Abscisic_acid (BioDeep_00000230838)

Main id: BioDeep_00000398555

Secondary id: BioDeep_00000000606, BioDeep_00000600338

PANOMIX_OTCML-2023 Plant Hormones BioNovoGene_Lab2019


代谢物信息卡片


(2Z,4E)-5-[(1S)-1-Hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl]-3-methyl-2,4-pentadienoic acid

化学式: C15H20O4 (264.1362)
中文名称: 脱落酸(天然), (+)-脱落酸, 脱落酸(ABA), 脱落酸
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC1=CC(=O)CC(C1(C=CC(=CC(=O)O)C)O)(C)C
InChI: InChI=1S/C15H20O4/c1-10(7-13(17)18)5-6-15(19)11(2)8-12(16)9-14(15,3)4/h5-8,19H,9H2,1-4H3,(H,17,18)/b6-5+,10-7-

描述信息

(+)-abscisic acid is the naturally occurring (1S)-(+) enantiomer of abscisic acid. It is an important sesquiterpenoid plant hormone which acts as a regulator of plant responses to environmental stresses such as drought and cold. It has a role as a plant hormone and a plant metabolite. It is a conjugate acid of a (+)-abscisate. It is an enantiomer of a (-)-abscisic acid.
Abscisic acid is a natural product found in Macaranga triloba, Cuscuta pentagona, and other organisms with data available.
Abscission-accelerating plant growth substance isolated from young cotton fruit, leaves of sycamore, birch, and other plants, and from potatoes, lemons, avocados, and other fruits.
The naturally occurring (1S)-(+) enantiomer of abscisic acid. It is an important sesquiterpenoid plant hormone which acts as a regulator of plant responses to environmental stresses such as drought and cold.
D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids
D006133 - Growth Substances > D010937 - Plant Growth Regulators
2-cis-abscisic acid is a member of the class of abscisic acids in which the double bond betweeen positions 2 and 3 has cis- (natural) geometry. It has a role as an abscisic acid receptor agonist. It is a conjugate acid of a 2-cis-abscisate.
Dormin is a natural product found in Axinella polypoides, Botrytis cinerea, and Leptosphaeria maculans with data available.
Abscission-accelerating plant growth substance isolated from young cotton fruit, leaves of sycamore, birch, and other plants, and from potatoes, lemons, avocados, and other fruits.
(±)-Abscisic acid is an orally active plant hormone that is present also in animals. (±)-Abscisic acid (ABA) contributes to the regulation of glycemia in mammals[1].
(±)-Abscisic acid is an orally active plant hormone that is present also in animals. (±)-Abscisic acid (ABA) contributes to the regulation of glycemia in mammals[1].
Abscisic acid ((S)-(+)-Abscisic acid), an orally active phytohormone in fruits and vegetables, is an endogenously produced mammalian hormone. Abscisic acid is a growth inhibitor and can regulate many aspects of plant growth and development. Abscisic acid inhibits proton pump (H+-ATPase) and leads to the plasma membrane depolarization in a Ca2+-dependent manner. Abscisic acid, a LANCL2 natural ligand, is a potent insulin-sensitizing compound and has the potential for pre-diabetes, type 2 diabetes and metabolic syndrome[1][2].
Abscisic acid ((S)-(+)-Abscisic acid), an orally active phytohormone in fruits and vegetables, is an endogenously produced mammalian hormone. Abscisic acid is a growth inhibitor and can regulate many aspects of plant growth and development. Abscisic acid inhibits proton pump (H+-ATPase) and leads to the plasma membrane depolarization in a Ca2+-dependent manner. Abscisic acid, a LANCL2 natural ligand, is a potent insulin-sensitizing compound and has the potential for pre-diabetes, type 2 diabetes and metabolic syndrome[1][2].

同义名列表

91 个代谢物同义名

(2Z,4E)-5-[(1S)-1-Hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl]-3-methyl-2,4-pentadienoic acid

