Trehalose (BioDeep_00000000820)

 

Secondary id: BioDeep_00000398136

natural product human metabolite PANOMIX_OTCML-2023 Endogenous BioNovoGene_Lab2019


代谢物信息卡片


(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxane-3,4,5-triol

化学式: C12H22O11 (342.1162)
中文名称: 海藻糖, α-D-吡喃葡萄糖基-α-D-吡喃葡萄糖苷, D-(+)-海藻糖 二水合物, D-海藻糖, D-海藻糖,无水, α,α-海藻糖,
谱图信息: 最多检出来源 Homo sapiens(feces) 35.58%

分子结构信息

SMILES: C(C1C(C(C(C(O1)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)O
InChI: InChI=1S/C12H22O11/c13-1-3-5(15)7(17)9(19)11(21-3)23-12-10(20)8(18)6(16)4(2-14)22-12/h3-20H,1-2H2

描述信息

Trehalose, also known as mycose, is a 1-alpha (disaccharide) sugar found extensively but not abundantly in nature. It is thought to be implicated in anhydrobiosis - the ability of plants and animals to withstand prolonged periods of desiccation. The sugar is thought to form a gel phase as cells dehydrate, which prevents disruption of internal cell organelles by effectively splinting them in position. Rehydration then allows normal cellular activity to be resumed without the major, generally lethal damage that would normally follow a dehydration/reyhdration cycle. Trehalose is a non-reducing sugar formed from two glucose units joined by a 1-1 alpha bond giving it the name of alpha-D-glucopyranoglucopyranosyl-1,1-alpha-D-glucopyranoside. The bonding makes trehalose very resistant to acid hydrolysis, and therefore stable in solution at high temperatures even under acidic conditions. The bonding also keeps non-reducing sugars in closed-ring form, such that the aldehyde or ketone end-groups do not bind to the lysine or arginine residues of proteins (a process called glycation). The enzyme trehalase, present but not abundant in most people, breaks it into two glucose molecules, which can then be readily absorbed in the gut. Trehalose is an important components of insects circulating fluid. It acts as a storage form of insect circulating fluid and it is important in respiration. Trehalose has also been found to be a metabolite of Burkholderia, Escherichia and Propionibacterium (PMID:12105274; PMID:25479689) (krishikosh.egranth.ac.in/bitstream/1/84382/1/88571\\\\%20P-1257.pdf).
Alpha,alpha-trehalose is a trehalose in which both glucose residues have alpha-configuration at the anomeric carbon. It has a role as a human metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite, a mouse metabolite and a geroprotector.
Cabaletta has been used in trials studying the treatment of Oculopharyngeal Muscular Dystrophy.
Trehalose is a metabolite found in or produced by Escherichia coli (strain K12, MG1655).
Trehalose is a natural product found in Cora pavonia, Selaginella nothohybrida, and other organisms with data available.
Trehalose is a metabolite found in or produced by Saccharomyces cerevisiae.
Occurs in fungi. EU and USA approved sweetener
Acquisition and generation of the data is financially supported in part by CREST/JST.
CONFIDENCE standard compound; INTERNAL_ID 149
D-(+)-Trehalose,which is widespread, can be used as a food ingredient and pharmaceutical excipient.
D-(+)-Trehalose,which is widespread, can be used as a food ingredient and pharmaceutical excipient.

