beta-Lactose (BioDeep_00000000298)

Main id: BioDeep_00000027528

 

human metabolite PANOMIX_OTCML-2023 BioNovoGene_Lab2019


代谢物信息卡片


(2R,3R,4R,5S,6R)-6-(Hydroxymethyl)-5-(((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2,3,4-triol

化学式: C12H22O11 (342.1162)
中文名称: D-乳糖 一水合物, 乳糖,无水, 乳糖, 乳糖单水合物, β-乳糖
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O
InChI: InChI=1S/C12H22O11/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17/h3-20H,1-2H2/t3-,4-,5+,6+,7-,8-,9-,10-,11-,12+/m1/s1

描述信息

Beta-lactose is the beta-anomer of lactose.
beta-Lactose contains a Lactosylceramide motif and is often attached to a Cer aglycon.
beta-Lactose is a natural product found in Hypericum perforatum with data available.
A disaccharide of GLUCOSE and GALACTOSE in human and cow milk. It is used in pharmacy for tablets, in medicine as a nutrient, and in industry.
Beta-Lactose is the beta-pyranose form of the compound lactose [CCD].
D000074385 - Food Ingredients > D005503 - Food Additives
D010592 - Pharmaceutic Aids > D005421 - Flavoring Agents
Beta-pyranose form of the compound lactose [CCD]
The beta-anomer of lactose.
Lactose, a major sugar in the milk of most species, could regulate human’s intestinal microflora.
Lactose, a major sugar in the milk of most species, could regulate human’s intestinal microflora.
α-Lactose (α-D-Lactose) is the major sugar present in milk. Lactose exists in the form of two anomers, α and β. The α form normally crystallizes as a monohydrate[1][2].
α-Lactose (α-D-Lactose) is the major sugar present in milk. Lactose exists in the form of two anomers, α and β. The α form normally crystallizes as a monohydrate[1][2].

同义名列表

88 个代谢物同义名

(2R,3R,4R,5S,6R)-6-(Hydroxymethyl)-5-(((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2,3,4-triol; (2R,3R,4R,5S,6R)-6-(hydroxymethyl)-5-((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)tetrahydro-2H-pyran-2,3,4-triol; (2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[(2R,3S,4R,5R,6R)-4,5,6-trihydroxy-2-(hydroxymethyl)tetrahydropyran-3-yl]oxy-tetrahydropyran-3,4,5-triol; (2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-{[(2R,3S,4R,5R,6R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}oxane-3,4,5-triol; (2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[(2R,3S,4R,5R,6R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol; beta-Lactose, <=30\\% alpha-anomer basis, >=99\\% total lactose basis; beta-D-Lactose, contains ca. 70\\% beta and ca. 30\\% alpha; WURCS=2.0/2,2,1/(a2122h-1b_1-5)(a2112h-1b_1-5)/1-2/a4-b1; WURCS=2.0/2,2,1/[a2122h-1b_1-5][a2112h-1b_1-5]/1-2/a4-b1; beta-Lactose, suitable for component for culture media; beta-D-galactopyranosyl-(1->4)-beta-D-glucopyranose; beta-D-Glucopyranose, 4-O-beta-D-galactopyranosyl-; 4-O-(beta-D-Galactopyranosyl)-beta-D-glucopyranose; 4-O-beta-D-Galactopyranosyl-beta-D-glucopyranose; beta-D-galactopyranosyl-(1->4)-beta-D-glucose; 4-O-b-D-Galactopyranosyl-b-D-glucopyranose; 4-O-Β-D-galactopyranosyl-β-D-glucopyranose; D-Glucose, 4-O-b-D-galactopyranosyl- (9CI); b-D-Galactopyranosyl-(1->4)-b-D-glucose; Β-D-galactopyranosyl-(1->4)-β-D-glucose; D-Glucose, 4-O-beta-D-galactopyranosyl; 4-O-beta-D-Galactopyranosyl-D-glucose; 60B85732-763B-4E21-BD67-6163315FD251; .beta.-D-Gal-(1-->4)-.beta.-D-Glc; 4-(beta-D-Galactosido)-D-glucose; Beta-d-lactose, with 30\\% alfa; beta-D-Galp-(1->4)-beta-D-Glcp; GUBGYTABKSRVRQ-DCSYEGIMSA-N; Β-D-galp-(1->4)-β-D-GLCP; b-D-Galp-(1->4)-b-D-GLCP; Lactin (carbohydrate); Lactose-electricitas; Lactosum anhydricum; Lactosum, anhydrous; Lactose, Anhydrous; Lactose anhydrous; Galbeta1-4Glcbeta; Pharmatosa DCL 21; Anhydrous lactose; Saccharum lactin; Lactose Fast-flo; .beta.-D-Lactose; Saccharum lactis; Fast-flo Lactose; UNII-13Q3A43E0S; Lactose, beta-; .beta.-Lactose; beta-D-Lactose; Lactose [JAN]; Tablettose 70; beta -lactose; Lactose (8CI); Tablettose 80; D-(+)-Lactose; Pharmatose 21; beta-Lactose; Tox21_301866; Β-D-lactose; b-D-Lactose; (+)-Lactose; Galb1-4Glcb; CAS-63-42-3; Lactobiose; Tablettose; Osmolactan; Milk sugar; Zeparox EP; Aletobiose; 13Q3A43E0S; Galactinum; Β-lactose; D-Lactose; b-Lactose; Super-Tab; α-Lactose; Lactose; Lactin; 1gwv; 2nn8; 2zgm; 1gzc; 1ax1; 1z3v; LAT; beta-Lactose; α-D-Lactose; Lactose; beta-Lactose