; 2,4-Pentadienoic acid, 5-[(1S)-1-hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl]-3-methyl-, (2Z,4E)-; 2,4-Pentadienoic acid,5-[(1S)-1-hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl]-3-methyl-,(2Z,4E)-; 2,4-Pentadienoic acid, 5-(1-hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl)-3-methyl-, (S-(Z,E))-; (2Z,4E)-5-[(1S)-1-Hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl]-3-methyl-2,4-pentadienoic acid; (2Z,4E)-5-((1S)-1-HYDROXY-2,6,6-TRIMETHYL-4-OXO-2-CYCLOHEXEN-1-YL)-3-METHYL-2,4-PENTADIENOIC ACID; (2Z,4E)-5-[(1S)-1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid; (2Z,4E)-5-((S)-1-Hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-3-methylpenta-2,4-dienoic acid; (S-(Z,E))-5-(1-Hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-3-methylpenta-2,4-dienoic acid; (2Z,4E)-5-((S)-1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-enyl)-3-methylpenta-2,4-dienoic acid; (S)-5-(1-Hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-3-methyl-[2Z,4E]-pentadienoic acid; (7E,9Z)-(6S)-6-hydroxy-3-oxo-11-apo-epsilon-caroten-11-oic acid; (+)-Abscisic acid, analytical reference material; Abscisic Acid Monoammonium Salt, (R)-Isomer; (.+/-.)-2-cis-4-trans-Abscisic acid; (+)-cis,trans-Abscisic Acid, 98\\%; Abscisic Acid, (E,Z)-(+,-)-Isomer; (+)-Abscisic acid, >=98\\% (HPLC); Abscisic Acid, (E,E)-(+-)-Isomer; Abscisic Acid (Dormin pound(c); cis-trans-(+)-Abscissic acid; 2-cis,4-trans-Abscisic acid; Abscisic Acid, (+,-)-Isomer; Abscisic Acid, (Z,E)-Isomer; (+)-cis,trans-Abscisic Acid; Dormin (abscission factor); Abscisic Acid, (R)-Isomer; Acide abscisique [French]; Abscisic Acid (Dormin); (S)-(+)-Abscisic acid; (+)-(S)-Abscisic Acid; ABSCISIC ACID [MI]; (+)-cis,trans ABA; (+)-Abscisic acid; Acide abscisique; UNII-72S9A8J5GW; Abscissic Acid; Abscisic Acid; Absicic Acid; Dormin (VAN); SMP2_000105; Abscisin II; (+)-(S)-ABA; 72S9A8J5GW; Abscissins; (+)-S-ABA; Abscisate; C15H20O4; (+)-ABA; Dormin; 3w9r; A8S; ABA; 2,4-pentadienoic acid, 5-(1-hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl)-3-methyl-, (2Z,4E)-; 2,4-Pentadienoic acid,5-(1-hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl)-3-methyl-,(2Z,4E)-; (2Z,4E)-5-(1-hydroxy-2,6,6-trimethyl-4-oxo-1-cyclohex-2-enyl)-3-methylpenta-2,4-dienoic acid; (2Z,4E)-5-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-3-methylpenta-2,4-dienoic acid; 5-[(1S)-1-HYDROXY-2,6,6-TRIMETHYL-4-OXO-2-CYCLOHEXEN-1-YL]-3-METHYL-2Z,4E-PENTADIENOIC ACID; (2Z,4E)-5-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-enyl)-3-methylpenta-2,4-d ienoic acid; (4E)-5-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-3-methylpenta-2,4-dienoic acid; (2Z,4E)-5-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-enyl)-3-methylpenta-2,4-dienoic acid; (2Z)-5-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-3-methylpenta-2,4-dienoic acid; 5-[1-Hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl]-3-methyl-[2Z,4e]-pentadienoic acid; (+/-)-Abscisic acid, BioReagent, plant cell culture tested, >=98.5\\% (HPLC); 2-cis,4-trans-Abscisic acid, synthetic, 98\\%; ( inverted exclamation markA)-Abscisic acid; Abscisic acid (+/-)-cis,trans-form [MI]; 13F617B4-6D52-4DAF-ADA1-A7FE2B84E828; (+/-)-2-cis-4-trans-Abscisic acid; (+/-)-(cis,Trans)-abscisic acid; ABSCISIC ACID (cis,trans; +/-); Abscisic acid, (+/-)-(2Z,4E)-; (+/-)-(2Z,4E)-abscisic acid; (+/-)-Abscisic acid; 2-cis-abscisic acid; (RS)-Abscisic acid; acide abscissique; (±)-Abscisic acid; Spectrum5_000342; acido abscisico; UNII-3B18Y5RNGK; Abscisinsaeure; Abszisinsaeure; Tox21_201137; 3B18Y5RNGK; (+/-)-Aba; Abscisic; PBI-57; (±)-ABA; (S)?-?(+)?-?Abscisic acid; Abscisate



数据库引用编号

26 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

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)

