Bibliographic Details
Title: |
The Efficacy and Underlying Mechanism of Sulfone Derivatives Containing 1,3,4-oxadiazole on Citrus Canker |
Authors: |
Pei Li, Yuhua Ma, Junliang Zhou, Hui Luo, Jiawen Yan, Yongya Mao, Zhuang Wang |
Source: |
Molecules, Vol 20, Iss 8, Pp 14103-14117 (2015) |
Publisher Information: |
MDPI AG, 2015. |
Publication Year: |
2015 |
Collection: |
LCC:Organic chemistry |
Subject Terms: |
sulfone derivatives, Xanthomonas citri subsp. citri, citrus canker, antibacterial bioassay, underlying mechanism, Organic chemistry, QD241-441 |
More Details: |
The objectives of the current study were to isolate and identify the pathogen responsible for citrus canker and investigate the efficacy of sulfone derivatives containing 1,3,4-oxadiazole moiety on controlling citrus canker caused by Xanthomonas citri subsp. citri (Xcc) under in vitro and field conditions. In an in vitro study, we tested eight sulfone derivatives against Xcc and the results demonstrated that compound 3 exhibited the best antibacterial activity against Xcc, with a half-maximal effective concentration (EC50) value of 1.23 μg/mL, which was even better than those of commercial bactericides Kocide 3000 (58.21 μg/mL) and Thiodiazole copper (77.04 μg/mL), respectively. Meanwhile, under field experiments, compound 3 treatments demonstrated the highest ability to reduce the disease of citrus canker in leaves and fruits in two different places relative to an untreated control as well as the commercial bactericides Kocide 3000 and Thiodiazole copper. Meanwhile, compound 3 could stimulate the increase in peroxidase (POD), polyphenol oxidase (PPO), and phenylalanine ammonia lyase (PAL) activities in the navel orange leaves, causing marked enhancement of plant resistance against citrus canker. Moreover, compound 3 could damage the cell membranes, destruct the biofilm formation, inhibit the production of extracellular polysaccharide (EPS), and affect the cell membrane permeability to restrain the growth of the bacteria. |
Document Type: |
article |
File Description: |
electronic resource |
Language: |
English |
ISSN: |
1420-3049 |
Relation: |
http://www.mdpi.com/1420-3049/20/8/14103; https://doaj.org/toc/1420-3049 |
DOI: |
10.3390/molecules200814103 |
Access URL: |
https://doaj.org/article/e1a15c202b7e4315b5aca300fb325768 |
Accession Number: |
edsdoj.1a15c202b7e4315b5aca300fb325768 |
Database: |
Directory of Open Access Journals |