表达表面重金属结合蛋白的重组大肠杆菌去除污染水中的Pb2+

M. Shehata, K. Yamazaki
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引用次数: 3

摘要

水污染仍然是全世界经济和公共卫生关切的一个严重问题。铅(Pb2+)是与慢性疾病相关的危险金属之一,在世界各地造成许多人死亡。尽管去除水中重金属(如Pb2+)的技术取得了进步,但目前所有的技术都显示出一些局限性,阻碍了它们的应用。考虑到需要开发一种去除水中重金属的新技术,我们开发了一种利用重组大肠杆菌死细胞快速、特异性和高效地去除水中Pb2+的方法。重组大肠杆菌在外膜上表达金属硫蛋白(SmtB)和铅结合蛋白(PbrR)。编码这些蛋白的DNA片段与编码抗原43 β结构域(Ag43)的DNA片段融合,从而实现两种重金属结合蛋白的易位。重组大肠杆菌能够成功地从含100 mg/L Pb2+的水样中吸附Pb2+, 18小时后Pb2+浓度达到检测不到的水平。热灭活的大肠杆菌在外膜上显示PbrR和SmtB,对活的大肠杆菌细胞的去除效率相当。这些观察结果表明,我们的方法可以作为一种有前途的、特定的和有效的方法来去除污染水中的Pb2+。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Using Recombinant E. coli Displaying Surface Heavy Metal Binding Proteins for Removal of Pb2+ from Contaminated Water
Water pollution remains a serious problem with economic and public health concerns worldwide. Lead (Pb2+) is one of the dangerous metals related to chronic diseases and is responsible for many deaths around the world. Despite the advances in technologies for removal of heavy metals e.g., Pb2+ from water, all current techniques have shown some limitations that obstructed their application. Bearing in mind that there is a need to develop a novel technique for removal of heavy metals from water, we developed a quick, specific and efficient method for removal of Pb2+ from water using dead cells of recombinant Escherichia coli. Recombinant E. coli were engineered to display metallothionein (SmtB) and lead binding protein (PbrR) onto outer membrane. DNA fragments encoding these proteins were fused to DNA fragment encoding β- domain of antigen 43 (Ag43) for translocation of both heavy metal binding proteins. The resultant recombinant E. coli exhibited a capability to adsorb Pb2+ successfully from water samples containing 100 mg/L of Pb2+, and concentrations of Pb2+ reached to undetectable level after 18 hours. Heat-inactivated E. coli displaying PbrR and SmtB on outer membrane showed comparable removal efficiencies to live E. coli cells. These observations suggest that our method can be used as a promising, specific and efficient approach for removal of Pb2+ from contaminated water.
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