Deoxynivalenol (BioDeep_00000002633)

   

human metabolite Endogenous natural product


代谢物信息卡片


3,10-dihydroxy-2-(hydroxymethyl)-1,5-dimethyl-8-oxaspiro[oxirane-2,12-tricyclo[7.2.1.0²,⁷]dodecan]-5-en-4-one

化学式: C15H20O6 (296.126)
中文名称: 脱氧雪腐镰刀菌烯醇
谱图信息: 最多检出来源 Homo sapiens(plant) 12.29%

分子结构信息

SMILES: CC1=CC2C(C(C1=O)O)(C3(CC(C(C34CO4)O2)O)C)CO
InChI: InChI=1S/C15H20O6/c1-7-3-9-14(5-16,11(19)10(7)18)13(2)4-8(17)12(21-9)15(13)6-20-15/h3,8-9,11-12,16-17,19H,4-6H2,1-2H3

描述信息

Deoxynivalenol is found in cereals and cereal products. Deoxynivalenol is produced by Fusarium graminearum and Fusarium roseum, responsible for headblight in cereals Vomitoxin, also known as deoxynivalenol (DON), is a type B trichothecene, an epoxy-sesquiterpeneoid. This mycotoxin occurs predominantly in grains such as wheat, barley, oats, rye, and maize, and less often in rice, sorghum, and triticale. The occurrence of deoxynivalenol is associated primarily with Fusarium graminearum (Gibberella zeae) and F. culmorum, both of which are important plant pathogens which cause Fusarium head blight in wheat and Gibberella ear rot in maize. Deoxynivalenol is a direct relationship between the incidence of Fusarium head blight and contamination of wheat with deoxynivalenol has been established. The incidence of Fusarium head blight is strongly associated with moisture at the time of flowering (anthesis), and the timing of rainfall, rather than the amount, is the most critical factor. Furthermore, deoxynivalenol contents are significantly affected by the susceptibility of cultivars towards Fusarium species, previous crop, tillage practices, and fungicide us
Production by Fusarium graminearum and Fusarium roseum, responsible for headblight in cereals
D009676 - Noxae > D011042 - Poisons > D014255 - Trichothecenes
D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins

同义名列表

7 个代谢物同义名

3,10-dihydroxy-2-(hydroxymethyl)-1,5-dimethyl-8-oxaspiro[oxirane-2,12-tricyclo[7.2.1.0²,⁷]dodecan]-5-en-4-one; 3-Epi-deoxynivalenol; DEOXYNIVALENOL; 3-Epi-DON; Vomitoxin; RD Toxin; Vomitoxin



数据库引用编号

18 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)

