Inhibition of mycotoxin deoxynivalenol generation by using selenized glucose
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* Corresponding authors.
E-mail addresses: taoli@yzu.edu.cn(T. Li) yulei@yzu.edu.cn (L. Yu).
Citation:
Xueyun Mao, Peizi Li, Tao Li, Minmeng Zhao, Chao Chen, Jian Liu, Zhiqiang Wang, Lei Yu. Inhibition of mycotoxin deoxynivalenol generation by using selenized glucose[J]. Chinese Chemical Letters,
;2020, 31(12): 3276-3278.
doi:
10.1016/j.cclet.2020.06.033
W.H. Bao, M. He, J.T. Wang, et al., J. Org. Chem. 84(2019) 6065-6071.
doi: 10.1021/acs.joc.9b00178
X. Deng, H.E. Cao, C. Chen, et al., Sci. Bull. 64(2019) 1280-1284.
doi: 10.1016/j.scib.2019.07.007
M.X. Liu, Y.M. Li, L. Yu, et al., Sci. China Chem. 61(2018) 294-299.
doi: 10.1007/s11426-017-9158-y
S. Kodama, T. Saeki, K. Mihara, et al., J. Org. Chem. 82(2017) 12477-12484.
doi: 10.1021/acs.joc.7b02276
L.H. Lu, Z. Wang, W. Xia, et al., Chin. Chem. Lett. 30(2019) 1237-1240.
doi: 10.1016/j.cclet.2019.04.033
L.H. Lu, S.J. Zhou, W.B. He, et al., Org. Biomol. Chem. 16(2018) 9064-9068.
doi: 10.1039/C8OB02368A
M. Wang, Q.L. Fan, X.F. Jiang, Org. Lett. 18(2016) 5756-5759.
doi: 10.1021/acs.orglett.6b03078
H.E. Cao, R.R. Qian, L. Yu, Catal. Sci. Technol. 10(2020) 3113-3121.
doi: 10.1039/D0CY00400F
C. Chen, Y.T. Cao, X.X. Wu, et al., Chin. Chem. Lett. 31(2020) 1078-1082.
doi: 10.1016/j.cclet.2019.12.019
Y.H. Zheng, A.Q. Wu, Y.Y. Ke, et al., Chin. Chem. Lett. 30(2019) 937-941.
doi: 10.1016/j.cclet.2019.01.012
H.E. Cao, M.X. Liu, R.R. Qian, et al., Appl. Organomet. Chem. 33(2019) e4599.
doi: 10.1002/aoc.4599
X. Liu, Y.Y. Liang, J.Y. Ji, et al., J. Am. Chem. Soc. 140(2018) 4782-4786.
doi: 10.1021/jacs.8b01513
T.T. Wang, X.B. Jing, C. Chen, et al., J. Org. Chem. 82(2017) 9342-9349.
doi: 10.1021/acs.joc.7b01245
F. Wang, L. Xu, C. Sun, et al., Chin. J. Org. Chem. 37(2017) 2115-2118.
doi: 10.6023/cjoc201701026
X.B. Jing, T.T. Wang, Y.H. Ding, et al., Appl. Catal. A-Gen. 541(2017) 107-111.
doi: 10.1016/j.apcata.2017.05.007
G.M. Fang, X.X. Chen, Q.Q. Yang, et al., Chin. Chem. Lett. 29(2018) 1033-1042.
doi: 10.1016/j.cclet.2018.02.002
L. Yu, H.E. Cao, X. Zhang, C. Yang, L. Yu, Sustain. Energ. Fuels 4(2020) 730-736.
doi: 10.1039/C9SE00850K
C. Liu, J.F. Mao, X. Zhang, L. Yu, Catal. Commun. 133(2020) 105828.
doi: 10.1016/j.catcom.2019.105828
K.H. Cao, X. Deng, T. Chen, Q.T. Zhang, L. Yu, J. Mater. Chem. A 7(2019) 10918-10923.
doi: 10.1039/C9TA00846B
X.B. Jing, C.Z. Chen, X. Deng, et al., Appl. Organomet. Chem. 32(2018) e4332.
doi: 10.1002/aoc.4332
Y. Wang, L. Yu, B. Zhu, L. Yu, J. Mater. Chem. A 4(2016) 10828-10833.
doi: 10.1039/C6TA02566H
H.E. Cao, Y.F. Yang, X.J. Chen, et al., Chin. Chem. Lett. 31(2020) 1887-1889.
doi: 10.1016/j.cclet.2020.01.027
M.P. Rayman, Lancet 379(2012) 1256-1268.
doi: 10.1016/S0140-6736(11)61452-9
US Pharmacopeial convention (USP), USP < 232> Elemental Impurities-Limits. 40-NF 35, First Supplement (2017). https://www.usp.org/sites/default/files/usp/document/ourwork/chemical-medicines/key-issues/232-40-35-1s.pdf.