同义名列表

76 个代谢物同义名

(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxane-3,4,5-triol; (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-3,4,5-triol; (2R,2R,3S,3S,4S,4S,5R,5R,6R,6R)-6,6-oxybis(2-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol); 1-[(1->4)-alpha-D-glucosyl]n-alpha-D-glucopyranoside; .alpha.-d-Glucopyranosyl-.alpha.-d-glucopyranoside; alpha-D-Glucopyranoside, a-D-glucopyranosyl (9CI); alpha-D-Glucopyranoside, alpha-D-glucopyranosyl; Alpha-D-Glucopyranosyl-Alpha-D-Glucopyranoside.; alpha-D-glucopyranosyl-alpha-D-glucopyranoside; alpha-D-glucopyranosyl alpha-D-glucopyranoside; O-D-Glucopyranosyl-(1→1)-D-glucopyranoside; a-d-glucopyranosyl-a-d-glucopyranoside; Α-D-glucopyranosyl-α-D-glucopyranoside; Α-D-glucopyranosyl α-D-glucopyranoside; a-D-Glucopyranosyl a-D-glucopyranoside; alpha-D-Glcp-(1↔1)-alpha-D-Glcp; alpha-D-Glcp-(1<->1)-alpha-D-Glcp; alpha-D-Glcp-(11)-alpha-D-Glcp; HDTRYLNUVZCQOY-LIZSDCNHSA-N; D-(+)-Trehalose, anhydrous; .alpha.,.alpha.-Trehalose; delta-trehalose-anhydrous; D-(+)-Trehalose Anhydrous; alpha,alpha-D-Trehalose; Trehalose, alpha,alpha-; Trehalose [INN:BAN:NF]; a-D-GLCP-(11)-a-D-GLCP; Α-D-GLCP-(11)-α-D-GLCP; D-trehalose-anhydrous; alpha,alpha-Trehalose; alpha,alpha-trehalose; TREHALOSE, DIHYDRATE; TREHALOSE [USP-RS]; TREHALOSE (USP-RS); TREHALOSE [WHO-DD]; Natural trehalose; Α,alpha-trehalose; alpha-D-Trehalose; a,Alpha-trehalose; TREHALOSE [INCI]; Α,α’-D-trehalose; UNII-B8WCK70T7I; Trehalose (8CI); D-(+)-Trehalose; alpha-Trehalose; Α,α-D-trehalose; TREHALOSE [FCC]; D(+)-Trehalose; TREHALOSE [MI]; Mushroom sugar; D(+)Trehalose; Α-D-trehalose; α,α-trehalose; Α,α-trehalose; a-D-Trehalose; a-Trehalose; Α-trehalose; Ergot sugar; D-Trehalose; Trehalose P; SMP1_000299; B8WCK70T7I; Cabaletta; Trehalose; Trehaose; Thealoz; Mycose; (GLC)2; Treha; 2b1q; TRE; D-(+)-Trehalose dihydrate,from Saccharomyces cerevisiae; α,α-Trehalose; Trehalose; Trehalose dihydrate; alpha,alpha-Trehalose



数据库引用编号

42 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(5)

BioCyc(21)

PlantCyc(3)

代谢反应

421 个相关的代谢反应过程信息。

Reactome(5)

BioCyc(81)

WikiPathways(0)

Plant Reactome(309)

INOH(0)

PlantCyc(12)

COVID-19 Disease Map(0)

PathBank(14)

PharmGKB(0)