70 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 9 ABI2, CDK16, HPGDS, ITPR3, LANCL2, PRKN, RBMS3, SFRP4, ZMYND8
Peripheral membrane protein 2 CDK16, CYP1B1
Endoplasmic reticulum membrane 5 CYP1B1, DEGS1, HSP90B1, ITPR3, RAB18
Mitochondrion membrane 1 DEGS1
Nucleus 11 ABI2, CDK16, HSP90B1, LANCL2, MYB, NFYB, PRKN, RBMS3, SFRP4, SNRK, ZMYND8
cytosol 11 ABI2, CDK16, GSR, HPGDS, HSP90B1, LANCL2, MYB, PRKN, RAB18, RBMS3, RGL2
mitochondrial membrane 1 DEGS1
nucleoplasm 8 ABI2, ATP2B1, HPGDS, ITPR3, LANCL2, MYB, NFYB, ZMYND8
RNA polymerase II transcription regulator complex 2 MYB, NFYB
Cell membrane 3 ATP2B1, CDK16, LANCL2
Lipid-anchor 1 RAB18
Cytoplasmic side 2 CDK16, RAB18
lamellipodium 1 ABI2
Multi-pass membrane protein 3 ATP2B1, DEGS1, ITPR3
Golgi apparatus membrane 1 RAB18
Synapse 1 ATP2B1
cell surface 1 SFRP4
dendritic shaft 1 ZMYND8
glutamatergic synapse 1 ATP2B1
Golgi apparatus 2 PRKN, RAB18
Golgi membrane 1 RAB18
neuronal cell body 1 ITPR3
presynaptic membrane 1 ATP2B1
smooth endoplasmic reticulum 1 HSP90B1
synaptic vesicle 1 CDK16
Cytoplasm, cytosol 1 PRKN
Cytoplasmic vesicle, secretory vesicle 1 CDK16
Presynapse 1 PRKN
plasma membrane 7 ATP2B1, CDK16, DEGS1, ITPR3, LANCL2, NPR1, RAB18
synaptic vesicle membrane 1 ATP2B1
Membrane 7 ATP2B1, CYP1B1, DEGS1, HSP90B1, ITPR3, MYB, NPR1
apical plasma membrane 1 RAB18
basolateral plasma membrane 1 ATP2B1
brush border 1 ITPR3
extracellular exosome 3 ATP2B1, GSR, HSP90B1
endoplasmic reticulum 4 DEGS1, HSP90B1, ITPR3, PRKN
extracellular space 1 SFRP4
perinuclear region of cytoplasm 2 HSP90B1, PRKN
adherens junction 1 ABI2
mitochondrion 4 CYP1B1, DEGS1, GSR, PRKN
protein-containing complex 1 HSP90B1
intracellular membrane-bounded organelle 4 ABI2, ATP2B1, CYP1B1, HPGDS
Microsome membrane 1 CYP1B1
filopodium 1 ABI2
postsynaptic density 1 PRKN
Secreted 1 SFRP4
extracellular region 2 HSP90B1, SFRP4
cytoplasmic side of plasma membrane 1 CDK16
Mitochondrion outer membrane 1 PRKN
mitochondrial outer membrane 1 PRKN
mitochondrial matrix 1 GSR
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane 1 ATP2B1
external side of plasma membrane 1 GSR
dendritic spine 2 ABI2, ZMYND8
microtubule cytoskeleton 1 CDK16
nucleolus 2 ITPR3, ZMYND8
midbody 1 HSP90B1
apical part of cell 1 ITPR3
Apical cell membrane 1 RAB18
Cell projection, lamellipodium 1 ABI2
filopodium tip 1 ABI2
Cytoplasm, cytoskeleton 1 ABI2
Cytoplasm, cytoskeleton, spindle 1 SNRK
focal adhesion 1 HSP90B1
Cell junction, adherens junction 1 ABI2
sarcoplasmic reticulum 1 ITPR3
collagen-containing extracellular matrix 1 HSP90B1
lateral plasma membrane 1 ATP2B1
nuclear speck 1 PRKN
nuclear outer membrane 1 ITPR3
Cell projection, filopodium 1 ABI2
receptor complex 2 ITPR3, NPR1
Cell projection, neuron projection 1 PRKN
neuron projection 2 CDK16, PRKN
chromatin 2 NFYB, ZMYND8
Cytoplasmic vesicle, autophagosome membrane 1 RAB18
autophagosome membrane 1 RAB18
cell projection 1 ATP2B1
Chromosome 1 ZMYND8
cytoskeleton 1 ABI2
Basolateral cell membrane 1 ATP2B1
Endomembrane system 2 DEGS1, RAB18
Lipid droplet 1 RAB18
specific granule membrane 1 DEGS1
Melanosome 1 HSP90B1
Presynaptic cell membrane 1 ATP2B1
sperm plasma membrane 1 HSP90B1
ubiquitin ligase complex 1 PRKN
secretory granule membrane 2 ITPR3, RAB18
endoplasmic reticulum lumen 1 HSP90B1
nuclear matrix 1 MYB
cortical actin cytoskeleton 1 LANCL2
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 RAB18
immunological synapse 1 ATP2B1
aggresome 1 PRKN
Sarcoplasmic reticulum lumen 1 HSP90B1
ribonucleoprotein complex 1 RBMS3
platelet dense tubular network membrane 1 ITPR3
Synapse, synaptosome 1 CDK16
protein-DNA complex 1 NFYB
dopaminergic synapse 1 PRKN
Cytoplasmic vesicle, secretory vesicle membrane 1 ITPR3
Lewy body 1 PRKN
Parkin-FBXW7-Cul1 ubiquitin ligase complex 1 PRKN
site of DNA damage 1 ZMYND8
cyclin-dependent protein kinase holoenzyme complex 1 CDK16
endocytic vesicle lumen 1 HSP90B1
transport vesicle membrane 1 ITPR3
endoplasmic reticulum chaperone complex 1 HSP90B1
photoreceptor ribbon synapse 1 ATP2B1
ANPR-A receptor complex 1 NPR1
cytoplasmic side of endoplasmic reticulum membrane 1 ITPR3
CCAAT-binding factor complex 1 NFYB
SCAR complex 1 ABI2
endoplasmic reticulum tubular network 1 RAB18
actin-based cell projection 1 ABI2
[Isoform 1]: Cell projection, lamellipodium 1 ABI2