B.A. Summerell, Annu. Rev. Phytopathol. 57(2019) 323-339.
doi: 10.1146/annurev-phyto-082718-100204
K. Nesic, S. Ivanovic, V. Nesic, Rev. Environ. Contam. Toxicol. 228(2014) 101-120.
B.L. Cheng, Y. Zhang, B. Tong, et al., Biol. Trace Elem. Res. 178(2017) 147-152.
doi: 10.1007/s12011-016-0900-3
F.Y. Sun, L. Yang, L. Li, et al., Curr. Biotech. 7(2017) 433-438.
Q.H. Wu, X. Wang, E. Nepovimova, et al., Oncotarget 8(2017) 110708-110726.
doi: 10.18632/oncotarget.22800
S.N. Chu, H.E. Cao, T. Chen, et al., Catal. Commun. 129(2019) 105730.
doi: 10.1016/j.catcom.2019.105730
Y.F. Yang, X. Fan, H.E. Cao, et al., Catal. Sci. Technol. 8(2018) 5017-5023.
doi: 10.1039/C8CY01413B
J.C. Peeler, J.A. Falco, R.E. Kelemen, et al., ACS Chem. Biol. 15(2020) 1535-1540.
doi: 10.1021/acschembio.0c00147
J. Qu, W. Wang, Q. Zhang, S. Li, Biol. Trace Elem. Res. 195(2020) 205-214.
doi: 10.1007/s12011-019-01841-0
W.J. Zhou, P.Z. Li, J. Liu, et al., Ind. Eng. Chem. Res. 59(2020) 10763-10767.
doi: 10.1021/acs.iecr.0c01147
Y. Chen, H.C. Kistler, Z.H. Ma, Annu. Rev. Phytopathol. 57(2019) 15-39.
doi: 10.1146/annurev-phyto-082718-100318
F. Jiao, A. Kawakami, T. Nakajima, FEMS Microbiol. Lett. 285(2008) 212-219.
doi: 10.1111/j.1574-6968.2008.01235.x
Cao Hongen , Yang Yufan , Chen Xijun , Liu Jian , Chen Chao , Yuan Shuzhong , Yu Lei . Synthesis of selenium-doped carbon from glucose: An efficient antibacterial material against Xcc. Chinese Chemical Letters, 2020, 31(7): 1887-1889. doi: 10.1016/j.cclet.2020.01.027
Xin Hua XU , Wen Qi LIU . Insertion of Selenium into Zinc Carbon Bond and Application in Synthesis of Arylselenoester. Chinese Chemical Letters, 2002, 13(4): 283-284.
Ying Jun Li , Li Jun Liu , Kun Jin , Yong Ting Xu , Su Qin Sun . Synthesis and bioactivity of a novel series of 3,6-disubstituted 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazoles. Chinese Chemical Letters, 2010, 21(3): 293-296. doi: 10.1016/j.cclet.2009.11.008
Xin-Yue Hu , Yong Chen , Yu Liu . Redox-responsive supramolecular nanoparticles based on amphiphilic sulfonatocalixarene and selenocystamine dihydrochloride. Chinese Chemical Letters, 2015, 26(7): 862-866. doi: 10.1016/j.cclet.2015.01.003
Guo-Jun Yan , Xin Mei , Jin Yang , Jenny Zhu , Jie-Ying Wu , Jin-Huo Pan . A novel real-time cell electronic analysis technology for the authentication and quality control of natural medicines. Chinese Chemical Letters, 2013, 24(12): 1140-1144.
Xi-Le Deng , Jin Xie , Yong-Qiang Li , De-Kai Yuan , Xue-Ping Hu , Li Zhang , Qing-Min Wang , Ming Chi , Xin-Ling Yang . Design, synthesis and biological activity of novel substituted pyrazole amide derivatives targeting EcR/USP receptor. Chinese Chemical Letters, 2016, 27(4): 566-570.