250 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 ATG5, CASP3, G6PD, GAPDH, HTT, PKM, PRKX, SOD1, TFEB
Peripheral membrane protein 2 ATG5, G6PD
Endosome membrane 1 HTT
Nucleus 7 CASP3, GAPDH, HTT, PKM, PRKX, SOD1, TFEB
autophagosome 3 ATG5, HTT, MAP1LC3A
cytosol 11 ATG5, CASP3, G6PD, GAPDH, GSR, HTT, LIPE, MAP1LC3A, PKM, SOD1, TFEB
dendrite 1 HTT
nucleoplasm 5 ATP2B1, CASP3, HTT, PRKX, SOD1
Cell membrane 5 ATP2B1, GPRC5A, HTT, LIPE, TNF
Lipid-anchor 1 MAP1LC3A
Multi-pass membrane protein 3 ATP2B1, GPRC5A, HTT
Synapse 2 ATP2B1, HTT
cell surface 1 TNF
glutamatergic synapse 4 ATG5, ATP2B1, CASP3, MAP1LC3A
Golgi apparatus 2 HTT, SI
Golgi membrane 1 INS
lysosomal membrane 1 TFEB
neuronal cell body 3 CASP3, SOD1, TNF
postsynapse 1 ATG5
presynaptic membrane 2 ATP2B1, HTT
Cytoplasm, cytosol 4 G6PD, GAPDH, LIPE, TFEB
plasma membrane 6 ATP2B1, GAPDH, GPRC5A, HTT, SI, TNF
synaptic vesicle membrane 1 ATP2B1
Membrane 6 ATG5, ATP2B1, G6PD, GAPDH, LIPE, SI
apical plasma membrane 1 SI
axon 2 ATG5, HTT
basolateral plasma membrane 1 ATP2B1
brush border 1 SI
caveola 1 LIPE
extracellular exosome 10 ATP2B1, BMP3, G6PD, GAPDH, GPRC5A, GSR, LYZ, PKM, SI, SOD1
Lysosome membrane 1 TFEB
endoplasmic reticulum 1 HTT
extracellular space 6 BMP3, IL6, INS, LYZ, SOD1, TNF
perinuclear region of cytoplasm 2 GAPDH, HTT
Schaffer collateral - CA1 synapse 1 ATG5
mitochondrion 3 GSR, PKM, SOD1
protein-containing complex 3 ATG5, HTT, SOD1
intracellular membrane-bounded organelle 5 ATP2B1, G6PD, GAPDH, GPRC5A, MAP1LC3A
postsynaptic density 1 CASP3
Secreted 3 BMP3, IL6, INS
extracellular region 7 BMP3, IL6, INS, LYZ, PKM, SOD1, TNF
cytoplasmic side of plasma membrane 1 G6PD
mitochondrial matrix 2 GSR, SOD1
centriolar satellite 1 G6PD
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane 1 ATP2B1
nuclear membrane 1 GAPDH
external side of plasma membrane 2 GSR, TNF
Extracellular vesicle 1 PKM
cytoplasmic vesicle 1 SOD1
microtubule cytoskeleton 1 GAPDH
nucleolus 1 GPRC5A
axon cytoplasm 1 SOD1
Early endosome 1 HTT
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
vesicle 3 GAPDH, GPRC5A, PKM
postsynaptic membrane 1 HTT
Cytoplasm, perinuclear region 1 GAPDH
Membrane raft 2 HTT, TNF
Cell junction, focal adhesion 1 HTT
Cytoplasm, cytoskeleton 2 GAPDH, MAP1LC3A
focal adhesion 1 HTT
microtubule 1 MAP1LC3A
Peroxisome 1 SOD1
mitochondrial intermembrane space 1 SOD1
collagen-containing extracellular matrix 1 PKM
lateral plasma membrane 1 ATP2B1
axoneme 1 ATG5
dendrite cytoplasm 1 SOD1
Late endosome 2 HTT, MAP1LC3A
receptor complex 1 GPRC5A
Cell projection, neuron projection 1 HTT
neuron projection 1 HTT
cilium 1 PKM
chromatin 1 TFEB
Cytoplasmic vesicle, autophagosome membrane 1 MAP1LC3A
autophagosome membrane 1 MAP1LC3A
cell projection 1 ATP2B1
phagocytic cup 1 TNF
phagocytic vesicle membrane 1 ATG5
cytoskeleton 1 GAPDH
centriole 1 HTT
Basolateral cell membrane 1 ATP2B1
organelle membrane 1 MAP1LC3A
Endomembrane system 2 HTT, MAP1LC3A
endosome lumen 1 INS
Lipid droplet 2 GAPDH, LIPE
Membrane, caveola 1 LIPE
Preautophagosomal structure membrane 1 ATG5
Atg12-Atg5-Atg16 complex 1 ATG5
mitochondria-associated endoplasmic reticulum membrane contact site 1 ATG5
phagophore assembly site membrane 1 ATG5
Cytoplasmic vesicle membrane 2 GPRC5A, HTT
Presynaptic cell membrane 1 ATP2B1
ficolin-1-rich granule lumen 1 PKM
secretory granule lumen 2 INS, PKM
Golgi lumen 1 INS
endoplasmic reticulum lumen 2 IL6, INS
specific granule lumen 1 LYZ
tertiary granule lumen 1 LYZ
transport vesicle 1 INS
azurophil granule lumen 1 LYZ
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
immunological synapse 1 ATP2B1
ribonucleoprotein complex 1 GAPDH
death-inducing signaling complex 1 CASP3
Rough endoplasmic reticulum 1 PKM
postsynaptic cytosol 1 HTT
