Malic_acid (BioDeep_00000001119)

Main id: BioDeep_00000001660

 

PANOMIX_OTCML-2023 BioNovoGene_Lab2019


代谢物信息卡片


Malic acid, Pharmaceutical Secondary Standard; Certified Reference Material

化学式: C4H6O5 (134.0215)
中文名称: L-羟基丁二酸-1-13C, DL-苹果酸, 苹果酸
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C(C(C(=O)O)O)C(=O)O
InChI: InChI=1S/C4H6O5/c5-2(4(8)9)1-3(6)7/h2,5H,1H2,(H,6,7)(H,8,9)

描述信息

Malic acid is a 2-hydroxydicarboxylic acid that is succinic acid in which one of the hydrogens attached to a carbon is replaced by a hydroxy group. It has a role as a food acidity regulator and a fundamental metabolite. It is a 2-hydroxydicarboxylic acid and a C4-dicarboxylic acid. It is functionally related to a succinic acid. It is a conjugate acid of a malate(2-) and a malate.
Malic acid has been used in trials studying the treatment of Xerostomia, Depression, and Hypertension.
See also: Hibiscus sabdariffa Flower (part of) ... View More ...
A 2-hydroxydicarboxylic acid that is succinic acid in which one of the hydrogens attached to a carbon is replaced by a hydroxy group.
Malic acid (Hydroxybutanedioic acid) is a dicarboxylic acid that is naturally found in fruits such as apples and pears. It plays a role in many sour or tart foods.
Malic acid (Hydroxybutanedioic acid) is a dicarboxylic acid that is naturally found in fruits such as apples and pears. It plays a role in many sour or tart foods.

同义名列表

112 个代谢物同义名

Malic acid, Pharmaceutical Secondary Standard; Certified Reference Material; Malic acid, United States Pharmacopeia (USP) Reference Standard; MALIC ACID (CONSTITUENT OF CRANBERRY LIQUID PREPARATION) [DSC]; MALIC ACID (CONSTITUENT OF CRANBERRY LIQUID PREPARATION); 4-ethoxyphenyltrans-4-propylcyclohexanecarboxylate; Malic acid, meets USP/NF testing specifications; DL-Malic acid, Vetec(TM) reagent grade, 98\\%; malic acid, monopotassium salt, (+-)-isomer; malic acid, calcium salt, (1:1), (S)-isomer; (+-)-1-Hydroxy-1,2-ethanedicarboxylic acid; DL-Malic acid, SAJ first grade, >=99.0\\%; malic acid, potassium salt, (R)-isomer; calcium (hydroxy-1-malate) hexahydrate; malic acid, disodium salt, (R)-isomer; DL-Malic acid, ReagentPlus(R), >=99\\%; malic acid, disodium salt, (S)-isomer; 