3-IAA (BioDeep_00000860911)

Main id: BioDeep_00000001353

 

PANOMIX_OTCML-2023 BioNovoGene_Lab2019


代谢物信息卡片


InChI=1\C10H9NO2\c12-10(13)5-7-6-11-9-4-2-1-3-8(7)9\h1-4,6,11H,5H2,(H,12,13

化学式: C10H9NO2 (175.0633)
中文名称: 吲哚乙酸(IAA), 3-吲哚乙酸(IAA), 吲哚-3-乙酸
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC=C2C(=C1)C(=CN2)CC(=O)O
InChI: InChI=1S/C10H9NO2/c12-10(13)5-7-6-11-9-4-2-1-3-8(7)9/h1-4,6,11H,5H2,(H,12,13)

描述信息

D006133 - Growth Substances > D010937 - Plant Growth Regulators > D007210 - Indoleacetic Acids
COVID info from COVID-19 Disease Map
Corona-virus
Coronavirus
SARS-CoV-2
COVID-19
SARS-CoV
COVID19
SARS2
SARS
3-Indoleacetic acid (Indole-3-acetic acid) is the most common natural plant growth hormone of the auxin class. It can be added to cell culture medium to induce plant cell elongation and division.
3-Indoleacetic acid (Indole-3-acetic acid) is the most common natural plant growth hormone of the auxin class. It can be added to cell culture medium to induce plant cell elongation and division.

同义名列表

75 个代谢物同义名

InChI=1\C10H9NO2\c12-10(13)5-7-6-11-9-4-2-1-3-8(7)9\h1-4,6,11H,5H2,(H,12,13; 2-(3-Indolyl)acetic acid 3-(Carboxymethyl)-1H-indole; EPA Pesticide Chemical Code 128915; 1H-Indole-3-acetic-a-t acid (9CI); Indole-3-acetic acid-carboxy-14C; Kyselina 3-indolyloctova [Czech]; .omega.-Skatole carboxylic acid; 2-(1H-indol-3-yl)ethanoic acid; .alpha.-Indol-3-yl-acetic acid; 3-Indolylmethylcarboxylic acid; omega-Skatole carboxylic acid; 1H-Indole-3-acetic acid (9CI); 2-(1H-indol-3-yl)Acetic acid; 2-(indol-3-yl)Ethanoic acid; .beta.-Indole-3-acetic acid; Heteroauxinhexteroauxiniaa; (1H-indol-3-yl)Acetic acid; Indole-3-acetic acid (8CI); .beta.-Indolylacetic acid; .beta.-Indoleacetic acid; 1H-Indol-3-ylacetic acid; 1H-Indole-3-acetic acid; Indoleacetic acid (VAN); 3-(Carboxymethyl)indole; beta-Indolylacetic acid; Indole-3-acetic-t acid; beta-Indoleacetic acid; indol-3-Ylacetic acid; Indolyl-3-acetic acid; Acetic acid, indolyl-; SDCCGMLS-0066204.P001; Indole-3-acetic acid; 3-Indolylessigsaeure; 3-Indolylacetic acid; 3-Indoleacetic acid; Maybridge1_006755; Indoleacetic acid; WLN: T56 BMJ D1VQ; EINECS 201-748-2; SR-01000596909-2; Oprea1_602123; I3750_ALDRICH; SMR000471855; 45533_RIEDEL; Hexteroauxin; MLS001066408; AIDS-009893; I8262_SIGMA; .alpha.-IAA; CHEBI:16411; I2886_SIGMA; Heteroauxin; Rhizopon a; AIDS009893; CCRIS 1014; EU-0099905; 54692-39-6; .beta.-IAA; alpha-IAA; ST5308201; AI3-24131; 6305-45-9; beta-IAA; NSC 3787; [3H]-IAA; Rhizopin; NSC3787; 87-51-4; C00954; 3-IAA; IES; IAC; IAA; Indole-3-acetic acid; Indole-3-acetate



