Cellobiose (BioDeep_00000014320)

Main id: BioDeep_00000014974

 

human metabolite PANOMIX_OTCML-2023 BioNovoGene_Lab2019 natural product


代谢物信息卡片


(2R,3S,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

化学式: C12H22O11 (342.1162)
中文名称: D(+)-纤维二糖, 纤维二糖, D-(+)-纤维二糖
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

Cellobiose, also known as GLCB1-4GLCB or cellose, is a disaccharide. It is also classified as a reducing sugar. In terms of its chemical structure, it is derived from the condensation of a pair beta-glucose molecules creating a beta (1‚Üí4) bond. It belongs to the class of organic compounds known as O-glycosyl compounds. These are glycosides in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. Cellobiose can be obtained by enzymatic hydrolysis of cellulose and cellulose-rich materials such as cotton, jute, or paper. Cellobiose is a plant metabolite found in flowering plants, conifers and other gymnosperms. Cellobiose can also be found in vertebrates that have consumed plant foods. It has been detected, but not quantified in, several different foods, such as okra, common chokecherries, cherry tomatoes, and welsh onions. Cellobiose can be used as an indicator carbohydrate for Crohns disease and malabsorption syndrome. Intestinal permeability to detect Crohns disease and malabsorption syndrome can be measured by the sugar absorption test. This test is based on determining the ratio of the urinary excretion of a large (a disaccharide such as cellobiose) and a small carbohydrate (a monosaccharide such as lactulose or rhamnose) after oral administration. Patients with Crohns disease or with ulcerative colitis have increased permeability indices in comparison to healthy controls (PMID: 15546811).
Cellobiose is a disaccharide consisting of two glucose units in a beta (1-4) glycosidic linkage. It is a microbial breakdown product from plant material (cellulose). It may be found in some food products (vegetables, fruits, corn syrups, etc.).
D-(+)-Cellobiose is an endogenous metabolite.
D-(+)-Cellobiose is an endogenous metabolite.

同义名列表

42 个代谢物同义名

(2R,3S,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; 4-beta-delta-Glucopyranosyl-delta-glucopyranose; 4-O-beta-D-Glucopyranosyl-beta-D-glucopyranose; 1-beta-D-Glucopyranosyl-4-beta-D-glucopyranose; 4-O-beta-delta-Glucopyranosyl-delta-glucose; 4 O beta D Glucopyranosyl D glucopyranose; 4-O-beta-D-Glucopyranosyl-D-glucopyranose; 4-O-Β-D-glucopyranosyl-β-D-glucopyranose; delta-Glucosyl-beta-(1->4)-delta-glucose; 1-Β-D-glucopyranosyl-4-β-D-glucopyranose; 4-O-b-D-Glucopyranosyl-b-D-glucopyranose; 1-b-D-Glucopyranosyl-4-b-D-glucopyranose; 4-beta-D-Glucopyranosyl-D-glucopyranose; delta-Glucosyl-beta-(1-4)-delta-glucose; 4-(beta-delta-Glucosido)-delta-glucose; beta-D-Glucosyl-(1->4)-beta-D-glucose; 4-O-beta-D-Glucopyranosyl-D-glucose; 4-(b-delta-Glucosido)-delta-glucose; D-Glucosyl-beta-(1->4)-D-glucose; 4-O-b-D-Glucopyranosyl-D-glucose; Β-D-glucosyl-(1->4)-β-D-glucose; b-D-Glucosyl-(1->4)-b-D-glucose; D-Glucosyl-beta-(1-4)-D-glucose; 4-(beta-D-Glucosido)-D-glucose; beta-D-GLCP-(1->4)-beta-D-GLCP; D-Glucosyl-b-(1->4)-D-glucose; beta-D-GLC-(1->4)-beta-D-GLC; 4-(b-D-Glucosido)-D-glucose; Β-D-GLCP-(1->4)-β-D-GLCP; b-D-GLCP-(1->4)-b-D-GLCP; Β-D-GLC-(1->4)-β-D-GLC; b-D-GLC-(1->4)-b-D-GLC; delta-(+)-Cellobiose; Glcbeta1-4glcbeta; D-(+)-Cellobiose; delta-Cellobiose; D-Cellobiose; b-Cellobiose; Β-cellobiose; GLCB1-4GLCB; Cellobiose; Cellose