2-Hydroxyethane-1,2-dicarboxylic acid; 0C9A2DC0-FEA2-4864-B98B-0597CDD0AD06; DL-Malic acid, >=98\\% (capillary GC); malic acid, sodium salt, (+-)-isomer; DL-Malic acid, ReagentPlus(R), 99\\%; Butanedioic acid, 2-hydroxy-, (2S)-; DL-Malic acid, analytical standard; Kyselina hydroxybutandiova [Czech]; malic acid, magnesium salt (2:1); BUTANEDIOIC ACID, HYDROXY-, (S)-; DL-Malic acid, USP, 99.0-100.5\\%; HYDROXYBUTANEDIOIC ACID, (+/-)-; HYDROXYBUTANEDIOIC ACID [HSDB]; (2S)-2-hydroxybutanedioic acid; Hydroxybutanedioic acid, (+-)-; Hydroxybutanedioic acid, (-)-; butanedioic acid, 2-hydroxy-; DL-2-hydroxybutanedioic acid; (R)-Hydroxybutanedioic acid; (S)-Hydroxybutanedioic acid; Butanedioic acid, hydroxy-; DL-Malic acid, FCC, >=99\\%; 2-Hydroxydicarboxylic acid; Kyselina hydroxybutandiova; 2-hydroxy-butanedioic acid; (+/-)-HYDROXYSUCCINIC ACID; dl-Hydroxybutanedioic acid; Monohydroxybernsteinsaeure; alpha-Hydroxysuccinic acid; MALIC ACID (USP IMPURITY); malic acid, disodium salt; MALIC ACID (EP MONOGRAPH); Butanedioic acid, (.+-.)-; (+-)-Hydroxysuccinic acid; MALIC ACID [USP IMPURITY]; MALIC ACID [EP MONOGRAPH]; Kyselina jablecna [Czech]; 2-Hydroxybutanedioic acid; 2-hydroxyl-succinic acid; 2-HYDROXY-SUCCINIC ACID; Succinic acid, hydroxy-; HYOSCYAMINEHYDROBROMIDE; hydroxybutanedioic acid; malic acid, (R)-isomer; DL-MALIC-2,3,3-D3 ACID; 2-Hydroxysuccinic acid; Malic acid-, (L-form)-; DL-Malic acid, >=99\\%; Hydroxybutandisaeure; hydroxysuccinic acid; MALIC ACID (USP-RS); MALIC ACID [USP-RS]; Musashi-no-Ringosan; DL-Malic acid, 99\\%; MALIC ACID [WHO-DD]; MALIC ACID [VANDF]; Racemic malic acid; R,S(+-)-Malic acid; L-Malic acid-1-13C; Deoxytetraric acid; MALIC ACID [INCI]; Kyselina jablecna; MALIC ACID [FCC]; (+/-)-Malic acid; MALIC ACID [MI]; Malic acid (NF); Malic acid, DL-; MALIC ACID (II); (+-)-Malic acid; L-(-)-MalicAcid; MALIC ACID,(DL); Malic acid [NF]; .+-.-Malic acid; MALIC ACID [II]; Malic acid, L-; (±)-Malic Acid; Malicum acidum; d,l-malic acid; Oprea1_130558; DL-malic acid; Oprea1_624131; DL-Apple Acid; Pomalous acid; Aepfelsaeure; Tox21_201536; Pomalus acid; Tox21_300372; R-Malic acid; Malic acid; Apple acid; AI3-06292; malate; H2mal; E 296; Malate; Malic acid