数据库引用编号

29 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(9)

BioCyc(8)

PlantCyc(3)

代谢反应

273 个相关的代谢反应过程信息。

Reactome(50)

BioCyc(30)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(193)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

18 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 6 APC, G6PD, GALT, LGALS1, PRL, TXN
Peripheral membrane protein 3 COQ10A, G6PD, GBA1
Endoplasmic reticulum membrane 1 LNPK
Nucleus 3 APC, PRL, TXN
cytosol 7 APC, G6PD, GALE, GALT, LGALS1, LGALS4, TXN
trans-Golgi network 1 GBA1
centrosome 1 APC
nucleoplasm 5 APC, ATP2B1, LNPK, PRL, TXN
RNA polymerase II transcription regulator complex 1 PRL
Cell membrane 3 APC, ATP2B1, CD79A
Cytoplasmic side 1 LNPK
lamellipodium 1 APC
ruffle membrane 1 APC
Multi-pass membrane protein 2 ATP2B1, LNPK
Synapse 1 ATP2B1
glutamatergic synapse 1 ATP2B1
Golgi apparatus 4 APC, GALT, GBA1, SI
Golgi membrane 1 INS
lysosomal membrane 1 GBA1
mitochondrial inner membrane 1 COQ10A
presynaptic membrane 1 ATP2B1
Cytoplasm, cytosol 1 G6PD
Lysosome 1 GBA1
plasma membrane 7 APC, ATP2B1, CD79A, GCG, LGALS1, LGALS4, SI
synaptic vesicle membrane 1 ATP2B1
Membrane 4 ATP2B1, G6PD, LNPK, SI
apical plasma membrane 1 SI
basolateral plasma membrane 1 ATP2B1
brush border 1 SI
extracellular exosome 7 AMY2A, ATP2B1, G6PD, GBA1, LGALS1, SI, TXN
Lysosome membrane 1 GBA1
Lumenal side 1 GBA1
endoplasmic reticulum 2 GBA1, LNPK
extracellular space 9 AMY2A, GCG, IGF1, IL10, INS, LGALS1, LGALS4, PRL, PTH
lysosomal lumen 1 GBA1
perinuclear region of cytoplasm 1 APC
adherens junction 1 APC
bicellular tight junction 1 APC
mitochondrion 1 COQ10A
intracellular membrane-bounded organelle 2 ATP2B1, G6PD
Single-pass type I membrane protein 1 CD79A
Secreted 7 GCG, IGF1, IL10, INS, LGALS1, PRL, TXN
extracellular region 9 AMY2A, GCG, IGF1, IL10, INS, LGALS1, PRL, PTH, TXN
cytoplasmic side of plasma membrane 1 G6PD
centriolar satellite 1 G6PD
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane 1 ATP2B1
external side of plasma membrane 1 CD79A
Secreted, extracellular space, extracellular matrix 1 LGALS1
multivesicular body 1 CD79A
beta-catenin destruction complex 1 APC
Wnt signalosome 1 APC
Cell projection, lamellipodium 1 APC
Cell projection, ruffle membrane 1 APC
Mitochondrion inner membrane 1 COQ10A
Matrix side 1 COQ10A
Membrane raft 1 CD79A
Cytoplasm, cytoskeleton 1 APC
microtubule 1 APC
Cell junction, adherens junction 1 APC
collagen-containing extracellular matrix 2 LGALS1, LGALS4
lateral plasma membrane 2 APC, ATP2B1
chromatin 1 PRL
cell projection 1 ATP2B1
cell periphery 1 APC
Basolateral cell membrane 1 ATP2B1
endosome lumen 2 INS, PRL
Presynaptic cell membrane 1 ATP2B1
exocytic vesicle 1 IGF1
secretory granule lumen 2 GCG, INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 3 GCG, INS, LGALS1
platelet alpha granule lumen 1 IGF1
kinetochore 1 APC
transport vesicle 1 INS
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
immunological synapse 1 ATP2B1
catenin complex 1 APC
[Glucagon-like peptide 1]: Secreted 1 GCG
IgM B cell receptor complex 1 CD79A
alphav-beta3 integrin-IGF-1-IGF1R complex 1 IGF1
insulin-like growth factor binding protein complex 1 IGF1
insulin-like growth factor ternary complex 1 IGF1
galectin complex 1 LGALS1
photoreceptor ribbon synapse 1 ATP2B1
B cell receptor complex 1 CD79A
endoplasmic reticulum tubular network 1 LNPK
endoplasmic reticulum tubular network membrane 1 LNPK