文献列表

  • Sanjay Singh Rawat, Shital Sandhya, Ashverya Laxmi. Complex genetic interaction between glucose sensor HXK1 and E3 SUMO ligase SIZ1 in regulating plant morphogenesis. Plant signaling & behavior. 2024 Dec; 19(1):2341506. doi: 10.1080/15592324.2024.2341506. [PMID: 38607960]
  • Qilin Yang, Jinheng Huang, Xiaofeng Nie, XiaoMin Tang, Peiran Liao, Quan Yang. Cloning and functional validation of DsWRKY6 gene from Desmodium styracifolium. Plant signaling & behavior. 2024 Dec; 19(1):2349868. doi: 10.1080/15592324.2024.2349868. [PMID: 38743594]
  • Kohei Kawaguchi, Michitaka Notaguchi, Koji Okayasu, Yu Sawai, Mikiko Kojima, Yumiko Takebayashi, Hitoshi Sakakibara, Shungo Otagaki, Shogo Matsumoto, Katsuhiro Shiratake. Plant hormone profiling of scion and rootstock incision sites and intra- and inter-family graft junctions in Nicotiana benthamiana. Plant signaling & behavior. 2024 Dec; 19(1):2331358. doi: 10.1080/15592324.2024.2331358. [PMID: 38513064]
  • Tianming Li, Wenjing Jia, Song Peng, Yanhui Guo, Jinrui Liu, Xue Zhang, Panyu Li, Hanfeng Zhang, Ruqiang Xu. Endogenous cAMP elevation in Brassica napus causes changes in phytohormone levels. Plant signaling & behavior. 2024 Dec; 19(1):2310963. doi: 10.1080/15592324.2024.2310963. [PMID: 38314783]
  • Jia Liu, Sumei Qiu, Tingting Xue, Yingdan Yuan. Physiology and transcriptome of Eucommia ulmoides seeds at different germination stages. Plant signaling & behavior. 2024 Dec; 19(1):2329487. doi: 10.1080/15592324.2024.2329487. [PMID: 38493506]
  • Ruotong Rao, Xiaoyu Huang, Xinting Wang, Xuelong Li, Huiping Liao, Nigara Abuduwaili, Xiuzhen Wei, Dengdi Li, Gengqing Huang. Genome-wide identification and analysis of DEAD-box RNA helicases in Gossypium hirsutum. Gene. 2024 Aug; 920(?):148495. doi: 10.1016/j.gene.2024.148495. [PMID: 38663690]
  • Kai Hou, Lu Cao, Wen Li, Zhi-Hui Fang, Daqiang Sun, Zhigang Guo, Lipeng Zhang. Overexpression of Rhodiola crenulata glutathione peroxidase 5 increases cold tolerance and enhances the pharmaceutical value of the hairy roots. Gene. 2024 Jul; 917(?):148467. doi: 10.1016/j.gene.2024.148467. [PMID: 38615983]
  • 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]
  • Caifeng Jiao, Jing Sun. SlbHLH1 mediates ABA treatment-retarded chilling injury by repressing SlPP2C29 in tomato fruit. Plant science : an international journal of experimental plant biology. 2024 Jul; 344(?):112086. doi: 10.1016/j.plantsci.2024.112086. [PMID: 38599246]
  • Liangxin Wang, Yuanxiu Lin, Guoyan Hou, Min Yang, Yuting Peng, Yuyan Jiang, Caixia He, Musha She, Qing Chen, Mengyao Li, Yong Zhang, Yunting Zhang, Yan Wang, Wen He, Xiaorong Wang, Haoru Tang, Ya Luo. A histone deacetylase, FaSRT1-2, plays multiple roles in regulating fruit ripening, plant growth and stresses resistance of cultivated strawberry. Plant, cell & environment. 2024 Jun; 47(6):2258-2273. doi: 10.1111/pce.14885. [PMID: 38482979]
  • Baoping Xue, Wen Duan, Luping Gong, Dongmei Zhu, Xueying Li, Xuemei Li, Yun-Kuan Liang. The OsDIR55 gene increases salt tolerance by altering the root diffusion barrier. The Plant journal : for cell and molecular biology. 2024 Jun; 118(5):1550-1568. doi: 10.1111/tpj.16696. [PMID: 38412303]
  • Xuping Lu, Yan Li, Maryam Akhtar, Caixia Liu, Tianli Ma, Weifang Min, Xiaorong Bai, Yangmengfei She, Liang Chen, Lei Tian, Peifu Li, Chengke Luo. A DUF966 gene family member OsDSR3 positively regulates alkali stress tolerance in rice. Plant science : an international journal of experimental plant biology. 2024 Jun; 343(?):112072. doi: 10.1016/j.plantsci.2024.112072. [PMID: 38513731]
  • Ying Li, Xifu Yang, Enping Feng, Kunming Zhao, Zhibin Zhang. Plant hormones mediate the interaction between oak acorn germination and rodent hoarding behaviour. The New phytologist. 2024 Jun; 242(5):2237-2250. doi: 10.1111/nph.19424. [PMID: 38037212]