数据库引用编号

22 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

34 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(2)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(32)

PharmGKB(0)

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

  • PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 11 ACLY, FH, G6PD, GLUL, HSPD1, MDH1, ME1, PC, PKM, SLC9A1, TXN
Peripheral membrane protein 2 G6PD, HSD17B6
Nucleus 5 CS, FH, GLUL, PKM, TXN
cytosol 11 ACLY, FH, G6PD, GLUL, GPT, HSPD1, MDH1, ME1, PC, PKM, TXN
centrosome 1 MDH1
nucleoplasm 4 ACLY, ATP2B1, SLC9A1, TXN
Cell membrane 4 ATP2B1, GLUL, GOT2, SLC9A1
Lipid-anchor 1 GLUL
lamellipodium 1 SLC9A1
Early endosome membrane 1 HSD17B6
Multi-pass membrane protein 3 ATP2B1, SLC25A13, SLC9A1
Synapse 1 ATP2B1
cell surface 2 HSPD1, SLC9A1
glutamatergic synapse 1 ATP2B1
Golgi membrane 1 INS
mitochondrial inner membrane 2 HSPD1, SLC25A13
presynaptic membrane 1 ATP2B1
Cytoplasm, cytosol 4 ACLY, G6PD, GLUL, MDH1
plasma membrane 8 ATP2B1, GCG, GLUL, GOT2, HSPD1, ME1, SLC25A13, SLC9A1
synaptic vesicle membrane 1 ATP2B1
Membrane 7 ACLY, ATP2B1, CS, G6PD, HSPD1, ME1, SLC9A1
apical plasma membrane 1 SLC9A1
basolateral plasma membrane 2 ATP2B1, SLC9A1
extracellular exosome 13 ACLY, ATP2B1, CS, FH, G6PD, GLUL, GOT2, GPT, HSPD1, MDH1, PKM, SLC9A1, TXN
Lumenal side 1 HSD17B6
endoplasmic reticulum 2 GLUL, HSD17B6
extracellular space 4 GCG, HSPD1, INS, MDH1
perinuclear region of cytoplasm 1 SLC9A1
intercalated disc 1 SLC9A1
mitochondrion 10 CS, FH, GLUL, GOT2, HSPD1, ME1, PC, PKM, SLC25A13, SLC9A1
protein-containing complex 1 HSPD1
intracellular membrane-bounded organelle 3 ATP2B1, G6PD, HSD17B6
Microsome membrane 1 HSD17B6
Secreted 3 GCG, INS, TXN
extracellular region 5 ACLY, GCG, INS, PKM, TXN
cytoplasmic side of plasma membrane 1 G6PD
Single-pass membrane protein 1 ME1
Mitochondrion matrix 3 CS, GOT2, PC
mitochondrial matrix 5 CS, FH, GOT2, HSPD1, PC
centriolar satellite 1 G6PD
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane 1 ATP2B1
Extracellular vesicle 1 PKM
T-tubule 1 SLC9A1
Early endosome 1 HSPD1
clathrin-coated pit 1 HSPD1
vesicle 1 PKM
Mitochondrion inner membrane 1 SLC25A13
Membrane raft 1 SLC9A1
focal adhesion 1 SLC9A1
Mitochondrion intermembrane space 1 SLC25A13
mitochondrial intermembrane space 1 SLC25A13
collagen-containing extracellular matrix 1 PKM
secretory granule 1 HSPD1
lateral plasma membrane 1 ATP2B1
cilium 1 PKM
cell projection 1 ATP2B1
Chromosome 1 FH
sperm midpiece 1 HSPD1
Basolateral cell membrane 2 ATP2B1, SLC9A1
site of double-strand break 1 FH
endosome lumen 1 INS
Presynaptic cell membrane 1 ATP2B1
cell body 1 GLUL
sperm plasma membrane 1 HSPD1
Microsome 1 GLUL
lipopolysaccharide receptor complex 1 HSPD1
ficolin-1-rich granule lumen 2 ACLY, PKM
secretory granule lumen 3 GCG, INS, PKM
Golgi lumen 1 INS
endoplasmic reticulum lumen 2 GCG, INS
transport vesicle 1 INS
azurophil granule lumen 1 ACLY
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
immunological synapse 1 ATP2B1
Rough endoplasmic reticulum 1 PKM
coated vesicle 1 HSPD1
glial cell projection 1 GLUL
[Glucagon-like peptide 1]: Secreted 1 GCG
[Isoform Mitochondrial]: Mitochondrion 1 FH
[Isoform Cytoplasmic]: Cytoplasm, cytosol 1 FH
migrasome 1 HSPD1
photoreceptor ribbon synapse 1 ATP2B1
[Isoform M2]: Cytoplasm 1 PKM
[Isoform M1]: Cytoplasm 1 PKM
cation-transporting ATPase complex 1 SLC9A1


