pyrrolostatin</metabolite_name><metabolite_name>Suberylglycine</metabolite_name><metabolite_name>Glu-Ile</metabolite_name><metabolite_name>Ataluren</metabolite_name><metabolite_name>2-Hydroxyestradiol</metabolite_name><metabolite_name>2-Propylglutaric Acid</metabolite_name><metabolite_name>Gly-Phe</metabolite_name><metabolite_name>Cycloheximide</metabolite_name><metabolite_name>3'-N-Acetyl-4'-O-(10,12-Octadecadienoyl)Fusarochromanone</metabolite_name><metabolite_name>Ineketone</metabolite_name><metabolite_name>Glutaminyl-Gamma-Glutamate</metabolite_name><metabolite_name>Gpetn(16:1/18:1)</metabolite_name><metabolite_name>Asp-Leu</metabolite_name><metabolite_name>((4-(4-Amidinophenoxy)Butanoyl)Aspartyl)Valine</metabolite_name><metabolite_name>3B,18B-3-Methoxy-11-Oxo-12-Oleanen-30-Oic Acid</metabolite_name><metabolite_name>Ganoderiol F</metabolite_name><metabolite_name>4-Hydroxy-5-Phenyltetrahydro-1,3-Oxazin-2-One</metabolite_name><metabolite_name>Peimine</metabolite_name><metabolite_name>Sucrose</metabolite_name><metabolite_name>Cyclic Adp-Ribose</metabolite_name><metabolite_name>Pgh1</metabolite_name><metabolite_name>Leu-Ile</metabolite_name><metabolite_name>N-Phenylacetyl Pyroglutamic Acid</metabolite_name><metabolite_name>Gpetn(18:2/18:2)</metabolite_name><metabolite_name>Bardoxolone</metabolite_name><metabolite_name>Trans-2-Trans-4-Heptadien-1-Ol</metabolite_name><metabolite_name>Ile-Phe</metabolite_name><metabolite_name>Polyanethole-Sulfate</metabolite_name><metabolite_name>Phosphonoacetate</metabolite_name><metabolite_name>Pe(40:5)</metabolite_name><metabolite_name>Minocycline</metabolite_name><metabolite_name>Dihydrodeoxy-8-Epiaustdiol</metabolite_name><metabolite_name>Clothianidin</metabolite_name><metabolite_name>Glycine-Betaxanthin</metabolite_name><metabolite_name>Gibberellin A4</metabolite_name><metabolite_name>Gibberellin A5</metabolite_name><metabolite_name>(R)-1-O-[B-D-Apiofuranosyl-(1->2)-B-D-Glucopyranoside]-1,3-Octanediol</metabolite_name><metabolite_name>Cis-Aconitic Acid</metabolite_name><metabolite_name>5-Methylthioribose</metabolite_name><metabolite_name>2,3,4,5-Tetrachloro-4'-Biphenylol</metabolite_name><metabolite_name>Pe(14:0/0:0)</metabolite_name><metabolite_name>5-(3',5'-Dihydroxyphenyl)-Gamma-Valerolactone Sulfate</metabolite_name><metabolite_name>S-Glutaryldihydrolipoamide</metabolite_name><metabolite_name>Bucladesine</metabolite_name><metabolite_name>Oseltamivir</metabolite_name><metabolite_name>8-Hydroxycarvedilol</metabolite_name><metabolite_name>Cholylhistidine</metabolite_name><metabolite_name>4-O-(Indole-3-Acetyl)-D-Glucopyranose</metabolite_name><metabolite_name>Glycyl-L-Leucine</metabolite_name><metabolite_name>Nelumboside</metabolite_name><metabolite_name>Ginkgolic Acid</metabolite_name><metabolite_name>11-Beta-Hydroxyandrosterone-3-Glucuronide</metabolite_name><metabolite_name>5-Chloro-2'-Deoxyuridine</metabolite_name><metabolite_name>Aflatoxin