GAIT complex 1 GAPDH
presynaptic cytosol 1 HTT
transferase complex 1 ATG5
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
Autolysosome 1 MAP1LC3A
inclusion body 1 HTT
interleukin-6 receptor complex 1 IL6
photoreceptor ribbon synapse 1 ATP2B1
[Isoform M2]: Cytoplasm 1 PKM
[Isoform M1]: Cytoplasm 1 PKM
serotonergic synapse 1 HTT
[Huntingtin]: Cytoplasm 1 HTT
[Huntingtin, myristoylated N-terminal fragment]: Cytoplasmic vesicle, autophagosome 1 HTT
phagophore 1 ATG5
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • Mohammad Alrosan, Ali Madi Almajwal, Ali Al-Qaisi, Sana Gammoh, Muhammad H Alu'datt, Farah R Al Qudsi, Thuan-Chew Tan, Ammar A Razzak Mahmood, Khalid Bani-Melhem. Trehalose-conjugated lentil-casein protein complexes prepared by structural interaction: Effects on water solubility and protein digestibility. Food chemistry. 2024 Jul; 447(?):138882. doi: 10.1016/j.foodchem.2024.138882. [PMID: 38452537]
  • Yakupjan Haxim, Ting Cao, Xiaoshuang Li, Xiujin Liu, Yuqing Liang, Amangul Hawar, Ruirui Yang, Daoyuan Zhang. Autophagy functions as a cytoprotective mechanism by regulating programmed cell death during desiccation in Syntrichia caninervis. Plant physiology and biochemistry : PPB. 2024 Jun; 211(?):108620. doi: 10.1016/j.plaphy.2024.108620. [PMID: 38714124]
  • 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]
  • Sayma Serine Chompa, Ali Tan Kee Zuan, Adibah Mohd Amin, Tan Geok Hun, Amir Hamzah Ahmad Ghazali, Buraq Musa Sadeq, Amaily Akter, Md Ekhlasur Rahman, Harun Or Rashid. Survival of beneficial microbes in liquid bioformulation and optimization of different carrier materials using RSM technique. International microbiology : the official journal of the Spanish Society for Microbiology. 2024 Jun; 27(3):697-706. doi: 10.1007/s10123-023-00423-4. [PMID: 37651053]
  • Xingxing Wang, Yingying Wei, Shu Jiang, Jianfen Ye, Yi Chen, Feng Xu, Xingfeng Shao. Transcriptome analysis reveals that trehalose alleviates chilling injury of peach fruit by regulating ROS signaling pathway and enhancing antioxidant capacity. Food research international (Ottawa, Ont.). 2024 Jun; 186(?):114331. doi: 10.1016/j.foodres.2024.114331. [PMID: 38729716]
  • Jantana Blanford, Zhiyang Zhai, Marcel D Baer, Gongrui Guo, Hui Liu, Qun Liu, Simone Raugei, John Shanklin. Molecular mechanism of trehalose 6-phosphate inhibition of the plant metabolic sensor kinase SnRK1. Science advances. 2024 May; 10(20):eadn0895. doi: 10.1126/sciadv.adn0895. [PMID: 38758793]
  • Sakthi Uma Devi Eswaran, Lalitha Sundaram, Kahkashan Perveen, Najat A Bukhari, R Z Sayyed. Osmolyte-producing microbial biostimulants regulate the growth of Arachis hypogaea L. under drought stress. BMC microbiology. 2024 May; 24(1):165. doi: 10.1186/s12866-024-03320-6. [PMID: 38745279]
  • Kazuhisa Maeda, Zheng Zhou, Miao Guo, Jinlong Zhang, Lang Chen, Fan Yang. Functional properties and skin care effects of sodium trehalose sulfate. Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI). 2024 Apr; 30(4):e13666. doi: 10.1111/srt.13666. [PMID: 38606717]
  • Ying Li, Shunjiao Wu, Yonghong Xu, Yaying Li, Yinghong Liu, Jia Wang. Transcriptomic Identification and Characterization of Trehalose-6-Phosphate Synthase in Fat Body of the Oriental Fruit Fly, Bactrocera dorsalis. Journal of agricultural and food chemistry. 2024 Mar; 72(11):5725-5733. doi: 10.1021/acs.jafc.3c06197. [PMID: 38452362]
  • Elena A Ianutsevich, Olga A Danilova, Olga A Grum-Grzhimaylo, Vera M Tereshina. Membrane Lipids and Osmolytes in the Response of the Acidophilic Basidiomycete Phlebiopsis gigantea to Heat, Cold, and Osmotic Shocks. International journal of molecular sciences. 2024 Mar; 25(6):. doi: 10.3390/ijms25063380. [PMID: 38542352]
