Dey Tuli, Basu Raunak, Ghosh Sudip K
Department of Biotechnology, Indian Institute of Technology Kharagpur, West Bengal 721302, India.
Exp Parasitol. 2009 Nov;123(3):244-9. doi: 10.1016/j.exppara.2009.07.008. Epub 2009 Jul 29.
Entamoeba histolytica, the causative agent of amebiasis infects through its cyst form and this transmission may be blocked using encystation specific protein as drug target. In this study, we have characterized the enzyme chitinase which express specifically during encystation. The reptilian parasite Entamoeba invadens, used as a model for encystation study contain three chitinases. We report the molecular cloning, over-expression and biochemical characterization of all three E. invadens chitinase. Cloned chitinases were over-expressed in bacterial system and purified by affinity chromatography. Their enzymatic profiles and substrate cleaving patterns were characterized. All of them showed binding affinity towards insoluble chitin though two of them lack the chitin binding domain. All the chitinases cleaved and released dimmers from the insoluble substrate and act as an exochitinase. Homology modeling was also done to understand the substrate binding and cleavage pattern.
溶组织内阿米巴是阿米巴病的病原体,通过其包囊形式进行感染,利用包囊化特异性蛋白作为药物靶点可阻断这种传播。在本研究中,我们对在包囊化过程中特异性表达的几丁质酶进行了表征。用作包囊化研究模型的爬行动物寄生虫侵袭内阿米巴含有三种几丁质酶。我们报告了所有三种侵袭内阿米巴几丁质酶的分子克隆、过表达及生化特性。克隆的几丁质酶在细菌系统中过表达,并通过亲和层析进行纯化。对它们的酶谱和底物切割模式进行了表征。尽管其中两种缺乏几丁质结合结构域,但它们都显示出对不溶性几丁质的结合亲和力。所有几丁质酶都从不溶性底物上切割并释放出二聚体,起外切几丁质酶的作用。还进行了同源建模以了解底物结合和切割模式。