  • Yuanyuan Wu, Ying Sun, Wanmin Wang, Zizhao Xie, Chenghang Zhan, Liang Jin, Junli Huang. OsJAZ10 negatively modulates the drought tolerance by integrating hormone signaling with systemic electrical activity in rice. Plant physiology and biochemistry : PPB. 2024 Jun; 211(?):108683. doi: 10.1016/j.plaphy.2024.108683. [PMID: 38714129]
  • Yun Yang, Aiqi Li, Yuqing Liu, Jianguo Shu, Jiarong Wang, Yuxin Guo, Quanzhi Li, Jiahui Wang, Ao Zhou, Chengyun Wu, Jiandong Wu. ZmASR1 negatively regulates drought stress tolerance in maize. Plant physiology and biochemistry : PPB. 2024 Jun; 211(?):108684. doi: 10.1016/j.plaphy.2024.108684. [PMID: 38710113]
  • Han Dong, Yuanyuan Wang, Yancui Di, Yingying Qiu, Zelin Ji, Tengfei Zhou, Shunshan Shen, Nanshan Du, Tao Zhang, Xiaoxing Dong, Zhixin Guo, Fengzhi Piao, Yonghua Li. Plant growth-promoting rhizobacteria Pseudomonas aeruginosa HG28-5 improves salt tolerance by regulating Na+/K+ homeostasis and ABA signaling pathway in tomato. Microbiological research. 2024 Jun; 283(?):127707. doi: 10.1016/j.micres.2024.127707. [PMID: 38582011]
  • Jing Li, Litao Zhang, Wenjie Yu, Mengjie Zhang, Feng Chen, Jianguo Liu. Mitochondrial alternative oxidase pathway accelerates non-motile cell germination by enhancing respiratory carbon metabolism and maintaining redox poise in Haematococcus pluvialis. Bioresource technology. 2024 Jun; 402(?):130729. doi: 10.1016/j.biortech.2024.130729. [PMID: 38657826]
  • Xiaoguang Lu, Fuzhi Zhang, Chenglong Zhang, Guorui Li, Yuchen Du, Cicong Zhao, Wei Zhao, Fengmei Gao, Lianshuang Fu, Xin Liu, Jun Liu, Xiaonan Wang. TaTPS11 enhances wheat cold resistance by regulating source-sink factor. Plant physiology and biochemistry : PPB. 2024 Jun; 211(?):108695. doi: 10.1016/j.plaphy.2024.108695. [PMID: 38744088]
  • Qiunan Zhu, Qinqin Tan, Qiyang Gao, Senlin Zheng, Weixin Chen, Jean-Philippe Galaud, Xueping Li, Xiaoyang Zhu. Calmodulin-like protein CML15 interacts with PP2C46/65 to regulate papaya fruit ripening via integrating calcium, ABA and ethylene signals. Plant biotechnology journal. 2024 Jun; 22(6):1703-1723. doi: 10.1111/pbi.14297. [PMID: 38319003]
  • Changan Zhu, Beiyu Jing, Teng Lin, Xinyan Li, Min Zhang, Yanhong Zhou, Jingquan Yu, Zhangjian Hu. Phosphorylation of sugar transporter TST2 by protein kinase CPK27 enhances drought tolerance in tomato. Plant physiology. 2024 May; 195(2):1005-1024. doi: 10.1093/plphys/kiae124. [PMID: 38431528]
  • Yang Yang, Yan-Qiu Tan, Xinyong Wang, Jia-Jun Li, Bo-Ya Du, Meijun Zhu, Pengcheng Wang, Yong-Fei Wang. OPEN STOMATA 1 phosphorylates CYCLIC NUCLEOTIDE-GATED CHANNELs to trigger Ca2+ signaling for abscisic acid-induced stomatal closure in Arabidopsis. The Plant cell. 2024 May; 36(6):2328-2358. doi: 10.1093/plcell/koae073. [PMID: 38442317]
  • Yamila Carla Agrofoglio, María José Iglesias, Soledad Perez-Santángelo, María José de Leone, Tino Koester, Rafael Catalá, Julio Salinas, Marcelo J Yanovsky, Dorothee Staiger, Julieta L Mateos. Arginine methylation of SM-LIKE PROTEIN 4 antagonistically affects alternative splicing during Arabidopsis stress responses. The Plant cell. 2024 May; 36(6):2219-2237. doi: 10.1093/plcell/koae051. [PMID: 38518124]
  • 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]
  • Jiaqi Zhang, Man Zhang, Mian Wang, Yixuan Wu, Yang Shi, Yujie Chen, Rui Feng, Xiaoling Yang, Xiaojiao Chen, Baomin Wang. High-Performance Liquid Chromatographic Quantification of the Plant Hormone Abscisic Acid at ppb Levels in Plant Samples after a Single Immunoaffinity Column Cleanup. Journal of agricultural and food chemistry. 2024 May; 72(20):11794-11803. doi: 10.1021/acs.jafc.4c01680. [PMID: 38739902]
  • Kay Gully, Alice Berhin, Damien De Bellis, Cornelia Herrfurth, Ivo Feussner, Christiane Nawrath. The GPAT4/6/8 clade functions in Arabidopsis root suberization nonredundantly with the GPAT5/7 clade required for suberin lamellae. Proceedings of the National Academy of Sciences of the United States of America. 2024 May; 121(21):e2314570121. doi: 10.1073/pnas.2314570121. [PMID: 38739804]