19 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 5 AIMP2, ALB, MAPK8, NFKB1, PTGS2
Peripheral membrane protein 1 PTGS2
Endoplasmic reticulum membrane 2 CD4, PTGS2
Nucleus 5 AIMP2, ALB, JUN, MAPK8, NFKB1
cytosol 5 AIMP2, ALB, ANK1, MAPK8, NFKB1
centrosome 1 ALB
nucleoplasm 3 JUN, MAPK8, NFKB1
RNA polymerase II transcription regulator complex 1 JUN
Cell membrane 4 CASR, CD4, CD8A, TNF
Multi-pass membrane protein 1 CASR
Synapse 1 MAPK8
cell surface 2 CASR, TNF
glutamatergic synapse 1 CASR
Golgi apparatus 1 ALB
neuronal cell body 2 CASR, TNF
presynaptic membrane 1 CASR
sarcolemma 1 ANK1
Cytoplasm, cytosol 1 AIMP2
plasma membrane 7 ANK1, CASR, CD4, CD8A, GCG, IGHE, TNF
Membrane 3 AIMP2, ANK1, CASR
apical plasma membrane 1 CASR
axon 2 CCK, MAPK8
basolateral plasma membrane 2 ANK1, CASR
caveola 1 PTGS2
extracellular exosome 1 ALB
endoplasmic reticulum 2 ALB, PTGS2
extracellular space 11 ALB, CCK, GCG, IGHE, IL10, IL2, IL4, IL5, IL6, PYY, TNF
mitochondrion 1 NFKB1
protein-containing complex 2 ALB, PTGS2
Microsome membrane 1 PTGS2
Single-pass type I membrane protein 3 CD4, CD8A, IGHE
Secreted 8 ALB, CCK, GCG, IL10, IL2, IL4, IL5, IL6
extracellular region 13 ALB, CCK, CD8A, GCG, IGHE, IL10, IL2, IL4, IL5, IL6, NFKB1, PYY, TNF
cytoplasmic side of plasma membrane 1 ANK1
[Isoform 2]: Secreted 1 CD8A
anchoring junction 1 ALB
transcription regulator complex 2 JUN, NFKB1
external side of plasma membrane 3 CD4, CD8A, TNF
Z disc 1 ANK1
Early endosome 1 CD4
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
postsynaptic membrane 1 ANK1
Membrane raft 2 CD4, TNF
Cytoplasm, cytoskeleton 1 ANK1
axolemma 1 ANK1
sarcoplasmic reticulum 1 ANK1
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
receptor complex 1 CD8A
neuron projection 2 ANK1, PTGS2
ciliary basal body 1 ALB
chromatin 2 JUN, NFKB1
IgE immunoglobulin complex 1 IGHE
phagocytic cup 1 TNF
cytoskeleton 1 ANK1
centriole 1 ALB
spindle pole 1 ALB
nuclear chromosome 1 JUN
blood microparticle 1 ALB
[Isoform 2]: Cell membrane 1 IGHE
M band 1 ANK1
euchromatin 1 JUN
plasma membrane raft 1 CD8A
secretory granule lumen 2 GCG, NFKB1
endoplasmic reticulum lumen 5 ALB, CD4, GCG, IL6, PTGS2
platelet alpha granule lumen 1 ALB
axon terminus 1 CASR
specific granule lumen 1 NFKB1
clathrin-coated endocytic vesicle membrane 1 CD4
basal dendrite 1 MAPK8
[Isoform 1]: Cell membrane 1 CD8A
aminoacyl-tRNA synthetase multienzyme complex 1 AIMP2
[Isoform 3]: Cell membrane 1 IGHE
transcription factor AP-1 complex 1 JUN
[Glucagon-like peptide 1]: Secreted 1 GCG
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
T cell receptor complex 2 CD4, CD8A
[Isoform 1]: Secreted 1 IGHE
IgE B cell receptor complex 1 IGHE
immunoglobulin complex, circulating 1 IGHE
spectrin-associated cytoskeleton 1 ANK1
ankyrin-1 complex 1 ANK1
interleukin-6 receptor complex 1 IL6
[Isoform Mu18]: Sarcoplasmic reticulum 1 ANK1
[Isoform Mu19]: Sarcoplasmic reticulum 1 ANK1
[Isoform Mu20]: Sarcoplasmic reticulum 1 ANK1
[Nuclear factor NF-kappa-B p105 subunit]: Cytoplasm 1 NFKB1
[Nuclear factor NF-kappa-B p50 subunit]: Nucleus 1 NFKB1
I-kappaB/NF-kappaB complex 1 NFKB1
NF-kappaB p50/p65 complex 1 NFKB1
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