数据库引用编号

22 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(1)

代谢反应

34 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(6)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(28)

  • starch degradation II: a glucan + maltotriose ⟶ D-glucopyranose + a glucan
  • starch degradation II: a glucan + maltotriose ⟶ D-glucopyranose + a glucan
  • starch degradation II: a glucan + maltotriose ⟶ D-glucopyranose + a glucan
  • starch degradation II: a glucan + maltotriose ⟶ D-glucopyranose + a glucan
  • starch degradation II: a glucan + maltotriose ⟶ D-glucopyranose + a glucan
  • starch degradation II: a glucan + maltotriose ⟶ D-glucopyranose + a glucan
  • starch degradation II: a glucan + maltotriose ⟶ D-glucopyranose + a glucan
  • starch degradation II: a glucan + maltotriose ⟶ D-glucopyranose + a glucan
  • starch degradation II: H2O + an exposed unphosphorylated, unbranched malto-oligosaccharide tail on amylopectin ⟶ amylopectin + maltose
  • starch degradation II: H2O + an exposed unphosphorylated, unbranched malto-oligosaccharide tail on amylopectin ⟶ amylopectin + maltose
  • starch degradation II: H2O + an exposed unphosphorylated, unbranched malto-oligosaccharide tail on amylopectin ⟶ amylopectin + maltose
  • starch degradation II: H2O + an exposed unphosphorylated, unbranched malto-oligosaccharide tail on amylopectin ⟶ amylopectin + maltose
  • starch degradation II: H2O + an exposed unphosphorylated, unbranched malto-oligosaccharide tail on amylopectin ⟶ amylopectin + maltose
  • starch degradation II: H2O + an exposed unphosphorylated, unbranched malto-oligosaccharide tail on amylopectin ⟶ amylopectin + maltose
  • starch degradation II: H2O + an exposed unphosphorylated, unbranched malto-oligosaccharide tail on amylopectin ⟶ amylopectin + maltose
  • starch degradation II: H2O + an exposed unphosphorylated, unbranched malto-oligosaccharide tail on amylopectin ⟶ amylopectin + maltose
  • starch degradation II: a glucan + maltotriose ⟶ D-glucopyranose + a glucan
  • starch degradation II: a glucan + maltotriose ⟶ D-glucopyranose + a glucan
  • starch degradation II: a glucan + maltotriose ⟶ D-glucopyranose + a glucan
  • starch degradation II: H2O + an exposed unphosphorylated, unbranched malto-oligosaccharide tail on amylopectin ⟶ amylopectin + maltose
  • starch degradation II: H2O + an exposed unphosphorylated, unbranched malto-oligosaccharide tail on amylopectin ⟶ amylopectin + maltose
  • starch degradation II: H2O + an exposed unphosphorylated, unbranched malto-oligosaccharide tail on amylopectin ⟶ amylopectin + maltose
  • starch degradation II: a glucan + maltotriose ⟶ D-glucopyranose + a glucan
  • starch degradation II: a glucan + maltotriose ⟶ D-glucopyranose + a glucan
  • starch degradation II: H2O + an exposed unphosphorylated, unbranched malto-oligosaccharide tail on amylopectin ⟶ an exposed unphosphorylated, (α-1,6)-branched malto-oligosaccharide tail on amylopectin + maltose
  • starch degradation II: a glucan + maltotriose ⟶ D-glucopyranose + a glucan
  • starch degradation II: a glucan + maltotriose ⟶ D-glucopyranose + a glucan
  • xyloglucan biosynthesis: UDP-α-D-glucose + a 1,4-β-D-glucan ⟶ UDP + a 1,4-β-D-glucan

