D-Xylose (BioDeep_00000405200)

Main id: BioDeep_00000002448

 

PANOMIX_OTCML-2023 BioNovoGene_Lab2019 natural product


代谢物信息卡片


D-(+)-Xylose

化学式: C5H10O5 (150.0528)
中文名称: D-木糖, D-(+)-木糖
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1C(C(C(C(O1)O)O)O)O
InChI: InChI=1S/C5H10O5/c6-2-1-10-5(9)4(8)3(2)7/h2-9H,1H2/t2-,3+,4-,5?/m1/s1

描述信息

D-Xylose is a flavouring ingredient; sweetener. It is found in straw, corncobs, pecan shells, carrot, dandelion, german camomile, and sweet orange. D-Xylose is a sugar first isolated from wood, and named for it. D-Xylose is classified as a monosaccharide of the aldopentose type, which means that it contains five carbon atoms and includes an aldehyde functional group. It is the precursor to hemicellulose, one of the main constituents of biomass (Wikipedia). Xylose in the urine is a biomarker for the consumption of fruits.
D-(+)-xylose (Xylose) is a natural compound that is catalyzed by xylose isomerase to form xylulose, which is a key step in the anaerobic ethanol fermentation of xylose.
D-(+)-xylose (Xylose) is a natural compound that is catalyzed by xylose isomerase to form xylulose, which is a key step in the anaerobic ethanol fermentation of xylose.

同义名列表

7 个代谢物同义名

D-Xylose; D-(+)-Xylose; (+)-Xylose; Wood sugar; Xylose; D-Xylose; D-Xylose



数据库引用编号

34 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(2)

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)