  • Philippe Guerre, Elodie Lassallette, Ugo Beaujardin-Daurian, Angelique Travel. Fumonisins alone or mixed with other fusariotoxins increase the C22-24:C16 sphingolipid ratios in chicken livers, while deoxynivalenol and zearalenone have no effect. Chemico-biological interactions. 2024 May; 395(?):111005. doi: 10.1016/j.cbi.2024.111005. [PMID: 38615975]
  • Yi He, Xiujuan Yang, Xiaobo Xia, Yuhua Wang, Yifan Dong, Lei Wu, Peng Jiang, Xu Zhang, Cong Jiang, Hongxiang Ma, Wujun Ma, Cong Liu, Ryan Whitford, Matthew R Tucker, Zhengguang Zhang, Gang Li. A phase-separated protein hub modulates resistance to Fusarium head blight in wheat. Cell host & microbe. 2024 May; 32(5):710-726.e10. doi: 10.1016/j.chom.2024.04.002. [PMID: 38657607]
  • Vishnukiran Thuraga, Farideh Ghadamgahi, Fantaye Ayele Dadi, Ramesh Raju Vetukuri, Aakash Chawade. A new bacterial consortia for management of Fusarium head blight in wheat. Scientific reports. 2024 05; 14(1):10131. doi: 10.1038/s41598-024-60356-4. [PMID: 38698085]
  • Xuzhao Mao, Lingping Li, Yakubu Saddeeq Abubakar, Yulong Li, Zenghong Luo, Meilian Chen, Wenhui Zheng, Zonghua Wang, Huawei Zheng. Nucleoside Diphosphate Kinase FgNdpk Is Required for DON Production and Pathogenicity by Regulating the Growth and Toxisome Formation of Fusarium graminearum. Journal of agricultural and food chemistry. 2024 May; 72(17):9637-9646. doi: 10.1021/acs.jafc.4c00593. [PMID: 38642053]
  • Weijie He, Tiantian Zhang, Mengru Zheng, Karim M Tabl, Tao Huang, Yucai Liao, Aibo Wu, Jingbo Zhang. Utilization of a Novel Soil-Isolated Strain Devosia insulae FS10-7 for Deoxynivalenol Degradation and Biocontrol of Fusarium Crown Rot in Wheat. Phytopathology. 2024 May; 114(5):1057-1067. doi: 10.1094/phyto-10-23-0412-kc. [PMID: 38451497]
  • Aliang Xia, Xuan Wang, Yingao Huang, Qing Yang, Meng Ye, Yankun Wang, Cong Jiang, Kaili Duan. The ING protein Fng2 associated with RPD3 HDAC complex for the regulation of fungal development and pathogenesis in wheat head blight fungus. International journal of biological macromolecules. 2024 May; 268(Pt 2):131938. doi: 10.1016/j.ijbiomac.2024.131938. [PMID: 38692539]
  • Gang Niu, Qing Yang, Yihui Liao, Daiyuan Sun, Zhe Tang, Guanghui Wang, Ming Xu, Chenfang Wang, Jiangang Kang. Advances in Understanding Fusarium graminearum: Genes Involved in the Regulation of Sexual Development, Pathogenesis, and Deoxynivalenol Biosynthesis. Genes. 2024 Apr; 15(4):. doi: 10.3390/genes15040475. [PMID: 38674409]
  • Akihiro Shirai, Ami Tanaka. Effects of ferulic acid combined with light irradiation on deoxynivalenol and its production in Fusarium graminearum. Fungal biology. 2024 04; 128(2):1684-1690. doi: 10.1016/j.funbio.2024.02.003. [PMID: 38575241]
  • Samia Berraies, Yuefeng Ruan, Ron Knox, Ron DePauw, Firdissa Bokore, Richard Cuthbert, Barbara Blackwell, Maria Antonia Henriquez, David Konkin, Bianyun Yu, Curtis Pozniak, Brad Meyer. Genetic mapping of deoxynivalenol and fusarium damaged kernel resistance in an adapted durum wheat population. BMC plant biology. 2024 Mar; 24(1):183. doi: 10.1186/s12870-023-04708-8. [PMID: 38475749]
