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消旋、R-和S-戊唑醇改变了大型溞的几丁质酶和壳二糖酶活性。

Racemic, R-, and S-tebuconazole altered chitinase and chitobiase activity of Daphnia magna.

作者信息

Qi Suzhen, Liu Xue, Zhu Lizhen, Chen Xiaofeng, Wang Chengju

机构信息

a Key Laboratory of Pesticide Chemistry & Application Technology, College of Sciences, China Agricultural University , Beijing , P.R. China.

b Institute of Apicultural Research, Chinese Academy of Agricultural Sciences , Beijing , P. R. China.

出版信息

J Environ Sci Health B. 2018 Mar 4;53(3):171-175. doi: 10.1080/03601234.2017.1399245. Epub 2017 Dec 11.

Abstract

Tebuconazole is a chiral trizole fungicide and widely used in many crops for controlling disease. Tebuconazole is potential toxic to some aquatic organisms but relative information of its isomers is scarce. To detect the endocrine disrupting effects and difference of rac-, R-, and S-tebuconazole, the chitinase activity in Daphnia magna and chitobiase activity in each test medium were used as biomonitors after a 14-day exposure. Results showed that chitinase activity was significantly reduced by rac-, R-, and S-tebuconazole. The chitobiase activity in the test medium was reduced by rac- and R-tebuconazole before day 10, and only one peak was observed at day 10 or day 12 compared with two obvious peaks in the control group (days 6 and 12). S-tebuconazole delayed and reduced the reproduction of D. magna, but did not delay the first chitobiase activity peak, whereas the second peak could not be characterized as the exposure concentration and time increased. Compared with chitinase activity, chitobiase activity can still be used as a rudimentary model for identifying molt-interfering xenobiotics, and further studies should focus on the analysis of correlations between these parameters.

摘要

戊唑醇是一种手性三唑类杀菌剂,广泛用于多种作物的病害防治。戊唑醇对一些水生生物具有潜在毒性,但其异构体的相关信息却很匮乏。为检测外消旋体、R-体和S-体戊唑醇的内分泌干扰效应及差异,在暴露14天后,将大型溞的几丁质酶活性及各试验介质中的壳二糖酶活性用作生物监测指标。结果表明,外消旋体、R-体和S-体戊唑醇均显著降低了几丁质酶活性。在第10天之前,外消旋体和R-体戊唑醇降低了试验介质中的壳二糖酶活性,与对照组(第6天和第12天出现两个明显峰值)相比,在第10天或第12天仅观察到一个峰值。S-体戊唑醇延迟并降低了大型溞的繁殖,但并未延迟壳二糖酶活性的第一个峰值,而随着暴露浓度和时间的增加,第二个峰值无法确定。与几丁质酶活性相比,壳二糖酶活性仍可作为识别干扰蜕皮的外源化合物的初步模型,进一步的研究应侧重于分析这些参数之间的相关性。

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