107 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 7 AKR1B1, ALB, CAT, G6PD, GAPDH, GCK, HAND1
Peripheral membrane protein 3 G6PD, GCK, HSD17B6
Endoplasmic reticulum membrane 1 TKT
Nucleus 5 ALB, GAPDH, GCK, HAND1, TAL1
cytosol 10 AKR1A1, AKR1B1, ALB, CAT, G6PD, GAPDH, GCK, LIPE, TKT, XYLB
nuclear body 1 TKT
centrosome 1 ALB
nucleoplasm 5 AKR1B1, GCK, HAND1, TAL1, TKT
RNA polymerase II transcription regulator complex 1 HAND1
Cell membrane 3 LIPE, TKT, TNF
Early endosome membrane 1 HSD17B6
Golgi apparatus membrane 1 GCK
Synapse 1 AKR1A1
cell surface 1 TNF
Golgi apparatus 1 ALB
Golgi membrane 2 GCK, INS
lysosomal membrane 2 EGF, GAA
neuronal cell body 1 TNF
Cytoplasm, cytosol 4 AKR1A1, G6PD, GAPDH, LIPE
Lysosome 1 GAA
plasma membrane 6 EGF, GAA, GAPDH, IGHE, TKT, TNF
Membrane 6 CAT, EGF, G6PD, GAA, GAPDH, LIPE
apical plasma membrane 2 AKR1A1, TKT
basolateral plasma membrane 1 GCK
caveola 1 LIPE
extracellular exosome 9 AKR1A1, AKR1B1, ALB, CAT, EGF, G6PD, GAA, GAPDH, TKT
Lysosome membrane 1 GAA
Lumenal side 1 HSD17B6
endoplasmic reticulum 2 ALB, HSD17B6
extracellular space 9 AKR1A1, AKR1B1, ALB, DCN, EGF, IGHE, IL6, INS, TNF
lysosomal lumen 2 DCN, GAA
perinuclear region of cytoplasm 1 GAPDH
mitochondrion 3 AKR1B1, CAT, GCK
protein-containing complex 2 ALB, CAT
intracellular membrane-bounded organelle 5 CAT, G6PD, GAA, GAPDH, HSD17B6
Microsome membrane 1 HSD17B6
Single-pass type I membrane protein 2 IGHE, TKT
Secreted 5 ALB, DCN, GAA, IL6, INS
extracellular region 9 ALB, CAT, DCN, EGF, GAA, IGHE, IL6, INS, TNF
cytoplasmic side of plasma membrane 1 G6PD
mitochondrial matrix 1 CAT
anchoring junction 1 ALB
transcription regulator complex 1 TAL1
centriolar satellite 1 G6PD
nuclear membrane 1 GAPDH
external side of plasma membrane 1 TNF
Secreted, extracellular space, extracellular matrix 1 DCN
actin cytoskeleton 1 TKT
microtubule cytoskeleton 1 GAPDH
nucleolus 1 HAND1
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
vesicle 2 GAPDH, TKT
Apical cell membrane 1 AKR1A1
Cytoplasm, perinuclear region 1 GAPDH
Membrane raft 1 TNF
Cytoplasm, cytoskeleton 1 GAPDH
focal adhesion 2 CAT, TKT
Peroxisome 2 CAT, TKT
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
collagen-containing extracellular matrix 1 DCN
receptor complex 1 TKT
ciliary basal body 1 ALB
chromatin 2 HAND1, TAL1
IgE immunoglobulin complex 1 IGHE
phagocytic cup 1 TNF
cytoskeleton 1 GAPDH
centriole 1 ALB
Nucleus, nucleolus 1 HAND1
spindle pole 1 ALB
blood microparticle 1 ALB
Basolateral cell membrane 1 GCK
[Isoform 2]: Cell membrane 1 IGHE
endosome lumen 1 INS
Lipid droplet 2 GAPDH, LIPE
Membrane, caveola 1 LIPE
Nucleus, nucleoplasm 1 HAND1
tertiary granule membrane 1 GAA
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 2 CAT, INS
Golgi lumen 2 DCN, INS
endoplasmic reticulum lumen 3 ALB, IL6, INS
platelet alpha granule lumen 2 ALB, EGF
transport vesicle 1 INS
azurophil granule membrane 1 GAA
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
clathrin-coated endocytic vesicle membrane 1 EGF
ribonucleoprotein complex 1 GAPDH
ficolin-1-rich granule membrane 1 GAA
GAIT complex 1 GAPDH
[Isoform 3]: Cell membrane 1 IGHE
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
[Isoform 1]: Secreted 1 IGHE
IgE B cell receptor complex 1 IGHE
immunoglobulin complex, circulating 1 IGHE
catalase complex 1 CAT
interleukin-6 receptor complex 1 IL6
autolysosome lumen 1 GAA
ciliary transition fiber 1 ALB
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • Viviane Maria de Sousa Fontes, Mércia de Sousa Galvão, Leila Moreira de Carvalho, Fabyan Laís do Nascimento Guedes, Marcos Dos Santos Lima, Taliana Kênia Alencar Bezerra, Marta Suely Madruga. Thiamine, cysteine and xylose added to the Maillard reaction of goat protein hydrolysate potentiates the formation of meat flavoring compounds. Food chemistry. 2024 Jul; 445(?):138398. doi: 10.1016/j.foodchem.2024.138398. [PMID: 38394903]
