Synthesis of Schiff bases modified inulin derivatives for potential antifungal and antioxidant applications
Chen, Y; Mi, YQ; Li, Q; Dong, F; Guo, ZY
刊名INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
2020-01-15
卷号143页码:714-723
关键词Inulin Schiff bases Chemical modification Antifungal Antioxidant
ISSN号0141-8130
DOI10.1016/j.ijbiomac.2019.09.127
产权排序[Chen, Yuan ; Mi, Yingqi ; Li, Qing ; Dong, Fang ; Guo, Zhanyong] Chinese Acad Sci, Yantai Inst Coastal Zone Res, Key Lab Coastal Biol & Bioresource Utilizat, Yantai 264003, Peoples R China ; [Chen, Yuan ; Mi, Yingqi ; Guo, Zhanyong] Chinese Acad Sci, Ctr Ocean Mega Sci, 7 Nanhai Rd, Qingdao 266071, Peoples R China ; [Chen, Yuan ; Mi, Yingqi ; Guo, Zhanyong] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
文献子类Article
英文摘要In this study, the structure of inulin was chemically modified by Schiff bases in order to improve its biological activity. A total of 6 kinds of inulin derivatives were synthesized according to aza-Wittig reaction. Their structures were confirmed by FIR, H-1 NMR, and C-13 NMR spectroscopy. The antioxidant activity of the inulin derivatives was evaluated in vitro. Their antifungal activities against three kinds of plant pathogenic fungi, including Botrytis cinerea, Fusarium oxysporum f. sp. cucumerium Owen, and Phomopsis asparagi, were also studied. The results showed that the biological activities of the derivatives were significantly improved compared to pure inulin. 3HBSAIL could completely scavenge hydroxyl radical and DPPH radical at 1.6 mg mL(-1). 3,4DHBSAIL and 2,3,4THBSAIL exhibited strong antioxidant activity as far as the four tested antioxidant systems. Moreover, the scavenging rates of 3,4DHBSAIL and 2,3,4THBSAIL against DPPH radicals were both 100% even at the lowest test concentration (0.1 mg mL(-1)). The synthetic inulin derivatives showed a broad antifungal spectrum against the tested fungi. At 1.6 mg mrL(-1), the inhibitory rates of 3HBSAIL against Botrytis cinerea, Fusarium oxysporum f. sp. cucumerium Owen, and Phomopsis asparagi were 93%, 83%, and 82%, respectively. The biological activities of the inulin derivatives were closely related to the DS, the number of phenolic hydroxyl groups and their substitutive positions. The products described in this paper have great potential as biomaterials with good bioactivity and biocompatibility. (C) 2019 Elsevier B.V. All rights reserved.
WOS关键词EFFICIENT SYNTHESIS ; POLYSACCHARIDES ; COMPOSITE ; DELIVERY ; CURDLAN
WOS研究方向Biochemistry & Molecular Biology ; Chemistry, Applied ; Polymer Science
语种英语
WOS记录号WOS:000515212500071
资助机构National Natural Science Foundation of China, ChinaNational Natural Science Foundation of China [41576156] ; Natural Science Foundation of Shandong Province, ChinaNatural Science Foundation of Shandong Province [ZR2017BD015] ; Science and Technology Service Network Initiative of Chinese Academy of Sciences, China [KFJ-STS-ZDTP-023] ; Public Science and Technology Research Funds Projects of Ocean, China [2015418022-3] ; Seed Project of Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, China [Y755031011]
内容类型期刊论文
源URL[http://ir.yic.ac.cn/handle/133337/24767]  
专题海岸带生物资源高效利用研究与发展中心
烟台海岸带研究所_海岸带生物学与生物资源利用所重点实验室
作者单位1.Chinese Acad Sci, Yantai Inst Coastal Zone Res, Key Lab Coastal Biol & Bioresource Utilizat, Yantai 264003, Peoples R China;
2.Chinese Acad Sci, Ctr Ocean Mega Sci, 7 Nanhai Rd, Qingdao 266071, Peoples R China;
3.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
推荐引用方式
GB/T 7714
Chen, Y,Mi, YQ,Li, Q,et al. Synthesis of Schiff bases modified inulin derivatives for potential antifungal and antioxidant applications[J]. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,2020,143:714-723.
APA Chen, Y,Mi, YQ,Li, Q,Dong, F,&Guo, ZY.(2020).Synthesis of Schiff bases modified inulin derivatives for potential antifungal and antioxidant applications.INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,143,714-723.
MLA Chen, Y,et al."Synthesis of Schiff bases modified inulin derivatives for potential antifungal and antioxidant applications".INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES 143(2020):714-723.
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