文献列表

  • Minghui Liu, Bili Cao, Jin-Wei Wei, Biao Gong. Redesigning a S-nitrosylated pyruvate-dependent GABA transaminase 1 to generate high-malate and saline-alkali-tolerant tomato. The New phytologist. 2024 Jun; 242(5):2148-2162. doi: 10.1111/nph.19693. [PMID: 38501546]
  • Shangguang Du, Jun Luo, Xutang Tu, Zuozuo Ai, Dong Wu, Zhengrong Zou, Liping Luo. Metabolic profiling of Oryza sativa seedlings under chilling stress using nanoliter electrospray ionization mass spectrometry. Food chemistry. 2024 Apr; 438(?):138005. doi: 10.1016/j.foodchem.2023.138005. [PMID: 37983997]
  • Yu-Lei Jia, Ying Zhang, Lu-Wei Xu, Zi-Xu Zhang, Ying-Shuang Xu, Wang Ma, Yang Gu, Xiao-Man Sun. Enhanced fatty acid storage combined with the multi-factor optimization of fermentation for high-level production of docosahexaenoic acid in Schizochytrium sp. Bioresource technology. 2024 Apr; 398(?):130532. doi: 10.1016/j.biortech.2024.130532. [PMID: 38447618]
  • Mingming Sun, Qi Feng, Qi Yan, Huifang Zhao, Haiyan Wang, Shuai Zhang, Changliang Shan, Shuangping Liu, Jiyan Wang, Hongyan Zhai. Malate, a natural inhibitor of 6PGD, improves the efficacy of chemotherapy in lung cancer. Lung cancer (Amsterdam, Netherlands). 2024 Apr; 190(?):107541. doi: 10.1016/j.lungcan.2024.107541. [PMID: 38531154]
  • Ye Miao, Xuan Hu, Linjie Wang, Rainer Schultze-Kraft, Wenqiang Wang, Zhijian Chen. Characterization of SgALMT genes reveals the function of SgALMT2 in conferring aluminum tolerance in Stylosanthes guianensis through the mediation of malate exudation. Plant physiology and biochemistry : PPB. 2024 Mar; 208(?):108535. doi: 10.1016/j.plaphy.2024.108535. [PMID: 38503187]
  • Jiaojiao Xue, Jianqing Su, Xueyan Wang, Rui Zhang, Xiaoli Li, Ying Li, Yi Ding, Xiuling Chu. Eco-Friendly and Efficient Extraction of Polysaccharides from Acanthopanax senticosus by Ultrasound-Assisted Deep Eutectic Solvent. Molecules (Basel, Switzerland). 2024 Feb; 29(5):. doi: 10.3390/molecules29050942. [PMID: 38474454]
  • Chase P Donnelly, Alexandra De Sousa, Bart Cuypers, Kris Laukens, Asma A Al-Huqail, Han Asard, Gerrit T S Beemster, Hamada AbdElgawad. Malate production, sugar metabolism, and redox homeostasis in the leaf growth zone of Rye (Secale cereale) increase stress tolerance to aluminum stress: A biochemical and genome-wide transcriptional study. Journal of hazardous materials. 2024 02; 464(?):132956. doi: 10.1016/j.jhazmat.2023.132956. [PMID: 37976853]
  • Harinderbir Kaur, Jean-Marie Teulon, Christian Godon, Thierry Desnos, Shu-Wen W Chen, Jean-Luc Pellequer. Correlation between plant cell wall stiffening and root extension arrest phenotype in the combined abiotic stress of Fe and Al. Plant, cell & environment. 2024 Feb; 47(2):574-584. doi: 10.1111/pce.14744. [PMID: 37876357]
  • Shuying Gu, Taju Wu, Junqi Zhao, Tao Sun, Zhen Zhao, Lu Zhang, Jingen Li, Chaoguang Tian. Rewiring metabolic flux to simultaneously improve malate production and eliminate by-product succinate accumulation by Myceliophthora thermophila. Microbial biotechnology. 2024 Jan; ?(?):e14410. doi: 10.1111/1751-7915.14410. [PMID: 38298109]