  • Yi-Wen Wang, Savithri U Nambeesan. Ethylene promotes fruit ripening initiation by downregulating photosynthesis, enhancing abscisic acid and suppressing jasmonic acid in blueberry (Vaccinium ashei). BMC plant biology. 2024 May; 24(1):418. doi: 10.1186/s12870-024-05106-4. [PMID: 38760720]
  • Liru Cao, Feiyu Ye, Abbas Muhammad Fahim, Chenchen Ma, Yunyun Pang, Xin Zhang, Qianjin Zhang, Xiaomin Lu. Transcription factor ZmDof22 enhances drought tolerance by regulating stomatal movement and antioxidant enzymes activities in maize (Zea mays L.). TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik. 2024 May; 137(6):132. doi: 10.1007/s00122-024-04625-w. [PMID: 38750241]
  • 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]
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  • Haoyang Sun, Chunping Li, Siyu Li, Jiaxin Ma, Shuo Li, Xin Li, Cai Gao, Rongchen Yang, Nan Ma, Jing Yang, Peizhi Yang, Xueqing He, Tianming Hu. Identification and validation of stable reference genes for RT-qPCR analyses of Kobresia littledalei seedlings. BMC plant biology. 2024 May; 24(1):389. doi: 10.1186/s12870-024-04924-w. [PMID: 38730341]
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  • Li Zhang, Yongmei Cui, Likun An, Jie Li, Youhua Yao, Yixiong Bai, Xin Li, Xiaohua Yao, Kunlun Wu. Genome-wide identification of the CNGC gene family and negative regulation of drought tolerance by HvCNGC3 and HvCNGC16 in transgenic Arabidopsis thaliana. Plant physiology and biochemistry : PPB. 2024 May; 210(?):108593. doi: 10.1016/j.plaphy.2024.108593. [PMID: 38615446]
  • Feng Zhang, Chunmeng Wang, Jia-Long Yao, Caihua Xing, Kang Xu, Zan Zhang, Qiming Chen, Qinghai Qiao, Huizhen Dong, Chenyang Han, Likun Lin, Shaoling Zhang, Xiaosan Huang. PbHsfC1a-coordinates ABA biosynthesis and H2O2 signalling pathways to improve drought tolerance in Pyrus betulaefolia. Plant biotechnology journal. 2024 May; 22(5):1177-1197. doi: 10.1111/pbi.14255. [PMID: 38041554]
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  • Hong Chen, Chao Han, Zemao Liu, Robert D Guy, Fangyuan Yu. Physiological and biochemical response analysis of Styrax tonkinensis seedlings to waterlogging stress. Plant physiology and biochemistry : PPB. 2024 May; 210(?):108587. doi: 10.1016/j.plaphy.2024.108587. [PMID: 38636255]
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  • Qi Tang, Xuan Wang, Shurui Ma, Shutian Fan, Fumei Chi, Yang Song. Molecular mechanism of abscisic acid signaling response factor VcbZIP55 to promote anthocyanin biosynthesis in blueberry (Vaccinium corymbosum). Plant physiology and biochemistry : PPB. 2024 May; 210(?):108611. doi: 10.1016/j.plaphy.2024.108611. [PMID: 38615439]
  • Xiaofeng Luo, Yujia Dai, Baoshan Xian, Jiahui Xu, Ranran Zhang, Muhammad Saad Rehmani, Chuan Zheng, Xiaoting Zhao, Kaitao Mao, Xiaotong Ren, Shaowei Wei, Lei Wang, Juan He, Weiming Tan, Junbo Du, Weiguo Liu, Shu Yuan, Kai Shu. PIF4 interacts with ABI4 to serve as a transcriptional activator complex to promote seed dormancy by enhancing ABA biosynthesis and signaling. Journal of integrative plant biology. 2024 May; 66(5):909-927. doi: 10.1111/jipb.13615. [PMID: 38328870]
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  • Liqun Tang, Guanghao Li, Huimei Wang, Juan Zhao, Zhiyong Li, Xixi Liu, Yazhou Shu, Wanning Liu, Shuang Wang, Jie Huang, Jiezheng Ying, Xiaohong Tong, Wenya Yuan, Xiangjin Wei, Shaoqing Tang, Yifeng Wang, Qingyun Bu, Jian Zhang. Exogenous abscisic acid represses rice flowering via SAPK8-ABF1-Ehd1/Ehd2 pathway. Journal of advanced research. 2024 May; 59(?):35-47. doi: 10.1016/j.jare.2023.06.012. [PMID: 37399924]
  • Veronika Berková, Miroslav Berka, Lenka Štěpánková, Ján Kováč, Susann Auer, Simona Menšíková, Jaroslav Ďurkovič, Stanislav Kopřiva, Jutta Ludwig-Müller, Břetislav Brzobohatý, Martin Černý. The fungus Acremonium alternatum enhances salt stress tolerance by regulating host redox homeostasis and phytohormone signaling. Physiologia plantarum. 2024 May; 176(3):e14328. doi: 10.1111/ppl.14328. [PMID: 38695265]