文献列表

  • C Gasser, J M Faurie, F Rul. Regulation of lactose, glucose and sucrose metabolisms in S. thermophilus. Food microbiology. 2024 Aug; 121(?):104487. doi: 10.1016/j.fm.2024.104487. [PMID: 38637064]
  • Virginia Gontijo Abreu Hochman, Regina Celia Fernandes de Abreu Nascimento, Camila Barros Melgaço da Silva, Pedro Noguchi Aragão Quinderé, Raquel Ximenes Melo, Luis Guillermo Coca Velarde, Arnaldo Costa Bueno, Alan Araújo Vieira. Relationship Between Maternal Age and Macronutrient Content of Colostrum. Journal of human lactation : official journal of International Lactation Consultant Association. 2024 05; 40(2):286-295. doi: 10.1177/08903344241233500. [PMID: 38411139]
  • Adam Poltorak, Xin Zhou, Takao Kasuga, Yong Xu, Zhiliang Fan. Conversion of Deproteinized Cheese Whey to Lactobionate by an Engineered Neurospora crassa Strain F5. Applied biochemistry and biotechnology. 2024 Mar; 196(3):1292-1303. doi: 10.1007/s12010-023-04583-x. [PMID: 37392323]
  • Xiàowěi Qí, Kirsten Gade Malmos, Frans W J van den Berg, Flemming Bjerg Grumsen, Serafim Bakalis. Crystal size, a key character of lactose crystallization affecting microstructure, surface chemistry and reconstitution of milk powder. Food research international (Ottawa, Ont.). 2024 Feb; 177(?):113872. doi: 10.1016/j.foodres.2023.113872. [PMID: 38225141]
  • K Bella, Sridhar Pilli, P Venkateswara Rao, R D Tyagi. Bio-conversion of whey lactose using enzymatic hydrolysis with β-galactosidase: an experimental and kinetic study. Environmental technology. 2024 Feb; 45(6):1234-1247. doi: 10.1080/09593330.2022.2139639. [PMID: 36282727]
  • Agnė Krupinskaitė, Rūta Stanislauskienė, Pijus Serapinas, Rasa Rutkienė, Renata Gasparavičiūtė, Rolandas Meškys, Jonita Stankevičiūtė. α-L-Fucosidases from an Alpaca Faeces Metagenome: Characterisation of Hydrolytic and Transfucosylation Potential. International journal of molecular sciences. 2024 Jan; 25(2):. doi: 10.3390/ijms25020809. [PMID: 38255883]
  • Jawad Alharake, Frédérique Bidard, Thiziri Aouam, Catherine Sénamaud-Beaufort, Antoine Margeot, Senta Heiss-Blanquet. Effect of the res2 transcription factor gene deletion on protein secretion and stress response in the hyperproducer strain Trichoderma reesei Rut-C30. BMC microbiology. 2023 Nov; 23(1):374. doi: 10.1186/s12866-023-03125-z. [PMID: 38036984]
  • Ake-Kavitch Siriatcharanon, Sawannee Sutheeworapong, Sirilak Baramee, Rattiya Waeonukul, Patthra Pason, Akihiko Kosugi, Ayaka Uke, Khanok Ratanakhanokchai, Chakrit Tachaapaikoon. Discovery of a Novel Cellobiose Dehydrogenase from Cellulomonas palmilytica EW123 and Its Sugar Acids Production. Journal of microbiology and biotechnology. 2023 Oct; 34(2):1-10. doi: 10.4014/jmb.2307.07004. [PMID: 38044713]
  • Muhammad Taufiq Firdausi Mazlee, Thorsten Heidelberg, Azhar Ariffin, Sharifuddin Md Zain. Cation-stimulated drug delivery via lipid assembly comprising macrocyclized disaccharides - A DFT study. Carbohydrate research. 2023 Oct; 532(?):108923. doi: 10.1016/j.carres.2023.108923. [PMID: 37598565]
