Department of Chemistry, University of Massachusetts, Amherst, Massachusetts 01003, USA.
Biochemistry. 2012 Oct 9;51(40):7816-32. doi: 10.1021/bi300981m. Epub 2012 Sep 28.
Nickel is an essential metal for a number of bacterial species that have developed systems for acquiring, delivering, and incorporating the metal into target enzymes and controlling the levels of nickel in cells to prevent toxic effects. As with other transition metals, these trafficking systems must be able to distinguish between the desired metal and other transition metal ions with similar physical and chemical properties. Because there are few enzymes (targets) that require nickel for activity (e.g., Escherichia coli transports nickel for hydrogenases made under anaerobic conditions, and Helicobacter pylori requires nickel for hydrogenase and urease that are essential for acid viability), the "traffic pattern" for nickel is relatively simple, and nickel trafficking therefore presents an opportunity to examine a system for the mechanisms that are used to distinguish nickel from other metals. In this review, we describe the details known for examples of uptake permeases, metallochaperones and proteins involved in metallocenter assembly, and nickel metalloregulators. We also illustrate a variety of mechanisms, including molecular recognition in the case of NikA protein and examples of allosteric regulation for HypA, NikR, and RcnR, employed to generate specific biological responses to nickel ions.
镍是许多细菌物种必需的金属,这些细菌已经开发出了获取、输送和将金属纳入靶酶的系统,并控制细胞内镍的水平以防止毒性作用。与其他过渡金属一样,这些运输系统必须能够区分所需的金属和具有相似物理化学性质的其他过渡金属离子。由于需要镍才能发挥活性的酶(例如,大肠杆菌在厌氧条件下运输用于氢化酶的镍,幽门螺杆菌需要镍用于氢化酶和脲酶,这些酶对酸性生存至关重要),因此镍的“运输模式”相对简单,镍运输因此提供了一个机会来研究用于将镍与其他金属区分开来的机制的系统。在这篇综述中,我们描述了摄取透性酶、金属伴侣蛋白和参与金属中心组装的蛋白以及镍金属调节蛋白的例子的详细信息。我们还说明了各种机制,包括 NikA 蛋白的分子识别以及 HypA、NikR 和 RcnR 的变构调节的例子,这些机制用于产生对镍离子的特定生物学反应。