  • Anitta Lutta, Matthias M Knopp, Matteo Tollemeto, Gabriel K Pedersen, Signe T Schmidt, Holger Grohganz, Line Hagner Nielsen. The interplay between trehalose and dextran as spray drying precursors for cationic liposomes. International journal of pharmaceutics. 2024 Mar; 652(?):123798. doi: 10.1016/j.ijpharm.2024.123798. [PMID: 38190949]
  • Javier A Miret, Cara A Griffiths, Matthew J Paul. Sucrose homeostasis: Mechanisms and opportunity in crop yield improvement. Journal of plant physiology. 2024 Mar; 294(?):154188. doi: 10.1016/j.jplph.2024.154188. [PMID: 38295650]
  • Shuyao Wang, Xin Hao, Yahui Liu, Yingying Chen, Yue Qu, Zhaoyuan Wang, Yingbai Shen. AnWRKY29 and AnHSP90 synergistically modulate trehalose levels in a desert shrub leaves during osmotic stress. Physiologia plantarum. 2024 Mar; 176(2):e14237. doi: 10.1111/ppl.14237. [PMID: 38433182]
  • Hao Chen, Suhua Huang, Changqian Quan, Zhining Chen, Meihua Xu, Fan Wei, Danfeng Tang. Effects of different colors of plastic-film mulching on soil temperature, yield, and metabolites in Platostoma palustre. Scientific reports. 2024 03; 14(1):5110. doi: 10.1038/s41598-024-55406-w. [PMID: 38429397]
  • Sana Parveen, Nasrin Akhtar, Teerasak E-Kobon, Richard Burchmore, Abdullah Ijaz Hussain, Kalsoom Akhtar. Biodesulfurization of organosulfur compounds by a trehalose biosurfactant producing Gordonia sp. isolated from crude oil contaminated soil. World journal of microbiology & biotechnology. 2024 Feb; 40(3):103. doi: 10.1007/s11274-024-03899-y. [PMID: 38372854]
  • Liangliang Li, Yan Li, Guijie Ding. Response mechanism of carbon metabolism of Pinus massoniana to gradient high temperature and drought stress. BMC genomics. 2024 Feb; 25(1):166. doi: 10.1186/s12864-024-10054-2. [PMID: 38347506]
  • Gongshan Chen, Anna Yang, Jianzhong Wang, Lixia Ke, Shaoxing Chen, Wentao Li. Effects of the synergistic treatments of arbuscular mycorrhizal fungi and trehalose on adaptability to salt stress in tomato seedlings. Microbiology spectrum. 2024 Jan; ?(?):e0340423. doi: 10.1128/spectrum.03404-23. [PMID: 38259091]
  • Yitong Chen, Liu Tang, Zhiyang Jiang, Shanshan Wang, Linlu Qi, Xiaolin Tian, Haiteng Deng, Zhiwei Kong, Wenqiang Gao, Xiaokang Zhang, Saijie Li, Meiqing Chen, Xin Zhang, Hongxia Duan, Jun Yang, You-Liang Peng, Dongli Wang, Junfeng Liu. Dual-Specificity Inhibitor Targets Enzymes of the Trehalose Biosynthesis Pathway. Journal of agricultural and food chemistry. 2024 Jan; 72(1):209-218. doi: 10.1021/acs.jafc.3c06946. [PMID: 38128269]
  • Benshui Shu, Xinyi Xie, Jinghua Dai, Luyang Liu, Xueming Cai, Zhongzhen Wu, Jintian Lin. Host plant-induced changes in metabolism and osmotic regulation gene expression in Diaphorina citri adults. Journal of insect physiology. 2024 01; 152(?):104599. doi: 10.1016/j.jinsphys.2023.104599. [PMID: 38072187]
  • Sara Lopes, Eva Fahr, João Costa, Andreia B Silva, M Manuel Lopes, Célia Faustino, Maria H L Ribeiro. Sustainable trehalose lipid production by Rhodotorula sp.: a promising bio-based alternative. Bioprocess and biosystems engineering. 2024 Jan; 47(1):145-157. doi: 10.1007/s00449-023-02949-3. [PMID: 38103079]
  • Mahima Misti Sarkar, Pritha Rudra, Paramita Paul, Tarun Kumar Dua, Swarnendu Roy. Enhanced adaptation to salinity stress in lentil seedlings through the use of trehalose-functionalized silica nanoparticles (TSiNPs): Exploring silica-sugar absorption and oxidative balance. Plant physiology and biochemistry : PPB. 2023 Dec; 206(?):108309. doi: 10.1016/j.plaphy.2023.108309. [PMID: 38169228]
  • Wenjing Shao, Xinlin Zhang, Zhiheng Zhou, Yue Ma, Duo Chu, Lei Wang, Yiming Yang, Lin Du, Yanli Du, Jidao Du, Qiang Zhao. Genome- and transcriptome-wide identification of trehalose-6-phosphate phosphatases (TPP) gene family and their expression patterns under abiotic stress and exogenous trehalose in soybean. BMC plant biology. 2023 Dec; 23(1):641. doi: 10.1186/s12870-023-04652-7. [PMID: 38082382]