  • Anthony J Zmuda, Xiaojun Kang, Katie B Wissbroecker, Katrina Freund Saxhaug, Kyle C Costa, Adrian D Hegeman, Thomas D Niehaus. A universal metabolite repair enzyme removes a strong inhibitor of the TCA cycle. Nature communications. 2024 Jan; 15(1):846. doi: 10.1038/s41467-024-45134-0. [PMID: 38287013]
  • Rodolfo A Maniero, Cristiana Picco, Anja Hartmann, Felipe Engelberger, Antonella Gradogna, Joachim Scholz-Starke, Michael Melzer, Georg Künze, Armando Carpaneto, Nicolaus von Wirén, Ricardo F H Giehl. Ferric reduction by a CYBDOM protein counteracts increased iron availability in root meristems induced by phosphorus deficiency. Nature communications. 2024 Jan; 15(1):422. doi: 10.1038/s41467-023-43912-w. [PMID: 38212310]
  • Shafeeq Ur Rahman, Jing-Cheng Han, Muhammad Ahmad, Muhammad Nadeem Ashraf, Muhammad Athar Khaliq, Maryam Yousaf, Yuchen Wang, Ghulam Yasin, Muhammad Farrakh Nawaz, Khalid Ali Khan, Zhenjie Du. Aluminum phytotoxicity in acidic environments: A comprehensive review of plant tolerance and adaptation strategies. Ecotoxicology and environmental safety. 2024 Jan; 269(?):115791. doi: 10.1016/j.ecoenv.2023.115791. [PMID: 38070417]
  • Ayhan Kocaman. Combined interactions of amino acids and organic acids in heavy metal binding in plants. Plant signaling & behavior. 2023 12; 18(1):2064072. doi: 10.1080/15592324.2022.2064072. [PMID: 35491815]
  • Maria Manzoor, Muhammad Shafiq, Iram Gul, Usman Rauf Kamboh, Dong-Xing Guan, Abdulrahman Ali Alazba, Sven Tomforde, Muhammad Arshad. Enhanced lead phytoextraction and soil health restoration through exogenous supply of organic ligands: Geochemical modeling". Journal of environmental management. 2023 Dec; 348(?):119435. doi: 10.1016/j.jenvman.2023.119435. [PMID: 37890401]
  • Yoko Yamaga-Hatakeyama, Masamitsu Okutani, Yuto Hatakeyama, Takayuki Yabiku, Tomohisa Yukawa, Osamu Ueno. Photosynthesis and leaf structure of F1 hybrids between Cymbidium ensifolium (C3) and C. bicolor subsp. pubescens (CAM). Annals of botany. 2023 11; 132(4):895-907. doi: 10.1093/aob/mcac157. [PMID: 36579478]
  • Xin Zhang, Weijie Xue, Lin Qi, Changbo Zhang, Changrong Wang, Yongchun Huang, Yanting Wang, Liangcai Peng, Zhongqi Liu. Malic acid inhibits accumulation of cadmium, lead, nickel and chromium by down-regulation of OsCESA and up-regulation of OsGLR3 in rice plant. Environmental pollution (Barking, Essex : 1987). 2023 Nov; ?(?):122934. doi: 10.1016/j.envpol.2023.122934. [PMID: 37967709]
  • Pan Pan, Huizhan Liu, Ang Liu, Xinchun Zhang, Qingmian Chen, Guihua Wang, Beibei Liu, Qinfen Li, Mei Lei. Rhizosphere environmental factors regulated the cadmium adsorption by vermicompost: Influence of pH and low-molecular-weight organic acids. Ecotoxicology and environmental safety. 2023 Nov; 266(?):115593. doi: 10.1016/j.ecoenv.2023.115593. [PMID: 37856985]
  • Qiqi Zhang, Shilong Tian, Genyun Chen, Qiming Tang, Yijing Zhang, Andrew J Fleming, Xin-Guang Zhu, Peng Wang. Regulatory NADH dehydrogenase-like complex optimizes C4 photosynthetic carbon flow and cellular redox in maize. The New phytologist. 2023 Oct; ?(?):. doi: 10.1111/nph.19332. [PMID: 37872738]
  • Alberto Burgos-Edwards, Sophia Miño, Nélida Nina, Cecilia Plaza, Fabiana Daza, Cristina Theoduloz, Hernán Paillán, Basilio Carrasco, Mónica Gajardo, Guillermo Schmeda-Hirschmann. Phenolic Composition, Antioxidant Capacity, and α-Glucosidase Inhibition of Boiled Green Beans and Leaves from Chilean Phaseolus vulgaris. Plant foods for human nutrition (Dordrecht, Netherlands). 2023 Oct; ?(?):. doi: 10.1007/s11130-023-01111-4. [PMID: 37812277]