数据库引用编号

16 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(1)

PlantCyc(8)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

75 个相关的物种来源信息

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 ABCB1, ABI3, AHR, HBS1L, HPGDS, NIT1, NIT2, PGP, PRKN, SKP1, SLC2A4RG
Golgi apparatus, trans-Golgi network membrane 1 ARF6
Endosome membrane 1 ARF6
Endoplasmic reticulum membrane 1 HSP90B1
Nucleus 7 AHR, HSP90B1, MYB, NIT1, PRKN, SKP1, SLC2A4RG
cytosol 12 AHR, ARF4, ARF6, GSR, HBS1L, HPGDS, HSP90B1, LIPE, MYB, NIT2, PRKN, SKP1
centrosome 2 NIT2, SKP1
nucleoplasm 5 AHR, ATP2B1, HPGDS, MYB, SKP1
RNA polymerase II transcription regulator complex 1 MYB
Cell membrane 4 ABCB1, ARF6, ATP2B1, LIPE
Lipid-anchor 2 ARF4, ARF6
Cleavage furrow 1 ARF6
lamellipodium 1 ABI3
ruffle membrane 1 ARF4
Early endosome membrane 1 ARF6
Multi-pass membrane protein 2 ABCB1, ATP2B1
Synapse 1 ATP2B1
cell cortex 1 ARF6
cell surface 2 ABCB1, TNR
dendritic shaft 1 ABI3
glutamatergic synapse 5 ABI3, ARF4, ARF6, ATP2B1, TNR
Golgi apparatus 4 ARF3, ARF4, ARF6, PRKN
Golgi membrane 2 ARF3, ARF4
postsynapse 1 ARF6
presynaptic membrane 1 ATP2B1
smooth endoplasmic reticulum 1 HSP90B1
Cytoplasm, cytosol 3 ARF6, LIPE, PRKN
Presynapse 2 ARF6, PRKN
endosome 1 ARF6
plasma membrane 5 ABCB1, ARF3, ARF4, ARF6, ATP2B1
synaptic vesicle membrane 1 ATP2B1
Membrane 9 ABCB1, ABI3, ARF4, ARF6, ATP2B1, HBS1L, HSP90B1, LIPE, MYB
apical plasma membrane 1 ABCB1
basolateral plasma membrane 1 ATP2B1
caveola 1 LIPE
extracellular exosome 9 ABCB1, ARF3, ARF4, ARF6, ATP2B1, GSR, HBS1L, HSP90B1, NIT2
endoplasmic reticulum 2 HSP90B1, PRKN
extracellular space 1 TNR
perinuclear region of cytoplasm 3 ARF3, HSP90B1, PRKN
Schaffer collateral - CA1 synapse 1 TNR
mitochondrion 4 GSR, NIT1, NIT2, PRKN
protein-containing complex 2 AHR, HSP90B1
intracellular membrane-bounded organelle 2 ATP2B1, HPGDS
postsynaptic density 2 ABI3, PRKN
extracellular region 3 HSP90B1, NIT2, TNR
Mitochondrion outer membrane 1 PRKN
mitochondrial outer membrane 1 PRKN