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

47 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


文献列表

  • Yazhe Liang, Wangli Ji, Xianhua Sun, Zhenzhen Hao, Xiaolu Wang, Yuan Wang, Wei Zhang, Yingguo Bai, Xing Qin, Huiying Luo, Bin Yao, Xiaoyun Su, Huoqing Huang. Production of cello-oligosaccharides from corncob residue by degradation-synthesis reactions. Applied microbiology and biotechnology. 2024 Dec; 108(1):13. doi: 10.1007/s00253-023-12832-6. [PMID: 38170309]
  • Bianca Oliva, Josman Velasco, Gabriela Leila Berto, Igor Polikarpov, Leandro Cristante de Oliveira, Fernando Segato. Recombinant cellobiose dehydrogenase from Thermothelomyces thermophilus: Its functional characterization and applicability in cellobionic acid production. Bioresource technology. 2024 Jun; 402(?):130763. doi: 10.1016/j.biortech.2024.130763. [PMID: 38692377]
  • Daguan Nong, Zachary K Haviland, Nerya Zexer, Sarah A Pfaff, Daniel J Cosgrove, Ming Tien, Charles T Anderson, William O Hancock. Single-molecule tracking reveals dual front door/back door inhibition of Cel7A cellulase by its product cellobiose. Proceedings of the National Academy of Sciences of the United States of America. 2024 Apr; 121(18):e2322567121. doi: 10.1073/pnas.2322567121. [PMID: 38648472]
  • Frédéric Kerff, Samuel Jourdan, Isolde M Francis, Benoit Deflandre, Silvia Ribeiro Monteiro, Nudzejma Stulanovic, Rosemary Loria, Sébastien Rigali. Common scab disease: structural basis of elicitor recognition in pathogenic Streptomyces species. Microbiology spectrum. 2023 Dec; 11(6):e0197523. doi: 10.1128/spectrum.01975-23. [PMID: 37791952]
  • 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]
  • Pamela B Besada-Lombana, Wilfred Chen, Nancy A Da Silva. An extracellular glucose sensor for substrate-dependent secretion and display of cellulose-degrading enzymes. Biotechnology and bioengineering. 2023 Sep; ?(?):. doi: 10.1002/bit.28549. [PMID: 37749915]
  • Xiao Guo, Yajing An, Fuping Lu, Fufeng Liu, Bo Wang. Efficient Secretory Production of Lytic Polysaccharide Monooxygenase BaLPMO10 and Its Application in Plant Biomass Conversion. International journal of molecular sciences. 2023 Jun; 24(11):. doi: 10.3390/ijms24119710. [PMID: 37298661]
  • Alizée Le Moigne, Florian Randegger, Anubhav Gupta, Owen L Petchey, Jakob Pernthaler. Stochasticity causes high β-diversity and functional divergence of bacterial assemblages in closed systems. Ecology. 2023 04; 104(4):e4005. doi: 10.1002/ecy.4005. [PMID: 36807130]
  • Jiuxing He, Meng Kong, Yuanchao Qian, Min Gong, Guohua Lv, Jiqing Song. Cellobiose elicits immunity in lettuce conferring resistance to Botrytis cinerea. Journal of experimental botany. 2023 Feb; 74(3):1022-1038. doi: 10.1093/jxb/erac448. [PMID: 36385320]
  • Sree Kavya Penneru, Moumita Saharay, Marimuthu Krishnan. CelS-Catalyzed Processive Cellulose Degradation and Cellobiose Extraction for the Production of Bioethanol. Journal of chemical information and modeling. 2022 12; 62(24):6628-6638. doi: 10.1021/acs.jcim.2c00239. [PMID: 35649216]
  • Lianyu Zhou, Lu Jiao, Jiasheng Ju, Xuelan Ma. Effect of Sodium Selenite on the Metabolite Profile of Epichloë sp. Mycelia from Festuca sinensis in Solid Culture. Biological trace element research. 2022 Nov; 200(11):4865-4879. doi: 10.1007/s12011-021-03054-w. [PMID: 34973128]