  • Alexander S Shashkov, Natalia V Potekhina, Elena M Tul'skaya, Andrey S Dmitrenok, Sof'ya N Senchenkova, Vladimir I Torgov, Lubov V Dorofeeva, Lyudmila I Evtushenko. New lactate- and pyruvate-containing polysaccharide and rhamnomannan with xylose residues from the cell wall of Rathayibacter oskolensis VKM Ac-2121T. Carbohydrate research. 2024 Jun; 540(?):109145. doi: 10.1016/j.carres.2024.109145. [PMID: 38759341]
  • Samantha A Crowe, Xixi Zhao, Fei Gan, Xiaoyue Chen, Graham A Hudson, Maria C T Astolfi, Henrik V Scheller, Yuzhong Liu, Jay D Keasling. Engineered Saccharomyces cerevisiae as a Biosynthetic Platform of Nucleotide Sugars. ACS synthetic biology. 2024 Apr; 13(4):1215-1224. doi: 10.1021/acssynbio.3c00666. [PMID: 38467016]
  • Lijun Li, Moshi Liu, Huiping Bi, Tao Liu. High-level production of Rhodiola rosea characteristic component rosavin from D-glucose and L-arabinose in engineered Escherichia coli. Metabolic engineering. 2024 Mar; 82(?):274-285. doi: 10.1016/j.ymben.2024.02.017. [PMID: 38428730]
  • Hajar Khaliliyan, Justine Lin, Paul Jusner, Sonja Schiehser, Markus Bacher, Mirjana Kostić, Thomas Rosenau, Antje Potthast, Stefan Böhmdorfer. Profiling of historical rag papers by their non-cellulosic polysaccharide composition. Carbohydrate polymers. 2024 Feb; 326(?):121611. doi: 10.1016/j.carbpol.2023.121611. [PMID: 38142095]
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  • Fan Li, Wenxin Bai, Yuan Zhang, Zijian Zhang, Deguo Zhang, Naidong Shen, Jingwei Yuan, Guomiao Zhao, Xiaoyan Wang. Construction of an economical Xylose-utilizing Saccharomyces cerevisiae and its ethanol fermentation. FEMS yeast research. 2024 Jan; ?(?):. doi: 10.1093/femsyr/foae001. [PMID: 38268490]
  • Rui Zhao, Hongshen Li, Qi Li, Zefang Jia, Shizhong Li, Ling Zhao, Shan Li, Yuwei Wang, Wenxin Fan, Ruoqi Ren, Zitong Yuan, Mengchan Yang, Xiaomei Wang, Xin Zhao, Weihua Xiao, Jian Zhao, Limin Cao. High titer (>100 g/L) ethanol production from pretreated corn stover hydrolysate by modified yeast strains. Bioresource technology. 2024 Jan; 391(Pt B):129993. doi: 10.1016/j.biortech.2023.129993. [PMID: 37944621]
  • Víctor Martín Zelaya Alvarez, Paula Virginia Fernández, Marina Ciancia. A novel substitution pattern in glucuronoarabinoxylans from woody bamboos. Carbohydrate polymers. 2024 Jan; 323(?):121356. doi: 10.1016/j.carbpol.2023.121356. [PMID: 37940262]
  • Huan Liu, Xiaolan Huang, Yangming Liu, Xinyun Jing, Yuchen Ning, Peng Xu, Li Deng, Fang Wang. Efficient Production of Triacetic Acid Lactone from Lignocellulose Hydrolysate by Metabolically Engineered Yarrowia lipolytica. Journal of agricultural and food chemistry. 2023 Dec; 71(48):18909-18918. doi: 10.1021/acs.jafc.3c06528. [PMID: 37999448]
  • Bhagwat Prasad Dewangan, Arunima Gupta, Rajan Kumar Sah, Shouvik Das, Sandeep Kumar, Saikat Bhattacharjee, Prashant Anupama-Mohan Pawar. Xylobiose treatment triggers a defense-related response and alters cell wall composition. Plant molecular biology. 2023 Dec; 113(6):383-400. doi: 10.1007/s11103-023-01391-z. [PMID: 37991689]
  • Emmanuel N Njoku, Walid Mottawea, Hebatoallah Hassan, Ahmed Gomaa, Nicolas Bordenave, Riadh Hammami. Bioengineered Wheat Arabinoxylan - Fostering Next-Generation Prebiotics Targeting Health-Related Gut Microbes. Plant foods for human nutrition (Dordrecht, Netherlands). 2023 Dec; 78(4):698-703. doi: 10.1007/s11130-023-01120-3. [PMID: 37919537]
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  • Jung Sik Lim, Sarang Cho, Peter Capek, Seong Cheol Kim, Roman Bleha, Doo Jin Choi, Jin Ree, Jisun Lee, Andriy Synytsya, Yong Il Park. Water-extractable polysaccharide fraction PNE-P1 from Pinus koraiensis pine nut: Structural features and immunostimulatory activity. Carbohydrate research. 2023 Nov; 534(?):108980. doi: 10.1016/j.carres.2023.108980. [PMID: 37952447]
