Zhang Yan, Rump Steffen, Gladyshev Vadim N
Division of Genetics, Department of Medicine, Brigham & Women's Hospital and Harvard Medical School, Boston, MA 02115, United States.
Coord Chem Rev. 2011 May;255(9-10):1206-1217. doi: 10.1016/j.ccr.2011.02.016.
The trace element molybdenum (Mo) is the catalytic component of important enzymes involved in global nitrogen, sulfur, and carbon metabolism in both prokaryotes and eukaryotes. With the exception of nitrogenase, Mo is complexed by a pterin compound thus forming the biologically active molybdenum cofactor (Moco) at the catalytic sites of molybdoenzymes. The physiological roles and biochemical functions of many molybdoenzymes have been characterized. However, our understanding of the occurrence and evolution of Mo utilization is limited. This article focuses on recent advances in comparative genomics of Mo utilization in the three domains of life. We begin with a brief introduction of Mo transport systems, the Moco biosynthesis pathway, the role of posttranslational modifications, and enzymes that utilize Mo. Then, we proceed to recent computational and comparative genomics studies of Mo utilization, including a discussion on novel Moco-binding proteins that contain the C-terminal domain of the Moco sulfurase and that are suggested to represent a new family of molybdoenzymes. As most molybdoenzymes need additional cofactors for their catalytic activity, we also discuss interactions between Mo metabolism and other trace elements and finish with an analysis of factors that may influence evolution of Mo utilization.
微量元素钼(Mo)是原核生物和真核生物中参与全球氮、硫和碳代谢的重要酶的催化成分。除了固氮酶外,钼与蝶呤化合物络合,从而在钼酶的催化位点形成生物活性钼辅因子(Moco)。许多钼酶的生理作用和生化功能已得到表征。然而,我们对钼利用的发生和进化的了解有限。本文重点介绍生命三域中钼利用的比较基因组学的最新进展。我们首先简要介绍钼转运系统、Moco生物合成途径、翻译后修饰的作用以及利用钼的酶。然后,我们继续介绍钼利用的最新计算和比较基因组学研究,包括对含有Moco硫酸化酶C末端结构域的新型Moco结合蛋白的讨论,这些蛋白被认为代表了一个新的钼酶家族。由于大多数钼酶需要额外的辅因子来发挥其催化活性,我们还讨论了钼代谢与其他微量元素之间的相互作用,并最后分析了可能影响钼利用进化的因素。