  • Xinyue Zhai, Xinwei Tao, Yuqian Wu, Kesun Jin, Huaping Tan, Tianle Zhou, Yong Chen. Injectable and Self-Adaptive Gel Scaffold Based on Heparin Microspheres for Adipogenesis of Human Adipose-Derived Stem Cells. Biomacromolecules. 2023 Sep; ?(?):. doi: 10.1021/acs.biomac.3c00348. [PMID: 37722066]
  • Chloe C Josefson, Lucelia De Moura Pereira, Amy L Skibiel. Chronic Stress Decreases Lactation Performance. Integrative and comparative biology. 2023 09; 63(3):557-568. doi: 10.1093/icb/icad044. [PMID: 37253624]
  • Chuting Shi, Haiyue Zhao, Ying Fang, Lan Shen, Lijie Zhao. Lactose in tablets: Functionality, critical material attributes, applications, modifications and co-processed excipients. Drug discovery today. 2023 09; 28(9):103696. doi: 10.1016/j.drudis.2023.103696. [PMID: 37419210]
  • Seham El-Kassas, Haitham G Abo-Al-Ela, Esraa Abdulraouf, Mohamed Atef Helal, A M Sakr, Safaa E Abdo. Detection of two SNPs of the LIPE gene in Holstein-Friesian cows with divergent milk production. The Journal of dairy research. 2023 Aug; ?(?):1-8. doi: 10.1017/s002202992300050x. [PMID: 37615121]
  • Yuang Wu, Yue Sun, Evelyne Richet, Zhifu Han, Jijie Chai. Structural basis for negative regulation of the Escherichia coli maltose system. Nature communications. 2023 08; 14(1):4925. doi: 10.1038/s41467-023-40447-y. [PMID: 37582800]
  • Patricia Benito, Javier Bellón, Rosa Porcel, Lynne Yenush, José M Mulet. The Biostimulant, Potassium Humate Ameliorates Abiotic Stress in Arabidopsis thaliana by Increasing Starch Availability. International journal of molecular sciences. 2023 Jul; 24(15):. doi: 10.3390/ijms241512140. [PMID: 37569516]
  • LiangFeng Wang, LiJie Zhao, YanLong Hong, Lan Shen, Xiao Lin. Attribute transmission and effects of diluents and granulation liquids on granule properties and tablet quality for high shear wet granulation and tableting process. International journal of pharmaceutics. 2023 Jul; 642(?):123177. doi: 10.1016/j.ijpharm.2023.123177. [PMID: 37364781]
  • Ke Wang, Yihong Xu, Zehui Xuan, Xina Xiao, Guofeng Gu, Lili Lu. Enzymatic synthesis of prebiotic galactooligosaccharides from galactose derived from gum arabic. Food chemistry. 2023 Jul; 429(?):136987. doi: 10.1016/j.foodchem.2023.136987. [PMID: 37523914]
  • Fábio Antunes Rizzo, Jorge Schafhauser Júnior, Rudolf Brand Scheibler, Ana Carolina Fluck, Diego Prado de Vargas, José Laerte Nörnberg, Vitor Ionatan Fioreze, Jamir Luís Silva da Silva, Olmar Antônio Denardin Costa. Biofortification of cow milk through dietary supplementation with sunflower oil: fatty acid profile, atherogenicity, and thrombogenic index. Tropical animal health and production. 2023 Jul; 55(4):269. doi: 10.1007/s11250-023-03670-9. [PMID: 37452970]
  • Yongqing Li, Li Liu, Abula Zunongjiang, Lijun Cao, Yikai Fan, Bo Hu, Shujun Zhang. Analysis of the relationship between short tandem repeats and lactation performance of Xinjiang Holstein cows. Tropical animal health and production. 2023 Jun; 55(4):238. doi: 10.1007/s11250-023-03651-y. [PMID: 37322113]
