Aulakh Simran Kaur, Varma Sreejith Jayasree, Ralser Markus
Molecular Biology of Metabolism Laboratory, The Francis Crick Institute, 1 Midland Road, NW1 1AT London, United Kingdom. Electronic address: https://twitter.com/@simranolak.
Department of Biochemistry, Charité - Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, Germany. Electronic address: https://twitter.com/@ajaanubahu.
Curr Opin Genet Dev. 2022 Dec;77:101987. doi: 10.1016/j.gde.2022.101987. Epub 2022 Sep 29.
Metal ions are potent catalysts and have been available for cellular biochemistry at all stages of evolution. Growing evidence suggests that metal catalysis was critical for the origin of the very first metabolic reactions. With approximately 80% of modern metabolic pathways being dependent on metal ions, metallocatalysis and homeostasis continue to be essential for intracellular metabolic networks and physiology. However, the genetic network that controls metal ion homeostasis and the impact of metal availability on metabolism is poorly understood. Here, we review recent work on gene and protein evolution relevant for better understanding metal ion biology and its role in metabolism. We highlight the importance of analysing the origin and evolution of enzyme catalysis in the context of catalytically relevant metal ions, summarise unanswered questions essential for developing a comprehensive understanding of metal ion homeostasis and advocate for the consideration of metal ion properties and availability in the design and directed evolution of novel enzymes and pathways.
金属离子是强效催化剂,在进化的各个阶段都参与细胞生物化学过程。越来越多的证据表明,金属催化对于最早的代谢反应的起源至关重要。现代约80%的代谢途径依赖金属离子,金属催化作用和体内平衡对于细胞内代谢网络和生理学仍然至关重要。然而,控制金属离子体内平衡的遗传网络以及金属可利用性对代谢的影响却鲜为人知。在此,我们综述了近期与更好理解金属离子生物学及其在代谢中的作用相关的基因和蛋白质进化研究工作。我们强调在催化相关金属离子的背景下分析酶催化起源和进化的重要性,总结对于全面理解金属离子体内平衡至关重要但尚未解答的问题,并提倡在设计新型酶和途径以及定向进化过程中考虑金属离子的特性和可利用性。