  • Mingkun Chen, Xiaoyun Cao, Yuanxing Huang, Wenting Zou, Xiaolong Liang, Yue Yang, Yu Wang, Jun Wei, Houhua Li. The bZIP transcription factor MpbZIP9 regulates anthocyanin biosynthesis in Malus 'Pinkspire' fruit. Plant science : an international journal of experimental plant biology. 2024 May; 342(?):112038. doi: 10.1016/j.plantsci.2024.112038. [PMID: 38367821]
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  • Zhenwei Yan, Fajun Zhang, Chunhua Mu, Changle Ma, Guoqi Yao, Yue Sun, Jing Hou, Bingying Leng, Xia Liu. The ZmbHLH47-ZmSnRK2.9 Module Promotes Drought Tolerance in Maize. International journal of molecular sciences. 2024 May; 25(9):. doi: 10.3390/ijms25094957. [PMID: 38732175]
  • Meiqi Zhao, Yijing Lei, Ling Wu, Haoran Qi, Zihe Song, Meng Xu. The miR159a-PeMYB33 module regulates poplar adventitious rooting through the abscisic acid signal pathway. The Plant journal : for cell and molecular biology. 2024 May; 118(3):879-891. doi: 10.1111/tpj.16643. [PMID: 38271219]
  • Qin Yang, Xiaojuan Deng, Ting Liu, Jiayun Qian, Penghong Zhang, Engao Zhu, Jingqi Wang, Xiaoxian Zhu, Guzel Kudoyarova, Jiangzhe Zhao, Kewei Zhang. Abscisic acid root-to-shoot translocation by transporter AtABCG25 mediates stomatal movements in Arabidopsis. Plant physiology. 2024 Apr; 195(1):671-684. doi: 10.1093/plphys/kiae073. [PMID: 38345859]
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  • Nanxin Xie, Haoyang Shi, Xiaoman Shang, Zixin Zhao, Yan Fang, Huimin Wu, Ping Luo, Yongyi Cui, Wen Chen. RhMED15a-like, a subunit of the Mediator complex, is involved in the drought stress response in Rosa hybrida. BMC plant biology. 2024 Apr; 24(1):351. doi: 10.1186/s12870-024-05059-8. [PMID: 38684962]
  • Shaoliang Mou, Weihong He, Haitao Jiang, Qianqian Meng, Tingting Zhang, Zhiqin Liu, Ailian Qiu, Shuilin He. Transcription factor CaHDZ15 promotes pepper basal thermotolerance by activating HEAT SHOCK FACTORA6a. Plant physiology. 2024 Apr; 195(1):812-831. doi: 10.1093/plphys/kiae037. [PMID: 38270532]
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  • Miron Gieniec, Zbigniew Miszalski, Piotr Rozpądek, Roman J Jędrzejczyk, Małgorzata Czernicka, Michał Nosek. How the Ethylene Biosynthesis Pathway of Semi-Halophytes Is Modified with Prolonged Salinity Stress Occurrence?. International journal of molecular sciences. 2024 Apr; 25(9):. doi: 10.3390/ijms25094777. [PMID: 38731994]
  • Daoyun Chen, Yuqing Xu, Jiawei Li, Hiroshi Shiba, Hiroshi Ezura, Ning Wang. ERECTA Modulates Seed Germination and Fruit Development via Auxin Signaling in Tomato. International journal of molecular sciences. 2024 Apr; 25(9):. doi: 10.3390/ijms25094754. [PMID: 38731974]
  • Xiao-Hua Lu, Ya-Jie Wang, Xing-Hou Zhen, Hui Yu, Mu Pan, Dong-Qing Fu, Rui-Mei Li, Jiao Liu, Hai-Yan Luo, Xin-Wen Hu, Yuan Yao, Jian-Chun Guo. Functional Characterization of the MeSSIII-1 Gene and Its Promoter from Cassava. International journal of molecular sciences. 2024 Apr; 25(9):. doi: 10.3390/ijms25094711. [PMID: 38731930]
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  • Shunyu Lin, Heng Zhang, Tao Ma, Kaiyue Yu, Ya Wang, Chunmei Zhao, Hong Zhu, Jingshan Wang, Lixian Qiao, Jiongming Sui. [Verification of the peanut vitamin C synthesis-related gene AhPMM and its role in stress resistance]. Sheng wu gong cheng xue bao = Chinese journal of biotechnology. 2024 Apr; 40(4):1089-1101. doi: 10.13345/j.cjb.230426. [PMID: 38658151]
  • Wei Gao, Yating Jiang, Xiaohu Yang, Ting Li, Litian Zhang, Shengnan Yan, Jiajia Cao, Jie Lu, Chuanxi Ma, Cheng Chang, Haiping Zhang. Functional analysis of a wheat class III peroxidase gene, TaPer12-3A, in seed dormancy and germination. BMC plant biology. 2024 Apr; 24(1):318. doi: 10.1186/s12870-024-05041-4. [PMID: 38654190]