mitochondrial matrix 1 GSR
transcription regulator complex 1 AHR
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane 1 ATP2B1
external side of plasma membrane 1 GSR
Secreted, extracellular space, extracellular matrix 1 TNR
dendritic spine 2 ABI3, ARF4
midbody 2 ARF6, HSP90B1
Apical cell membrane 1 ABCB1
Cytoplasm, perinuclear region 1 ARF3
Membrane raft 1 TNR
focal adhesion 2 ARF6, HSP90B1
collagen-containing extracellular matrix 2 HSP90B1, TNR
lateral plasma membrane 1 ATP2B1
nuclear speck 2 PRKN, SLC2A4RG
Cell projection, ruffle 1 ARF6
ruffle 1 ARF6
Cell projection, neuron projection 1 PRKN
neuron projection 1 PRKN
chromatin 1 AHR
cell projection 1 ATP2B1
Flemming body 1 ARF6
[Isoform 2]: Mitochondrion 1 NIT1
Basolateral cell membrane 1 ATP2B1
Recycling endosome membrane 1 ARF6
Lipid droplet 1 LIPE
Membrane, caveola 1 LIPE
aryl hydrocarbon receptor complex 1 AHR
Melanosome 1 HSP90B1
Presynaptic cell membrane 1 ATP2B1
sperm plasma membrane 1 HSP90B1
Midbody, Midbody ring 1 ARF6
ubiquitin ligase complex 1 PRKN
filopodium membrane 1 ARF6
[Isoform 1]: Cytoplasm 1 NIT1
endoplasmic reticulum lumen 1 HSP90B1
nuclear matrix 1 MYB
PcG protein complex 1 SKP1
specific granule lumen 1 NIT2
tertiary granule lumen 1 NIT2
endocytic vesicle 1 ARF6
immunological synapse 1 ATP2B1
perineuronal net 1 TNR
aggresome 1 PRKN
[Isoform 2]: Cytoplasm 1 HBS1L
Sarcoplasmic reticulum lumen 1 HSP90B1
external side of apical plasma membrane 1 ABCB1
dopaminergic synapse 1 PRKN
Lewy body 1 PRKN
Parkin-FBXW7-Cul1 ubiquitin ligase complex 1 PRKN
cytosolic ribosome 1 HBS1L
Cell projection, filopodium membrane 1 ARF6
endocytic vesicle lumen 1 HSP90B1
endoplasmic reticulum chaperone complex 1 HSP90B1
SCF ubiquitin ligase complex 1 SKP1
photoreceptor ribbon synapse 1 ATP2B1
tenascin complex 1 TNR
nuclear aryl hydrocarbon receptor complex 1 AHR
cytosolic aryl hydrocarbon receptor complex 1 AHR
SCAR complex 1 ABI3
Cul7-RING ubiquitin ligase complex 1 SKP1
actin-based cell projection 1 ABI3
Dom34-Hbs1 complex 1 HBS1L