  • Anshu Deewan, Jing-Jing Liu, Sujit Sadashiv Jagtap, Eun Ju Yun, Hanna Walukiewicz, Yong-Su Jin, Christopher V Rao. System analysis of Lipomyces starkeyi during growth on various plant-based sugars. Applied microbiology and biotechnology. 2022 Sep; 106(17):5629-5642. doi: 10.1007/s00253-022-12084-w. [PMID: 35906440]
  • Hassan Mohamed, Mohamed F Awad, Aabid Manzoor Shah, Beenish Sadaqat, Yusuf Nazir, Tahira Naz, Wu Yang, Yuanda Song. Coculturing of Mucor plumbeus and Bacillus subtilis bacterium as an efficient fermentation strategy to enhance fungal lipid and gamma-linolenic acid (GLA) production. Scientific reports. 2022 07; 12(1):13111. doi: 10.1038/s41598-022-17442-2. [PMID: 35908106]
  • Victoria Pastor, Raquel Cervero, Jordi Gamir. The simultaneous perception of self- and non-self-danger signals potentiates plant innate immunity responses. Planta. 2022 Jun; 256(1):10. doi: 10.1007/s00425-022-03918-y. [PMID: 35697869]
  • Jiwei Zhang, Lye Meng Markillie, Hugh D Mitchell, Matthew J Gaffrey, Galya Orr, Jonathan S Schilling. Distinctive carbon repression effects in the carbohydrate-selective wood decay fungus Rhodonia placenta. Fungal genetics and biology : FG & B. 2022 04; 159(?):103673. doi: 10.1016/j.fgb.2022.103673. [PMID: 35150839]
  • Marta Acin-Albiac, Pasquale Filannino, Rossana Coda, Carlo Giuseppe Rizzello, Marco Gobbetti, Raffaella Di Cagno. How water-soluble saccharides drive the metabolism of lactic acid bacteria during fermentation of brewers' spent grain. Microbial biotechnology. 2022 03; 15(3):915-930. doi: 10.1111/1751-7915.13846. [PMID: 34132488]
  • Susanne Zibek, Gloria Soberón-Chávez. Overview on Glycosylated Lipids Produced by Bacteria and Fungi: Rhamno-, Sophoro-, Mannosylerythritol and Cellobiose Lipids. Advances in biochemical engineering/biotechnology. 2022; 181(?):73-122. doi: 10.1007/10_2021_200. [PMID: 35526186]
  • Benoit Deflandre, Nudzejma Stulanovic, Sören Planckaert, Sinaeda Anderssen, Beatrice Bonometti, Latifa Karim, Wouter Coppieters, Bart Devreese, Sébastien Rigali. The virulome of Streptomyces scabiei in response to cello-oligosaccharide elicitors. Microbial genomics. 2022 01; 8(1):. doi: 10.1099/mgen.0.000760. [PMID: 35040428]
  • Yanguo Xu, Min Yang, Rong Yin, Luotao Wang, Lifen Luo, Bianxian Zi, Haijiao Liu, Huichuan Huang, Yixiang Liu, Xiahong He, Shusheng Zhu. Autotoxin Rg1 Induces Degradation of Root Cell Walls and Aggravates Root Rot by Modifying the Rhizospheric Microbiome. Microbiology spectrum. 2021 12; 9(3):e0167921. doi: 10.1128/spectrum.01679-21. [PMID: 34908454]
  • Clara Kampik, Nian Liu, Mohamed Mroueh, Nathalie Franche, Romain Borne, Yann Denis, Séverine Gagnot, Chantal Tardif, Sandrine Pagès, Stéphanie Perret, Nicolas Vita, Pascale de Philip, Henri-Pierre Fierobe. Handling Several Sugars at a Time: a Case Study of Xyloglucan Utilization by Ruminiclostridium cellulolyticum. mBio. 2021 12; 12(6):e0220621. doi: 10.1128/mbio.02206-21. [PMID: 34749527]
  • Sören Planckaert, Benoit Deflandre, Anne-Mare de Vries, Maarten Ameye, José C Martins, Kris Audenaert, Sébastien Rigali, Bart Devreese. Identification of Novel Rotihibin Analogues in Streptomyces scabies, Including Discovery of Its Biosynthetic Gene Cluster. Microbiology spectrum. 2021 09; 9(1):e0057121. doi: 10.1128/spectrum.00571-21. [PMID: 34346752]