P1</metabolite_name><metabolite_name>Adrenoylcarnitine</metabolite_name><metabolite_name>Phthalate</metabolite_name><metabolite_name>Dehydrocyanaropicrin</metabolite_name><metabolite_name>7,8-Dehydro-Beta-Micropteroxanthin</metabolite_name><metabolite_name>1,4-Dihydroxy-2-Naphthoic Acid</metabolite_name><metabolite_name>Diflucortolone</metabolite_name><metabolite_name>Beta-D-Glucopyranuronic Acid</metabolite_name><metabolite_name>P-Toluenesulfonic Acid</metabolite_name><metabolite_name>D-Dopachrome</metabolite_name><metabolite_name>(S)-2,3-Dihydrodipicolinate</metabolite_name><metabolite_name>Leu-Met</metabolite_name><metabolite_name>4-Nitrophenol</metabolite_name><metabolite_name>Thr-Leu</metabolite_name><metabolite_name>Aspartylglycosamine</metabolite_name><metabolite_name>Apigenin</metabolite_name><metabolite_name>N-(1-Deoxy-1-Fructosyl)Valine</metabolite_name><metabolite_name>Xanthosine 5'-Monophosphate</metabolite_name><metabolite_name>Luteolin</metabolite_name><metabolite_name>4-Nitroquinoline-1-Oxide</metabolite_name><metabolite_name>Tetradecanedioic Acid</metabolite_name><metabolite_name>N-Acetyl-9-Aminominocycline, (4R)-</metabolite_name><metabolite_name>Noreugenin</metabolite_name><metabolite_name>Phyllanthusol B</metabolite_name><metabolite_name>Pe(34:3)</metabolite_name><metabolite_name>(S,E)-2-(5-Hydroxy-8,9-Dihydro-5H-Benzo[7]Annulen-6(7H)-Ylidene)Acetic Acid</metabolite_name><metabolite_name>Cappariloside A</metabolite_name><metabolite_name>Urea Citrate</metabolite_name><metabolite_name>Glycyrrhetinic Acid</metabolite_name><metabolite_name>Asp-Ile</metabolite_name><metabolite_name>Ibritumomab Tiuxetan</metabolite_name><metabolite_name>1,3,5-Trichloro-2-Methoxybenzene</metabolite_name><metabolite_name>Desmethyl Bosentan</metabolite_name><metabolite_name>1,4-Dihydro-2-Methylbenzoicacid</metabolite_name><metabolite_name>Purpurogallin</metabolite_name><metabolite_name>Abietinal</metabolite_name><metabolite_name>Glu-Val</metabolite_name><metabolite_name>Abscisic Acid</metabolite_name><metabolite_name>Xanthine</metabolite_name><metabolite_name>Sulfobutyl Ether</metabolite_name><metabolite_name>Laurenoniolide</metabolite_name><metabolite_name>N-Acetylneuraminic Acid</metabolite_name><metabolite_name>Cordycepin</metabolite_name><metabolite_name>Fraxin</metabolite_name><metabolite_name>Sagecoumarin</metabolite_name><metabolite_name>Pc(33:0)</metabolite_name><metabolite_name>Vaccarin</metabolite_name><metabolite_name>S-(2-Hydroxyethyl)Glutathione</metabolite_name><metabolite_name>Indicine-N-Oxide</metabolite_name><metabolite_name>8H-1,3-Dioxolo[4,5-H][1]Benzopyran-8-One</metabolite_name><metabolite_name>Sobetirome</metabolite_name><metabolite_name>Bilobalide A</metabolite_name><metabolite_name>3'-N-Acetyl-4'-O-(14-Methylpentadecanoyl)Fusarochromanone</metabolite_name><metabolite_name>1,2-Dioleoyl-Sn-Glycero-3-Phosphoethanolamine</metabolite_name><metabolite_name>5-(4'-Hydroxyphenyl)-Gamma-Valerolactone 4'-Sulfate</metabolite_name><metabolite_name>Sinapic Acid