文献列表

  • Sareeka Kumari, Anil Kumar, Ayush Lepcha, Rakshak Kumar. Cold-adapted Exiguobacterium sibiricum K1 as a potential bioinoculant in cold regions: Physiological and genomic elucidation of biocontrol and plant growth promotion. Gene. 2024 Jul; 916(?):148439. doi: 10.1016/j.gene.2024.148439. [PMID: 38583819]
  • Zhikai Wang, Ruihua Wang, Huanran Yuan, Fengfeng Fan, Shaoqing Li, Mingxing Cheng, Zhihong Tian. Comprehensive identification and analysis of DUF640 genes associated with rice growth. Gene. 2024 Jul; 914(?):148404. doi: 10.1016/j.gene.2024.148404. [PMID: 38521113]
  • Yanling Wang, Qi Wang, Fanhang Zhang, Chenyang Han, Wen Li, Mei Ren, Yueyang Wang, Kaijie Qi, Zhihua Xie, Shaoling Zhang, Shutian Tao. PbARF19-mediated auxin signaling regulates lignification in pear fruit stone cells. Plant science : an international journal of experimental plant biology. 2024 Jul; 344(?):112103. doi: 10.1016/j.plantsci.2024.112103. [PMID: 38657909]
  • Rajkumar Vasanthkumar, Venkidasamy Baskar, Sathasivam Vinoth, Kattilaparambil Roshna, Thomas Nancy Mary, Raman Alagupandi, Krishnagowdu Saravanan, Ramalingam Radhakrishnan, Muthukrishnan Arun, Packiaraj Gurusaravanan. Biogenic carbon quantum dots from marine endophytic fungi (Aspergillus flavus) to enhance the curcumin production and growth in Curcuma longa L. Plant physiology and biochemistry : PPB. 2024 Jun; 211(?):108644. doi: 10.1016/j.plaphy.2024.108644. [PMID: 38710114]
  • Xi-Tao Wang, Kai Yan, Tian-Hua Yu, Zhan-Nan Yang, Shi-Qiong Luo. A Single Latent Plant Growth-Promoting Endophyte BH46 Enhances Houttuynia cordata Thunb. Yield and Quality. Journal of agricultural and food chemistry. 2024 May; 72(21):12057-12071. doi: 10.1021/acs.jafc.3c08177. [PMID: 38753758]
  • Khammool Khamsuk, Bernard Dell, Wasu Pathom-Aree, Wanwarang Pathaichindachote, Nungruthai Suphrom, Nareeluk Nakaew, Juangjun Jumpathong. Screening Plant Growth-Promoting Bacteria with Antimicrobial Properties for Upland Rice. Journal of microbiology and biotechnology. 2024 May; 34(5):1029-1039. doi: 10.4014/jmb.2402.02008. [PMID: 38563101]
  • Craig L Cowling, Arielle L Homayouni, Jodi B Callwood, Maxwell R McReynolds, Jasper Khor, Haiyan Ke, Melissa A Draves, Katayoon Dehesh, Justin W Walley, Lucia C Strader, Dior R Kelley. ZmPILS6 is an auxin efflux carrier required for maize root morphogenesis. Proceedings of the National Academy of Sciences of the United States of America. 2024 May; 121(22):e2313216121. doi: 10.1073/pnas.2313216121. [PMID: 38781209]
  • Jin Wang, Lei Liu, Haiyan Zhang, Dilian Zhang, Zhen Dai, Xian Luo, Xiaoli Zhang, Hui Xia, Dong Liang, Xiulan Lv, Lijin Lin. Exogenous indole-3-acetic acid promotes the plant growth and accumulation of selenium in grapevine under selenium stress. BMC plant biology. 2024 May; 24(1):426. doi: 10.1186/s12870-024-05105-5. [PMID: 38769488]
  • Wenwen Li, Jie Li, Khateeb Hussain, Kaihao Peng, Jiaming Yu, Miaoqing Xu, Shiyong Yang. Transporters and phytohormones analysis reveals differential regulation of ryegrass (Lolium perenne L.) in response to cadmium and arsenic stresses. Journal of hazardous materials. 2024 May; 470(?):134228. doi: 10.1016/j.jhazmat.2024.134228. [PMID: 38626683]