  • Simon Schiwek, Matthäus Slonka, Mohammad Alhussein, Dennis Knierim, Paolo Margaria, Hanna Rose, Katja R Richert-Pöggeler, Michael Rostás, Petr Karlovsky. Mycoviruses Increase the Attractiveness of Fusarium graminearum for Fungivores and Suppress Production of the Mycotoxin Deoxynivalenol. Toxins. 2024 Mar; 16(3):. doi: 10.3390/toxins16030131. [PMID: 38535797]
  • Min Zhu, En-Qing Lu, Yong-Xia Fang, Guo-Wei Liu, Yu-Jie Cheng, Ke Huang, E Xu, Yi-Yu Zhang, Xiao-Jing Wang. Piceatannol Alleviates Deoxynivalenol-Induced Damage in Intestinal Epithelial Cells via Inhibition of the NF-κB Pathway. Molecules (Basel, Switzerland). 2024 Feb; 29(4):. doi: 10.3390/molecules29040855. [PMID: 38398607]
  • Laura Righetti, Francesca Vanara, Renato Bruni, Claudia Sardella, Massimo Blandino, Chiara Dall'Asta. Investigating Metabolic Plant Response toward Deoxynivalenol Accumulation in Four Winter Cereals. Journal of agricultural and food chemistry. 2024 Feb; 72(6):3200-3209. doi: 10.1021/acs.jafc.3c06111. [PMID: 38315448]
  • Panpan Huang, Xiao Yu, Huiquan Liu, Mingyu Ding, Zeyi Wang, Jin-Rong Xu, Cong Jiang. Regulation of TRI5 expression and deoxynivalenol biosynthesis by a long non-coding RNA in Fusarium graminearum. Nature communications. 2024 Feb; 15(1):1216. doi: 10.1038/s41467-024-45502-w. [PMID: 38332031]
  • Jenna-Lee Price, Cobus Meyer Visagie, Hannalien Meyer, Neriman Yilmaz. Fungal Species and Mycotoxins Associated with Maize Ear Rots Collected from the Eastern Cape in South Africa. Toxins. 2024 02; 16(2):. doi: 10.3390/toxins16020095. [PMID: 38393173]
  • Milos Sevarika, Giovanni Beccari, Francesco Tini, Luisa Ederli, Ilaria Bellezza, Lorenzo Covarelli, Roberto Romani. Effect of the mycotoxins enniatin B and deoxynivalenol on the wheat aphid Sitobion avenae and on the predatory lacewing Chrysoperla carnea. Pest management science. 2024 Feb; ?(?):. doi: 10.1002/ps.8005. [PMID: 38312069]
  • Chao Sun, Chuncai Mao, Zhie Zhou, Jianhui Xiao, Wenwen Zhou, Juan Du, Jun Li. In Vitro Assessment of Ozone-Treated Deoxynivalenol by Measuring Cytotoxicity and Wheat Quality. Toxins. 2024 01; 16(2):. doi: 10.3390/toxins16020064. [PMID: 38393142]
  • Tianshuai Qi, Fumeng He, Xinqi Zhang, Jiaqi Wang, Zengli Zhang, Heran Jiang, Biao Zhao, Chong Du, Yunzhu Che, Xu Feng, Yingnan Wang, Fenglan Li. Genome-Wide Identification and Expression Profiling of Potato (Solanum tuberosum L.) Universal Stress Proteins Reveal Essential Roles in Mechanical Damage and Deoxynivalenol Stress. International journal of molecular sciences. 2024 Jan; 25(2):. doi: 10.3390/ijms25021341. [PMID: 38279341]