  • Ruben Halfwerk, Louise Verdonk, Doekle Yntema, Jaap Van Spronsen, Albert Van der Padt. Scaling up continuous eutectic freeze crystallization of lactose from whey permeate: A pilot plant study at sub-zero temperatures. Food research international (Ottawa, Ont.). 2023 06; 168(?):112764. doi: 10.1016/j.foodres.2023.112764. [PMID: 37120213]
  • Joan Teichenné, Úrsula Catalán, Roger Mariné-Casadó, Cristina Domenech-Coca, Anna Mas-Capdevila, Juan María Alcaide-Hidalgo, Gertruda Chomiciute, Ana Rodríguez-García, Ana Hernández, Vanessa Gutierrez, Francesc Puiggròs, Josep M Del Bas, Antoni Caimari. Bacillus coagulans GBI-30, 6086 (BC30) improves lactose digestion in rats exposed to a high-lactose meal. European journal of nutrition. 2023 May; ?(?):. doi: 10.1007/s00394-023-03183-z. [PMID: 37249602]
  • Roberta Giugliano, Noemi Musolino, Valentina Ciccotelli, Carla Ferraris, Valentina Savio, Barbara Vivaldi, Carlo Ercolini, Daniela Manila Bianchi, Lucia Decastelli. Soy, Rice and Oat Drinks: Investigating Chemical and Biological Safety in Plant-Based Milk Alternatives. Nutrients. 2023 May; 15(10):. doi: 10.3390/nu15102258. [PMID: 37242141]
  • Karolina Drężek, Maria Krystyna Sobczyk, Zoltán Kállai, Anna Detman, Paula Bardadyn, Jolanta Mierzejewska. Valorisation of Whey Permeate in Sequential Bioprocesses towards Value-Added Products-Optimisation of Biphasic and Classical Batch Cultures of Kluyveromyces marxianus. International journal of molecular sciences. 2023 Apr; 24(8):. doi: 10.3390/ijms24087560. [PMID: 37108722]
  • Ayako Wada-Katsumata, Eduardo Hatano, Coby Schal. Gustatory polymorphism mediates a new adaptive courtship strategy. Proceedings. Biological sciences. 2023 03; 290(1995):20222337. doi: 10.1098/rspb.2022.2337. [PMID: 36987637]
  • Dinesh Jhamb, Thirumala Rao Talluri, Sunanda Sharma, Rohit Juneja, Surendar Singh Nirwan, Deepak, Kalpesh Kumar Pargi, Aashish Tanwer, Pramod Kumar, Ramesh Kumar, Sharat Chandra Mehta, Mukesh Parashar, Mitesh Gaur. Freezability and fertility rates of stallion semen supplemented with trehalose in lactose extender. Journal of equine veterinary science. 2023 Mar; ?(?):104293. doi: 10.1016/j.jevs.2023.104293. [PMID: 36958410]
  • Blerina Shkembi, Thom Huppertz. Impact of Dairy Products and Plant-Based Alternatives on Dental Health: Food Matrix Effects. Nutrients. 2023 Mar; 15(6):. doi: 10.3390/nu15061469. [PMID: 36986199]
  • D Ott, D Manneck, K T Schrapers, J Rosendahl, J R Aschenbach. Blood calcium concentration and performance in periparturient and early lactating dairy cows is influenced by plant bioactive lipid compounds. Journal of dairy science. 2023 Mar; ?(?):. doi: 10.3168/jds.2022-22387. [PMID: 36907757]
  • Samantha McPherson, Ayako Wada-Katsumata, Jules Silverman, Coby Schal. Glucose- and disaccharide-containing baits impede secondary mortality in glucose-averse German cockroaches. Journal of economic entomology. 2023 Mar; ?(?):. doi: 10.1093/jee/toad030. [PMID: 36888567]
