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« Previous AbstractPhysiological and biochemical effects of allelochemical ethyl 2-methyl acetoacetate (EMA) on cyanobacterium Microcystis aeruginosa    Next AbstractThe role of anthropogenic chlorine emission in surface ozone formation during different seasons over eastern China »

J Plant Physiol


Title:Responses of enzymatic antioxidants and non-enzymatic antioxidants in the cyanobacterium Microcystis aeruginosa to the allelochemical ethyl 2-methyl acetoacetate (EMA) isolated from reed (Phragmites communis)
Author(s):Hong Y; Hu HY; Xie X; Li FM;
Address:"Environmental Simulation and Pollution Control State Key Joint Laboratory, Department of Environmental Science and Engineering, Tsinghua University, Beijing 100084, PR China"
Journal Title:J Plant Physiol
Year:2008
Volume:20071231
Issue:12
Page Number:1264 - 1273
DOI: 10.1016/j.jplph.2007.10.007
ISSN/ISBN:1618-1328 (Electronic) 0176-1617 (Linking)
Abstract:"Macrophytic allelochemicals are considered an environment-friendly and promising alternative to control algal bloom. However, studies examining the potential mechanisms of inhibitory allelochemicals on algae are few. The allelochemical ethyl 2-methyl acetoacetate (EMA), isolated from reed (Phragmites communis), was a strong allelopathic inhibitor on the growth of Microcystis aeruginosa. EMA-induced antioxidant responses were investigated in the cyanobacterium M. aeruginosa to understand the mechanism of EMA inhibition on algal growth. The activities of enzymatic antioxidants superoxide dismutase (SOD) and catalase (CAT), and the contents of non-enzymatic antioxidants reduced glutathione (GSH) and ascorbic acid (AsA) of M. aeruginosa cells were analyzed after treatments with different concentrations of EMA. Exposure of M. aeruginosa to EMA caused changes in enzyme activities and contents of non-enzymatic antioxidants in different manners. The decrease in SOD activity occurred first after 4 h of EMA exposure, and more markedly after 40 h. CAT activity did not change after 4 h of EMA exposure, but increased obviously after 40 h. The contents of AsA and GSH were increased greatly by EMA after 4 h. After 60 h, low EMA concentrations still increased the CAT activity and the contents of AsA and GSH, but high EMA concentrations started to impose a marked suppression on them. EMA increased dehydroascorbate (DHAsA) and oxidized glutathione (GSSG) contents during all exposure times. After 60 h, the regeneration rates of AsA and GSH (represented by the AsA/DHAsA ratio and GSH/GSSG ratio, respectively) were reduced by high EMA concentrations. These results suggest that the activation of CAT and the availability of AsA and GSH at early exposure are important to counteract the oxidative stress induced by EMA, and the inactivation of SOD may be crucial to the growth inhibition of M. aeruginosa by EMA"
Keywords:"Acetoacetates/chemistry/metabolism/*pharmacology Antioxidants/*metabolism Ascorbic Acid/metabolism Catalase/metabolism Dose-Response Relationship, Drug Glutathione/metabolism Glutathione Disulfide/metabolism Microcystis/chemistry/drug effects/*enzymology;"
Notes:"MedlineHong, Yu Hu, Hong-Ying Xie, Xing Li, Feng-Min eng Research Support, Non-U.S. Gov't Germany 2008/01/01 J Plant Physiol. 2008 Aug 25; 165(12):1264-73. doi: 10.1016/j.jplph.2007.10.007. Epub 2007 Dec 31"

 
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