  • Ewa Skała, Monika A Olszewska, Przemysław Tabaka, Agnieszka Kicel. Light-Emitting Diodes and Liquid System Affect the Caffeoylquinic Acid Derivative and Flavonoid Production and Shoot Growth of Rhaponticum carthamoides (Willd.) Iljin. Molecules (Basel, Switzerland). 2024 May; 29(9):. doi: 10.3390/molecules29092145. [PMID: 38731636]
  • Carlos Cortés-Albayay, Mabel Delgado-Torres, Giovanni Larama, Cecilia Paredes-Negron, María de la Luz Mora, Paola Durán, Patricio Javier Barra. Comparative genomics of plant growth promoting phosphobacteria isolated from acidic soils. Antonie van Leeuwenhoek. 2024 May; 117(1):76. doi: 10.1007/s10482-024-01961-1. [PMID: 38705910]
  • Jia Liu, Sumei Qiu, Tingting Xue, Yingdan Yuan. Physiology and transcriptome of Sapindus mukorossi seeds at different germination stages. Genomics. 2024 May; 116(3):110822. doi: 10.1016/j.ygeno.2024.110822. [PMID: 38471577]
  • Hongling Zeng, Kaiwei He, Qin He, Liting Xu, Wei Zhang, Xiang Lu, Yongyan Tang, Xiaobo Zhu, Junjie Yin, Min He, Xuewei Chen, Weitao Li. Exogenous Indole-3-Acetic Acid Suppresses Rice Infection of Magnaporthe oryzae by Affecting Plant Resistance and Fungal Growth. Phytopathology. 2024 May; 114(5):1050-1056. doi: 10.1094/phyto-10-23-0365-kc. [PMID: 38709298]
  • Meng-Yao Ma, Li-Li Hu, Wen-Yan Xu, Wei Zhang. L-tryptophan anaerobic fermentation for indole acetic acid production: Bacterial enrichment and effects of zero valent iron. Bioresource technology. 2024 May; 400(?):130691. doi: 10.1016/j.biortech.2024.130691. [PMID: 38599347]
  • S P Ramya Ranjan Nayak, Seenivasan Boopathi, Munisamy Chandrasekar, B Yamini, Vellapandian Chitra, Bader O Almutairi, Selvaraj Arokiyaraj, Ajay Guru, Jesu Arockiaraj. Indole-3 acetic acid induced cardiac hypertrophy in Wistar albino rats. Toxicology and applied pharmacology. 2024 May; 486(?):116917. doi: 10.1016/j.taap.2024.116917. [PMID: 38555004]
  • Yuanzhou Xu, Yunyun Li, Zhuoliang Xiao, Xinyue Zhang, Jiaguo Jiao, Huijuan Zhang, Huixin Li, Feng Hu, Li Xu. Endogenous IAA affected fluoranthene accumulation by regulating H+-ATPase and SOD activity in ryegrass. Ecotoxicology and environmental safety. 2024 May; 276(?):116315. doi: 10.1016/j.ecoenv.2024.116315. [PMID: 38614001]
  • Jiaxin Chen, Run Cai, Lu Tang, Dan Wang, Ruiwei Lv, Changhong Guo. Antagonistic activity and mechanism of Bacillus subtilis CG-6 suppression of root rot and growth promotion in Alfalfa. Microbial pathogenesis. 2024 May; 190(?):106616. doi: 10.1016/j.micpath.2024.106616. [PMID: 38492826]
  • Tiangang Qi, Weiqiang Yang, Muhammad Jawad Hassan, Jiefang Liu, Yujiao Yang, Qinyu Zhou, Hang Li, Yan Peng. Genome-wide identification of Aux/IAA gene family in white clover (Trifolium repens L.) and functional verification of TrIAA18 under different abiotic stress. BMC plant biology. 2024 Apr; 24(1):346. doi: 10.1186/s12870-024-05034-3. [PMID: 38684940]
  • Jinqing Zhang, Shuxia Li, Xueqin Gao, Yaling Liu, BingZhe Fu. Genome-wide identification and expression pattern analysis of the Aux/IAA (auxin/indole-3-acetic acid) gene family in alfalfa (Medicago sativa) and the potential functions under drought stress. BMC genomics. 2024 Apr; 25(1):382. doi: 10.1186/s12864-024-10313-2. [PMID: 38637768]
  • Nidhi Kandhol, Aakriti Srivastava, Padmaja Rai, Shivesh Sharma, Sangeeta Pandey, Vijay Pratap Singh, Durgesh Kumar Tripathi. Cytokinin and indole-3-acetic acid crosstalk is indispensable for silicon mediated chromium stress tolerance in roots of wheat seedlings. Journal of hazardous materials. 2024 Apr; 468(?):133134. doi: 10.1016/j.jhazmat.2023.133134. [PMID: 38387171]