  • Zhuolei Tang, Xiaoyan Huang, Kaifeng Huang. Strigolactones affect the yield of Tartary buckwheat by regulating endogenous hormone levels. BMC plant biology. 2024 Apr; 24(1):320. doi: 10.1186/s12870-024-05029-0. [PMID: 38654155]
  • Dacheng Wang, Lirong Wei, Jinbiao Ma, Yingqiao Wan, Keyi Huang, Yiqiong Sun, Huili Wen, Zhipeng Chen, Zijie Li, Dongli Yu, Haitao Cui, Jingni Wu, Yufeng Wu, Sun Tae Kim, Jing Zhao, Jane E Parker, Kenichi Tsuda, Chunhao Jiang, Yiming Wang. Bacillus cereus NJ01 induces SA- and ABA-mediated immunity against bacterial pathogens through the EDS1-WRKY18 module. Cell reports. 2024 Apr; 43(4):113985. doi: 10.1016/j.celrep.2024.113985. [PMID: 38517890]
  • Fan Yan, Junchi Ma, Manjiang Peng, Congfang Xi, Sheng Chang, Ying Yang, Suohui Tian, Bo Zhou, Tao Liu. Lactic acid induced defense responses in tobacco against Phytophthora nicotianae. Scientific reports. 2024 04; 14(1):9338. doi: 10.1038/s41598-024-60037-2. [PMID: 38654120]
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  • Rong Li, Lingzhi Zhu, Peizhen Chen, Yu Chen, Qingqing Hao, Peihuang Zhu, Kongshu Ji. Functional Characterization of PmDXR, a Critical Rate-Limiting Enzyme, for Turpentine Biosynthesis in Masson Pine (Pinus massoniana Lamb.). International journal of molecular sciences. 2024 Apr; 25(8):. doi: 10.3390/ijms25084415. [PMID: 38673998]
  • Shen Huang, Chunli Wang, Zixuan Ding, Yaqian Zhao, Jing Dai, Jia Li, Haining Huang, Tongkai Wang, Min Zhu, Mingfeng Feng, Yinghua Ji, Zhongkai Zhang, Xiaorong Tao. A plant NLR receptor employs ABA central regulator PP2C-SnRK2 to activate antiviral immunity. Nature communications. 2024 Apr; 15(1):3205. doi: 10.1038/s41467-024-47364-8. [PMID: 38615015]
  • Youju Ye, Shuangshuang Wen, Jiali Ying, Yunfei Cai, Renjuan Qian. Screening and Preliminary Identification of Asparagus officinalis Varieties under Low-Temperature Stress. Genes. 2024 Apr; 15(4):. doi: 10.3390/genes15040486. [PMID: 38674420]
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  • Yu Kong, Xianbin Hou, Zhenglu Liu, Yufeng Li. Cold-stress induced metabolomic and transcriptomic changes in leaves of three mango varieties with different cold tolerance. BMC plant biology. 2024 Apr; 24(1):266. doi: 10.1186/s12870-024-04983-z. [PMID: 38600447]
  • Yaqian Chen, Jinfeng Wu, Changrui Ma, Dawei Zhang, Dinggang Zhou, Jihong Zhang, Mingli Yan. Metabolome and transcriptome analyses reveal changes of rapeseed in response to ABA signal during early seedling development. BMC plant biology. 2024 Apr; 24(1):245. doi: 10.1186/s12870-024-04918-8. [PMID: 38575879]
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  • Adnan Sami, Muhammad Zeeshan Haider, Muhammad Shafiq, Saleh Sadiq, Farooq Ahmad. Genome-wide identification and in-silico expression analysis of CCO gene family in sunflower (Helianthus annnus) against abiotic stress. Plant molecular biology. 2024 Apr; 114(2):34. doi: 10.1007/s11103-024-01433-0. [PMID: 38568355]
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  • Lin He, Zixuan Wu, Xueheyuan Wang, Changjiang Zhao, Dianjun Cheng, Chuhuai Du, Haoyu Wang, Yuan Gao, Ruijia Zhang, Jienan Han, Jingyu Xu. A novel maize F-bZIP member, ZmbZIP76, functions as a positive regulator in ABA-mediated abiotic stress tolerance by binding to ACGT-containing elements. Plant science : an international journal of experimental plant biology. 2024 Apr; 341(?):111952. doi: 10.1016/j.plantsci.2023.111952. [PMID: 38072329]
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  • Xiaoxue Yang, Meiyun Wang, Qian Zhou, Xinfeng Xu, Ying Li, Xilin Hou, Dong Xiao, Tongkun Liu. BcABF1 Plays a Role in the Feedback Regulation of Abscisic Acid Signaling via the Direct Activation of BcPYL4 Expression in Pakchoi. International journal of molecular sciences. 2024 Mar; 25(7):. doi: 10.3390/ijms25073877. [PMID: 38612692]
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