  • Xia Wang, Yudie Fu, Meiyan Wang, Guoqing Niu. Synthetic Cellobiose-Inducible Regulatory Systems Allow Tight and Dynamic Controls of Gene Expression in Streptomyces. ACS synthetic biology. 2021 08; 10(8):1956-1965. doi: 10.1021/acssynbio.1c00152. [PMID: 34347449]
  • Parthasarathy Santhanam, Caroline Labbé, Luciano Gomes Fietto, Richard R Bélanger. A reassessment of flocculosin-mediated biocontrol activity of Pseudozyma flocculosa through CRISPR/Cas9 gene editing. Fungal genetics and biology : FG & B. 2021 08; 153(?):103573. doi: 10.1016/j.fgb.2021.103573. [PMID: 34029708]
  • Sun-Ki Kim, Jordan Russell, Minseok Cha, Michael E Himmel, Yannick J Bomble, Janet Westpheling. Coexpression of a β-d-Xylosidase from Thermotoga maritima and a Family 10 Xylanase from Acidothermus cellulolyticus Significantly Improves the Xylan Degradation Activity of the Caldicellulosiruptor bescii Exoproteome. Applied and environmental microbiology. 2021 06; 87(14):e0052421. doi: 10.1128/aem.00524-21. [PMID: 33990300]
  • Daiki Tanaka, Ken-Ichiro Ohnishi, Seiya Watanabe, Satoru Suzuki. Isolation of cellulase-producing Microbulbifer sp. from marine teleost blackfish (Girella melanichthys) intestine and the enzyme characterization. The Journal of general and applied microbiology. 2021 Jun; 67(2):47-53. doi: 10.2323/jgam.2020.05.001. [PMID: 33250506]
  • Ai-Ping Pang, Haiyan Wang, Yongsheng Luo, Zihuayuan Yang, Zhiyu Liu, Zhao Wang, Bingzhi Li, Song Yang, Zhihua Zhou, Xiaolin Lu, Fu-Gen Wu, Zuhong Lu, Fengming Lin. Dissecting Cellular Function and Distribution of β-Glucosidases in Trichoderma reesei. mBio. 2021 05; 12(3):. doi: 10.1128/mbio.03671-20. [PMID: 33975944]
  • Nadine Paßlack, Barbara Kohn, Wilfried Vahjen, Jürgen Zentek. Effects of dietary cellobiose on the intestinal microbiota and excretion of nitrogen metabolites in healthy adult dogs. Journal of animal physiology and animal nutrition. 2021 May; 105(3):569-578. doi: 10.1111/jpn.13485. [PMID: 33480132]
  • Shangshang Sun, Xinlei Wei, Xigui Zhou, Chun You. Construction of an Artificial In Vitro Synthetic Enzymatic Platform for Upgrading Low-Cost Starch to Value-Added Disaccharides. Journal of agricultural and food chemistry. 2021 Jan; 69(1):302-314. doi: 10.1021/acs.jafc.0c06936. [PMID: 33371670]
  • Chih-Hao Huang, Tzu-Ling Huang, Yu-Chang Liu, Ting-Chieh Chen, Shih-Ming Lin, Shyh-Yu Shaw, Ching-Chun Chang. Overexpression of a multifunctional β-glucosidase gene from thermophilic archaeon Sulfolobus solfataricus in transgenic tobacco could facilitate glucose release and its use as a reporter. Transgenic research. 2020 12; 29(5-6):511-527. doi: 10.1007/s11248-020-00212-z. [PMID: 32776308]
  • Lan Liu, Jian-Yu Jiao, Bao-Zhu Fang, Ai-Ping Lv, Yu-Zhen Ming, Meng-Meng Li, Nimaichand Salam, Wen-Jun Li. Isolation of Clostridium from Yunnan-Tibet hot springs and description of Clostridium thermarum sp. nov. with lignocellulosic ethanol production. Systematic and applied microbiology. 2020 Sep; 43(5):126104. doi: 10.1016/j.syapm.2020.126104. [PMID: 32847779]
  • May Thin Kyu, Shunsuke Nishio, Koki Noda, Bay Dar, San San Aye, Tsukasa Matsuda. Predominant secretion of cellobiohydrolases and endo-β-1,4-glucanases in nutrient-limited medium by Aspergillus spp. isolated from subtropical field. Journal of biochemistry. 2020 Sep; 168(3):243-256. doi: 10.1093/jb/mvaa049. [PMID: 32330257]
