Preparation, characterization, and antifungal activity of hymexazol-linked chitosan derivatives

Yan Li; Yukun Qin; Song Liu; Pengcheng Li; Rong’e Xing

doi:10.1007/s00343-017-6100-y

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Preparation, characterization, and antifungal activity of hymexazol-linked chitosan derivatives

OriginalPaper | Updated：2023-05-16

- Preparation, characterization, and antifungal activity of hymexazol-linked chitosan derivatives
- Preparation, characterization, and antifungal activity of hymexazol-linked chitosan derivatives
- 海洋湖沼学报（英文） 2017年35卷第5期页码：1079-1085
- Affiliations：
  
  1. Institute of Oceanology Chinese Academy of Sciences
  2. University of Chinese Academy of Sciences
  3. Key Laboratory of Experimental Marine Biology Institute of Oceanology Chinese Academy of Sciences
- Author bio：
- Funds：
  
  Supported by the National Natural Science Foundation of China (No. 41306071), the Public Science and Technology Research Funds Projects of Ocean (No. 201305016-2), and the Science and Technology Development Program of Shandong Province (No. 2012GHY11530)
- DOI：10.1007/s00343-017-6100-y
  中图分类号：
- 网络首发：2016-09-29，
  
  纸质出版：2017
- Accepted：
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Preparation, characterization, and antifungal activity of hymexazol-linked chitosan derivatives[J]. 海洋湖沼学报（英文）, 2017,35(5):1079-1085.

Li, Y., Qin, Y., Liu, S. et al. Preparation, characterization, and antifungal activity of hymexazol-linked chitosan derivatives., Chin. J. Ocean. Limnol. 35, 1079–1085 (2017). https://doi.org/10.1007/s00343-017-6100-y
Preparation, characterization, and antifungal activity of hymexazol-linked chitosan derivatives[J]. 海洋湖沼学报（英文）, 2017,35(5):1079-1085. DOI： 10.1007/s00343-017-6100-y.

Li, Y., Qin, Y., Liu, S. et al. Preparation, characterization, and antifungal activity of hymexazol-linked chitosan derivatives., Chin. J. Ocean. Limnol. 35, 1079–1085 (2017). https://doi.org/10.1007/s00343-017-6100-y DOI：

摘要

Abstract

In this study

three hymexazol-linked chitosan derivatives (HML-CS) were synthesized and their structures confirmed by Fourier transform infrared and elemental analysis. Linkage ratios were measured by high performance liquid chromatography. The derivatives’ antifungal activity against the plant pathogenic fungi Rhizoctonia solani CGMCC 3.28 and Gibberella zeae CGMCC 3.42 were investigated at concentrations of 100

200

and 400 mg/L. These HML-CS derivatives exhibited stronger antifungal activity than CS alone. HML-CS-1 showed the best antifungal activity against G. zeae

whose antifungal index was 65.9% at 400 mg/L

and also showed the best antifungal activity against R. solani

whose antifungal index was 52.7% at 400 mg/L. This conjugation of CS and HML suggested the presence of synergistic effects between the moieties and indicated that these derivatives possessed great potential as novel fungicides and require further research for the development of applications in crop protection.

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references

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