Sulfate</metabolite_name><metabolite_name>Pe(36:2)</metabolite_name><metabolite_name>Leu-Glu</metabolite_name><metabolite_name>Dialdehyde</metabolite_name><metabolite_name>10-Octacosene-1,12-Diol</metabolite_name><metabolite_name>Gpetn(18:1/18:1)</metabolite_name><metabolite_name>Lpc(18:3)</metabolite_name><metabolite_name>3,4-Dihydroxyphenylpyruvate</metabolite_name><metabolite_name>2-Hydroxy-6-[(8Z,11Z)-Pentadeca-8,11-Dienyl]Benzoic Acid</metabolite_name><metabolite_name>Gamma-Glutamylmethionine</metabolite_name><metabolite_name>Dimercaptosuccinic Acid Monomethyl Ester</metabolite_name><metabolite_name>Triethylene Glycol Bis(3-Tert-Butyl-4-Hydroxy-5-Methylphenyl)Propionate</metabolite_name><metabolite_name>Gibberellin A8-Catabolite</metabolite_name><metabolite_name>5-(3',5'-Dihydroxyphenyl)-Gamma-Valerolactone-O-Sulphate-O-Methyl</metabolite_name><metabolite_name>11-Deacetylvaltrate 11-(3-Hydroxy-3-Methylbutanoate)</metabolite_name><metabolite_name>10-Hydroxydecanoic Acid</metabolite_name><metabolite_name>Cefpirome</metabolite_name><metabolite_name>Piscidic Acid</metabolite_name><metabolite_name>Pg(34:1)</metabolite_name><metabolite_name>Pe(P-16:0/18:2)</metabolite_name><metabolite_name>7,8-Dichloro-1,2,3,4-Tetrahydroisoquinoline</metabolite_name><metabolite_name>Phenylalanylaspartic Acid</metabolite_name><metabolite_name>(Imidazolylbiphenylyl)Sulfonylurea</metabolite_name><metabolite_name>Indole-3-Acetyl-Tryptophan</metabolite_name><metabolite_name>3-(2-Propenoic Acid)-O-Benzoquinone</metabolite_name><metabolite_name>Vulgarin</metabolite_name><metabolite_name>Coriandrone E</metabolite_name><metabolite_name>2,4-Dihydroxybenzophenone</metabolite_name><metabolite_name>Fasoracetam</metabolite_name><metabolite_name>Ser-Leu</metabolite_name><metabolite_name>Atorvastatin</metabolite_name><metabolite_name>N(Alpha)-Phosphorylalanylproline</metabolite_name><metabolite_name>Trans-3,5-Diethyl-1,2,4,-Trithiolane</metabolite_name><metabolite_name>Ethyl Cellulose</metabolite_name><metabolite_name>Daphnoretin</metabolite_name><metabolite_name>Pa(5-Iso Pgf2Vi/19:2(10Z,13Z))</metabolite_name><metabolite_name>Gemcitabine</metabolite_name><metabolite_name>5-Cholesten-3Beta-25-Diol-3-Sulfate</metabolite_name><metabolite_name>17A,21-Dihydroxy-5B-Pregnane-3,11,20-Trione</metabolite_name><metabolite_name>Trans-P-Menthane-7,8-Diol 7-Glucoside</metabolite_name><metabolite_name>3',6'-Dihydroxy-4,5-Diaminospiro[Isobenzofuran-1(3H),9'-[9H]Xanthene]-3-One</metabolite_name><metabolite_name>2-Methylcitric Acid</metabolite_name><metabolite_name>Raffinose</metabolite_name><metabolite_name>Docosanal</metabolite_name><metabolite_name>Coumachlor</metabolite_name><metabolite_name>Toluidine</metabolite_name><metabolite_name>Alectrol</metabolite_name><metabolite_name>Leu-Ser</metabolite_name><metabolite_name>17Z-Hexacosenoic Acid</metabolite_name><metabolite_name>Decane-1-Sulfonic Acid</metabolite_name><metabolite_name>2,5-Furandicarboxylic