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检测用蜂胶处理后的十二指肠贾第鞭毛虫滋养体分泌的细胞外产物中的蛋白酶活性。

Characterisation of protease activity in extracellular products secreted by Giardia duodenalis trophozoites treated with propolis.

机构信息

Department of Parasitology, Biosciences Institute, Universidade Estadual Paulista, Botucatu, SP, Brazil.

出版信息

Nat Prod Res. 2012;26(4):370-4. doi: 10.1080/14786419.2010.515547. Epub 2011 Jun 27.

DOI:10.1080/14786419.2010.515547
PMID:21707229
Abstract

Results from our laboratory revealed propolis activity on Giardia trophozoites proliferation. Since therapeutic agents can inhibit the activity of proteases related to relevant biologic and physiologic processes of parasites, this study was undertaken to characterise the proteolytic activity of excretory/secretory products (ESP) of trophozoites treated with propolis. ESP was obtained from culture supernatants of trophozoites exposed to 250 and 500 µg mL(-1) of propolis. ESP were tested in sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the protein profiles and the protease activity was assayed in gelatin-containing gels. Synthetic inhibitors were used to characterise the protease classes. Treated and non-treated ESP showed a similar protein and hydrolysis pattern. A simple pattern of protein composed by five evident bands of approximately 167, 132, 79, 61 and 51 kDa was found, and the zymograms comprised hydrolysis zones distributed from >170 to 23 kDa. No inhibition was seen on protease activity of propolis-treated trophozoites, whose hydrolysis pattern was similar to control. One may conclude that both ESP degraded gelatin and the activity was predominantly due to cysteine proteases. Although propolis had no effect on the proteolytic activity, further studies could identify the active constituents responsible for propolis antigiardial activity and their mechanisms of action.

摘要

我们实验室的研究结果表明,蜂胶对贾第鞭毛虫滋养体的增殖有活性。由于治疗药物可以抑制与寄生虫相关的生物学和生理学过程相关的蛋白酶的活性,因此进行了这项研究,以表征用蜂胶处理的滋养体的分泌/排泄产物(ESP)的蛋白水解活性。ESP 是从暴露于 250 和 500µg mL(-1) 蜂胶的滋养体的培养上清液中获得的。ESP 在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳中进行蛋白质图谱测试,并在含有明胶的凝胶中测定蛋白酶活性。使用合成抑制剂来表征蛋白酶类。处理和未处理的 ESP 显示出相似的蛋白质和水解模式。发现了一种由五个明显的约 167、132、79、61 和 51 kDa 条带组成的简单蛋白质图谱,并且同工酶图谱包含从>170 到 23 kDa 的水解区。蜂胶处理的滋养体的蛋白酶活性没有抑制,其水解模式与对照相似。可以得出结论,ESP 均降解明胶,并且该活性主要归因于半胱氨酸蛋白酶。尽管蜂胶对蛋白水解活性没有影响,但进一步的研究可以鉴定出蜂胶抗贾第鞭毛虫活性的活性成分及其作用机制。

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