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  • Samuel T Coradetti, Paul A Adamczyk, Di Liu, Yuqian Gao, Peter B Otoupal, Gina M Geiselman, Bobbie-Jo M Webb-Robertson, Meagan C Burnet, Young-Mo Kim, Kristin E Burnum-Johnson, Jon Magnuson, John M Gladden. Engineering transcriptional regulation of pentose metabolism in Rhodosporidium toruloides for improved conversion of xylose to bioproducts. Microbial cell factories. 2023 Aug; 22(1):144. doi: 10.1186/s12934-023-02148-5. [PMID: 37537586]
  • Paul A Adamczyk, Samuel T Coradetti, John M Gladden. Non-canonical D-xylose and L-arabinose metabolism via D-arabitol in the oleaginous yeast Rhodosporidium toruloides. Microbial cell factories. 2023 Aug; 22(1):145. doi: 10.1186/s12934-023-02126-x. [PMID: 37537595]
  • Juan A Méndez-Líter, Laura I de Eugenio, Manuel Nieto-Domínguez, Alicia Prieto, María Jesús Martínez. Expression and Characterization of Two α-l-Arabinofuranosidases from Talaromyces amestolkiae: Role of These Enzymes in Biomass Valorization. International journal of molecular sciences. 2023 Jul; 24(15):. doi: 10.3390/ijms241511997. [PMID: 37569374]
  • Vandierly Sampaio de Melo, Brisa Moreira Gomes, Felipe Santiago Chambergo. Biochemical characterization of a xylose-tolerant GH43 β-xylosidase from Geobacillus thermodenitrificans. Carbohydrate research. 2023 Jul; 532(?):108901. doi: 10.1016/j.carres.2023.108901. [PMID: 37487384]
  • Kailash Yadav, Meenakshi Arya, Satya Prakash, Bhavana Sharma Jha, Preet Manchanda, Abhishek Kumar, Renu Deswal. Brassica juncea leaf cuticle contains xylose and mannose (xylomannan) which inhibit ice recrystallization on the leaf surface. Planta. 2023 Jul; 258(2):44. doi: 10.1007/s00425-023-04203-2. [PMID: 37460860]
  • André Vessoni Alexandrino, Evandro Luis Prieto, Nicole Castro Silva Nicolela, Tamiris Garcia da Silva Marin, Talita Alves Dos Santos, João Pedro Maia de Oliveira da Silva, Anderson Ferreira da Cunha, Franklin Behlau, Maria Teresa Marques Novo-Mansur. Xylose Isomerase Depletion Enhances Virulence of Xanthomonas citri subsp. citri in Citrus aurantifolia. International journal of molecular sciences. 2023 Jul; 24(14):. doi: 10.3390/ijms241411491. [PMID: 37511250]
  • Takehiro Watanabe, Kohki Fujikawa, Soichiro Urai, Kazunari Iwaki, Tadayoshi Hirai, Katsuro Miyagawa, Hiroshi Uratani, Tohru Yamagaki, Koji Nagao, Yoshiaki Yokoo, Keiko Shimamoto. Identification, Chemical Synthesis, and Sweetness Evaluation of Rhamnose or Xylose Containing Steviol Glycosides of Stevia (Stevia rebaudiana) Leaves. Journal of agricultural and food chemistry. 2023 Jul; ?(?):. doi: 10.1021/acs.jafc.3c01753. [PMID: 37432401]
  • Eunah Jeong, Wonyong Kim, Seungju Son, Sungyeon Yang, Dasom Gwon, Jihee Hong, Yoonhee Cho, Chang-Young Jang, Martin Steinegger, Young Woon Lim, Kyo Bin Kang. Qualitative metabolomics-based characterization of a phenolic UDP-xylosyltransferase with a broad substrate spectrum from Lentinus brumalis. Proceedings of the National Academy of Sciences of the United States of America. 2023 07; 120(28):e2301007120. doi: 10.1073/pnas.2301007120. [PMID: 37399371]
  • G Platamone, S Procacci, O Maccioni, I Borromeo, M Rossi, Loretta Bacchetta, C Forni. Arthrobacter sp. Inoculation Improves Cactus Pear Growth, Quality of Fruits, and Nutraceutical Properties of Cladodes. Current microbiology. 2023 Jul; 80(8):266. doi: 10.1007/s00284-023-03368-z. [PMID: 37400738]
  • Ellen R Wagner, Nicole M Nightingale, Annie Jen, Katherine A Overmyer, Mick McGee, Joshua J Coon, Audrey P Gasch. PKA regulatory subunit Bcy1 couples growth, lipid metabolism, and fermentation during anaerobic xylose growth in Saccharomyces cerevisiae. PLoS genetics. 2023 07; 19(7):e1010593. doi: 10.1371/journal.pgen.1010593. [PMID: 37410771]