Acid</metabolite_name><metabolite_name>Glycyrrhizaisoflavone B</metabolite_name><metabolite_name>Tryptophyl-Serine</metabolite_name><metabolite_name>Isopropyl Beta-D-Glucoside</metabolite_name><metabolite_name>5,7-Dihydroxy-4H-1-Benzopyran-4-One</metabolite_name><metabolite_name>Indophenol</metabolite_name><metabolite_name>Prostaglandin J2</metabolite_name><metabolite_name>Traumatic Acid</metabolite_name><metabolite_name>Kuguacin B</metabolite_name><metabolite_name>N-Acetyl-Dl-Penicillamine</metabolite_name><metabolite_name>Vicenin 2</metabolite_name><metabolite_name>Dynorphin A (6-8)</metabolite_name><metabolite_name>Indenolol</metabolite_name><metabolite_name>Chondroitin</metabolite_name><metabolite_name>4-P-Coumaroylquinic Acid</metabolite_name><metabolite_name>Hematein</metabolite_name><metabolite_name>Franguloside</metabolite_name><metabolite_name>Isolinderenolide</metabolite_name><metabolite_name>Pe(40:6)</metabolite_name><metabolite_name>Glycylphenylalanylleucylglycine</metabolite_name><metabolite_name>N-Feruloylaspartic Acid</metabolite_name><metabolite_name>3-Keto-B-D-Galactose</metabolite_name><metabolite_name>Henatinib</metabolite_name><metabolite_name>Gemopatrilat</metabolite_name></additional><is_claimable>false</is_claimable><name>Intercropping with Peucedanum praeruptorum enhances the growth and quality of Pseudostellaria heterophylla</name><description>&lt;p>Pseudostellaria heterophylla, a valued shade-loving traditional Chinese medicinal herb, faces severe yield and quality decline under continuous monocropping, threatening industry sustainability. Intercropping, which leverages niche complementarity, offers an eco-friendly mitigation strategy, but its regulatory mechanisms on P. heterophylla remain unclear. Here, we evaluated the influence on P. heterophylla intercropped with Peucedanum praeruptorum via field/hydroponic experiments, integrating phenotypic, photosynthetic, metabolomic, and transcriptomic analyses. Intercropping significantly promoted P. heterophylla growth and yield in a density-dependent manner. High-density intercropping (IS3) increased the fresh weight of plant by 202.80%,and increased the yield of tuberous root by 82.67% compared to monoculture (MPh). Despite reduced photosynthetic rate, intercropping sustained chlorophyll content and reduced damping rate by up to 58.33%, prolonging the effective photosynthetic period to compensate for light limitation. Medicinal quality was concurrently improved. Heterophyllin B, the core bioactive component, rose from 0.0064% (MPh) to 0.0099% (IS1), 0.0093% (IS2), and 0.0096% (IS3), with total saponins and crude polysaccharides also elevated slightly. Additionally, metabolomic analysis identified 1157 differentially accumulated metabolites (DAMs). Peptides, terpenoids, and intermediate products of polysaccharide biosynthesis were enriched under intercropping treatment, promoting quality metabolites biosynthesis. Transcriptomic profiling revealed 141 shared differentially expressed