  • Raheel Khan, Muhammad Junaid Sarwar, Muhammad Shabaan, Hafiz Naeem Asghar, Usman Zulfiqar, Irfan Iftikhar, Nazish Aijaz, Fasih Ullah Haider, Talha Chaudhary, Walid Soufan. Exploring the synergistic effects of indole acetic acid (IAA) and compost in the phytostabilization of nickel (Ni) in cauliflower rhizosphere. BMC plant biology. 2024 Apr; 24(1):275. doi: 10.1186/s12870-024-04920-0. [PMID: 38605329]
  • Raifa Abdul Aziz, Poornima Ramesh, Kokkarambath Vannadil Suchithra, Paul Stothard, Vanya Kadla Narayana, Shamprasad Varija Raghu, Fo-Ting Shen, Chiu-Chung Young, T S Keshava Prasad, Asif Hameed. Comprehensive insights into the impact of bacterial indole-3-acetic acid on sensory preferences in Drosophila melanogaster. Scientific reports. 2024 04; 14(1):8311. doi: 10.1038/s41598-024-58829-7. [PMID: 38594449]
  • Min Ji Byun, Hee Seung Seo, Joonghak Lee, Kitae Ban, Serim Oh, Yun Young Lee, Jaesung Lim, Na Kyeong Lee, Chi-Pin James Wang, Minjeong Kim, Jun-Hyeok Han, Juwon Park, Taejong Paik, Hee Ho Park, Tae-Eun Park, Wooram Park, Se-Na Kim, Dae-Hwan Park, Chun Gwon Park. Biofunctional Inorganic Layered Double Hydroxide Nanohybrid Enhances Immunotherapeutic Effect on Atopic Dermatitis Treatment. Small (Weinheim an der Bergstrasse, Germany). 2024 Apr; 20(17):e2304862. doi: 10.1002/smll.202304862. [PMID: 38050931]
  • Xiurong Chen, Xiaoyun Ye, Xiao Yu, Jiamin Zhao, Meijing Song, Danning Yin, Jiayu Yu. Analysis of the regulatory mechanism of exogenous IAA-mediated tryptophan accumulation and synthesis of endogenous IAA in Chlorococcum humicola. Chemosphere. 2024 Apr; 354(?):141633. doi: 10.1016/j.chemosphere.2024.141633. [PMID: 38442772]
  • Tatsuki Akabane, Nobuhiro Suzuki, Kazuyoshi Ikeda, Tomoki Yonezawa, Satoru Nagatoishi, Hiroyoshi Matsumura, Takuya Yoshizawa, Wataru Tsuchiya, Satoshi Kamino, Kouhei Tsumoto, Ken Ishimaru, Etsuko Katoh, Naoki Hirotsu. THOUSAND-GRAIN WEIGHT 6, which is an IAA-glucose hydrolase, preferentially recognizes the structure of the indole ring. Scientific reports. 2024 03; 14(1):6778. doi: 10.1038/s41598-024-57506-z. [PMID: 38514802]
  • Pooja Singh, Saumya Jaiswal, Durgesh Kumar Tripathi, Vijay Pratap Singh. Nitric oxide acts upstream of indole-3-acetic acid in ameliorating arsenate stress in tomato seedlings. Plant physiology and biochemistry : PPB. 2024 Mar; 208(?):108461. doi: 10.1016/j.plaphy.2024.108461. [PMID: 38461754]
  • Xinyan Qu, Yingying Song, Qingjun Li, Qi Xu, Yanru Li, Huimin Zhang, Xuemei Cheng, Charles R Mackay, Quanbo Wang, Wei Liu. Indole-3-acetic acid ameliorates dextran sulfate sodium-induced colitis via the ERK signaling pathway. Archives of pharmacal research. 2024 Mar; 47(3):288-299. doi: 10.1007/s12272-024-01488-z. [PMID: 38489148]
  • Jiayu Yu, Biao Ding, Renjie Li, Xiurong Chen, Danning Yin, Meijing Song, Xiaoyun Ye. The efficient capture of polysaccharides in Tetradesmus obliquus of indole-3-acetic acid coupling sludge extraction. The Science of the total environment. 2024 Feb; 912(?):168963. doi: 10.1016/j.scitotenv.2023.168963. [PMID: 38065504]