  • Yulu Ran, Qingzhuoma Yang, Jie Zeng, Fazhi Li, Yu Cao, Qingrui Xu, Dairong Qiao, Hui Xu, Yi Cao. Potential xylose transporters regulated by CreA improved lipid yield and furfural tolerance in oleaginous yeast Saitozyma podzolica zwy-2-3. Bioresource technology. 2023 Jun; ?(?):129413. doi: 10.1016/j.biortech.2023.129413. [PMID: 37390935]
  • Carolina Victal Garbelotti, Adriana Grandis, Eduardo Crevelin, Marcos Silveira Buckeridge, Luiz Alberto Beraldo de Moraes, Richard John Ward. Glycomic profiling identifies key-structural differences in three arabinoxylan fractions from sugarcane culms. Carbohydrate polymers. 2023 Jun; 310(?):120694. doi: 10.1016/j.carbpol.2023.120694. [PMID: 36925235]
  • Danfeng Shen, Xinrong Lu, Wenjie Li, Lin Zou, Yongliang Tong, Lei Wang, Lin Rao, Yuxin Zhang, Linlin Hou, Guiqin Sun, Li Chen. Identification and characterization of an α-1,3 mannosidase from Elizabethkingia meningoseptica and its potential attenuation impact on allergy associated with cross-reactive carbohydratedeterminant. Biochemical and biophysical research communications. 2023 Jun; 672(?):17-26. doi: 10.1016/j.bbrc.2023.06.035. [PMID: 37331167]
  • Rishitha L Nalabothu, Kaitlin J Fisher, Abigail Leavitt LaBella, Taylor A Meyer, Dana A Opulente, John F Wolters, Antonis Rokas, Chris Todd Hittinger. Codon Optimization Improves the Prediction of Xylose Metabolism from Gene Content in Budding Yeasts. Molecular biology and evolution. 2023 06; 40(6):. doi: 10.1093/molbev/msad111. [PMID: 37154525]
  • Ignacio Álvarez-Martínez, Colin Ruprecht, Deborah Senf, Hsin-Tzu Wang, Breeanna R Urbanowicz, Fabian Pfrengle. Chemo-Enzymatic Synthesis of Long-Chain Oligosaccharides for Studying Xylan-Modifying Enzymes. Chemistry (Weinheim an der Bergstrasse, Germany). 2023 May; 29(26):e202203941. doi: 10.1002/chem.202203941. [PMID: 36791391]
  • Italo de Andrade Bianchini, Fanny Machado Jofre, Sarah de Souza Queiroz, Talita Martins Lacerda, Maria das Graças de Almeida Felipe. Relation of xylitol formation and lignocellulose degradation in yeast. Applied microbiology and biotechnology. 2023 May; 107(10):3143-3151. doi: 10.1007/s00253-023-12495-3. [PMID: 37039848]
  • Alīna Reķēna, Marina J Pinheiro, Nemailla Bonturi, Isma Belouah, Eliise Tammekivi, Koit Herodes, Eduard J Kerkhoven, Petri-Jaan Lahtvee. Genome-scale metabolic modeling reveals metabolic trade-offs associated with lipid production in Rhodotorula toruloides. PLoS computational biology. 2023 Apr; 19(4):e1011009. doi: 10.1371/journal.pcbi.1011009. [PMID: 37099621]
  • Yao Zhang, Yueping Yang, Qing Liu, Shaoqi Li, Yuanda Song. Lipid Accumulation by Snf-β Engineered Mucor circinelloides Strains on Glucose and Xylose. Applied biochemistry and biotechnology. 2023 Apr; ?(?):. doi: 10.1007/s12010-023-04531-9. [PMID: 37086376]
  • Saumashish Mukherjee, Tushar Dilipchand Lodha, Jogi Madhuprakash. Comprehensive Genome Analysis of Cellulose and Xylan-Active CAZymes from the Genus Paenibacillus: Special Emphasis on the Novel Xylanolytic Paenibacillus sp. LS1. Microbiology spectrum. 2023 Apr; ?(?):e0502822. doi: 10.1128/spectrum.05028-22. [PMID: 37071006]
  • Shang-Ting Tsai, Hsu-Chen Hsu, Chi-Kung Ni. A simple tandem mass spectrometry method for structural identification of pentose oligosaccharides. The Analyst. 2023 Apr; 148(8):1712-1731. doi: 10.1039/d3an00068k. [PMID: 36929945]
  • Kun Wang, Xujie Cui, Xiaocui Ling, Jiarui Chen, Jiachen Zheng, Yuling Xiang, Weihui Li. D-Xylose Blocks the Broad Negative Regulation of XylR on Lipid Metabolism and Affects Multiple Physiological Characteristics in Mycobacteria. International journal of molecular sciences. 2023 Apr; 24(8):. doi: 10.3390/ijms24087086. [PMID: 37108247]