genes (DEGs) across intercropping treatments, with upregulation of light-harvesting complex (LHCA4/LHCB1), chlorophyll metabolism (chlE/chlH), and bioactive component synthesis (PREP/CTSF/SQLE) genes. Weighted gene co-expression network analysis (WGCNA) identified the MEred module correlated with biomass and key transcription factors (GRAS,GATA,BHLH1) regulating growth and metabolites biosynthesis. Collectively,P. praeruptorum intercropping creates a favorable microenvironment, triggering adaptive photosynthetic reprogramming and activating hormone-signaling, secondary metabolism, and nutrient transport pathways to synergistically improve P. heterophylla growth, yield, and quality. This study reveals the adaptive mechanism of shade-tolerant medicinal plants to the environment under intercropping conditions, and has provided theoretical and practical guidance for the ecological cultivation of P. heterophylla.&lt;/p></description><dates><publication>2026-05-06</publication><submission>2026-03-21</submission></dates><accession>MTBLS14102</accession><cross_references><HMDB>HMDB0028893</HMDB><HMDB>HMDB0000148;PW_C000095</HMDB><HMDB>HMDB0002113</HMDB><HMDB>HMDB0038625</HMDB><HMDB>HMDB0012267</HMDB><HMDB>HMDB0037759</HMDB><HMDB>HMDB0257954</HMDB><HMDB>HMDB0060617</HMDB><HMDB>HMDB0000001</HMDB><HMDB>HMDB0000283</HMDB><HMDB>HMDB0001185</HMDB><HMDB>HMDB0000034;PW_C000024</HMDB><HMDB>HMDB0248497</HMDB><HMDB>HMDB0000132</HMDB><HMDB>HMDB0259142</HMDB><HMDB>HMDB0014634</HMDB><HMDB>HMDB0255658</HMDB><HMDB>HMDB0028684</HMDB><HMDB>HMDB0253490</HMDB><HMDB>HMDB0060410</HMDB><HMDB>HMDB0256878</HMDB><HMDB>HMDB0248452</HMDB><HMDB>HMDB0028886</HMDB><HMDB>HMDB0258379</HMDB><HMDB>HMDB0041379</HMDB><HMDB>HMDB0003950</HMDB><HMDB>HMDB0250970</HMDB><HMDB>HMDB0255983</HMDB><HMDB>HMDB0028839</HMDB><HMDB>HMDB0000050;HMDB0247583;PW_C000034</HMDB><HMDB>HMDB0253048</HMDB><HMDB>HMDB0001991;PW_C001335</HMDB><HMDB>HMDB0258970</HMDB><HMDB>HMDB0000089</HMDB><HMDB>HMDB0036583;LMFA02020010</HMDB><HMDB>HMDB0041419</HMDB><HMDB>HMDB0303767</HMDB><HMDB>HMDB0002017</HMDB><HMDB>HMDB0028691</HMDB><HMDB>HMDB0015132</HMDB><HMDB>HMDB0013062</HMDB><HMDB>HMDB0035372</HMDB><HMDB>HMDB0015122</HMDB><HMDB>HMDB0243530</HMDB><HMDB>HMDB0256045</HMDB><HMDB>HMDB0033691</HMDB><HMDB>HMDB0011741</HMDB><HMDB>HMDB0253109</HMDB><HMDB>HMDB0000210;HMDB0250782;PW_C000136</HMDB><HMDB>HMDB0246838</HMDB><HMDB>HMDB0254740</HMDB><HMDB>HMDB0241109</HMDB><HMDB>HMDB0000671</HMDB><HMDB>HMDB0034777</HMDB><HMDB>HMDB0061822</HMDB><HMDB>HMDB0015441</HMDB><HMDB>HMDB0240458</HMDB><HMDB>HMDB0002089</HMDB><HMDB>HMDB0060442</HMDB><HMDB>HMDB0302755</HMDB><HMDB>HMDB0001938</HMDB><HMDB>HMDB0001901</HMDB><HMDB>HMDB0029737</HMDB><HMDB>HMDB0000037</HMDB><HMDB>HMDB0005796</HMDB><HMDB>HMDB0246756</HMDB><HMDB>HMDB0037592</HMDB><HMDB>HMDB0304788</HMDB><HMDB>HMDB0258292</HMDB><HMDB>HMDB0246429</HMDB><HMDB>HMDB0000594</HMDB><HMDB>HMDB0014825</HMDB><HMDB>HMDB0004081</HMDB><HMDB>HMDB0254838</HMDB><HMDB>HMDB0255464</HMDB><HMDB>HMDB0032764</HMDB><HMDB>HMDB0256780</HMDB><HMDB>HMDB0002706</HMDB><HMDB>HMDB0250877</HMDB><HMDB>HMDB0002390</HMDB><HMDB>HMDB0062645</HMDB><HMDB>HMDB0036157</HMDB><HMDB>HMDB0304408</HMDB><HMDB>HMDB0029448</HMDB><HMDB>HMDB0257599</HMDB><HMDB>HMDB0041920</HMDB><HMDB>HMDB0015321</HMDB><HMDB>HMDB0250616</HMDB><HMDB>HMDB0258230</HMDB><HMDB>HMDB0060852;PW_C040611</HMDB><HMDB>HMDB0250954</HMDB><HMDB>HMDB0251157</HMDB><HMDB>HMDB0003556</HMDB><HMDB>HMDB0036434</HMDB><HMDB>HMDB0252432</HMDB><HMDB>HMDB0245544</HMDB><HMDB>HMDB0015095</HMDB><HMDB>HMDB0032012</HMDB><HMDB>HMDB0030641</HMDB><HMDB>HMDB0037582</HMDB><HMDB>HMDB0033965</HMDB><HMDB>HMDB0014322</HMDB><HMDB>HMDB0255226</HMDB><HMDB>HMDB0252833</HMDB><HMDB>HMDB0028981</HMDB><HMDB>HMDB0240687</HMDB><HMDB>HMDB0248298</HMDB><HMDB>HMDB0038995</HMDB><HMDB>HMDB0015485</HMDB><HMDB>HMDB0249137</HMDB><HMDB>HMDB0036317</HMDB><HMDB>HMDB0247867</HMDB><HMDB>HMDB0258290</HMDB><HMDB>HMDB0032997</HMDB><HMDB>HMDB0251007</HMDB><HMDB>HMDB0247595</HMDB><HMDB>HMDB0005771</HMDB><HMDB>HMDB0257938</HMDB><HMDB>HMDB0303942</HMDB><HMDB>HMDB0302720;HMDB0034277</HMDB><HMDB>HMDB0258812</HMDB><HMDB>HMDB0014514;PW_C008891</HMDB><HMDB>HMDB0038516</HMDB><HMDB>HMDB0060826</HMDB><HMDB>HMDB0248001</HMDB><HMDB>HMDB0004708</HMDB><HMDB>HMDB0036648;LMPR0103410006</HMDB><HMDB>HMDB0035612</HMDB><HMDB>HMDB0006294</HMDB><HMDB>HMDB0005020</HMDB><HMDB>HMDB0301837</HMDB><HMDB>HMDB0059764</HMDB><HMDB>HMDB0258876</HMDB><HMDB>HMDB0257249</HMDB><HMDB>HMDB0000086</HMDB><HMDB>HMDB0254704</HMDB><HMDB>HMDB0060850</HMDB><HMDB>HMDB0015043;HMDB0243537;PW_C009355</HMDB><HMDB>HMDB0252101</HMDB><HMDB>HMDB0258235</HMDB><HMDB>HMDB0257571</HMDB><HMDB>HMDB0014376</HMDB><HMDB>HMDB0253475</HMDB><HMDB>HMDB0250941</HMDB><HMDB>HMDB0257277</HMDB><HMDB>HMDB0031763</HMDB><HMDB>HMDB0036456</HMDB><HMDB>HMDB0304223</HMDB><HMDB>HMDB0251890</HMDB><HMDB>HMDB0003072</HMDB><HMDB>HMDB0001932</HMDB><HMDB>HMDB0034146</HMDB><HMDB>HMDB0242408</HMDB><HMDB>HMDB0015281</HMDB><HMDB>HMDB0038122</HMDB><HMDB>HMDB0301821</HMDB><HMDB>HMDB0012220</HMDB><HMDB>HMDB0036453</HMDB><HMDB>HMDB0031936</HMDB><HMDB>HMDB0033135</HMDB><HMDB>HMDB0015002</HMDB><HMDB>HMDB0030466</HMDB><HMDB>HMDB0252324</HMDB><HMDB>HMDB0037559</HMDB><HMDB>HMDB0015193</HMDB><HMDB>HMDB0302864</HMDB><HMDB>HMDB0038202</HMDB><HMDB>HMDB0033243</HMDB><HMDB>HMDB0033960</HMDB><HMDB>HMDB0036423</HMDB><HMDB>HMDB0248818</HMDB><HMDB>HMDB0248395</HMDB><HMDB>HMDB0248559</HMDB><HMDB>HMDB0040615</HMDB><HMDB>HMDB0035934</HMDB><HMDB>HMDB0036685</HMDB><HMDB>HMDB0035915;LMFA12000039</HMDB><HMDB>HMDB0012283</HMDB><HMDB>HMDB0039522</HMDB><HMDB>HMDB0034714</HMDB><HMDB>HMDB0258762</HMDB><HMDB>HMDB0034889</HMDB><HMDB>HMDB0002825</HMDB><HMDB>HMDB0010697</HMDB><HMDB>HMDB0036789</HMDB><HMDB>HMDB0113986</HMDB><HMDB>HMDB0036791</HMDB><HMDB>HMDB0010388</HMDB><HMDB>HMDB0009702</HMDB><HMDB>HMDB0256501</HMDB><HMDB>HMDB0033244</HMDB><HMDB>HMDB0263298</HMDB><HMDB>HMDB0060928</HMDB><HMDB>HMDB0007735</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