  • Nadine Paßlack, Wilfried Vahjen, Jürgen Zentek. Impact of Dietary Cellobiose on the Fecal Microbiota of Horses. Journal of equine veterinary science. 2020 08; 91(?):103106. doi: 10.1016/j.jevs.2020.103106. [PMID: 32684251]
  • Dan Liu, Yisong Liu, Duoduo Zhang, Xiaoting Chen, Qian Liu, Bentao Xiong, Lihui Zhang, Linfang Wei, Yifan Wang, Hao Fang, Johannes Liesche, Yahong Wei, N Louise Glass, Zhiqi Hao, Shaolin Chen. Quantitative Proteome Profiling Reveals Cellobiose-Dependent Protein Processing and Export Pathways for the Lignocellulolytic Response in Neurospora crassa. Applied and environmental microbiology. 2020 07; 86(15):. doi: 10.1128/aem.00653-20. [PMID: 32471912]
  • Michael Brysch-Herzberg, Marizeth Groenewald, Dénes Dlauchy, Martin Seidel, Gábor Péter. Hyphopichia lachancei, f.a., sp. nov., a yeast species from diverse origins. Antonie van Leeuwenhoek. 2020 Jun; 113(6):773-778. doi: 10.1007/s10482-020-01387-5. [PMID: 32086682]
  • Xiangjun Zhou, Kun Jiang, Haijun Luo, Cheng Wu, Weimin Yu, Fan Cheng. Novel lncRNA XLOC_032768 alleviates cisplatin-induced apoptosis and inflammatory response of renal tubular epithelial cells through TNF-α. International immunopharmacology. 2020 Jun; 83(?):106472. doi: 10.1016/j.intimp.2020.106472. [PMID: 32278129]
  • Ching-Yi Cheng, Ashanul Haque, Ming-Fa Hsieh, Syed Imran Hassan, Md Serajul Haque Faizi, Necmi Dege, Muhammad S Khan. 1,4-Disubstituted 1H-1,2,3-Triazoles for Renal Diseases: Studies of Viability, Anti-Inflammatory, and Antioxidant Activities. International journal of molecular sciences. 2020 May; 21(11):. doi: 10.3390/ijms21113823. [PMID: 32481556]
  • Qingling Gou, Mou Tang, Yanan Wang, Wenting Zhou, Yi Liu, Zhiwei Gong. Deficiency of β-Glucosidase Beneficial for the Simultaneous Saccharification and Lipid Production by the Oleaginous Yeast Lipomyces starkeyi. Applied biochemistry and biotechnology. 2020 Feb; 190(2):745-757. doi: 10.1007/s12010-019-03129-4. [PMID: 31485895]
  • Nagendra P Kurumbang, Jessica M Vera, Alexander S Hebert, Joshua J Coon, Robert Landick. Heterologous expression of a glycosyl hydrolase and cellular reprogramming enable Zymomonas mobilis growth on cellobiose. PloS one. 2020; 15(8):e0226235. doi: 10.1371/journal.pone.0226235. [PMID: 32797046]
  • Tobie D Lee, Olivia W Lee, Kyle R Brimacombe, Lu Chen, Rajarshi Guha, Sabrina Lusvarghi, Bethilehem G Tebase, Carleen Klumpp-Thomas, Robert W Robey, Suresh V Ambudkar, Min Shen, Michael M Gottesman, Matthew D Hall. A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. Molecular pharmacology. 2019 11; 96(5):629-640. doi: 10.1124/mol.119.115964. [PMID: 31515284]
  • Weijun Wang, Tania Archbold, Joseph S Lam, Matthew S Kimber, Ming Z Fan. A processive endoglucanase with multi-substrate specificity is characterized from porcine gut microbiota. Scientific reports. 2019 09; 9(1):13630. doi: 10.1038/s41598-019-50050-1. [PMID: 31541154]
  • Sun-Ki Kim, Daehwan Chung, Michael E Himmel, Yannick J Bomble, Janet Westpheling. Heterologous co-expression of two β-glucanases and a cellobiose phosphorylase resulted in a significant increase in the cellulolytic activity of the Caldicellulosiruptor bescii exoproteome. Journal of industrial microbiology & biotechnology. 2019 May; 46(5):687-695. doi: 10.1007/s10295-019-02150-0. [PMID: 30783893]
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