  • Yao Zhang, Yueping Yang, Silu Zhang, Qing Liu, Wenrui Dang, Yuanda Song. Lipid accumulation and SNF1 transcriptional analysis of Mucor circinelloides on xylose under nitrogen limitation. Antonie van Leeuwenhoek. 2023 Apr; 116(4):383-391. doi: 10.1007/s10482-023-01810-7. [PMID: 36656419]
  • Yang Liu, Qiwei Guo, Saimin Zhang, Yilin Bao, Mengling Chen, Lin Gao, Yang Zhang, Hongli Zhou. Polysaccharides from Discarded Stems of Trollius chinensis Bunge Elicit Promising Potential in Cosmetic Industry: Characterization, Moisture Retention and Antioxidant Activity. Molecules (Basel, Switzerland). 2023 Mar; 28(7):. doi: 10.3390/molecules28073114. [PMID: 37049877]
  • Tao Sun, Yizi Yu, Lexin Wang, Yichun Qi, Tian Xu, Zhe Wang, Lu Lin, Rodrigo Ledesma-Amaro, Xiao-Jun Ji. Combination of a Push-Pull-Block Strategy with a Heterologous Xylose Assimilation Pathway toward Lipid Overproduction from Lignocellulose in Yarrowia lipolytica. ACS synthetic biology. 2023 03; 12(3):761-767. doi: 10.1021/acssynbio.2c00550. [PMID: 36789673]
  • Friederike Mierke, Daniel P Brink, Joakim Norbeck, Verena Siewers, Thomas Andlid. Functional genome annotation and transcriptome analysis of Pseudozyma hubeiensis BOT-O, an oleaginous yeast that utilizes glucose and xylose at equal rates. Fungal genetics and biology : FG & B. 2023 Mar; ?(?):103783. doi: 10.1016/j.fgb.2023.103783. [PMID: 36870442]
  • Theodora Tryfona, Matthieu Bourdon, Rita Delgado Marques, Marta Busse-Wicher, Francisco Vilaplana, Katherine Stott, Paul Dupree. Grass xylan structural variation suggests functional specialization and distinctive interaction with cellulose and lignin. The Plant journal : for cell and molecular biology. 2023 03; 113(5):1004-1020. doi: 10.1111/tpj.16096. [PMID: 36602010]
  • Ao Sun, Lining Chen, Wei Wu, Olugbenga P Soladoye, Yuhao Zhang, Yu Fu. The potential meat flavoring generated from Maillard reaction products of wheat gluten protein hydrolysates-xylose: Impacts of different thermal treatment temperatures on flavor. Food research international (Ottawa, Ont.). 2023 03; 165(?):112512. doi: 10.1016/j.foodres.2023.112512. [PMID: 36869515]
  • Ronivaldo Rodrigues da Silva, Mohammed Anas Zaiter, Maurício Boscolo, Roberto da Silva, Eleni Gomes. Xylose consumption and ethanol production by Pichia guilliermondii and Candida oleophila in the presence of furans, phenolic compounds, and organic acids commonly produced during the pre-treatment of plant biomass. Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]. 2023 Feb; ?(?):. doi: 10.1007/s42770-023-00937-z. [PMID: 36826705]
  • Diptarka Dasgupta, Vishal Ahuja, Raghuvir Singh, Snehal More, Sandeep Mudliar, Madan Kumar. Food-grade xylitol production from corncob biomass with acute oral toxicity studies. World journal of microbiology & biotechnology. 2023 Feb; 39(4):102. doi: 10.1007/s11274-023-03542-2. [PMID: 36797527]
  • Li Tan, Liang Zhang, Ian Black, John Glushka, Breeanna Urbanowicz, Christian Heiss, Parastoo Azadi. Most of the rhamnogalacturonan-I from cultured Arabidopsis cell walls is covalently linked to arabinogalactan-protein. Carbohydrate polymers. 2023 Feb; 301(Pt B):120340. doi: 10.1016/j.carbpol.2022.120340. [PMID: 36446508]
  • Mee-Rye Park, Rahul Gauttam, Bonnie Fong, Yan Chen, Hyun Gyu Lim, Adam M Feist, Aindrila Mukhopadhyay, Christopher J Petzold, Blake A Simmons, Steven W Singer. Revealing oxidative pentose metabolism in new Pseudomonas putida isolates. Environmental microbiology. 2023 Feb; 25(2):493-504. doi: 10.1111/1462-2920.16296. [PMID: 36465038]
  • Rahele Panahabadi, Asadollah Ahmadikhah, Naser Farrokhi. Genetic dissection of monosaccharides contents in rice whole grain using genome-wide association study. The plant genome. 2023 Jan; ?(?):e20292. doi: 10.1002/tpg2.20292. [PMID: 36691363]
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