  • Matthias Sipiczki, Valéria Hrabovszki. Galactomyces candidus diversity in the complex mycobiota of cow-milk bryndza cheese comprising antagonistic and sensitive strains. International journal of food microbiology. 2023 Mar; 388(?):110088. doi: 10.1016/j.ijfoodmicro.2023.110088. [PMID: 36689829]
  • Dylan Jabeguero, Lina Siukstaite, Chunyue Wang, Anna Mitrovic, Serge Pérez, Olga Makshakova, Ralf P Richter, Winfried Römer, Christelle Breton. Enzymatic Glyco-Modification of Synthetic Membrane Systems. Biomolecules. 2023 Feb; 13(2):. doi: 10.3390/biom13020335. [PMID: 36830704]
  • Qin Qin Gong, Justin Yong Soon Tay, Natalia Veronica, Jian Xu, Paul Wan Sia Heng, Yong Ping Zhang, Celine Valeria Liew. Surface Modification of lactose carrier particles using a fluid bed coater to improve fine particle fraction for dry powder inhalers. Pharmaceutical development and technology. 2023 Feb; 28(2):164-175. doi: 10.1080/10837450.2023.2171434. [PMID: 36683577]
  • Liangke Chen, Xiangbai Dong, Huifang Yang, Yaru Chai, Yan Xia, Lihong Tian, Le Qing Qu. Cytosolic disproportionating enzyme2 is essential for pollen germination and pollen tube elongation in rice. Plant physiology. 2023 01; 191(1):96-109. doi: 10.1093/plphys/kiac496. [PMID: 36282529]
  • Rana Kamei, Oinam Sangita Devi, Sorokhaibam Jibankumar Singh, Wayenbam Sobhachandra Singh, Senjam Sunil Singh. Purification and Characterization of a Novel D-Galactose Binding Lectin from Seeds of Meizotropis buteiformis. Current pharmaceutical biotechnology. 2023; 24(5):665-675. doi: 10.2174/1389201023666220517145338. [PMID: 35585818]
  • Iftikhar Khan, Ali Al-Hasani, Mohsin H Khan, Aamir N Khan, Fakhr-E -Alam, Sajid K Sadozai, Abdelbary Elhissi, Jehanzeb Khan, Sakib Yousaf. Impact of dispersion media and carrier type on spray-dried proliposome powder formulations loaded with beclomethasone dipropionate for their pulmonary drug delivery via a next generation impactor. PloS one. 2023; 18(3):e0281860. doi: 10.1371/journal.pone.0281860. [PMID: 36913325]
  • Mikel Redin Hurtado, Ida Fischer, Matthias Laska. Is sugar as sweet to the palate as seeds are appetizing to the belly? Taste responsiveness to five food-associated carbohydrates in zoo-housed white-faced sakis, Pithecia pithecia. PloS one. 2023; 18(10):e0292175. doi: 10.1371/journal.pone.0292175. [PMID: 37906563]
  • Tengfei Liu, Md Abu Kawochar, Shengxuan Liu, Yunxia Cheng, Shahnewaz Begum, Enshuang Wang, Tingting Zhou, Tiantian Liu, Xingkui Cai, Botao Song. Suppression of the tonoplast sugar transporter, StTST3.1, affects transitory starch turnover and plant growth in potato. The Plant journal : for cell and molecular biology. 2023 01; 113(2):342-356. doi: 10.1111/tpj.16050. [PMID: 36444716]
  • A Ruiz-Gayosso, I Rodríguez-Cruz, E Martínez-Barajas, P Coello. Phosphorylation of DPE2 at S786 partially regulates starch degradation. Plant physiology and biochemistry : PPB. 2022 Dec; 193(?):70-77. doi: 10.1016/j.plaphy.2022.10.024. [PMID: 36335878]
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