  • Valentino Casolo, Marco Zancani, Elisa Pellegrini, Antonio Filippi, Sara Gargiulo, Dennis Konnerup, Piero Morandini, Ole Pedersen. Restricted O2 consumption in pea roots induced by hexanoic acid is linked to depletion of Krebs cycle substrates. Physiologia plantarum. 2023 Sep; 175(5):e14024. doi: 10.1111/ppl.14024. [PMID: 37882315]
  • Natalia Oleinik, Onder Albayram, Mohamed Faisal Kassir, F Cansu Atilgan, Chase Walton, Eda Karakaya, John Kurtz, Alexander Alekseyenko, Habeeb Alsudani, Megan Sheridan, Zdzislaw M Szulc, Besim Ogretmen. Alterations of lipid-mediated mitophagy result in aging-dependent sensorimotor defects. Aging cell. 2023 Aug; ?(?):e13954. doi: 10.1111/acel.13954. [PMID: 37614052]
  • Da Guo, Peng Liu, Qianwen Liu, Lihua Zheng, Sikai Liu, Chen Shen, Li Liu, Shasha Fan, Nan Li, Jiangli Dong, Tao Wang. Legume-specific SnRK1 promotes malate supply to bacteroids for symbiotic nitrogen fixation. Molecular plant. 2023 Aug; ?(?):. doi: 10.1016/j.molp.2023.08.009. [PMID: 37598296]
  • Kashif Saeed, Fatiha Kalam Nisa, Muna Ali Abdalla, Karl Hermann Mühling. The Interplay of Sulfur and Selenium Enabling Variations in Micronutrient Accumulation in Red Spinach. International journal of molecular sciences. 2023 Aug; 24(16):. doi: 10.3390/ijms241612766. [PMID: 37628947]
  • Deepika Kandoi, Baishnab C Tripathy. Overexpression of chloroplastic Zea mays NADP-malic enzyme (ZmNADP-ME) confers tolerance to salt stress in Arabidopsis thaliana. Photosynthesis research. 2023 Aug; ?(?):. doi: 10.1007/s11120-023-01041-x. [PMID: 37561272]
  • Enrico Martinoia, Ekkehard Neuhaus. A complex network regulating malate contents during fruit ripening in climacteric fruits. The New phytologist. 2023 08; 239(3):821-823. doi: 10.1111/nph.18962. [PMID: 37203357]
  • Meiyi Yang, Junxing Song, Xu Zhang, Ruitao Lu, Azheng Wang, Rui Zhai, Zhigang Wang, Chengquan Yang, Lingfei Xu. PbWRKY26 positively regulates malate accumulation in pear fruit by activating PbMDH3. Journal of plant physiology. 2023 Aug; 288(?):154061. doi: 10.1016/j.jplph.2023.154061. [PMID: 37562312]
  • Ahmed Alabd, Haiyan Cheng, Mudassar Ahmad, Xinyue Wu, Lin Peng, Lu Wang, Shulin Yang, Songling Bai, Junbei Ni, Yuanwen Teng. ABRE-BINDING FACTOR3-WRKY DNA-BINDING PROTEIN44 module promotes salinity-induced malate accumulation in pear. Plant physiology. 2023 07; 192(3):1982-1996. doi: 10.1093/plphys/kiad168. [PMID: 36932703]
  • Litong Zheng, Liao Liao, Chenbo Duan, Wenfang Ma, Yunjing Peng, Yangyang Yuan, Yuepeng Han, Fengwang Ma, Mingjun Li, Baiquan Ma. Allelic variation of MdMYB123 controls malic acid content by regulating MdMa1 and MdMa11 expression in apple. Plant physiology. 2023 07; 192(3):1877-1891. doi: 10.1093/plphys/kiad111. [PMID: 36810940]
  • Valéria F Lima, Francisco Bruno S Freire, Silvio A Cândido-Sobrinho, Nicole P Porto, David B Medeiros, Alexander Erban, Joachim Kopka, Markus Schwarzländer, Alisdair R Fernie, Danilo M Daloso. Unveiling the dark side of guard cell metabolism. Plant physiology and biochemistry : PPB. 2023 Jun; 201(?):107862. doi: 10.1016/j.plaphy.2023.107862. [PMID: 37413941]