  • Shijie Fan, Luxi Lin, Pingyang Li, Huihui Tian, Jialu Shen, Longzhu Zhou, Qingyu Zhao, Junmin Zhang, Yuchang Qin, Chaohua Tang. Selenomethionine protects the liver from dietary deoxynivalenol exposure via Nrf2/PPARγ-GPX4-ferroptosis pathway in mice. Toxicology. 2024 Jan; 501(?):153689. doi: 10.1016/j.tox.2023.153689. [PMID: 38040082]
  • Cong Zhang, Fengjuan Chen, Youshuang Wang, Kefei Zhang, Xu Yang, Xuebing Wang. Tanshinone IIA protects intestinal epithelial cells from deoxynivalenol-induced pyroptosis. Ecotoxicology and environmental safety. 2024 Jan; 269(?):115743. doi: 10.1016/j.ecoenv.2023.115743. [PMID: 38035519]
  • Meiling Gao, Mohamed F Abdallah, Minggui Song, Yiqian Xu, Daiyuan Sun, Ping Lu, Jianhua Wang. Novel Endophytic Pseudescherichia sp. GSE25 Strain Significantly Controls Fusarium graminearum and Reduces Deoxynivalenol in Wheat. Toxins. 2023 12; 15(12):. doi: 10.3390/toxins15120702. [PMID: 38133206]
  • Jing Jin, Bingxin Huangfu, Fuguo Xing, Wentao Xu, Xiaoyun He. Combined exposure to deoxynivalenol facilitates lipid metabolism disorder in high-fat-diet-induced obesity mice. Environment international. 2023 Dec; 182(?):108345. doi: 10.1016/j.envint.2023.108345. [PMID: 38008010]
  • DanDan Meng, Xu Dong, XianFang He, Rui Pan, MingNa Sun, Yue Chu, Zhou Tong, XiaoTong Yi, Hui Fan, TongChun Gao, JinSheng Duan. Effects of wheat varieties, fungicides and application time on Fusarium head blight and deoxynivalenol contamination control in wheat. Pest management science. 2023 Dec; 79(12):4784-4794. doi: 10.1002/ps.7674. [PMID: 37471098]
  • Pengju Wang, Qin Yao, Xiangwen Meng, Xiaosong Yang, Xu Wang, Qirong Lu, Aimei Liu. Effective protective agents against organ toxicity of deoxynivalenol and their detoxification mechanisms: A review. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2023 Dec; 182(?):114121. doi: 10.1016/j.fct.2023.114121. [PMID: 37890761]
  • Yuang Tu, Shiqi Liu, Peiran Cai, Tizhong Shan. Global distribution, toxicity to humans and animals, biodegradation, and nutritional mitigation of deoxynivalenol: A review. Comprehensive reviews in food science and food safety. 2023 09; 22(5):3951-3983. doi: 10.1111/1541-4337.13203. [PMID: 37421323]
  • Lifang Hu, Cong Guo, Jing Chen, Ruimin Jia, Yan Sun, Shang Cao, Ping Xiang, Yang Wang. Venturicidin A Is a Potential Fungicide for Controlling Fusarium Head Blight by Affecting Deoxynivalenol Biosynthesis, Toxisome Formation, and Mitochondrial Structure. Journal of agricultural and food chemistry. 2023 Aug; 71(33):12440-12451. doi: 10.1021/acs.jafc.3c02683. [PMID: 37566096]
  • Pengju Wang, Qing Yao, Dan Zhu, Xiaosong Yang, Qingjie Chen, Qirong Lu, Aimei Liu. Resveratrol protects against deoxynivalenol-induced ferroptosis in HepG2 cells. Toxicology. 2023 08; 494(?):153589. doi: 10.1016/j.tox.2023.153589. [PMID: 37419272]
  • Mubashar Hassan, Yanan Wang, Shahid Ali Rajput, Aftab Shaukat, Ping Yang, Muhammad Zahid Farooq, Qianhui Cheng, Mehboob Ali, Xiaomei Mi, Yu An, Desheng Qi. Ameliorative Effects of Luteolin and Activated Charcoal on Growth Performance, Immunity Function, and Antioxidant Capacity in Broiler Chickens Exposed to Deoxynivalenol. Toxins. 2023 Jul; 15(8):. doi: 10.3390/toxins15080478. [PMID: 37624235]