  • Yuan Zhong, Ali Maruf, Kai Qu, Małgorzata Milewska, Ilona Wandzik, Nianlian Mou, Yu Cao, Wei Wu. Nanogels with covalently bound and releasable trehalose for autophagy stimulation in atherosclerosis. Journal of nanobiotechnology. 2023 Dec; 21(1):472. doi: 10.1186/s12951-023-02248-9. [PMID: 38066538]
  • Huihui Yu, Zhenning Teng, Bohan Liu, Jiahan Lv, Yinke Chen, Zhonge Qin, Yan Peng, Shuan Meng, Yuchi He, Meijuan Duan, Jianhua Zhang, Nenghui Ye. Transcription factor OsMYB30 increases trehalose content to inhibit α-amylase and seed germination at low temperature. Plant physiology. 2023 Dec; ?(?):. doi: 10.1093/plphys/kiad650. [PMID: 38057158]
  • Moritz Göbel, Franziska Fichtner. Functions of sucrose and trehalose 6-phosphate in controlling plant development. Journal of plant physiology. 2023 Dec; 291(?):154140. doi: 10.1016/j.jplph.2023.154140. [PMID: 38007969]
  • Tiantian Liu, Jin Wang, Lin Chen, Shengxuan Liu, Tengfei Liu, Liu Yu, Jingjing Guo, Ye Chen, Yiling Zhang, Botao Song. ScAREB4 promotes potato constitutive and acclimated freezing tolerance associated with enhancing trehalose synthesis and oxidative stress tolerance. Plant, cell & environment. 2023 Dec; 46(12):3839-3857. doi: 10.1111/pce.14707. [PMID: 37651608]
  • Qingqing Liu, Ningning Wang, Minli Qiu, Jun Cheng, Huajun Zhou, Feihu Che, Yan Hu, Yinghui He, Yuzhu Dai, Yingjie Zhang. Development and application of a universal extraction-free reagent based on an algal glycolipid. Analytical methods : advancing methods and applications. 2023 11; 15(44):6061-6072. doi: 10.1039/d3ay01246h. [PMID: 37921204]
  • Nattavat Sukko, Saowalak Kalapanulak, Treenut Saithong. Trehalose metabolism coordinates transcriptional regulatory control and metabolic requirements to trigger the onset of cassava storage root initiation. Scientific reports. 2023 11; 13(1):19973. doi: 10.1038/s41598-023-47095-8. [PMID: 37968317]
  • Yunxiao Wei, Yuhan Song, Muhammad Aamir Khan, Chengzhen Liang, Zhigang Meng, Yuan Wang, Sandui Guo, Rui Zhang. GhTPPA_2 Enhancement of Tobacco Sugar Accumulation and Drought Tolerance. Gene. 2023 Nov; ?(?):147969. doi: 10.1016/j.gene.2023.147969. [PMID: 37931857]
  • Changxia Li, Xuefang Lu, Yunzhi Liu, Junrong Xu, Wenjin Yu. Trehalose alleviates the inhibition of adventitious root formation caused by drought stress in cucumber through regulating ROS metabolism and activating trehalose and plant hormone biosynthesis. Plant physiology and biochemistry : PPB. 2023 Nov; 205(?):108159. doi: 10.1016/j.plaphy.2023.108159. [PMID: 37944244]
  • L Soltani. Role of oleic acid and trehalose on frozen-thawed ram semen. Cryo letters. 2023 Nov; 44(6):343-351. doi: . [PMID: 38311928]
  • Sandra Mae-Lin Kerbler, Vinicio Armijos-Jaramillo, John Edward Lunn, Rubén Vicente. The trehalose 6-phosphate phosphatase family in plants. Physiologia plantarum. 2023 Nov; 175(6):e14096. doi: 10.1111/ppl.14096. [PMID: 38148193]
  • Kun Cao, Yufeng Sun, Xiaoyan Zhang, Yue Zhao, Jing Bian, Hao Zhu, Pan Wang, Baochang Gao, Xiaoli Sun, Ming Hu, Yongxia Guo, Xiaonan Wang. The miRNA-mRNA regulatory networks of the response to NaHCO3 stress in industrial hemp (Cannabis sativa L.). BMC plant biology. 2023 Oct; 23(1):509. doi: 10.1186/s12870-023-04463-w. [PMID: 37875794]
  • Orpheus M Butler, Stefano Manzoni, Charles R Warren. Community composition and physiological plasticity control microbial carbon storage across natural and experimental soil fertility gradients. The ISME journal. 2023 Oct; ?(?):. doi: 10.1038/s41396-023-01527-5. [PMID: 37853184]
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