  • Mengmeng Zhou, Guanqi Wang, Ruoyu Bai, Huiping Zhao, Zhongyuan Ge, Haitao Shi. The self-association of cytoplasmic malate dehydrogenase 1 promotes malate biosynthesis and confers disease resistance in cassava. Plant physiology and biochemistry : PPB. 2023 Jun; 201(?):107814. doi: 10.1016/j.plaphy.2023.107814. [PMID: 37321041]
  • Dongpu Lin, Xuzixin Zhou, Huan Zhao, Xiaoguang Tao, Sanmiao Yu, Xiaopeng Zhang, Yaoqiang Zang, Lingli Peng, Li Yang, Shuyue Deng, Xiyan Li, Xinjing Mao, Aiping Luan, Junhu He, Jun Ma. The Synergistic Mechanism of Photosynthesis and Antioxidant Metabolism between the Green and White Tissues of Ananas comosus var. bracteatus Chimeric Leaves. International journal of molecular sciences. 2023 May; 24(11):. doi: 10.3390/ijms24119238. [PMID: 37298190]
  • Yunjing Peng, Yangyang Yuan, Wenjing Chang, Litong Zheng, Wenfang Ma, Hang Ren, Peipei Liu, Lingcheng Zhu, Jing Su, Fengwang Ma, Mingjun Li, Baiquan Ma. Transcriptional repression of MdMa1 by MdMYB21 in Ma Locus decreases malic acid content in apple fruit. The Plant journal : for cell and molecular biology. 2023 May; ?(?):. doi: 10.1111/tpj.16314. [PMID: 37219375]
  • Bei-Ling Fu, Wen-Qiu Wang, Xiang Li, Tong-Hui Qi, Qiu-Fang Shen, Kun-Feng Li, Xiao-Fen Liu, Shao-Jia Li, Andrew C Allan, Xue-Ren Yin. A dramatic decline in fruit citrate induced by mutagenesis of a NAC transcription factor, AcNAC1. Plant biotechnology journal. 2023 May; ?(?):. doi: 10.1111/pbi.14070. [PMID: 37161940]
  • Sławomir Dresler, Maciej Strzemski, Izabela Baczewska, Mateusz Koselski, Mohammad Bagher Hassanpouraghdam, Dariusz Szczepanek, Ireneusz Sowa, Magdalena Wójciak, Agnieszka Hanaka. Extraction of Isoflavones, Alpha-Hydroxy Acids, and Allantoin from Soybean Leaves-Optimization by a Mixture Design of the Experimental Method. Molecules (Basel, Switzerland). 2023 May; 28(9):. doi: 10.3390/molecules28093963. [PMID: 37175385]
  • Joanna Szablińska-Piernik, Lesław Bernard Lahuta. Polar Metabolites Profiling of Wheat Shoots (Triticum aestivum L.) under Repeated Short-Term Soil Drought and Rewatering. International journal of molecular sciences. 2023 May; 24(9):. doi: 10.3390/ijms24098429. [PMID: 37176136]
  • Xin Tang, Fengzhu Ling, Jianxin Zhao, Haiqin Chen, Wei Chen. Overexpression of Citrate-Malate Carrier Promoted Lipid Accumulation in Oleaginous Filamentous Fungus Mortierella alpina. Journal of agricultural and food chemistry. 2023 May; ?(?):. doi: 10.1021/acs.jafc.3c01577. [PMID: 37155830]
  • Karuna Sharma, Rupam Kapoor. Arbuscular mycorrhiza differentially adjusts central carbon metabolism in two contrasting genotypes of Vigna radiata (L.) Wilczek in response to salt stress. Plant science : an international journal of experimental plant biology. 2023 Apr; 332(?):111706. doi: 10.1016/j.plantsci.2023.111706. [PMID: 37054921]
  • Tong Jiang, Kaitong Du, Jipeng Xie, Geng Sun, Pei Wang, Xi Chen, Zhiyan Cao, Baichen Wang, Qing Chao, Xiangdong Li, Zaifeng Fan, Tao Zhou. Activated malate circulation contributes to the manifestation of light-dependent mosaic symptoms. Cell reports. 2023 Apr; 42(4):112333. doi: 10.1016/j.celrep.2023.112333. [PMID: 37018076]
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