  • Yingrong Ye, Mingzhen Jiang, Xinyao Hong, Yiwu Fu, Yichun Chen, Hanpeng Wu, Youpeng Sun, Xia Wang, Ershun Zhou, Jingjing Wang, Zhengtao Yang. Quercetin Alleviates Deoxynivalenol-Induced Intestinal Damage by Suppressing Inflammation and Ferroptosis in Mice. Journal of agricultural and food chemistry. 2023 Jul; 71(28):10761-10772. doi: 10.1021/acs.jafc.3c02027. [PMID: 37392437]
  • Ruifen Kang, Honglei Qu, Yanxin Guo, Chuanliang Ji, Jie Cheng, Yantao Wang, Shimeng Huang, Lihong Zhao, Cheng Ji, Qiugang Ma. Toxicokinetics of Deoxynivalenol in Dezhou Male Donkeys after Oral Administration. Toxins. 2023 06; 15(7):. doi: 10.3390/toxins15070426. [PMID: 37505695]
  • Sigita Janaviciene, Eimantas Venslovas, Grazina Kadziene, Neringa Matelioniene, Zane Berzina, Vadims Bartkevics, Skaidre Suproniene. Diversity of Mycotoxins Produced by Fusarium Strains Infecting Weeds. Toxins. 2023 06; 15(7):. doi: 10.3390/toxins15070420. [PMID: 37505689]
  • Magdalena Gajęcka, Iwona Otrocka-Domagała, Paweł Brzuzan, Łukasz Zielonka, Michał Dąbrowski, Maciej T Gajęcki. Influence of deoxynivalenol and zearalenone on the immunohistochemical expression of oestrogen receptors and liver enzyme genes in vivo in prepubertal gilts. Archives of toxicology. 2023 Jun; ?(?):. doi: 10.1007/s00204-023-03502-7. [PMID: 37328583]
  • Bilal Murtaza, Xiaoyu Li, Liming Dong, Muhammad Kashif Saleemi, Mazhar Iqbal, Saima Majeed, Ashiq Ali, Gen Li, Bowen Jin, Lili Wang, Yongping Xu. In-vitro assessment of a novel plant rhizobacterium, Citrobacter freundii, for degrading and biocontrol of food mycotoxin deoxynivalenol. Toxicon : official journal of the International Society on Toxinology. 2023 May; 227(?):107095. doi: 10.1016/j.toxicon.2023.107095. [PMID: 36972839]
  • Irene Valenti, Francesco Tini, Milos Sevarika, Alessandro Agazzi, Giovanni Beccari, Ilaria Bellezza, Luisa Ederli, Silvia Grottelli, Matias Pasquali, Roberto Romani, Marco Saracchi, Lorenzo Covarelli. Impact of Enniatin and Deoxynivalenol Co-Occurrence on Plant, Microbial, Insect, Animal and Human Systems: Current Knowledge and Future Perspectives. Toxins. 2023 04; 15(4):. doi: 10.3390/toxins15040271. [PMID: 37104209]
  • Xu Yang, Tingyu Huang, Yunhe Chen, Fengjuan Chen, Yu Liu, Youshuang Wang, Wenxi Song, Juntao Zhang, Yibao Jiang, Fangyu Wang, Cong Zhang. Deoxynivalenol induces testicular ferroptosis by regulating the Nrf2/System Xc-/GPX4 axis. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2023 Mar; 175(?):113730. doi: 10.1016/j.fct.2023.113730. [PMID: 36925038]
  • Cristina Miguel-Rojas, Brad Cavinder, Jeffrey P Townsend, Frances Trail. Comparative Transcriptomics of Fusarium graminearum and Magnaporthe oryzae Spore Germination Leading up To Infection. mBio. 2023 02; 14(1):e0244222. doi: 10.1128/mbio.02442-22. [PMID: 36598191]
