School of Physical and Chemical Sciences, Biomolecular Interaction Centre, and Maurice Wilkins Centre for MolecularBiodiscovery, University of Canterbury, Christchurch 8041, New Zealand.
Laboratory of Structural Biology, School of Biological Sciences and Maurice Wilkins Centre for MolecularBiodiscovery, University of Auckland, Private Bag 92019, Auckland, New Zealand.
Curr Opin Struct Biol. 2020 Dec;65:33-41. doi: 10.1016/j.sbi.2020.05.005. Epub 2020 Jul 5.
Menaquinones (vitamin K2) are a family of redox-active small molecules with critical functions across all domains of life, including energy generation in bacteria and bone health in humans. The enzymes involved in menaquinone biosynthesis also have bioengineering applications and are potential antimicrobial drug targets. New insights into the essential roles of menaquinones, and their potential to cause redox-related toxicity, have highlighted the need for this pathway to be tightly controlled. Here, we provide an overview of our current understanding of the classical menaquinone biosynthesis pathway in bacteria. We also review recent discoveries on protein-level allostery and sublocalisation of membrane-bound enzymes that have provided insight into the regulation of flux through this biosynthetic pathway.
甲萘醌(维生素 K2)是一类具有氧化还原活性的小分子,在所有生命领域都具有关键功能,包括细菌中的能量生成和人类骨骼健康。参与甲萘醌生物合成的酶也具有生物工程应用,并且是潜在的抗菌药物靶点。对甲萘醌的重要作用及其潜在的氧化还原相关毒性的新认识,突出表明需要严格控制该途径。在这里,我们提供了对细菌中经典甲萘醌生物合成途径的当前理解的概述。我们还回顾了最近在蛋白质水平变构和膜结合酶的亚定位方面的发现,这些发现为该生物合成途径中通量的调节提供了深入的了解。