Zhang Xiaopeng , Dong Shuxiang , Ding Qianqian , Fan Xuesen , Zhang Guisheng . Selenium-catalyzed oxidative carbonylation of 1, 2, 3-thiadiazol-5-amine with amines to 1, 2, 3-thiadiazol-5- ylureas. Chinese Chemical Letters, 2019, 30(2): 375-378. doi: 10.1016/j.cclet.2018.07.017
Ren Hui-Hui , Zhao Hui-Yu , Cui Yang , Ao Xiang , Li Ai-Ling , Zhang Zhong-Min , Qiu Dong . Poly(1, 8-octanediol citrate)/bioactive glass composite with improved mechanical performance and bioactivity for bone regeneration. Chinese Chemical Letters, 2017, 28(11): 2116-2120. doi: 10.1016/j.cclet.2017.07.014
Chen Chao , Cao Yitao , Wu Xixi , Cai Yuanli , Liu Jian , Xu Lin , Ding Kehong , Yu Lei . Energy saving and environment-friendly element-transfer reactions with industrial application potential. Chinese Chemical Letters, 2020, 31(5): 1078-1082. doi: 10.1016/j.cclet.2019.12.019
Ren Huihui , Cui Yang , Li Ailing , Qiu Dong . Bioactive glass sol as a dual function additive for chitosan-alginate hybrid scaffold. Chinese Chemical Letters, 2018, 29(3): 395-398. doi: 10.1016/j.cclet.2018.01.023
Li Da-Wei , Guo Qing-Lan , Meng Xian-Hua , Zhu Cheng-Gen , Xu Cheng-Bo , Shi Jian-Gong . Two pairs of unusual scalemic enantiomers from Isatis indigotica leaves. Chinese Chemical Letters, 2016, 27(12): 1745-1750. doi: 10.1016/j.cclet.2016.08.006
Yan Cheng-Nong , Liu Yi , Qu Song-Sheng , Chen Chun-Ying , Xu Hui-Bi . Studies on Cell Kinetics Ⅷ. Characteristics of the Action of Na2SeO3 on Rhizopus Nigrocans. Acta Physico-Chimica Sinica, 1997, 13(04): 354-357. doi: 10.3866/PKU.WHXB19970413
ZHAI Tongyi , ZHU Yaxian . Resume of Sister Selenium. University Chemistry, 2018, 33(7): 33-36. doi: 10.3866/PKU.DXHX201803050
TAO Chen , LI Chun-Sheng , CHU Wei-Cheng , GAO Ran-Ran , ZHOU Zhi-Heng , LI Yun-Meng , MA Zhen-Yu , TIAN DI . Correction Method of Light Source Interference for Simultaneous Determination of Selenium and Lead by Non-dispersive Hydride Generation-Atomic Fluorescence Spectrometry. Chinese Journal of Analytical Chemistry, 2019, 47(1): 163-168. doi: 10.19756/j.issn.0253-3820.181542
ZHU Yuelu , ZHAO Xinyang , WU Qian , CHEN Ying , ZHAO Jing . Research Advances in C―H Bond Activation of Multitasking N-Phenoxyamides. Acta Physico-Chimica Sinica, 2019, 35(9): 989-1004. doi: 10.3866/PKU.WHXB201812016
Chen Fuheng , Wuang Qin . THE SYNTHESIS OF NEW PYRETHROIDS. Chinese Journal of Applied Chemistry, 1988, 5(3): 43-47.
CHEN Zhenzhen , YANG Yanmei , JIANG Zhongyao , TANG Bo . The Magic Element of Life: Selenium. University Chemistry, 2019, 34(12): 79-85. doi: 10.3866/PKU.DXHX201911015
Ming Zhu LIU , Sheng Yi ZHANG , Yu Hua SHEN , Ming Liang ZHANG . Selenium Nanoparticles Prepared from Reverse Microemulsion Process. Chinese Chemical Letters, 2004, 15(10): 1249-1252.
Jin Hao Zhao , Ming Hua Ji , Xu Hui Xu , Jing Li Cheng , Guo Nian Zhu . Synthesis analogues of milbemycin and their bioactivity evaluation. Chinese Chemical Letters, 2010, 21(12): 1391-1394. doi: 10.1016/j.cclet.2010.06.035
Jin Hao Zhao , Ming Hua Ji , Xu Hui Xu , Jing Li Cheng , Guo Nian Zhu . Synthetic derivatives of spiromesifen and their bioactivity research. Chinese Chemical Letters, 2009, 20(11): 1307-1310. doi: 10.1016/j.cclet.2009.06.028