Department of Chemistry, The University of Iowa, E274 Chemistry Building, Iowa City, IA 52245, USA.
Bioorg Chem. 2012 Aug;43:37-43. doi: 10.1016/j.bioorg.2011.11.005. Epub 2011 Nov 27.
Uracil methylation is essential for survival of organisms and passage of information from generation to generation with high fidelity. Two alternative uridyl methylation enzymes, flavin-dependent thymidylate synthase and folate/FAD-dependent RNA methyltransferase, have joined the long-known classical enzymes, thymidylate synthase and SAM-dependent RNA methyltransferase. These alternative enzymes differ significantly from their classical counterparts in structure, cofactor requirements and chemical mechanism. This review covers the available structural and mechanistic knowledge of the classical and alternative enzymes in biological uracil methylation, and offers a possibility of using inhibitors specifically aiming at microbial thymidylate production as antimicrobial drugs.
尿嘧啶甲基化对于生物的生存和世代间信息的高保真传递至关重要。两种替代的尿嘧啶甲基化酶,黄素依赖性胸苷酸合成酶和叶酸/FAD 依赖性 RNA 甲基转移酶,与已知的经典酶,胸苷酸合成酶和 SAM 依赖性 RNA 甲基转移酶一起加入。这些替代酶在结构、辅助因子要求和化学机制方面与经典酶有很大的不同。本文综述了生物尿嘧啶甲基化中经典和替代酶的结构和机制方面的现有知识,并提出了使用专门针对微生物胸苷酸生成的抑制剂作为抗菌药物的可能性。