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Engineering outer-membrane proteins in Pseudomonas putida for enhanced heavy-metal bioadsorption

机译:工程恶臭假单胞菌的外膜蛋白可增强重金属的生物吸附

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摘要

Metallothioneins (MTs) are small, cysteine-rich proteins with a strong metal-binding capacity that are ubiquitous in the animal kingdom. Recombinant expression of MT fused to outer-membrane components of Gram-negative bacteria may provide new methods to treat heavy-metal pollution in industrial sewage. In this work, we have engineered Pseudomonas putida, a per se highly robust microorganism able to grow in highly contaminated habitats in order to further increase its metal-chelating ability. We report the expression of a hybrid protein between mouse MT and the beta domain of the IgA protease of Neisseria in the outer membrane of Pseudomonas cells. The metal-binding capacity of such cells was increased three-fold. The autotranslocating capacity of the beta domain of the IgA protease of Neisseria, as well as the correct anchoring of the transported protein into the outer membrane, have been demonstrated for the first time in a member of the Pseudomonas genus. (C) 2000 Elsevier Science Inc. All rights reserved. [References: 26]
机译:金属硫蛋白(MTs)是小的,富含半胱氨酸的蛋白质,具有很强的金属结合能力,在动物界很普遍。重组表达与革兰氏阴性菌外膜成分融合可能为治疗工业污水中的重金属污染提供新的方法。在这项工作中,我们设计了恶臭假单胞菌(Pseudomonas putida),它本身是一种高度健壮的微生物,能够在高度污染的栖息地中生长,以进一步提高其金属螯合能力。我们报告了假单胞菌细胞外膜中的小鼠MT和奈瑟氏球菌IgA蛋白酶的β域之间的杂交蛋白的表达。这种细胞的金属结合能力增加了三倍。假单胞菌属的成员首次证明了奈瑟氏球菌IgA蛋白酶β结构域的自转位能力,以及转运蛋白正确锚定在外膜中。 (C)2000 Elsevier Science Inc.保留所有权利。 [参考:26]

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