  • Haoyue Zhang, Jiuxia Zhao, Jingling Zhang, Shuhan Wen, Shiqing Xie, Shengchao Yang, Junwen Chen, Yanli Zhou, Guangqiang Long. Low-concentration exogenous 3-indoleacetic acid improves fruit-setting rate of Marsdenia tenacissima by inhibiting the expression of embryo abortion-related genes. Gene. 2024 Jan; 893(?):147930. doi: 10.1016/j.gene.2023.147930. [PMID: 38381505]
  • Eliandro Espindula, Luciane Maria Pereira Passaglia. Maize-Azospirillum brasilense interaction: accessing maize's miRNA expression under the effect of an inhibitor of indole-3-acetic acid production by the plant. Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]. 2024 Jan; ?(?):. doi: 10.1007/s42770-023-01236-3. [PMID: 38214876]
  • Hassan Etesami, Bernard R Glick. Bacterial indole-3-acetic acid: A key regulator for plant growth, plant-microbe interactions, and agricultural adaptive resilience. Microbiological research. 2024 Jan; 281(?):127602. doi: 10.1016/j.micres.2024.127602. [PMID: 38228017]
  • Jin-Long Zhou, Ashiwin Vadiveloo, Dong-Zhi Chen, Feng Gao. Regulation effects of indoleacetic acid on lipid production and nutrient removal of Chlorella pyrenoidosa in seawater-containing wastewater. Water research. 2024 Jan; 248(?):120864. doi: 10.1016/j.watres.2023.120864. [PMID: 37979569]
  • Kaniz Fatema, Nur Uddin Mahmud, Dipali Rani Gupta, Md Nurealam Siddiqui, Tahsin Islam Sakif, Aniruddha Sarker, Andrew G Sharpe, Tofazzal Islam. Enhancing rice growth and yield with weed endophytic bacteria Alcaligenes faecalis and Metabacillus indicus under reduced chemical fertilization. PloS one. 2024; 19(5):e0296547. doi: 10.1371/journal.pone.0296547. [PMID: 38753661]
  • Qian Tang, Molly Tillmann, Jerry D Cohen. Analytical methods for stable isotope labeling to elucidate rapid auxin kinetics in Arabidopsis thaliana. PloS one. 2024; 19(5):e0303992. doi: 10.1371/journal.pone.0303992. [PMID: 38776314]
  • Tatjana Popržen, Ivan Nikolić, Dijana Krstić-Milošević, Branka Uzelac, Milana Trifunović-Momčilov, Marija Marković, Olga Radulović. Characterization of the IAA-Producing and -Degrading Pseudomonas Strains Regulating Growth of the Common Duckweed (Lemna minor L.). International journal of molecular sciences. 2023 Dec; 24(24):. doi: 10.3390/ijms242417207. [PMID: 38139036]
  • Zi-Ang Li, Yi Li, Dan Liu, David P Molloy, Zhou-Fei Luo, Hai-Ou Li, Jing Zhao, Jing Zhou, Yi Su, Ruo-Zhong Wang, Chao Huang, Lang-Tao Xiao. YUCCA2 (YUC2)-Mediated 3-Indoleacetic Acid (IAA) Biosynthesis Regulates Chloroplast RNA Editing by Relieving the Auxin Response Factor 1 (ARF1)-Dependent Inhibition of Editing Factors in Arabidopsis thaliana. International journal of molecular sciences. 2023 Nov; 24(23):. doi: 10.3390/ijms242316988. [PMID: 38069311]
  • Lingjuan Tang, Daodong Li, Wei Liu, Yafang Sun, Ying Dai, Wenjing Cui, Xinliu Geng, Dayong Li, Fengming Song, Lijun Sun. Continuous In Vivo Monitoring of Indole-3-Acetic Acid and Salicylic Acid in Tomato Leaf Veins Based on an Electrochemical Microsensor. Biosensors. 2023 Nov; 13(12):. doi: 10.3390/bios13121002. [PMID: 38131762]
  • Renjie Li, Meijing Song, Danning Yin, Xiaoyun Ye, Jiayu Yu, Xiurong Chen. Indole-3-acetic acid mediated removal of sludge toxicity by microalgae: Focus on the role of extracellular polymeric substances. Bioresource technology. 2023 Nov; 387(?):129700. doi: 10.1016/j.biortech.2023.129700. [PMID: 37604255]
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