  • Wanderson Bucker Moraes, Laurence V Madden, Byung-Kee Baik, James Gillespie, Pierce A Paul. Environmental Conditions After Fusarium Head Blight Visual Symptom Development Affect Contamination of Wheat Grain with Deoxynivalenol and Deoxynivalenol-3-Glucoside. Phytopathology. 2023 Feb; 113(2):206-224. doi: 10.1094/phyto-06-22-0199-r. [PMID: 36131392]
  • Rizky Pasthika Kirana, Kumar Gaurav, Sanu Arora, Gerlinde Wiesenberger, Maria Doppler, Sebastian Michel, Simone Zimmerl, Magdalena Matic, Chinedu E Eze, Mukesh Kumar, Ajla Topuz, Marc Lemmens, Rainer Schuhmacher, Gerhard Adam, Brande B H Wulff, Hermann Buerstmayr, Barbara Steiner. Identification of a UDP-glucosyltransferase conferring deoxynivalenol resistance in Aegilops tauschii and wheat. Plant biotechnology journal. 2023 01; 21(1):109-121. doi: 10.1111/pbi.13928. [PMID: 36121345]
  • Z A Chalyy, M G Kiseleva, I B Sedova, V A Tutelyan. [Mycotoxins in spices consumed in Russia]. Voprosy pitaniia. 2023; 92(2):26-34. doi: 10.33029/0042-8833-2023-92-2-26-34. [PMID: 37346017]
  • Antoni Femenias, Polina Fomina, Valeria Tafintseva, Stephan Freitag, Volha Shapaval, Michael Sulyok, Boris Zimmermann, Sonia Marín, Rudolf Krska, Achim Kohler, Boris Mizaikoff. Optimizing extraction solvents for deoxynivalenol analysis in maize via infrared attenuated total reflection spectroscopy and chemometric methods. Analytical methods : advancing methods and applications. 2022 12; 15(1):36-47. doi: 10.1039/d2ay00995a. [PMID: 36448527]
  • Xiaoxiang Xu, Juan Chang, Ping Wang, Chaoqi Liu, Mengjie Liu, Ting Zhou, Qingqiang Yin, Guorong Yan. Glycyrrhizic Acid and Compound Probiotics Supplementation Alters the Intestinal Transcriptome and Microbiome of Weaned Piglets Exposed to Deoxynivalenol. Toxins. 2022 12; 14(12):. doi: 10.3390/toxins14120856. [PMID: 36548753]
  • Beibei Li, Jiaqi Duan, Jie Ren, Frédéric Francis, Guangyue Li. Isolation and Characterization of Two New Deoxynivalenol-Degrading Strains, Bacillus sp. HN117 and Bacillus sp. N22. Toxins. 2022 11; 14(11):. doi: 10.3390/toxins14110781. [PMID: 36356030]
  • Yuting Hu, Rui Hou, Zeyi Wang, Weiwei Zhang, Jin-Rong Xu. Nitrogen repression of deoxynivalenol biosynthesis is mediated by Mep2 ammonium permease in Fusarium graminearum. Environmental microbiology. 2022 11; 24(11):5392-5407. doi: 10.1111/1462-2920.16233. [PMID: 36200537]
  • Cintia Adácsi, Szilvia Kovács, István Pócsi, Tünde Pusztahelyi. Elimination of Deoxynivalenol, Aflatoxin B1, and Zearalenone by Gram-Positive Microbes (Firmicutes). Toxins. 2022 08; 14(9):. doi: 10.3390/toxins14090591. [PMID: 36136529]
  • Akos Mesterhazy, Balázs Szabó, Sándor Szél, Zoltán Nagy, Attila Berényi, Beata Tóth. Novel Insights into the Inheritance of Gibberella Ear Rot (GER), Deoxynivalenol (DON) Accumulation, and DON Production. Toxins. 2022 08; 14(9):. doi: 10.3390/toxins14090583. [PMID: 36136521]
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